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Category   Symbol Source: HGNC EntrezGene Ensembl GeneCards RNA genes CroW21
GIFtS

TSPAN32 Gene

protein-coding   GIFtS: 49
GCID: GC11P002323

tetraspanin 32

(Previous name: pan-hematopoietic expression )
(Previous symbols: TSSC6, PHEMX)
 Explore 42 diseases affiliated with
TSPAN32 via our new
 Human Malady Compendium 
Biological research products
for TSPAN32
    

(According to 1HGNC, 2Entrez Gene,
3UniProtKB/Swiss-Prot, 4UniProtKB/TrEMBL, 5OMIM, 6GeneLoc, 7Ensembl, 8DME, 9miRBase, and/or 10fRNAdb)
About This Section

Aliases
Tetraspanin 321 2     Pan-Hematopoietic Expression Protein2
PHEMX1 2 3 5     Tetraspanin-321
TSSC61 2 3 5     Tspan-323
Protein Phemx2 3     Tumor-Suppressing STF CDNA 62
Pan-Hematopoietic Expression1     Tumor-Suppressing Subchromosomal Transferable Fragment CDNA 62
ART12     Tumor-Suppressing Subtransferable Candidate 62
PHMX2     Tspan-323

External Ids:    HGNC: 134101   Entrez Gene: 100772   Ensembl: ENSG000000642017   OMIM: 6038535   UniProtKB: Q96QS13   

Export aliases for TSPAN32 gene to outside databases

Previous GC identifers: GC11P002280 GC11P002113


(According to Entrez Gene, Tocris Bioscience, Wikipedia's Gene Wiki, PharmGKB,
UniProtKB/Swiss-Prot, and/or UniProtKB/TrEMBL)
About This Section

Entrez Gene summary for TSPAN32:
This gene, which is a member of the tetraspanin superfamily, is one of several tumor-suppressing subtransferable
fragments located in the imprinted gene domain of chromosome 11p15.5, an important tumor-suppressor gene region.
Alterations in this region have been associated with Beckwith-Wiedemann syndrome, Wilms tumor, rhabdomyosarcoma,
adrenocortical carcinoma, and lung, ovarian and breast cancers. This gene is located among several imprinted genes;
however, this gene, as well as the tumor-suppressing subchromosomal transferable fragment 4, escapes imprinting. This
gene may play a role in malignancies and diseases that involve this region, and it is also involved in hematopoietic
cell function. Alternatively spliced transcript variants have been described, but their biological validity has not
been determined. (provided by RefSeq, Jul 2008)

Gene Wiki entry for TSPAN32


(According to GeneLoc and/or HGNC, and/or
Entrez Gene (NCBI build 37),
and/or miRBase,
Genomic Views according to UCSC (hg19) and Ensembl (release 69), Regulatory elements and Epigenetics data according to QIAGEN, SABiosciences, and/or SwitchGear Genomics)
About This Section
RefSeq DNA sequence:
NC_000011.9  NC_018922.1  NT_009237.18  
Regulatory elements:
   SABiosciences Regulatory transcription factor binding sites in the TSPAN32 gene promoter:
         Elk-1   RP58   GATA-3   NCX/Ncx   MyoD   CREB   GATA-6   deltaCREB   HOXA5   TGIF   
         Other transcription factors

SwitchGear Promoter luciferase reporter plasmids (see all 2): TSPAN32 promoter sequence
   Search SABiosciences Chromatin IP Primers for TSPAN32

Epigenetics:
QIAGEN PyroMark CpG Assay predesigned Pyrosequencing DNA Methylation assays in human, mouse, rat TSPAN32


Genomic Location:
Genomic View: UCSC Golden Path with GeneCards custom track

Entrez Gene cytogenetic band: 11p15.5   Ensembl cytogenetic band:  11p15.5   HGNC cytogenetic band: 11p15

TSPAN32 Gene in genomic location: bands according to Ensembl, locations according to (and/or Entrez Gene and/or Ensembl if different)
TSPAN32 gene location

GeneLoc information about chromosome 11         GeneLoc Exon Structure

GeneLoc location for GC11P002323:  view genomic region     (about GC identifiers)

Start:
2,323,227 bp from pter      End:
2,339,430 bp from pter
Size:
16,204 bases      Orientation:
plus strand

(According to 1UniProtKB, HORDE, neXtProt, Ensembl, and/or Reactome, Modification sites according to 2PhosphoSitePlus, Specific Peptides from DME, Protein expression images according to data from SPIRE MOPED and PaxDb, RefSeq according to NCBI, PDB rendering according to OCA and/or Proteopedia, Recombinant Proteins from EMD Millipore, R&D Systems, GenScript, Enzo Life Sciences, OriGene, Novus Biologicals, Sino Biological, ProSpec, and/or Uscn,
Biochemical Assays by EMD Millipore, R&D Systems, OriGene, GenScript, Cell Signaling Technology, Enzo Life Sciences, and/or Uscn, Ontologies according to Gene Ontology Consortium 01 Mar 2013 and Entrez Gene, Antibodies by EMD Millipore, R&D Systems, GenScript, Cell Signaling Technology, OriGene, Novus Biologicals, Thermo Fisher Scientific, Abcam, and/or Uscn)
About This Section

UniProtKB/Swiss-Prot: TSN32_HUMAN, Q96QS1 (See protein sequence)
Recommended Name: Tetraspanin-32  
Size: 320 amino acids; 34631 Da
Subcellular location: Membrane; Multi-pass membrane protein (Potential)
Developmental stage: Expressed from early embryogenesis through to adulthood
Secondary accessions: Q96KX4 Q9HC50 Q9HC51 Q9Y5U1
Alternative splicing: 5 isoforms:  Q96QS1-1   Q96QS1-2   Q96QS1-3   Q96QS1-4   Q96QS1-5   (May be produced at very low levels due to a premature stop codon in the mRNA, leading to nonsense-mediated mRNA decay)

Explore the universe of human proteins at neXtProt for TSPAN32: NX_Q96QS1

Post-translational modifications:

  • View modification sites using PhosphoSitePlus2
  • View neXtProt modification sites for NX_Q96QS1

  • TSPAN32 Protein expression data from MOPED and PaxDb:    About this image 
    TSPAN32 Protein Expression
    REFSEQ proteins: NP_620591.3  
    ENSEMBL proteins: 
     ENSP00000405001   ENSP00000182290   ENSP00000395018   ENSP00000370513   ENSP00000343285  
     ENSP00000405205   ENSP00000388033   ENSP00000370509  

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    Uscn Proteins for TSPAN32

    Gene Ontology (GO): 2 cellular component terms (GO ID links to tree view):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0005622intracellular IEA--
    GO:0016021integral to membrane NAS--

    TSPAN32 for ontologies           About GeneDecksing



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    (According to InterPro, ProtoNet, UniProtKB, and/or BLOCKS, Sets of similar genes according to GeneDecks)
    About This Section

    TSPAN32 for domains           About GeneDecksing

    3 InterPro domains/families:
     IPR018499 Tetraspanin/Peripherin
     IPR000301 Tetraspanin
     IPR008952 Tetraspanin_EC2

    Graphical View of Domain Structure for InterPro Entry Q96QS1

    ProtoNet protein and cluster: Q96QS1

    UniProtKB/Swiss-Prot: TSN32_HUMAN, Q96QS1
    Similarity: Belongs to the tetraspanin (TM4SF) family


    (According to 1UniProtKB, Genatlas, LifeMap Discovery™, IUBMB, and/or 2DME, Human phenotypes from GenomeRNAi, Animal models from MGI Mar 06 2013, inGenious Targeting Laboratory,
    bound targets from SABiosciences, miRNA Gene Targets from miRTarBase, shRNA from OriGene, Sirion Biotech, RNAi from EMD Millipore, siRNAs from OriGene, QIAGEN, microRNA from QIAGEN, Gene Editing from DNA2.0, Sirion Biotech, Clones from EMD Millipore, OriGene, SwitchGear Genomics, GenScript, Sino Biological, DNA2.0, and Vector BioLabs, Cell Lines from GenScript, LifeMap BioReagents, Sirion Biotech, In Situ Hybridization Assays from Advanced Cell Diagnostics, Ontologies according to Gene Ontology Consortium 01 Mar 2013 via Entrez Gene.)
    About This Section

         Gene Ontology (GO): 1 molecular function term (GO ID links to tree view):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0003674molecular_function ND--
         
    TSPAN32 for ontologies           About GeneDecksing


    Phenotypes:
         3 MGI mutant phenotypes (inferred from 1 allele(MGI details for Tspan32):
     cellular  hematopoietic system  immune system 

    TSPAN32 for phenotypes           About GeneDecksing

    Animal Models:
       inGenious Targeting Laboratory - Customizable classic, inducible, and humanized mouse model solutions for TSPAN32 

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    In Situ Assay
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    (Pathways according to EMD Millipore, R&D Systems, Cell Signaling Technology, KEGG, PharmGKB, BioSystems, Reactome, Tocris Bioscience, GeneGo (Thomson Reuters), QIAGEN, and/or UniProtKB, Sets of similar genes according to GeneDecks, Interaction Networks according to SABiosciences, and/or STRING, Interactions according to 1UniProtKB, 2MINT, 3I2D, and/or 4STRING, with links to IntAct and Ensembl, Ontologies according to Gene Ontology Consortium 01 Mar 2013 via Entrez Gene).
    About This Section



    Interactions:

        Search SABiosciences Gene Network CentralTM Interacting Genes and Proteins Networks for TSPAN32

    Gene Ontology (GO): 1 biological process term (GO ID links to tree view):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0007267cell-cell signaling TAS10950922

    TSPAN32 for ontologies           About GeneDecksing



    (Chemical Compounds according to UniProtKB, Enzo Life Sciences, EMD Millipore, Tocris Bioscience HMDB, BitterDB, and/or Novoseek, and Drugs according to DrugBank, Enzo Life Sciences, and/or PharmGKB, with drugs/clinical trials/news search links to CenterWatch)
    About This Section

    TSPAN32 for compounds           About GeneDecksing

    Browse Small Molecules at EMD Millipore
    Browse drugs & compounds from Enzo Life Sciences

    Browse Tocris compounds for TSPAN32
    7 Novoseek chemical compound relationships for TSPAN32 gene    About this table
    Compound   -log (P-Val)   Hits   PubMed IDs for Articles with Shared Sentences (# sentences)
    ganglioside 44.3 4 15334254 (1), 12068006 (1), 15710618 (1), 19559406 (1)
    tyrosine 31 6 10427099 (1), 12938224 (1), 12110679 (1), 19166707 (1) (see all 5)
    lipid 27.3 9 15454569 (1), 15496196 (1), 16785325 (1), 19497983 (1) (see all 9)
    phosphatidylinositol 23.4 2 12110679 (1), 11739647 (1)
    cysteine 23.2 5 20171294 (2), 11907260 (1), 14556650 (1), 12575999 (1)
    cholesterol 5.22 23 12938224 (5), 15184367 (2), 15454569 (1), 19497983 (1) (see all 5)
    polysaccharide 0 1 12701754 (1)

    Search CenterWatch for drugs/clinical trials and news about TSPAN32 / TSN32 

    (Secondary structures according to fRNAdb,
    GenBank/EMBL/DDBJ Accessions according to
    Unigene (Build 235 Homo sapiens; Mar 10 2013) or GenBank,
    RefSeq according to Entrez Gene,
    DOTS (version 10), and/or AceView, transcript ids from Ensembl with links to UCSC,
    exon structure from GeneLoc, alternative splicing isoforms according to ASD and/or ECgene,
    RNAi Products from EMD Millipore,
    siRNAs from OriGene, QIAGEN, shRNA from OriGene, Sirion Biotech, microRNA from QIAGEN,
    Tagged/untagged cDNA clones from OriGene, SwitchGear Genomics, GenScript, DNA2.0, Vector BioLabs, Primers from OriGene, SABiosciences, and/or QIAGEN )
    About This Section

    REFSEQ mRNAs for TSPAN32 gene (3 alternative transcripts): 
    NM_139022.2  NM_005705.4  NM_139024.3  

    Unigene Cluster for TSPAN32:

    Tetraspanin 32
    Hs.271954  [show with all ESTs]
    Unigene Representative Sequence: AK298692
    18 Ensembl transcripts including schematic representations, and UCSC links where relevant:
    ENST00000437313 ENST00000461200(uc001lvx.1 uc009ydk.1 uc010qxk.2 uc001lvy.1 uc009ydl.1 uc001lwb.1 uc001lwc.1 uc001lwd.1)
    ENST00000182290 ENST00000446063 ENST00000493924 ENST00000484104 ENST00000479508
    ENST00000498313 ENST00000483227 ENST00000381121 ENST00000493948 ENST00000339046
    ENST00000451520(uc001lvz.1) ENST00000444307 ENST00000468578 ENST00000381117
    ENST00000484523 ENST00000486011

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    Additional cDNA sequence: 

    AF176071.1 AK298692.1 AK307638.1 AK310116.1 AY039001.1 AY303780.1 BC016693.1 

    11 DOTS entries:

    DT.95168325  DT.111418  DT.95094062  DT.111419  DT.91648803  DT.97812022  DT.91656368  DT.120684722 
    DT.95168321  DT.95168322  DT.40314344 

    24/49 AceView cDNA sequences (see all 49):

    AW440888 AA701395 BI906333 AY039001 AF176070 BX117724 NM_139024 NM_139022 
    CR606621 BG506933 AF125569 AA913945 N99620 BI909345 BI907377 AK128812 
    NM_005705 AF176071 BI518496 AY303780 BC016693 BI909447 BV196160 BM926073 

    GeneLoc Exon Structure

    5/12 Alternative Splicing Database (ASD) splice patterns (SP) for TSPAN32 (see all 12)    About this scheme

    ExUns: 1a · 1b · 1c ^ 2a · 2b · 2c · 2d ^ 3 ^ 4 ^ 5 ^ 6 ^ 7a · 7b ^ 8a · 8b ^ 9a · 9b ^ 10 ^ 11 ^ 12 ^ 13 ^ 14a · 14b · 14c
    SP1:              -     -     -                 -           -                             -     -     -                                             
    SP2:              -     -     -                 -           -                             -     -     -           -                                 
    SP3:                                            -           -                 -           -     -     -                                             
    SP4:                                            -           -                             -     -     -                                             
    SP5:                                            -           -     -                       -     -     -                                             


    ECgene alternative splicing isoforms for TSPAN32

    (RNA expression data according to H-InvDB, NONCODE, miRBase, and RNAdb, Expression images according to data from BioGPS, Illumina Human BodyMap, and CGAP SAGE, Sets of similar genes according to GeneDecks, in vivo and in vitro expression data from LifeMap Discovery™, plus additional links to Genevestigator, and/or SOURCE, and/or BioGPS, and/or UniProtKB,
    PCR Arrays from SABiosciences, Primers from OriGene, SABiosciences, and/or QIAGEN, In Situ Hybridization Assays from Advanced Cell Diagnostics)
    About This Section

    TSPAN32 expression in normal human tissues (normalized intensities)
    See probesets specificity/sensitivity at GeneAnnot
    About this imageBioGPS
    CGAP TAG: GCTGTAGGAC
    TSPAN32 Expression
    About this image

    TSPAN32 expression in embryonic tissues and stem cells
    Expression by the Database of Embryonic development, Stem cell research, and Regenerative medicine    About this table

    1 LifeMap In Vivo Development Anatomical Compartment/Cell 
    Tissue Anatomical Compartment CellCategory (developmental path)
    Extraembryonic MesodermExtraembryonic Capillary PlexusExtraembryonic AngioblastsEndothelium
    Expression: Positive    Negative     Selective marker
    Experimental details: Curated     Microarrays     In-situ hybridization
    Stem Cell Differentiation: 2 LifeMap Cells 
    NameCategory
    PureStem™ progenitor EN7 (Embryonic Progenitor Cell)
    Blimp1- mVenus and stella-ECFP genetically modified stem cells (Embryonic Stem Cell)Early Embryo, Inner Cell Mass

    See TSPAN32 Protein Expression from SPIRE MOPED and PaxDB
    Genevestigator expression for TSPAN32

    SOURCE GeneReport for Unigene cluster: Hs.271954

    UniProtKB/Swiss-Prot: TSN32_HUMAN, Q96QS1
    Tissue specificity: Expressed ubiquitously at low levels. High levels of expression are confined to hematopoietic
    tissues including peripheral blood leukocytes, thymus and spleen

        SABiosciences Custom PCR Arrays for TSPAN32
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    In Situ
    Assay Products:
     

     
    Advanced Cell Diagnostics RNAscope RNA in situ hybridization assays for TSPAN32

    (Orthologs according to 1,2HomoloGene (2older version, for species not in 1newer version), 3euGenes, 4SGD , 5MGI Mar 06 2013, with possible further links to Flybase and/or WormBase, and/or 6Ensembl pan taxonomic compara , Gene Trees according to Ensembl and TreeFam)
    About This Section

    This gene was present in the common ancestor of chordates.

    Orthologs for TSPAN32 gene from 3/7 species (see all 7)    About this table
    Organism Taxonomic
    classification
    Gene Description Human
    Similarity
    Orthology
    Type
    Details
    mouse
    (Mus musculus)
    Mammalia Tspan321 , 5 tetraspanin 321, 5 76.02(n)1
    64.03(a)1
      7 (88.09 cM)5
    270271  NM_001128080.21  NP_001121552.11 
     1430050465 
    chicken
    (Gallus gallus)
    Aves TSPAN321 tetraspanin 32 59.82(n)
    47.49(a)
      395087  XM_421025.2  XP_421025.2 
    lizard
    (Anolis carolinensis)
    Reptilia TSPAN326
    --
    52(a)
    1 ↔ 1
    1(69690114-69698244)


    ENSEMBL Gene Tree for TSPAN32 (if available)
    TreeFam Gene Tree for TSPAN32 (if available) 

    (Paralogs according to 1HomoloGene,
    2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
    About This Section
      --

    (SNPs/Variants according to the 1NCBI SNP Database, 2Ensembl, 3PupaSUITE, UniProtKB, and DNA2.0, Linkage Disequilibrium by HapMap, Structural Variations(CNVs/InDels/Inversions) from the Database of Genomic Variants, Mutations from the Human Gene Mutation Database (HGMD) and the Locus Specific Mutation Databases (LSDB), Blood group antigen gene mutations by BGMUT, Resequencing Primers from QIAGEN, Cancer Mutation PCR Arrays and Assays and Copy Number PCR Arrays from SABiosciences)
    About This Section

    368/411 NCBI SNPs in TSPAN32 are shown (see all 411    About this table
    Genomic DataTranscription Related DataAllele Frequencies
    SNP IDValidClinical
    significance
    Chr 11 posSequence#AA
    Chg
    TypeMore#Allele
    freq
    PopTotal
    sample
    More
    ----------
    rs763951941,2
    C--2321250(+) AACCCG/ACTGCT 3 -- int1 us2k12Minor allele frequency- A:0.07NA 122
    rs1114476041,2
    C--2321279(+) CCCAGC/TGGCCG 3 -- int1 us2k11Minor allele frequency- T:0.50NA 2
    rs1475056221,2
    --2321283(+) GCGGCC/TGGCAC 3 -- us2k1 int10--------
    rs122249671,2
    C,F--2321284(+) CGGCCA/GGCACC 3 -- int1 us2k15Minor allele frequency- G:0.45NA CSA EA 245
    rs734044791,2
    C--2321306(+) AGGTGG/CGCAGG 3 -- int1 us2k11Minor allele frequency- C:0.50WA 2
    rs618715611,2
    --2321392(+) GGGGCA/GTGTGG 3 -- int1 us2k10--------
    rs26518231,2
    C,F--2321650(+) GAGGGG/AATGTT 3 -- us2k1 int111Minor allele frequency- A:0.39NA WA CSA EA 372
    rs128021871,2
    H--2321677(+) GCTCAG/TCAAAG 3 -- us2k1 int1 tfbs34Minor allele frequency- T:0.00NS EA 420
    rs797197141,2
    --2321693(+) GGGGGA/TTCCAC 3 -- int1 us2k10--------
    rs22855681,2
    C,F,H--2321899(+) TGCTCC/TGAAAT 3 -- int1 us2k19Minor allele frequency- T:0.05EA NS NA CSA 2100
    rs20770781,2
    C,F,H--2322136(+) ACCTGC/TGCCCC 3 -- us2k1 int116Minor allele frequency- T:0.14NS EA NA WA 2116
    rs777810091,2
    --2322383(+) TGAGCG/AGGCGG 3 -- us2k1 int12Minor allele frequency- A:0.13CSA WA 120
    rs2006718251,2
    C--2322403(+) CCTCTC/TCCCAC 3 -- us2k1 int10--------
    rs7569211,2
    C,F,A,H--2322415(+) GCCACT/GCTGGG 3 -- us2k1 int114Minor allele frequency- G:0.20NS NA WA CSA EA 598
    rs1887138041,2
    --2322458(+) CCCCTC/TGATGA 3 -- int1 us2k10--------
    rs7569221,2
    C,F,O,A--2322561(+) GAATGA/GTGGAT 3 -- int1 us2k121Minor allele frequency- N:0.00NA EA WA CSA 1578
    rs1169325921,2
    F--2322614(+) AGAGGC/TCCACG 3 -- int1 us2k11Minor allele frequency- T:0.03NA 120
    rs1142275971,2
    F--2322648(+) GCAGCG/ACTGCC 3 -- int1 us2k11Minor allele frequency- A:0.04WA 118
    rs7569231,2
    C,F,A,H--2322662(+) ACCCAC/TACGTA 3 -- us2k1 int130Minor allele frequency- A:0.00EA NA NS WA CSA 2673
    rs1927723621,2
    --2322680(+) GGCTCA/GGTGTA 3 -- us2k1 int10--------
    rs1487995091,2
    --2322697(+) AATTCA/GAGGTT 3 -- int1 us2k10--------
    rs740482201,2
    --2322741(+) GTGAGG/CGAGGC 3 -- us2k1 int11Minor allele frequency- C:0.50WA 2
    rs1422473391,2
    --2322782(+) TCTGCA/GACAAA 3 -- us2k1 int10--------
    rs1843414301,2
    --2322803(+) GTGCCA/GCCCAC 3 -- us2k1 int10--------
    rs110221571,2
    C,F,H--2322829(+) AACGAA/CCTTCT 3 -- int1 us2k128Minor allele frequency- N:0.00EA NA NS WA 2980
    rs1871684331,2
    C,F--2322935(+) GATTAC/TGCCCC 3 -- int1 us2k11Minor allele frequency- T:0.01EU 445
    rs169280841,2
    C,F--2322954(+) AGTCCA/GCACTT 3 -- int1 us2k110Minor allele frequency- G:0.13NA WA EU 810
    rs7340951,2
    C,F--2323198(+) CCTCCC/GCTTCC 3 -- us2k1 tfbs3 trp36Minor allele frequency- G:0.17MN NA CSA WA 428
    rs7340941,2
    C,F,A--2323220(+) CTTCCG/AGGGCA 3 -- us2k111Minor allele frequency- A:0.30NA EA WA CSA 2097
    rs784656851,2
    --2323304(+) AGCTGC/TGGTCT 3 -- us2k1 ut511Minor allele frequency- T:0.01WA 118
    rs1488612751,2
    C,F--2323396(+) GAGTCG/AAGTCA 4 /Q /R us2k1 mis12Minor allele frequency- A:0.00NA EU 4919
    rs20740211,2
    C,F,H--2323528(+) GATTAC/TCCCTC 3 -- us2k1 int1 trp325Minor allele frequency- T:0.40EA NS NA WA CSA 3599
    rs22342881,2
    H--2323557(+) CCCTAC/TTGTCC 3 -- us2k1 int14Minor allele frequency- T:0.00NS EA 412
    rs22342891,2
    F,H--2323588(+) TGTGTC/TCTGCC 3 -- us2k1 int16Minor allele frequency- T:0.02NS EA CSA WA 522
    rs22342901,2
    C,F,A--2323619(+) GGCAGG/TGACCA 3 -- us2k1 int18Minor allele frequency- T:0.31NA CSA WA EA 370
    rs22342911,2
    --2323628(+) CACCAC/TGAGCA 3 -- us2k1 int10--------
    rs22342931,2
    --2323680(+) AGGCCC/TGAGTG 3 -- us2k1 int11Minor allele frequency- T:0.50CSA 2
    rs1443328681,2
    --2323744(+) GGGATC/GTTCTC 3 -- us2k1 int10--------
    rs1902876071,2
    --2323763(+) GCCCCA/GGAGGG 3 -- us2k1 int10--------
    rs2019167381,2
    --2324029(+) GCTCCA/TGCAGC 3 -- us2k1 int10--------
    rs2013411951,2
    --2324031(+) TCCTGC/TAGCAG 3 -- us2k1 int10--------
    rs20740221,2
    C,F,O,A,H--2324041(+) GTCCCG/ATGCCC 3 -- int1 us2k1 ese331Minor allele frequency- A:0.31EA NS NA WA CSA EU 4640
    rs1464809451,2
    C,F--2324118(+) TACTTC/TGGGGC 4 F us2k1 syn11Minor allele frequency- T:0.00NA 4550
    rs1459050961,2
    C,F--2324173(+) ACCAGG/CCTGTG 4 /P /A us2k1 mis11Minor allele frequency- C:0.00NA 4552
    rs1810675591,2
    --2324183(+) GCACCA/CATGGG 4 Q P us2k1 mis10--------
    rs1138608121,2
    C--2324217(+) GCATCA/GGGAGG 3 -- int1 us2k12Minor allele frequency- G:0.33CSA 3
    rs1999992811,2
    --2324219(+) ATCGGA/GAGGGG 3 -- int1 us2k10--------
    rs2005367691,2
    --2324229(+) GCCTCA/GGGTGC 3 -- us2k1 int10--------
    rs71063341,2
    A--2324249(+) TGGCAC/GGAGCC 3 -- int1 us2k10--------
    rs22342941,2
    --2324322(+) GGCAGC/GGAGGG 3 -- us2k1 int10--------
    rs1433956251,2
    --2324331(+) GGGCTG/TCCCTG 3 -- us2k1 int10--------
    rs556488101,2
    C,F--2324347(+) CTAGCT/CCCCCT 3 -- us2k1 int14Minor allele frequency- C:0.32NA WA 242
    rs556458181,2
    C--2324364(+) GGCCTC/TGGGTC 3 -- us2k1 int11Minor allele frequency- T:0.50WA 2
    rs1887087711,2
    --2324365(+) GCCTCA/GGGTCT 3 -- int1 us2k10--------
    rs1137142971,2
    --2324402(+) TTCTCG/ATGCCC 3 -- us2k1 int11Minor allele frequency- A:0.50CSA 2
    rs108317331,2
    C,F,A,H--2324440(+) TATGTC/TGGGCA 3 -- int1 us2k121Minor allele frequency- T:0.28NS EA NA WA CSA 2348
    rs15014671,2
    C,F,A,H--2324692(+) CAGAGC/TCTGCT 3 -- us2k1 int19Minor allele frequency- T:0.23NA EA 254
    rs1861770801,2
    --2324741(+) ATGAGA/GGGATG 3 -- us2k1 int10--------
    rs799274841,2
    --2324761(+) GATCTG/ACAGGG 3 -- us2k1 int12Minor allele frequency- A:0.13CSA WA 120
    rs1455970031,2
    --2324799(+) CAGGAA/GGGCTG 3 -- us2k1 int10--------
    rs1489147341,2
    --2324806(+) GCTGCA/CGCCCG 3 -- us2k1 int10--------
    rs773933101,2
    --2324810(+) CAGCCC/TGGTGG 3 -- us2k1 int12Minor allele frequency- T:0.18CSA WA 120
    rs1130765941,2
    --2324816(+) GGTGGG/ACAGAT 3 -- int1 us2k11Minor allele frequency- A:0.50CSA 2
    rs26518241,2
    C,H--2324852(+) CAGGGC/ATACTG 3 -- us2k1 int112Minor allele frequency- A:0.02NA WA CSA 139
    rs1916955091,2
    --2324922(+) CCTGGA/GGCCCA 3 -- us2k1 int10--------
    rs25212701,2
    C,A--2325108(+) AGGCAG/TGGAGG 3 -- us2k1 int112Minor allele frequency- T:0.25NA WA CSA EA 375
    rs1833384091,2
    --2325165(+) AGTCCC/TACCTC 1 -- int10--------
    rs1176003571,2
    F--2325192(+) GGGCCG/ATCTGA 1 -- int11Minor allele frequency- A:0.05NA 120
    rs22342951,2
    F--2325239(+) CCTCAC/TGGCCC 1 -- int11Minor allele frequency- T:0.03NA 120
    rs2021894711,2
    --2325290(+) TCAGGA/GCCTGT 1 -- int10--------
    rs2015309101,2
    --2325347(+) TCTGCA/GGGGTT 2 A syn10--------
    rs2006317811,2
    --2325378(+) CTCTGA/GGAGCC 2 R G mis10--------
    rs22342961,2
    C,F,H--2325384(+) GAGCCG/ATGCTG 2 /M /V mis1 ese38Minor allele frequency- A:0.01NS EA CSA NA EU 4985
    rs1996509871,2
    --2325392(+) CTGAGC/TGCTGC 2 S syn10--------
    rs2016344191,2
    --2325393(+) TGAGCA/GCTGCA 2 T A mis10--------
    rs2006246621,2
    --2325414(+) GGGAGG/TCCCAG 2 A S mis10--------
    rs617449291,2
    C,F--2325427(+) CCTCAT/CGGCAG 2 /T /M mis15Minor allele frequency- C:0.01NS NA EU 4371
    rs767230041,2
    C--2325436(+) AGGGGG/TGAGTT 1 -- spd10--------
    rs2001177051,2
    --2325468(+) GGCCCC/GCAGAA 1 -- int10--------
    rs754725351,2
    C--2325518(+) CCACCC/TCCACA 1 -- int10--------
    rs20740231,2
    C,F,A,H--2325581(+) CCCCAC/TGTCAA 1 -- int121Minor allele frequency- T:0.27EA NS NA WA 3818
    rs1458417531,2
    --2325708(+) ACGCCC/TAACAA 1 -- int10--------
    rs1387392271,2
    --2325729(+) AGGAGA/CTCTGA 1 -- int10--------
    rs26518251,2
    H--2325746(+) GAGACG/AGCCCT 1 -- int14Minor allele frequency- A:0.00NS EA 396
    rs563446181,2
    C--2325798(+) GGTTC-/TATGCC 1 -- int11Minor allele frequency- T:0.00NA 2
    rs1389066681,2
    C--2325798(+) GGTTC-/TATTGCC 1 -- int10--------
    rs562953181,2
    C--2325800(+) TTCTA-/TTGCCC 1 -- int11Minor allele frequency- T:0.00NA 2
    rs25212711,2
    C,F,A,H--2325868(+) CAGGCA/TCAGGA 1 -- int117Minor allele frequency- T:0.26NS EA NA WA CSA 764
    rs128070611,2
    C,F,A--2325901(+) CTGGGT/CTCTCC 1 -- int112Minor allele frequency- C:0.27NA WA CSA EA 374
    rs588339301,2
    C,F--2325997(+) NNNNCC/TTCTTG 1 -- int14Minor allele frequency- T:0.17WA NA 242
    rs1124987471,2
    --2326081(+) CCTGGC/AGGCAG 1 -- int12Minor allele frequency- A:0.09CSA WA 120
    rs108317371,2
    C,A--2326129(+) CCCTCC/TTCTCT 1 -- int1 trp313Minor allele frequency- T:0.25NA WA CSA EA 375
    rs728441981,2
    C--2326364(+) AATGAC/TCCTGG 1 -- int10--------
    rs781634281,2
    C--2326405(+) GTCACC/TTCCTG 1 -- int10--------
    rs1144208431,2
    C--2326422(+) CTGCCA/GGGCCA 1 -- int10--------
    rs20771121,2
    C,A,H--2326451(+) CATGGG/TGGGCA 1 -- int111Minor allele frequency- T:0.24NA WA CSA EA 375
    rs2019915241,2
    --2326605(+) CCCCC-/CGCCCCC 1 -- int10--------
    rs745238691,2
    C--2326608(+) CCCCC-/ACCCAG 1 -- int10--------
    rs285376081,2
    F--2326612(+) CCCCCC/AGAGGG 1 -- int11Minor allele frequency- A:0.50NA 4
    rs118236821,2
    C,F,H--2326614(+) CCCAGA/GGGGTG 1 -- int14Minor allele frequency- G:0.25NA WA 246
    rs20771131,2
    C,F,A,H--2326657(+) AAAGGC/TTGGCA 1 -- int114Minor allele frequency- T:0.24NA WA CSA EA 381
    rs20771141,2
    C,F,A,H--2326714(+) GAACCG/AGCGCT 1 -- int114Minor allele frequency- A:0.43NA WA CSA EA 381
    rs1389431861,2
    --2326734(+) GTACCA/GTCCAC 1 -- int10--------
    rs755516201,2
    --2326742(+) CACCAG/AGGGGT 1 -- int12Minor allele frequency- A:0.10CSA WA 120
    rs790645321,2
    --2326800(+) GCCACG/AGGGCT 1 -- int12Minor allele frequency- A:0.04CSA WA 120
    rs9376141,2
    C,F,A,H--2326920(+) GTGTCC/GCCAGC 1 -- int116Minor allele frequency- G:0.30EA NA NS WA CSA 926
    rs25212721,2
    C,A--2327151(+) CCTGCC/TCCATT 1 -- int113Minor allele frequency- T:0.25NA WA CSA EA 375
    rs26518191,2
    C,A--2327188(+) GGTGAA/GCCTAT 1 -- int17Minor allele frequency- G:0.00NA WA CSA 12
    rs49300781,2
    C,F,A--2327190(+) TGAGCT/CTATGT 1 -- int13Minor allele frequency- C:0.33NA 6
    rs1141120481,2
    --2327202(+) TATGCG/ATGTGC 1 -- int11Minor allele frequency- A:0.01WA 118
    rs1822287971,2
    --2327209(+) GTGCAA/CATATA 1 -- int10--------
    rs2011562831,2
    --2327216(+) TATAC-/ATGTGTG 1 -- int10--------
    rs49299771,2
    H--2327222(+) tgtgtG/Atgtgc 1 -- int14Minor allele frequency- A:0.00NS EA 416
    rs1468126941,2
    C--2327238(+) CATGA-/GTGTGTG 1 -- int10--------
    rs1483860171,2
    --2327276(+) GCCTC-/TGTGTG
            
    TGTGT
    1 -- int10--------
    rs1864624291,2
    --2327338(+) GTTGCC/TATACG 1 -- int10--------
    rs1494421301,2
    --2327394(+) TGCACA/GCATGA 1 -- int10--------
    rs1446703711,2
    --2327454(+) TCCAAG/TGGGCT 1 -- int10--------
    rs618715771,2
    --2327511(+) CCCTCC/TGGCCT 1 -- int12Minor allele frequency- T:0.06NA 122
    rs21886591,2
    C,A,H--2327587(+) AGCGCT/CGCCCA 1 -- int111Minor allele frequency- C:0.25NA WA CSA EA 372
    rs49300791,2
    C,F,A--2327601(+) AAGCAC/GATTCA 1 -- int15Minor allele frequency- G:0.22NA EA 246
    rs1917629301,2
    --2327678(+) CCTGAA/CCACCC 1 -- int10--------
    rs22378581,2
    C--2327706(+) AAGGCC/TCTGGG 1 -- int10--------
    rs2009546521,2
    --2327778(+) GGGAG-/AGA   
       GAGAA
    AGAGA
    1 -- int10--------
    rs1380750641,2
    C--2327782(+) GAGAG-/AGAA  
            
    AGAGA
    1 -- int10--------
    rs714641791,2
    C--2327785(+) AGAGAAAGA/-  
            
    GAGAA
    1 -- int11Minor allele frequency- -:0.50NA 2
    rs728457061,2
    C--2327785(+) AGAGAG/AAGAGA 1 -- int11Minor allele frequency- A:0.50WA 2
    rs1392606321,2
    C--2328067(+) AGGGG-/GAGGGA
            
    GAGGG
    1 -- int10--------
    rs1171673951,2
    F--2328105(+) AGGGAG/AGGGGA 1 -- int11Minor allele frequency- A:0.12NA 120
    rs1118839751,2
    C--2328156(+) GGAGAT/AGNNNN 1 -- int13Minor allele frequency- A:0.37WA NA 240
    rs561469261,2
    C--2328188(+) GAGGGG/AGAAGG 1 -- int13Minor allele frequency- A:0.06CSA WA NA 239
    rs1401794431,2
    C--2328201(+) GAGGA-/AAGAG 
            
    AAAAG
    1 -- int10--------
    rs22378591,2
    C,A--2328364(+) CCATGA/CGGAGC 1 -- int110Minor allele frequency- C:0.48EA NA WA CSA 1831
    rs1824033141,2
    --2328572(+) TGGGGA/CCCCAG 1 -- int10--------
    rs601329011,2
    --2328628(+) CAGGCG/AGGCAC 1 -- int12Minor allele frequency- A:0.04CSA WA 120
    rs1460823341,2
    --2328656(+) CTGGCA/GTTTCA 1 -- int10--------
    rs1869368821,2
    --2328667(+) CCGGGA/GCCTCA 1 -- int10--------
    rs22378601,2
    C,A--2328693(+) CTGCCT/CGGTCG 1 -- int112Minor allele frequency- C:0.26NA WA CSA EA 373
    rs22378611,2
    C,A--2328707(+) GCTAGG/ACTCAC 1 -- int113Minor allele frequency- A:0.25NA WA CSA EA 375
    rs1931853241,2
    --2328759(+) AAGGCA/GGCTGC 1 -- int10--------
    rs1406499471,2
    C--2328764(+) GGCTG-/CCCAGA 1 -- int10--------
    rs22378621,2
    C,F--2328795(+) CCAGGG/ATTCTT 1 -- int18Minor allele frequency- A:0.06EA NA WA CSA 1652
    rs7569251,2
    C,F,A--2328948(+) AGTGCT/CGGGGG 1 -- int112Minor allele frequency- C:0.38NA WA CSA EA 376
    rs1400834591,2
    --2329007(+) GGCACA/GGGCAT 1 -- int10--------
    rs7569261,2
    C,F,A,H--2329078(+) GAAAGG/TGAGGT 1 -- int125Minor allele frequency- T:0.38NS EA NA WA CSA 3836
    rs7569271,2
    C,A--2329119(+) GGCCAT/CAGCAT 1 -- int114Minor allele frequency- C:0.50EA NA WA CSA 1313
    rs79354831,2
    C,H--2329423(+) AGCGCC/AGGGGA 1 -- int1 trp310Minor allele frequency- A:0.25NA WA CSA EA 370
    rs49950511,2
    C--2329694(+) GCCCCA/C/GAACAG 1 -- int11NA 2
    rs1908056461,2
    --2329706(+) GACCAC/GCCCCC 1 -- int10--------
    rs1930237321,2
    --2329714(+) CCCCAC/TAGTGA 1 -- int10--------
    rs127987991,2
    A--2329739(+) TGACCA/GGCCCC 1 -- int10--------
    rs1837884361,2
    --2329762(+) GCCCCC/GAACAG 1 -- int10--------
    rs1881778321,2
    --2329774(+) GACCAC/GCCCCC 1 -- int10--------
    rs1813291801,2
    --2329782(+) CCCCAC/TAGTGA 1 -- int10--------
    rs1858105091,2
    --2329818(+) CCGCAA/GTGACC 1 -- int10--------
    rs349751241,2
    --2329830(+) GCCCCG/CAACAG 1 -- int11Minor allele frequency- C:0.00NA 2
    rs127969571,2
    C--2329880(+) GGCCCC/GCCCAC 1 -- int11Minor allele frequency- G:0.00NA 2
    rs344006241,2
    C--2329895(+) ACCGG-/CCCCCC 1 -- int11Minor allele frequency- C:0.00NA 2
    rs1865744131,2
    --2329908(+) AGCAGC/TGACCA 1 -- int10--------
    rs2019407061,2
    --2329941(+) CAACAC/GTGACC 1 -- int10--------
    rs115549471,2
    C,F--2329995(+) TTCTGA/C/G/
            
    GCACA
    4 * C W stg1 mis1 syn1 ese311NS NA CSA WA EA EU 4310
    rs22342971,2
    C,A--2330077(+) AGGGTG/CCCCCA 1 -- int17Minor allele frequency- C:0.42NA CSA WA EA 366
    rs1922982551,2
    --2330165(+) GTGGGC/GTGGGG 1 -- int10--------
    rs1433288741,2
    --2330246(+) GCAGCC/TCCCTG 1 -- int10--------
    rs25212731,2
    C,A--2330400(+) CCTTAA/GGGGTT 1 -- int112Minor allele frequency- G:0.24NA WA CSA EA 374
    rs25212741,2
    C,A--2330479(+) CAGACA/GGTACC 1 -- int111Minor allele frequency- G:0.25NA WA CSA EA 371
    rs71088981,2
    C--2330518(+) ACTGGG/AGTGTC 1 -- int15Minor allele frequency- A:0.08NA CSA WA EA 361
    rs25212751,2
    C,F,A--2330563(+) CCTTCT/CGTCCT 1 -- int110Minor allele frequency- C:0.41NA WA CSA EA 372
    rs71129191,2
    C,F--2330596(+) GGGTCC/TGGCCT 1 -- int15Minor allele frequency- T:0.10NA CSA WA EA 362
    rs1512058681,2
    --2330634(+) GTCCCA/CGTGGA 1 -- int10--------
    rs1391904581,2
    --2330647(+) GGCCAG/TCAGCT 1 -- int10--------
    rs1129807121,2
    --2330766(+) CGGGCG/AGCACC 1 -- int12Minor allele frequency- A:0.03CSA WA 119
    rs789425211,2
    --2330801(+) GGAGTG/AGGGCA 1 -- int11Minor allele frequency- A:0.01NA 120
    rs1499641241,2
    --2330865(+) TAGTGA/GCCTCG 1 -- int10--------
    rs1831355081,2
    --2330896(+) CCCAGA/GGCCCT 1 -- int10--------
    rs740482461,2
    C,F--2330919(+) TGGCCA/CTGAGA 1 -- int14Minor allele frequency- C:0.07WA CSA EA 242
    rs26518211,2
    C,F,A,H--2330930(-) GCCTCA/GGTATC 1 -- int117Minor allele frequency- G:0.27NS EA NA WA CSA 785
    rs25212761,2
    C,A--2330977(+) GGGCCT/CGCTGT 1 -- int112Minor allele frequency- C:0.47EA NA WA CSA 1651
    rs25212771,2
    C,A--2331050(+) GGGGAA/CTCAGG 1 -- int18Minor allele frequency- C:0.25NA WA EA 368
    rs22517111,2
    C,A--2331053(-) GGGCCC/TGAGTC 1 -- int19Minor allele frequency- T:0.27NA WA EA 370
    rs25212781,2
    C,A--2331096(+) GCAGTG/ACCGGG 1 -- int114Minor allele frequency- A:0.47EA NA WA CSA 1859
    rs25212791,2
    C,A--2331214(+) ATTTTA/CTCAGG 1 -- int112Minor allele frequency- C:0.47EA WA NA CSA 1855
    rs25212801,2
    C,F,A--2331307(+) GAGCTC/GGGCCA 1 -- int113Minor allele frequency- G:0.25NA WA CSA EA 376
    rs1851306301,2
    --2331409(+) ACAGCG/TGCCAG 1 -- int10--------
    rs110222181,2
    C,F--2331416(+) CCAGGG/ATTCCC 1 -- int15Minor allele frequency- A:0.06WA CSA EA 244
    rs25212811,2
    C,F,A,H--2331444(+) GCTGCT/GGCCCA 1 -- int111Minor allele frequency- G:0.40NA WA CSA EA 374
    rs15484321,2
    C,F,A,H--2331547(+) CTGGGA/GCCTGC 1 -- int112Minor allele frequency- G:0.43MN WA NA CSA EA 558
    rs757943411,2
    C,F--2331597(+) CAGCCG/AGGCTC 1 -- int11Minor allele frequency- A:0.17EA 120
    rs1451122321,2
    --2331662(+) TGGCCA/CGTGCG 1 -- int10--------
    rs1419260071,2
    --2331709(+) GCCTGA/GCCCCA 1 -- int10--------
    rs740482601,2
    C--2331771(+) CAGTGG/AGTCTT 1 -- int12Minor allele frequency- A:0.04WA 120
    rs1457776051,2
    --2331865(+) TGGGCC/TGCCCT 1 -- int10--------
    rs1149636691,2
    --2331868(+) GCCGCC/TCTTGG 1 -- int11Minor allele frequency- T:0.01WA 118
    rs1477852561,2
    --2331872(+) CCCTTA/GGGCAA 1 -- int10--------
    rs1898386681,2
    --2331930(+) ACCAAC/GATCCA 1 -- int10--------
    rs1412771421,2
    --2331960(+) TGGCCA/CGGTGT 1 -- int10--------
    rs8089631,2
    C,F,A,H--2332037(+) AGGACA/GTGGGA 1 -- int122Minor allele frequency- G:0.49MN NS EA NA WA CSA 2255
    rs1160256391,2
    F--2332115(+) GGGGCG/AGCTGC 1 -- int11Minor allele frequency- A:0.03WA 118
    rs1433375791,2
    --2332387(+) CCTGCA/GGATGG 1 -- int10--------
    rs1134321531,2
    --2332422(+) GGGACC/AAGCCA 1 -- int12Minor allele frequency- A:0.02CSA WA 120
    rs734067831,2
    C--2332462(+) GACCCG/AGGCCC 1 -- int11Minor allele frequency- A:0.50WA 2
    rs796627541,2
    --2332619(+) CTCCTC/TGAGGG 1 -- int11Minor allele frequency- T:0.01WA 118
    rs1483600251,2
    --2332666(+) CTGACG/TAGTCT 1 -- int10--------
    rs801201621,2
    C,F--2332694(+) TGCTCA/GAATTA 1 -- int17Minor allele frequency- G:0.13NA WA CSA EA 365
    rs734067851,2
    C--2332726(+) GCCTCG/ATCCTC 1 -- int14Minor allele frequency- A:0.08NA WA EA 360
    rs1821389661,2
    --2333024(+) TCCCCC/TAGGTG 1 -- int10--------
    rs8001391,2
    C,F,A,H--2333124(+) CCGTGG/AAGAGC 1 -- int111Minor allele frequency- A:0.40EA NA WA CSA 1875
    rs1415645211,2
    --2333303(+) AGGCAA/GGGCAG 1 -- int10--------
    rs1161795431,2
    F--2333460(+) GGGAGG/AGAAGC 1 -- int11Minor allele frequency- A:0.02WA 118
    rs1504754661,2
    --2333491(+) ACCCCA/CGGGCC 1 -- int10--------
    rs1384891541,2
    --2333610(+) GCCCCC/TGCCCT 1 -- int10--------
    rs8001401,2
    C,F,A,H--2333675(+) AGGACA/GAGGCT 1 -- int122Minor allele frequency- G:0.42EA NS NA WA 3084
    rs1427254181,2
    --2333732(+) CATCAA/GTGGGA 1 -- int10--------
    rs22831451,2
    C--2333846(+) ACTGCC/TCGCCC 1 -- int10--------
    rs22831461,2
    C,F--2333860(+) TGGCCG/ACTGTC 1 -- int16Minor allele frequency- A:0.23NA WA EA 364
    rs1884611451,2
    --2333910(+) CCGCCA/GTAAGC 1 -- int10--------
    rs79368571,2
    C,F--2333987(+) GCCCTT/CTGGGG 1 -- int11Minor allele frequency- C:0.02WA 118
    rs49300801,2
    C,F,A--2334039(+) TGGCAT/CTTGGG 1 -- int16Minor allele frequency- C:0.10NA WA CSA EA 364
    rs1400715001,2
    --2334130(+) ACCAGC/TGACTC 1 -- int10--------
    rs768728071,2
    C--2334315(+) CTTCAC/TCCCCT 1 -- int12Minor allele frequency- T:0.08CSA WA 120
    rs753143311,2
    F--2334336(+) GGCCTC/TGTCCA 1 -- int11Minor allele frequency- T:0.03WA 118
    rs756663431,2
    F--2334404(+) CAGCTG/ACCCGG 1 -- int11Minor allele frequency- A:0.02EA 120
    rs1493857341,2
    --2334407(+) CTGCCC/TGGGCT 1 -- int10--------
    rs1926855981,2
    --2334525(+) CCCATC/TCCCCA 1 -- int10--------
    rs1174093741,2
    --2334550(+) GTAGCG/ATGCTG 1 -- int11Minor allele frequency- A:0.01NA 120
    rs1445353561,2
    --2334574(+) GCCAAA/CCTTGT 1 -- int10--------
    rs1484473101,2
    --2334667(+) GGCCAC/TTGTGT 1 -- int10--------
    rs7395461,2
    C,F,A--2334740(+) TTTGGA/GGAGAT 1 -- int114Minor allele frequency- G:0.48NA EA MN WA CSA 786
    rs22342991,2
    --2334828(+) GGGGGA/CTGTGT 1 -- int10--------
    rs22343001,2
    C--2334892(+) GAGGAC/TGCCAT 2 D syn1 ese30--------
    rs22343011,2
    C--2334893(+) AGGACG/ACCATG 2 /T /A mis1 ese32Minor allele frequency- A:0.00EA NA 4574
    rs1476304811,2
    --2334910(+) ACCTAC/TGACCT 2 Y syn10--------
    rs1124559171,2
    C,F--2334939(+) GAAAGG/TTACGT 2 G V mis12Minor allele frequency- T:0.00CSA NA 4425
    rs1381294691,2
    C--2334954(+) CGTCCG/AGCGGC 2 /Q /R mis11Minor allele frequency- A:0.00NA 4350
    rs22343021,2
    C,F--2334957(+) CCGGCG/AGCAGG 2 /Q /R mis1 ese31Minor allele frequency- A:0.00NA 4324
    rs22343031,2
    H--2334991(+) GTGAGC/AGTGGG 1 -- int14Minor allele frequency- A:0.00NS EA 408
    rs2004394081,2
    --2334995(+) GCGTGA/GGGACG 1 -- int10--------
    rs22343041,2
    C,F--2335015(+) CAGGGC/TGGTCA 1 -- int11Minor allele frequency- T:0.12WA 118
    rs557561781,2
    C--2335054(+) CAGGCG/ACAGGG 1 -- int12Minor allele frequency- A:0.03WA 120
    rs1837180801,2
    --2335187(+) ATTCTC/TGAGGC 1 -- int10--------
    rs1170352091,2
    --2335188(+) TTCTCG/AAGGCC 1 -- int11Minor allele frequency- A:0.01NA 120
    rs1155702561,2
    F--2335195(+) GGCCCA/CGTGCA 1 -- int11Minor allele frequency- C:0.05WA 118
    rs1881919111,2
    --2335204(+) CAAAAC/TGAGAG 1 -- int10--------
    rs1925896891,2
    --2335219(+) GGGCCC/TTGTAT 1 -- int10--------
    rs1406130751,2
    --2335266(+) AATACA/GGGGCC 1 -- int10--------
    rs1123627421,2
    --2335279(+) ACATAG/ATGGCT 1 -- int12Minor allele frequency- A:0.04CSA WA 119
    rs1847741441,2
    --2335343(+) AGCCCA/GGGAGT 1 -- int10--------
    rs350280821,2
    C--2335393(+) AAAAAA/-AAAAA 1 -- int11Minor allele frequency- -:0.00NA 2
    rs2001115741,2
    C--2335409(-) CTTTTC/TTNNNN 1 -- int10--------
    rs792974921,2
    C--2335436(+) TACAGC/TGCACA 1 -- int12Minor allele frequency- T:0.02WA 120
    rs7395471,2
    C,F,A,H--2335444(-) ACAGGC/GCCTGT 1 -- int111Minor allele frequency- G:0.49WA NA CSA EA 372
    rs1441968331,2
    C--2335489(+) NNNNCC/TGTCAC 1 -- int10--------
    rs784375861,2
    C,F--2335541(+) GGGCCC/TGGCTG 1 -- int11Minor allele frequency- T:0.03EA 120
    rs740482611,2
    C--2335560(+) CTGGAG/ACCCCA 1 -- int11Minor allele frequency- A:0.50WA 2
    rs1412136121,2
    --2335625(+) CTGGAG/TACTTG 1 -- int10--------
    rs2020944881,2
    --2335678(+) TCTCGC/GGAGCA 1 -- int10--------
    rs1486013111,2
    C,F--2335748(+) TCAGCC/TGTCTG 2 R C mis12Minor allele frequency- T:0.00NA EU 4627
    rs1420568901,2
    C,F--2335749(+) CAGCCG/ATCTGG 2 /H /R mis11Minor allele frequency- A:0.00NA 4480
    rs2004782991,2
    --2335795(+) GCGGCA/GAGAGA 2 A syn10--------
    rs1995723861,2
    --2335807(+) GTGAGG/TGGGGG 1 -- int10--------
    rs1916044361,2
    C--2335809(+) GAGGGA/GGGGAC 1 -- int10--------
    rs22343051,2
    C,H--2335840(+) ACCCTC/TGGGGG 1 -- int15Minor allele frequency- T:0.01NS EA WA 520
    rs762411111,2
    F--2336042(+) CCTTTG/CCCCAG 1 -- int11Minor allele frequency- C:0.12WA 118
    rs1503311621,2
    --2336106(+) GACTTC/GCCAAG 1 -- int10--------
    rs1141484801,2
    C,F--2336124(+) AAGTCC/TACAGA 1 -- int11Minor allele frequency- T:0.02WA 118
    rs1837461461,2
    --2336164(+) TGTGCC/TAAGGG 1 -- int10--------
    rs1449587001,2
    --2336217(+) CAGGCA/GTCCTG 1 -- int10--------
    rs74827551,2
    H--2336240(+) AGGAGT/ATGAAG 1 -- int14Minor allele frequency- A:0.00NS EA 420
    rs1898767381,2
    --2336246(+) TGAAGA/GGCACT 1 -- int10--------
    rs1414501991,2
    C--2336264(+) AAGAA-/GCCAGGCT
    GGAGGGTCGGC
    GTAGG
    1 -- int10--------
    rs1997625491,2
    --2336264(+) GAAGA-/AGTAGGCC 1 -- int10--------
    rs1810910061,2
    --2336432(+) CCGCTC/TCCCTC 1 -- int10--------
    rs1853640531,2
    --2336618(+) CGGCAC/TTGGGG 1 -- int10--------
    rs1898435461,2
    --2336680(+) CCCCCC/GACTGA 1 -- int10--------
    rs1163706181,2
    F--2336835(+) GCAGAC/ACTGCC 1 -- int11Minor allele frequency- A:0.03WA 118
    rs110222521,2
    C,H--2337012(+) AGGAAC/GCTGGG 1 -- int112Minor allele frequency- G:0.00NA WA CSA 141
    rs740482621,2
    C--2337022(+) GACTGT/CGCGGG 1 -- int12Minor allele frequency- C:0.04WA 120
    rs1814764361,2
    --2337211(+) GGAGAC/TGGCAC 1 -- int10--------
    rs125768241,2
    C,F,H--2337218(+) GCACCG/AGCCGG 1 -- int11Minor allele frequency- A:0.27EA 120
    rs1437700321,2
    --2337221(+) CCGGCC/TGGGCC 1 -- int10--------
    rs755746771,2
    F--2337272(+) CACTGG/AGCTTC 1 -- int11Minor allele frequency- A:0.16WA 118
    rs22343061,2
    F--2337334(+) CCGCAC/TCCGCC 1 -- int11Minor allele frequency- T:0.03WA 118
    rs1507314131,2
    F--2337506(+) CAGGTC/TGCCTC 2 V syn11Minor allele frequency- T:0.00NA 4322
    rs2014003871,2
    --2337534(+) GCCTGG/TCCCTC 2 A S mis10--------
    rs22343071,2
    F--2337650(+) TTGAGC/TCTCAC 1 -- int11Minor allele frequency- T:0.02NA 120
    rs22343081,2
    C,F,A--2337693(+) GACAGG/AGCCTG 1 -- int16Minor allele frequency- A:0.12NA CSA WA EA 364
    rs22343091,2
    C,F--2337758(+) AGGGGC/TGCCCG 1 -- int11Minor allele frequency- T:0.06WA 118
    rs2006782681,2
    --2337820(+) TTGCTC/GTTCAG 2 L syn10--------
    rs2000260821,2
    --2337848(+) CCATCC/TGCTGT 2 R C mis10--------
    rs1431121751,2
    --2337858(+) TGGCTA/GCAGCT 2 Y C mis10--------
    rs1863723891,2
    --2338000(+) CCAAGA/CCCCAG 1 -- int10--------
    rs22343101,2
    --2338038(+) GGGTGG/ACTGAG 1 -- int13Minor allele frequency- A:0.10CSA WA NA 239
    rs22343111,2
    C,F--2338043(+) GCTGAG/ACACCA 1 -- int11Minor allele frequency- A:0.06WA 118
    rs22343131,2
    --2338091(+) TGCACC/TGCACC 1 -- int10--------
    rs1908909321,2
    --2338109(+) CCACAA/TGGGGA 1 -- int10--------
    rs1388271481,2
    --2338156(+) GGAGAG/TGGATG 1 -- int10--------
    rs110222581,2
    C,F,A,H--2338240(+) GGGGCT/AGGGAG 1 -- int113Minor allele frequency- A:0.50NA WA CSA EA 381
    rs110222591,2
    C,F,A,H--2338256(+) AACCCG/ACAGCC 1 -- int113Minor allele frequency- A:0.29NA WA CSA EA 379
    rs1810078571,2
    --2338296(+) GGCCCA/GTCTCT 1 -- int10--------
    rs1158722251,2
    F--2338381(+) CTACAA/GTAGCC 1 -- int11Minor allele frequency- G:0.06WA 118
    rs773625671,2
    F--2338386(+) ATAGCC/TTCACA 1 -- int11Minor allele frequency- T:0.03WA 118
    rs1152630151,2
    F--2338397(+) GTCCCG/ATCTAG 1 -- int11Minor allele frequency- A:0.07WA 118
    rs22343141,2
    C--2338469(+) CCAGAA/TCATTC 1 -- int10--------
    rs595482601,2
    C--2338529(+) GTCCCG/CTGTAG 1 -- int11Minor allele frequency- C:0.50WA 2
    rs1857993411,2
    --2338542(+) CATTCA/CACCAC 1 -- int10--------
    rs31801601,2
    H--2338615(+) GAGATG/TCTCCC 2 C F mis1 ese34Minor allele frequency- T:0.00NS EA 402
    rs1390818151,2
    C,F--2338621(+) CTCCCA/TGGGTG 2 Q L mis12Minor allele frequency- T:0.00NA EU 4877
    rs1468377541,2
    F--2338639(+) ACATTG/ATCTCC 2 /Y /C mis11Minor allele frequency- A:0.00NA 4362
    rs347452341,2
    C,F--2338677(+) GAGGAT/CGCTCG 2 /R /C mis12Minor allele frequency- C:0.00NA 4500
    rs1492303961,2
    C--2338681(+) ATGCTC/TGGGTA 2 S L mis11Minor allele frequency- T:0.00NA 4400
    rs1432253481,2
    C--2338692(+) GTCTTC/TGGTGG 2 R W mis11Minor allele frequency- T:0.00NA 4354
    rs1914386511,2
    C--2338709(+)