Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 100506127 |
| ensemblid | ENSG00000179240.13 |
| hgncid | 51239 |
| symbol | GVQW3 |
| name | GVQW motif containing 3 |
| refseq_nuc | NM_001347885.2 |
| refseq_prot | NP_001334814.1 |
| ensembl_nuc | ENST00000529331.2 |
| ensembl_prot | ENSP00000489195.1 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 76381323 |
| end | 76408132 |
| strand | + |
| ver | v1.2 |
| region | chr11:76381323-76408132 |
| region5000 | chr11:76376323-76413132 |
| regionname0 | GVQW3_chr11_76381323_76408132 |
| regionname5000 | GVQW3_chr11_76376323_76413132 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 187 | 380 | 88 | 57 | 182 | 14 | 37 | 144 | GVQW3_chr11_76376323_76413132 | GVQW3 | MSDRY others(182): Show |
chr11 | 76376323 | 76413132 |
| a0002 | 0/0 | 187 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | MSDRY others(182): Show |
chr11 | 76376323 | 76413132 |
| a0003 | 0/0 | 187 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | MSDRY others(182): Show |
chr11 | 76376323 | 76413132 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 561 | 370 | 78 | 57 | 182 | 14 | 37 | GVQW3_chr11_76376323_76413132 | GVQW3 | ATGAG others(556): Show |
chr11 | 76376323 | 76413132 | ||
| a0001c0002 | 0/0 | 561 | 10 | 10 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | ATGAG others(556): Show |
chr11 | 76376323 | 76413132 | ||
| a0002c0003 | 0/0 | 561 | 1 | 0 | 1 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | ATGAG others(556): Show |
chr11 | 76376323 | 76413132 | ||
| a0003c0004 | 0/0 | 561 | 1 | 0 | 0 | 0 | 0 | 1 | GVQW3_chr11_76376323_76413132 | GVQW3 | ATGAG others(556): Show |
chr11 | 76376323 | 76413132 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 5445 | 75 | 5 | 16 | 41 | 1 | 11 | GVQW3_chr11_76376323_76413132 | GVQW3 | ATGCG others(5440): Show |
chr11 | 76376323 | 76413132 |
| a0001c0001t0002 | 0/0 | 5438 | 74 | 12 | 12 | 40 | 4 | 6 | GVQW3_chr11_76376323_76413132 | GVQW3 | ATGCG others(5433): Show |
chr11 | 76376323 | 76413132 |
| a0001c0001t0003 | 0/0 | 5446 | 41 | 10 | 12 | 11 | 2 | 6 | GVQW3_chr11_76376323_76413132 | GVQW3 | ATGCG others(5441): Show |
chr11 | 76376323 | 76413132 |
| a0001c0001t0004 | 0/0 | 5445 | 19 | 0 | 2 | 11 | 5 | 1 | GVQW3_chr11_76376323_76413132 | GVQW3 | ATGCG others(5440): Show |
chr11 | 76376323 | 76413132 |
| a0001c0001t0005 | 0/0 | 5439 | 18 | 7 | 1 | 10 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | ATGCG others(5434): Show |
chr11 | 76376323 | 76413132 |
| a0001c0001t0006 | 0/0 | 5446 | 12 | 0 | 0 | 11 | 1 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | ATGCG others(5441): Show |
chr11 | 76376323 | 76413132 |
| a0001c0001t0007 | 0/0 | 5443 | 9 | 1 | 0 | 8 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | ATGCG others(5438): Show |
chr11 | 76376323 | 76413132 |
| a0001c0001t0008 | 1/0 | 5444 | 8 | 6 | 1 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | ATGCG others(5439): Show |
chr11 | 76376323 | 76413132 |
| a0001c0001t0009 | 0/0 | 5446 | 8 | 6 | 1 | 0 | 0 | 1 | GVQW3_chr11_76376323_76413132 | GVQW3 | ATGCG others(5441): Show |
chr11 | 76376323 | 76413132 |
| a0001c0001t0010 | 0/0 | 5443 | 8 | 2 | 3 | 2 | 0 | 1 | GVQW3_chr11_76376323_76413132 | GVQW3 | ATGCG others(5438): Show |
chr11 | 76376323 | 76413132 |
| a0001c0001t0011 | 0/0 | 5444 | 7 | 0 | 0 | 7 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | ATGCG others(5439): Show |
chr11 | 76376323 | 76413132 |
| a0001c0001t0012 | 0/0 | 5446 | 5 | 0 | 3 | 2 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | ATGCG others(5441): Show |
chr11 | 76376323 | 76413132 |
| a0001c0001t0013 | 0/0 | 5446 | 5 | 0 | 0 | 4 | 0 | 1 | GVQW3_chr11_76376323_76413132 | GVQW3 | ATGCG others(5441): Show |
chr11 | 76376323 | 76413132 |
| a0001c0001t0014 | 0/0 | 5446 | 4 | 0 | 0 | 4 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | ATGCG others(5441): Show |
chr11 | 76376323 | 76413132 |
| a0001c0001t0015 | 0/0 | 5445 | 3 | 0 | 0 | 3 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | ATGCG others(5440): Show |
chr11 | 76376323 | 76413132 |
| a0001c0001t0016 | 0/0 | 5447 | 3 | 0 | 0 | 3 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | ATGCG others(5442): Show |
chr11 | 76376323 | 76413132 |
| a0001c0001t0017 | 0/0 | 5438 | 3 | 0 | 0 | 3 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | ATGCG others(5433): Show |
chr11 | 76376323 | 76413132 |
| a0001c0001t0018 | 0/0 | 5439 | 3 | 0 | 0 | 2 | 0 | 1 | GVQW3_chr11_76376323_76413132 | GVQW3 | ATGCG others(5434): Show |
chr11 | 76376323 | 76413132 |
| a0001c0001t0019 | 0/0 | 5445 | 3 | 3 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | ATGCG others(5440): Show |
chr11 | 76376323 | 76413132 |
| a0001c0001t0020 | 0/0 | 5444 | 2 | 2 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | ATGCG others(5439): Show |
chr11 | 76376323 | 76413132 |
| a0001c0001t0021 | 0/0 | 5438 | 2 | 0 | 0 | 0 | 0 | 2 | GVQW3_chr11_76376323_76413132 | GVQW3 | ATGCG others(5433): Show |
chr11 | 76376323 | 76413132 |
| a0001c0001t0022 | 0/0 | 5438 | 2 | 0 | 0 | 0 | 1 | 1 | GVQW3_chr11_76376323_76413132 | GVQW3 | ATGCG others(5433): Show |
chr11 | 76376323 | 76413132 |
| a0001c0001t0023 | 0/0 | 5438 | 2 | 0 | 0 | 0 | 0 | 2 | GVQW3_chr11_76376323_76413132 | GVQW3 | ATGCG others(5433): Show |
chr11 | 76376323 | 76413132 |
| a0001c0001t0024 | 0/0 | 5445 | 2 | 2 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | ATGCG others(5440): Show |
chr11 | 76376323 | 76413132 |
| a0001c0001t0025 | 0/0 | 5444 | 2 | 2 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | ATGCG others(5439): Show |
chr11 | 76376323 | 76413132 |
| a0001c0001t0026 | 0/0 | 5446 | 2 | 0 | 0 | 0 | 0 | 2 | GVQW3_chr11_76376323_76413132 | GVQW3 | ATGCG others(5441): Show |
chr11 | 76376323 | 76413132 |
| a0001c0001t0027 | 0/0 | 5443 | 2 | 0 | 0 | 2 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | ATGCG others(5438): Show |
chr11 | 76376323 | 76413132 |
| a0001c0001t0028 | 0/0 | 5428 | 1 | 1 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | ATGCG others(5423): Show |
chr11 | 76376323 | 76413132 |
| a0001c0001t0029 | 0/0 | 5438 | 1 | 1 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | ATGCG others(5433): Show |
chr11 | 76376323 | 76413132 |
| a0001c0001t0030 | 0/0 | 5428 | 1 | 1 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | ATGCG others(5423): Show |
chr11 | 76376323 | 76413132 |
| a0001c0001t0031 | 0/0 | 5445 | 1 | 0 | 0 | 1 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | ATGCG others(5440): Show |
chr11 | 76376323 | 76413132 |
| a0001c0001t0032 | 0/0 | 5444 | 1 | 1 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | ATGCG others(5439): Show |
chr11 | 76376323 | 76413132 |
| a0001c0001t0033 | 0/0 | 5447 | 1 | 0 | 0 | 1 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | ATGCG others(5442): Show |
chr11 | 76376323 | 76413132 |
| a0001c0001t0034 | 0/0 | 5439 | 1 | 1 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | ATGCG others(5434): Show |
chr11 | 76376323 | 76413132 |
| a0001c0001t0035 | 0/0 | 5446 | 1 | 1 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | ATGCG others(5441): Show |
chr11 | 76376323 | 76413132 |
| a0001c0001t0036 | 0/0 | 5467 | 1 | 0 | 0 | 1 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | ATGCG others(5462): Show |
chr11 | 76376323 | 76413132 |
| a0001c0001t0037 | 0/0 | 5446 | 1 | 0 | 0 | 1 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | ATGCG others(5441): Show |
chr11 | 76376323 | 76413132 |
| a0001c0001t0038 | 0/0 | 5445 | 1 | 1 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | ATGCG others(5440): Show |
chr11 | 76376323 | 76413132 |
| a0001c0001t0039 | 0/0 | 5445 | 1 | 0 | 0 | 1 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | ATGCG others(5440): Show |
chr11 | 76376323 | 76413132 |
| a0001c0001t0040 | 0/0 | 5438 | 1 | 0 | 1 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | ATGCG others(5433): Show |
chr11 | 76376323 | 76413132 |
| a0001c0001t0041 | 0/0 | 5437 | 1 | 0 | 0 | 1 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | ATGCG others(5432): Show |
chr11 | 76376323 | 76413132 |
| a0001c0001t0042 | 0/0 | 5445 | 1 | 0 | 0 | 1 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | ATGCG others(5440): Show |
chr11 | 76376323 | 76413132 |
| a0001c0001t0043 | 0/0 | 5439 | 1 | 0 | 0 | 1 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | ATGCG others(5434): Show |
chr11 | 76376323 | 76413132 |
| a0001c0001t0044 | 0/0 | 5447 | 1 | 1 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | ATGCG others(5442): Show |
chr11 | 76376323 | 76413132 |
| a0001c0001t0045 | 0/0 | 5445 | 1 | 0 | 1 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | ATGCG others(5440): Show |
chr11 | 76376323 | 76413132 |
| a0001c0001t0046 | 0/0 | 5446 | 1 | 0 | 0 | 0 | 0 | 1 | GVQW3_chr11_76376323_76413132 | GVQW3 | ATGCG others(5441): Show |
chr11 | 76376323 | 76413132 |
| a0001c0001t0047 | 0/0 | 5445 | 1 | 0 | 1 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | ATGCG others(5440): Show |
chr11 | 76376323 | 76413132 |
| a0001c0001t0048 | 0/0 | 5446 | 1 | 1 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | ATGCG others(5441): Show |
chr11 | 76376323 | 76413132 |
| a0001c0001t0049 | 0/0 | 5447 | 1 | 0 | 0 | 1 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | ATGCG others(5442): Show |
chr11 | 76376323 | 76413132 |
| a0001c0001t0050 | 0/0 | 5445 | 1 | 0 | 0 | 1 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | ATGCG others(5440): Show |
chr11 | 76376323 | 76413132 |
| a0001c0001t0051 | 0/0 | 5446 | 1 | 0 | 1 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | ATGCG others(5441): Show |
chr11 | 76376323 | 76413132 |
| a0001c0001t0052 | 0/0 | 5442 | 1 | 1 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | ATGCG others(5437): Show |
chr11 | 76376323 | 76413132 |
| a0001c0001t0053 | 0/0 | 5445 | 1 | 1 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | ATGCG others(5440): Show |
chr11 | 76376323 | 76413132 |
| a0001c0001t0054 | 0/0 | 5445 | 1 | 0 | 0 | 1 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | ATGCG others(5440): Show |
chr11 | 76376323 | 76413132 |
| a0001c0001t0055 | 0/0 | 5438 | 1 | 1 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | ATGCG others(5433): Show |
chr11 | 76376323 | 76413132 |
| a0001c0001t0056 | 0/0 | 5445 | 1 | 0 | 0 | 1 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | ATGCG others(5440): Show |
chr11 | 76376323 | 76413132 |
| a0001c0001t0057 | 0/0 | 5447 | 1 | 0 | 0 | 1 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | ATGCG others(5442): Show |
chr11 | 76376323 | 76413132 |
| a0001c0001t0058 | 0/0 | 5438 | 1 | 1 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | ATGCG others(5433): Show |
chr11 | 76376323 | 76413132 |
| a0001c0001t0059 | 0/0 | 5444 | 1 | 1 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | ATGCG others(5439): Show |
chr11 | 76376323 | 76413132 |
| a0001c0001t0060 | 0/0 | 5447 | 1 | 1 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | ATGCG others(5442): Show |
chr11 | 76376323 | 76413132 |
| a0001c0001t0061 | 0/0 | 5445 | 1 | 1 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | ATGCG others(5440): Show |
chr11 | 76376323 | 76413132 |
| a0001c0001t0062 | 0/0 | 5443 | 1 | 1 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | ATGCG others(5438): Show |
chr11 | 76376323 | 76413132 |
| a0001c0001t0063 | 0/0 | 5447 | 1 | 1 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | ATGCG others(5442): Show |
chr11 | 76376323 | 76413132 |
| a0001c0001t0064 | 0/0 | 5444 | 1 | 0 | 0 | 0 | 0 | 1 | GVQW3_chr11_76376323_76413132 | GVQW3 | ATGCG others(5439): Show |
chr11 | 76376323 | 76413132 |
| a0001c0001t0065 | 0/0 | 5440 | 1 | 1 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | ATGCG others(5435): Show |
chr11 | 76376323 | 76413132 |
| a0001c0001t0066 | 0/0 | 5446 | 1 | 0 | 0 | 1 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | ATGCG others(5441): Show |
chr11 | 76376323 | 76413132 |
| a0001c0001t0067 | 0/0 | 5444 | 1 | 0 | 0 | 1 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | ATGCG others(5439): Show |
chr11 | 76376323 | 76413132 |
| a0001c0001t0068 | 0/0 | 5444 | 1 | 1 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | ATGCG others(5439): Show |
chr11 | 76376323 | 76413132 |
| a0001c0001t0069 | 0/0 | 5438 | 1 | 0 | 1 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | ATGCG others(5433): Show |
chr11 | 76376323 | 76413132 |
| a0001c0001t0070 | 0/0 | 5445 | 1 | 0 | 0 | 1 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | ATGCG others(5440): Show |
chr11 | 76376323 | 76413132 |
| a0001c0001t0071 | 0/0 | 5439 | 1 | 0 | 0 | 1 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | ATGCG others(5434): Show |
chr11 | 76376323 | 76413132 |
| a0001c0001t0072 | 0/0 | 5445 | 1 | 0 | 0 | 1 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | ATGCG others(5440): Show |
chr11 | 76376323 | 76413132 |
| a0001c0001t0083 | 0/0 | 5438 | 1 | 0 | 1 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | ATGCG others(5433): Show |
chr11 | 76376323 | 76413132 |
| a0001c0002t0073 | 0/0 | 5445 | 1 | 1 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | ATGCG others(5440): Show |
chr11 | 76376323 | 76413132 |
| a0001c0002t0074 | 0/0 | 5444 | 1 | 1 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | ATGCG others(5439): Show |
chr11 | 76376323 | 76413132 |
| a0001c0002t0075 | 0/0 | 5443 | 1 | 1 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | ATGCG others(5438): Show |
chr11 | 76376323 | 76413132 |
| a0001c0002t0076 | 0/0 | 5438 | 1 | 1 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | ATGCG others(5433): Show |
chr11 | 76376323 | 76413132 |
| a0001c0002t0077 | 0/0 | 5444 | 1 | 1 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | ATGCG others(5439): Show |
chr11 | 76376323 | 76413132 |
| a0001c0002t0078 | 0/0 | 5438 | 1 | 1 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | ATGCG others(5433): Show |
chr11 | 76376323 | 76413132 |
| a0001c0002t0079 | 0/0 | 5438 | 1 | 1 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | ATGCG others(5433): Show |
chr11 | 76376323 | 76413132 |
| a0001c0002t0080 | 0/0 | 5446 | 1 | 1 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | ATGCG others(5441): Show |
chr11 | 76376323 | 76413132 |
| a0001c0002t0081 | 0/0 | 5440 | 1 | 1 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | ATGCG others(5435): Show |
chr11 | 76376323 | 76413132 |
| a0001c0002t0082 | 0/0 | 5445 | 1 | 1 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | ATGCG others(5440): Show |
chr11 | 76376323 | 76413132 |
| a0002c0003t0001 | 0/0 | 5445 | 1 | 0 | 1 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | ATGCG others(5440): Show |
chr11 | 76376323 | 76413132 |
| a0003c0004t0001 | 0/0 | 5445 | 1 | 0 | 0 | 0 | 0 | 1 | GVQW3_chr11_76376323_76413132 | GVQW3 | ATGCG others(5440): Show |
chr11 | 76376323 | 76413132 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 19 | 0 | 5 | 12 | 0 | 2 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0001g0003 | 0/0 | 14 | 0 | 0 | 14 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0001g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0001g0066 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0002g0001 | 0/0 | 36 | 1 | 9 | 21 | 2 | 3 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0002g0005 | 0/0 | 8 | 8 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0002g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0002g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0003g0002 | 0/0 | 5 | 0 | 2 | 1 | 0 | 2 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0003g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0003g0004 | 0/0 | 7 | 1 | 6 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0003g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0003g0014 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0003g0015 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0003g0016 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0003g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0003g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0003g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0003g0038 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0003g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0003g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0003g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0003g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0003g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0003g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0003g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0004g0006 | 0/0 | 8 | 0 | 1 | 4 | 3 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0004g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0004g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0004g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0004g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0004g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0004g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0004g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0004g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0005g0008 | 0/0 | 7 | 0 | 1 | 6 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0005g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0005g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0005g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0005g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0005g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0005g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0005g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0006g0007 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0006g0034 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0006g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0007g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0007g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0007g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0007g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0007g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0007g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0007g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0008g0009 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0008g0068 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0008g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0008g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0008g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0009g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0009g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0009g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0009g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0009g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0009g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0010g0011 | 0/0 | 5 | 0 | 3 | 2 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0010g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0010g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0010g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0011g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0011g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0011g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0011g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0011g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0012g0012 | 0/0 | 5 | 0 | 3 | 2 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0013g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0013g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0013g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0013g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0013g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0014g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0014g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0014g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0015g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0016g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0017g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0018g0001 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0018g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0019g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0020g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0021g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0022g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0022g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0023g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0023g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0024g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0025g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0025g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0026g0030 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0027g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0027g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0028g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0029g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0030g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0031g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0032g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0033g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0034g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0035g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0036g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0037g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0038g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0039g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0040g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0041g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0042g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0043g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0044g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0045g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0046g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0047g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0048g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0049g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0050g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0051g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0052g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0053g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0054g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0055g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0056g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0057g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0058g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0059g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0060g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0061g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0062g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0063g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0064g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0065g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0066g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0067g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0068g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0069g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0070g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0071g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0072g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0001t0083g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0002t0073g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0002t0074g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0002t0075g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0002t0076g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0002t0077g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0002t0078g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0002t0079g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0002t0080g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0002t0081g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0001c0002t0082g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0002c0003t0001g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| a0003c0004t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0004 | g0093 | EUR | GBR | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | GBR | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG00280 | hp1 | a0001 | c0001 | t0004 | g0075 | EUR | FIN | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG00280 | hp2 | a0001 | c0001 | t0003 | g0038 | EUR | FIN | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0107 | EUR | FIN | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG00323 | hp2 | a0001 | c0001 | t0006 | g0034 | EUR | FIN | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG00438 | hp1 | a0001 | c0001 | t0070 | g0001 | EAS | CHS | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | CHS | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG00544 | hp1 | a0001 | c0001 | t0012 | g0012 | EAS | CHS | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG00558 | hp1 | a0001 | c0001 | t0015 | g0006 | EAS | CHS | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | CHS | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG00597 | hp1 | a0001 | c0001 | t0007 | g0013 | EAS | CHS | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | CHS | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG00609 | hp1 | a0001 | c0001 | t0005 | g0008 | EAS | CHS | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG00621 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | CHS | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | CHS | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG00639 | hp2 | a0001 | c0001 | t0008 | g0148 | AMR | PUR | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG00642 | hp2 | a0001 | c0001 | t0083 | g0058 | AMR | PUR | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | CHS | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG00673 | hp2 | a0001 | c0001 | t0027 | g0133 | EAS | CHS | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG00733 | hp1 | a0001 | c0001 | t0040 | g0112 | AMR | PUR | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG00733 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0134 | AMR | PUR | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0100 | AMR | PUR | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG01106 | hp1 | a0001 | c0001 | t0005 | g0008 | AMR | PUR | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG01109 | hp1 | a0002 | c0003 | t0001 | g0002 | AMR | PUR | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG01167 | hp2 | a0001 | c0001 | t0069 | g0001 | AMR | PUR | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0015 | AMR | PUR | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG01175 | hp1 | a0001 | c0001 | t0051 | g0006 | AMR | PUR | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG01192 | hp1 | a0001 | c0001 | t0047 | g0002 | AMR | PUR | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG01243 | hp1 | a0001 | c0001 | t0009 | g0061 | AMR | PUR | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG01243 | hp2 | a0001 | c0001 | t0004 | g0006 | AMR | PUR | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | CLM | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | CLM | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0016 | AMR | CLM | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG01257 | hp1 | a0001 | c0001 | t0045 | g0004 | AMR | CLM | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG01261 | hp1 | a0001 | c0001 | t0010 | g0011 | AMR | CLM | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | CLM | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG01358 | hp1 | a0001 | c0001 | t0010 | g0011 | AMR | CLM | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG01358 | hp2 | a0001 | c0001 | t0003 | g0149 | AMR | CLM | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0159 | AMR | CLM | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | CLM | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG01433 | hp2 | a0001 | c0001 | t0010 | g0011 | AMR | CLM | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG01496 | hp1 | a0001 | c0001 | t0004 | g0073 | AMR | CLM | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0032 | EUR | IBS | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0096 | EUR | IBS | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG01516 | hp1 | a0001 | c0001 | t0022 | g0057 | EUR | IBS | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG01516 | hp2 | a0001 | c0001 | t0004 | g0006 | EUR | IBS | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0001 | EUR | IBS | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG01517 | hp2 | a0001 | c0001 | t0004 | g0006 | EUR | IBS | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG01884 | hp1 | a0001 | c0001 | t0005 | g0019 | AFR | ACB | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG01884 | hp2 | a0001 | c0001 | t0053 | g0009 | AFR | ACB | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG01891 | hp1 | a0001 | c0001 | t0008 | g0009 | AFR | ACB | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0103 | AFR | ACB | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG01975 | hp1 | a0001 | c0001 | t0012 | g0012 | AMR | PEL | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG01993 | hp2 | a0001 | c0001 | t0012 | g0012 | AMR | PEL | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG02015 | hp1 | a0001 | c0001 | t0006 | g0007 | EAS | KHV | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG02040 | hp1 | a0001 | c0001 | t0011 | g0002 | EAS | KHV | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG02040 | hp2 | a0001 | c0001 | t0037 | g0007 | EAS | KHV | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG02055 | hp1 | a0001 | c0001 | t0008 | g0156 | AFR | ACB | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG02055 | hp2 | a0001 | c0001 | t0009 | g0008 | AFR | ACB | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG02056 | hp2 | a0001 | c0001 | t0017 | g0001 | EAS | KHV | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | KHV | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG02080 | hp2 | a0001 | c0001 | t0004 | g0079 | EAS | KHV | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG02129 | hp1 | a0001 | c0001 | t0005 | g0008 | EAS | KHV | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG02129 | hp2 | a0001 | c0001 | t0010 | g0011 | EAS | KHV | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG02135 | hp1 | a0001 | c0001 | t0072 | g0003 | EAS | KHV | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG02135 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | KHV | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG02155 | hp1 | a0001 | c0001 | t0039 | g0002 | EAS | CDX | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG02155 | hp2 | a0001 | c0001 | t0005 | g0090 | EAS | CDX | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG02165 | hp1 | a0001 | c0001 | t0005 | g0060 | EAS | CDX | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | ACB | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG02257 | hp2 | a0001 | c0001 | t0025 | g0143 | AFR | ACB | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG02258 | hp1 | a0001 | c0001 | t0005 | g0019 | AFR | ACB | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG02258 | hp2 | a0001 | c0001 | t0010 | g0152 | AFR | ACB | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG02280 | hp1 | a0001 | c0001 | t0009 | g0008 | AFR | ACB | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0055 | AFR | ACB | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG02293 | hp1 | a0001 | c0001 | t0012 | g0012 | AMR | PEL | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG02300 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PEL | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0114 | AMR | PEL | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG02451 | hp1 | a0001 | c0001 | t0062 | g0047 | AFR | ACB | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG02451 | hp2 | a0001 | c0001 | t0009 | g0049 | AFR | ACB | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | KHV | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG02572 | hp1 | a0001 | c0001 | t0068 | g0048 | AFR | GWD | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG02572 | hp2 | a0001 | c0001 | t0060 | g0008 | AFR | GWD | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG02622 | hp1 | a0001 | c0002 | t0080 | g0162 | AFR | GWD | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG02622 | hp2 | a0001 | c0001 | t0038 | g0086 | AFR | GWD | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0009 | AFR | GWD | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG02630 | hp2 | a0001 | c0001 | t0059 | g0077 | AFR | GWD | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG02647 | hp1 | a0001 | c0001 | t0008 | g0009 | AFR | GWD | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG02647 | hp2 | a0001 | c0002 | t0078 | g0040 | AFR | GWD | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG02698 | hp2 | a0001 | c0001 | t0004 | g0072 | SAS | PJL | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG02717 | hp1 | a0001 | c0001 | t0065 | g0018 | AFR | GWD | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG02717 | hp2 | a0001 | c0001 | t0048 | g0004 | AFR | GWD | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG02723 | hp1 | a0001 | c0001 | t0063 | g0064 | AFR | GWD | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | GWD | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG02738 | hp2 | a0001 | c0001 | t0021 | g0005 | SAS | PJL | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG02809 | hp1 | a0001 | c0001 | t0055 | g0052 | AFR | GWD | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG02809 | hp2 | a0001 | c0001 | t0005 | g0018 | AFR | GWD | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG02818 | hp1 | a0001 | c0002 | t0082 | g0042 | AFR | GWD | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG02818 | hp2 | a0001 | c0001 | t0010 | g0045 | AFR | GWD | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0009 | AFR | GWD | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0153 | AFR | GWD | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG02895 | hp1 | a0001 | c0001 | t0019 | g0004 | AFR | GWD | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | GWD | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG02896 | hp1 | a0001 | c0002 | t0073 | g0017 | AFR | GWD | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0062 | AFR | GWD | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0063 | AFR | GWD | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG02897 | hp2 | a0001 | c0001 | t0019 | g0004 | AFR | GWD | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG02922 | hp1 | a0001 | c0001 | t0005 | g0024 | AFR | ESN | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG02922 | hp2 | a0001 | c0001 | t0028 | g0025 | AFR | ESN | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | ESN | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG02965 | hp2 | a0001 | c0001 | t0044 | g0053 | AFR | ESN | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG02970 | hp1 | a0001 | c0001 | t0030 | g0044 | AFR | ESN | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | ESN | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0081 | AFR | ESN | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG02976 | hp2 | a0001 | c0002 | t0075 | g0017 | AFR | ESN | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG03017 | hp1 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG03098 | hp1 | a0001 | c0001 | t0061 | g0065 | AFR | MSL | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG03098 | hp2 | a0001 | c0001 | t0008 | g0009 | AFR | MSL | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG03130 | hp1 | a0001 | c0002 | t0077 | g0163 | AFR | ESN | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG03130 | hp2 | a0001 | c0002 | t0074 | g0017 | AFR | ESN | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | ESN | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG03139 | hp2 | a0001 | c0001 | t0009 | g0008 | AFR | ESN | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG03195 | hp1 | a0001 | c0001 | t0005 | g0024 | AFR | ESN | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG03195 | hp2 | a0001 | c0001 | t0008 | g0157 | AFR | ESN | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG03209 | hp1 | a0001 | c0001 | t0020 | g0027 | AFR | MSL | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG03209 | hp2 | a0001 | c0001 | t0035 | g0085 | AFR | MSL | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | MSL | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG03225 | hp2 | a0001 | c0001 | t0020 | g0027 | AFR | MSL | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG03239 | hp1 | a0001 | c0001 | t0023 | g0001 | SAS | PJL | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG03239 | hp2 | a0001 | c0001 | t0021 | g0005 | SAS | PJL | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | MSL | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG03453 | hp2 | a0001 | c0001 | t0024 | g0005 | AFR | MSL | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | MSL | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG03486 | hp2 | a0001 | c0001 | t0029 | g0025 | AFR | MSL | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG03490 | hp1 | a0001 | c0001 | t0009 | g0109 | SAS | PJL | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG03490 | hp2 | a0001 | c0001 | t0026 | g0030 | SAS | PJL | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG03491 | hp2 | a0001 | c0001 | t0046 | g0004 | SAS | PJL | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG03492 | hp2 | a0001 | c0001 | t0026 | g0030 | SAS | PJL | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0054 | AFR | ESN | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG03516 | hp2 | a0001 | c0002 | t0076 | g0041 | AFR | ESN | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG03540 | hp1 | a0001 | c0001 | t0009 | g0050 | AFR | GWD | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG03540 | hp2 | a0001 | c0001 | t0025 | g0142 | AFR | GWD | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG03579 | hp1 | a0001 | c0002 | t0081 | g0039 | AFR | MSL | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG03579 | hp2 | a0001 | c0002 | t0079 | g0043 | AFR | MSL | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0094 | SAS | PJL | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | STU | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0016 | SAS | STU | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0108 | SAS | PJL | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG03710 | hp1 | a0001 | c0001 | t0064 | g0011 | SAS | PJL | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0164 | SAS | PJL | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0002 | SAS | BEB | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG03831 | hp2 | a0001 | c0001 | t0013 | g0071 | SAS | BEB | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG03942 | hp1 | a0001 | c0001 | t0010 | g0151 | SAS | BEB | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0038 | SAS | BEB | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG04184 | hp1 | a0001 | c0001 | t0022 | g0005 | SAS | BEB | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | BEB | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG04199 | hp1 | a0001 | c0001 | t0003 | g0029 | SAS | STU | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0161 | SAS | STU | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | STU | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG04204 | hp2 | a0003 | c0004 | t0001 | g0015 | SAS | STU | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG04228 | hp1 | a0001 | c0001 | t0018 | g0001 | SAS | STU | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | STU | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA18522 | hp1 | a0001 | c0001 | t0008 | g0009 | AFR | YRI | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA18522 | hp2 | a0001 | c0001 | t0019 | g0004 | AFR | YRI | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA18747 | hp1 | a0001 | c0001 | t0004 | g0010 | EAS | CHB | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | CHB | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA18906 | hp1 | a0001 | c0001 | t0034 | g0024 | AFR | YRI | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA18906 | hp2 | a0001 | c0001 | t0024 | g0005 | AFR | YRI | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA18939 | hp1 | a0001 | c0001 | t0011 | g0002 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA18939 | hp2 | a0001 | c0001 | t0018 | g0122 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA18940 | hp1 | a0001 | c0001 | t0016 | g0007 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA18941 | hp1 | a0001 | c0001 | t0071 | g0001 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA18941 | hp2 | a0001 | c0001 | t0006 | g0007 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA18942 | hp1 | a0001 | c0001 | t0004 | g0076 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA18945 | hp2 | a0001 | c0001 | t0003 | g0120 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA18946 | hp1 | a0001 | c0001 | t0006 | g0144 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA18948 | hp1 | a0001 | c0001 | t0011 | g0137 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA18948 | hp2 | a0001 | c0001 | t0007 | g0026 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA18950 | hp1 | a0001 | c0001 | t0016 | g0007 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA18952 | hp1 | a0001 | c0001 | t0017 | g0001 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA18953 | hp1 | a0001 | c0001 | t0007 | g0013 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA18957 | hp2 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA18959 | hp1 | a0001 | c0001 | t0003 | g0126 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA18959 | hp2 | a0001 | c0001 | t0014 | g0031 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA18961 | hp2 | a0001 | c0001 | t0011 | g0003 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA18962 | hp1 | a0001 | c0001 | t0011 | g0003 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA18962 | hp2 | a0001 | c0001 | t0007 | g0069 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA18964 | hp2 | a0001 | c0001 | t0049 | g0014 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA18965 | hp1 | a0001 | c0001 | t0016 | g0007 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA18967 | hp1 | a0001 | c0001 | t0041 | g0095 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA18969 | hp1 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA18970 | hp2 | a0001 | c0001 | t0007 | g0082 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA18973 | hp1 | a0001 | c0001 | t0004 | g0074 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA18974 | hp1 | a0001 | c0001 | t0005 | g0008 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA18977 | hp1 | a0001 | c0001 | t0005 | g0008 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA18977 | hp2 | a0001 | c0001 | t0014 | g0080 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA18979 | hp1 | a0001 | c0001 | t0005 | g0008 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA18979 | hp2 | a0001 | c0001 | t0057 | g0014 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA18983 | hp2 | a0001 | c0001 | t0005 | g0091 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA18985 | hp1 | a0001 | c0001 | t0014 | g0089 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA18986 | hp2 | a0001 | c0001 | t0050 | g0002 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA18987 | hp1 | a0001 | c0001 | t0042 | g0036 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA18987 | hp2 | a0001 | c0001 | t0011 | g0004 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA18988 | hp1 | a0001 | c0001 | t0003 | g0131 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA18988 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA18992 | hp1 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA18992 | hp2 | a0001 | c0001 | t0006 | g0007 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA18994 | hp1 | a0001 | c0001 | t0018 | g0001 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA18995 | hp1 | a0001 | c0001 | t0010 | g0011 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA18995 | hp2 | a0001 | c0001 | t0014 | g0031 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA18999 | hp1 | a0001 | c0001 | t0003 | g0136 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA19001 | hp1 | a0001 | c0001 | t0013 | g0070 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA19001 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA19002 | hp2 | a0001 | c0001 | t0031 | g0146 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA19003 | hp1 | a0001 | c0001 | t0003 | g0140 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA19003 | hp2 | a0001 | c0001 | t0012 | g0012 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA19004 | hp1 | a0001 | c0001 | t0006 | g0007 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA19005 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA19005 | hp2 | a0001 | c0001 | t0005 | g0008 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA19006 | hp1 | a0001 | c0001 | t0036 | g0092 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA19006 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA19009 | hp1 | a0001 | c0001 | t0013 | g0117 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA19011 | hp1 | a0001 | c0001 | t0006 | g0034 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | LWK | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0051 | AFR | LWK | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | LWK | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA19043 | hp2 | a0001 | c0001 | t0005 | g0019 | AFR | LWK | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA19056 | hp1 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA19056 | hp2 | a0001 | c0001 | t0066 | g0013 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA19057 | hp2 | a0001 | c0001 | t0015 | g0006 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA19060 | hp1 | a0001 | c0001 | t0006 | g0007 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA19060 | hp2 | a0001 | c0001 | t0011 | g0130 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA19062 | hp1 | a0001 | c0001 | t0027 | g0013 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA19066 | hp1 | a0001 | c0001 | t0017 | g0001 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA19066 | hp2 | a0001 | c0001 | t0006 | g0007 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA19067 | hp1 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA19067 | hp2 | a0001 | c0001 | t0013 | g0010 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA19068 | hp2 | a0001 | c0001 | t0005 | g0129 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA19070 | hp2 | a0001 | c0001 | t0013 | g0006 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA19074 | hp1 | a0001 | c0001 | t0054 | g0010 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA19074 | hp2 | a0001 | c0001 | t0006 | g0007 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA19077 | hp2 | a0001 | c0001 | t0007 | g0026 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA19078 | hp1 | a0001 | c0001 | t0043 | g0032 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA19078 | hp2 | a0001 | c0001 | t0067 | g0013 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA19079 | hp2 | a0001 | c0001 | t0033 | g0012 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA19082 | hp2 | a0001 | c0001 | t0006 | g0007 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA19083 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA19085 | hp1 | a0001 | c0001 | t0015 | g0006 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA19085 | hp2 | a0001 | c0001 | t0007 | g0084 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA19088 | hp2 | a0001 | c0001 | t0007 | g0083 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA19089 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA19089 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA19090 | hp2 | a0001 | c0001 | t0056 | g0003 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA19240 | hp1 | a0001 | c0001 | t0005 | g0018 | AFR | YRI | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA19240 | hp2 | a0001 | c0001 | t0058 | g0078 | AFR | YRI | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0014 | AFR | ASW | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA20129 | hp2 | a0001 | c0001 | t0052 | g0158 | AFR | ASW | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0035 | EUR | TSI | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA20752 | hp2 | a0001 | c0001 | t0004 | g0006 | EUR | TSI | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA20905 | hp1 | a0001 | c0001 | t0023 | g0067 | SAS | GIH | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | GIH | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG02109 | hp1 | a0001 | c0001 | t0003 | g0004 | AFR | ACB | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | ACB | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG02486 | hp1 | a0001 | c0001 | t0009 | g0046 | AFR | ACB | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | ACB | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | ACB | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| HG02559 | hp2 | a0001 | c0001 | t0032 | g0105 | AFR | ACB | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA18955 | hp1 | a0001 | c0001 | t0006 | g0007 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA21309 | hp1 | a0001 | c0001 | t0007 | g0087 | AFR | LWK | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| NA21309 | hp2 | a0001 | c0001 | t0003 | g0015 | AFR | LWK | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0066 | REF | REF | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0008 | g0068 | REF | REF | GVQW3_chr11_76376323_76413132 | GVQW3 | chr11 | 76376323 | 76413132 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:76382116 | G | C | 1 | a0002 | 1 | HG01109.hp1 | missense_variant | MODERATE | c.288G>C | p.Glu96Asp | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/2 | 794/5444 | 288/564 | 96/187 | chr11 | 76382116 | |||
| chr11:76382246 | G | T | 1 | a0003 | 1 | HG04204.hp2 | missense_variant | MODERATE | c.418G>T | p.Asp140Tyr | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/2 | 924/5444 | 418/564 | 140/187 | chr11 | 76382246 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:76382098 | G | T | 1 | a0001c0002 | 10 | HG02622.hp1 HG02647.hp2 HG02818.hp1 others(7): Show |
synonymous_variant | LOW | c.270G>T | p.Val90Val | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/2 | 776/5444 | 270/564 | 90/187 | chr11 | 76382098 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:76381343 | A | G | 1 | a0001c0001t0083 | 1 | HG00642.hp2 | 5_prime_UTR_variant | MODIFIER | c.-486A>G | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/2 | 486 | chr11 | 76381343 | ||||||
| chr11:76381344 | C | T | 10 | a0001c0002t0073 a0001c0002t0074 a0001c0002t0075 others(7): Show |
10 | HG02622.hp1 HG02647.hp2 HG02818.hp1 others(7): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-485C>T | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/2 | chr11 | 76381344 | |||||||
| chr11:76381363 | T | C | 25 | a0001c0001t0006 a0001c0001t0012 a0001c0001t0015 others(22): Show |
45 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(42): Show |
5_prime_UTR_variant | MODIFIER | c.-466T>C | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/2 | 466 | chr11 | 76381363 | ||||||
| chr11:76381403 | G | T | 1 | a0001c0001t0072 | 1 | HG02135.hp1 | 5_prime_UTR_variant | MODIFIER | c.-426G>T | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/2 | 426 | chr11 | 76381403 | ||||||
| chr11:76403841 | T | C | 3 | a0001c0001t0021 a0001c0001t0022 a0001c0001t0083 |
5 | HG00642.hp2 HG01516.hp1 HG02738.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*83T>C | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 2/2 | 83 | chr11 | 76403841 | ||||||
| chr11:76403942 | T | A | 1 | a0001c0001t0038 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*184T>A | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 2/2 | 184 | chr11 | 76403942 | ||||||
| chr11:76403947 | A | G | 2 | a0001c0001t0070 a0001c0001t0071 |
2 | HG00438.hp1 NA18941.hp1 |
3_prime_UTR_variant | MODIFIER | c.*189A>G | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 2/2 | 189 | chr11 | 76403947 | ||||||
| chr11:76403962 | G | T | 1 | a0001c0001t0069 | 1 | HG01167.hp2 | 3_prime_UTR_variant | MODIFIER | c.*204G>T | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 2/2 | 204 | chr11 | 76403962 | ||||||
| chr11:76403981 | G | A | 1 | a0001c0001t0039 | 1 | HG02155.hp1 | 3_prime_UTR_variant | MODIFIER | c.*223G>A | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 2/2 | 223 | chr11 | 76403981 | ||||||
| chr11:76404187 | G | A | 16 | a0001c0001t0002 a0001c0001t0017 a0001c0001t0018 others(13): Show |
97 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*429G>A | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 2/2 | 429 | chr11 | 76404187 | ||||||
| chr11:76404440 | G | C | 1 | a0001c0001t0025 | 2 | HG02257.hp2 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*682G>C | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 2/2 | 682 | chr11 | 76404440 | ||||||
| chr11:76404443 | A | G | 1 | a0001c0001t0037 | 1 | HG02040.hp2 | 3_prime_UTR_variant | MODIFIER | c.*685A>G | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 2/2 | 685 | chr11 | 76404443 | ||||||
| chr11:76404545 | G | C | 1 | a0001c0001t0045 | 1 | HG01257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*787G>C | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 2/2 | 787 | chr11 | 76404545 | ||||||
| chr11:76404655 | A | G | 26 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0007 others(23): Show |
83 | HG00323.hp2 HG00544.hp1 HG00597.hp1 others(80): Show |
3_prime_UTR_variant | MODIFIER | c.*897A>G | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 2/2 | 897 | chr11 | 76404655 | ||||||
| chr11:76404731 | A | G | 2 | a0001c0001t0068 a0001c0002t0082 |
2 | HG02572.hp1 HG02818.hp1 |
3_prime_UTR_variant | MODIFIER | c.*973A>G | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 2/2 | 973 | chr11 | 76404731 | ||||||
| chr11:76404838 | C | G | 4 | a0001c0001t0007 a0001c0001t0027 a0001c0001t0066 others(1): Show |
13 | HG00597.hp1 HG00673.hp2 NA18948.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1080C>G | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 2/2 | 1080 | chr11 | 76404838 | ||||||
| chr11:76404886 | G | C | 1 | a0001c0001t0027 | 2 | HG00673.hp2 NA19062.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1128G>C | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 2/2 | 1128 | chr11 | 76404886 | ||||||
| chr11:76404908 | T | C | 1 | a0001c0001t0040 | 1 | HG00733.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1150T>C | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 2/2 | 1150 | chr11 | 76404908 | ||||||
| chr11:76405042 | A | G | 27 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0007 others(24): Show |
87 | HG00323.hp2 HG00544.hp1 HG00597.hp1 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*1284A>G | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 2/2 | 1284 | chr11 | 76405042 | ||||||
| chr11:76405118 | G | A | 1 | a0001c0001t0041 | 1 | NA18967.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1360G>A | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 2/2 | 1360 | chr11 | 76405118 | ||||||
| chr11:76405133 | C | A | 3 | a0001c0001t0028 a0001c0001t0029 a0001c0001t0030 |
3 | HG02922.hp2 HG02970.hp1 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1375C>A | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 2/2 | 1375 | chr11 | 76405133 | ||||||
| chr11:76405156 | G | T | 1 | a0001c0001t0036 | 1 | NA19006.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1398G>T | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 2/2 | 1398 | chr11 | 76405156 | ||||||
| chr11:76405189 | T | C | 1 | a0001c0001t0046 | 1 | HG03491.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1431T>C | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 2/2 | 1431 | chr11 | 76405189 | ||||||
| chr11:76405200 | C | T | 1 | a0001c0001t0025 | 2 | HG02257.hp2 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1442C>T | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 2/2 | 1442 | chr11 | 76405200 | ||||||
| chr11:76405319 | G | T | 27 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0007 others(24): Show |
87 | HG00323.hp2 HG00544.hp1 HG00597.hp1 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*1561G>T | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 2/2 | 1561 | chr11 | 76405319 | ||||||
| chr11:76405322 | C | T | 20 | a0001c0001t0002 a0001c0001t0017 a0001c0001t0018 others(17): Show |
102 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(99): Show |
3_prime_UTR_variant | MODIFIER | c.*1564C>T | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 2/2 | 1564 | chr11 | 76405322 | ||||||
| chr11:76405669 | T | G | 50 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0006 others(47): Show |
192 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(189): Show |
3_prime_UTR_variant | MODIFIER | c.*1911T>G | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 2/2 | 1911 | chr11 | 76405669 | ||||||
| chr11:76405710 | C | T | 1 | a0001c0001t0030 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1952C>T | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 2/2 | 1952 | chr11 | 76405710 | ||||||
| chr11:76405753 | A | C | 1 | a0001c0001t0026 | 2 | HG03490.hp2 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1995A>C | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 2/2 | 1995 | chr11 | 76405753 | ||||||
| chr11:76405800 | C | T | 2 | a0001c0001t0025 a0001c0001t0058 |
3 | HG02257.hp2 HG03540.hp2 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2042C>T | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 2/2 | 2042 | chr11 | 76405800 | ||||||
| chr11:76405873 | G | C | 1 | a0001c0001t0021 | 2 | HG02738.hp2 HG03239.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2115G>C | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 2/2 | 2115 | chr11 | 76405873 | ||||||
| chr11:76405941 | C | T | 23 | a0001c0001t0002 a0001c0001t0017 a0001c0001t0018 others(20): Show |
105 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(102): Show |
3_prime_UTR_variant | MODIFIER | c.*2183C>T | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 2/2 | 2183 | chr11 | 76405941 | ||||||
| chr11:76406117 | C | T | 16 | a0001c0001t0002 a0001c0001t0017 a0001c0001t0018 others(13): Show |
97 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*2359C>T | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 2/2 | 2359 | chr11 | 76406117 | ||||||
| chr11:76406147 | A | AT | 28 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0007 others(25): Show |
88 | HG00323.hp2 HG00544.hp1 HG00597.hp1 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*2395dupT | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 2/2 | 2396 | INFO_REALIGN_3_PRIME | chr11 | 76406147 | |||||
| chr11:76406169 | C | T | 24 | a0001c0001t0002 a0001c0001t0017 a0001c0001t0018 others(21): Show |
106 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(103): Show |
3_prime_UTR_variant | MODIFIER | c.*2411C>T | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 2/2 | 2411 | chr11 | 76406169 | ||||||
| chr11:76406423 | A | G | 1 | a0001c0001t0057 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2665A>G | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 2/2 | 2665 | chr11 | 76406423 | ||||||
| chr11:76406470 | T | G | 1 | a0001c0001t0047 | 1 | HG01192.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2712T>G | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 2/2 | 2712 | chr11 | 76406470 | ||||||
| chr11:76406582 | A | C | 1 | a0001c0001t0030 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2824A>C | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 2/2 | 2824 | chr11 | 76406582 | ||||||
| chr11:76406620 | C | A | 13 | a0001c0001t0006 a0001c0001t0009 a0001c0001t0012 others(10): Show |
37 | HG00323.hp2 HG00544.hp1 HG01243.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*2862C>A | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 2/2 | 2862 | chr11 | 76406620 | ||||||
| chr11:76406728 | G | T | 1 | a0001c0001t0056 | 1 | NA19090.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2970G>T | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 2/2 | 2970 | chr11 | 76406728 | ||||||
| chr11:76406737 | G | A | 20 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0011 others(17): Show |
142 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(139): Show |
3_prime_UTR_variant | MODIFIER | c.*2979G>A | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 2/2 | 2979 | chr11 | 76406737 | ||||||
| chr11:76406784 | C | G | 19 | a0001c0001t0006 a0001c0001t0007 a0001c0001t0009 others(16): Show |
55 | HG00323.hp2 HG00544.hp1 HG00597.hp1 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*3026C>G | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 2/2 | 3026 | chr11 | 76406784 | ||||||
| chr11:76406835 | C | T | 26 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0010 others(23): Show |
129 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(126): Show |
3_prime_UTR_variant | MODIFIER | c.*3077C>T | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 2/2 | 3077 | chr11 | 76406835 | ||||||
| chr11:76406880 | T | C | 19 | a0001c0001t0006 a0001c0001t0007 a0001c0001t0009 others(16): Show |
55 | HG00323.hp2 HG00544.hp1 HG00597.hp1 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*3122T>C | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 2/2 | 3122 | chr11 | 76406880 | ||||||
| chr11:76406994 | C | T | 1 | a0001c0001t0054 | 1 | NA19074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3236C>T | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 2/2 | 3236 | chr11 | 76406994 | ||||||
| chr11:76407232 | A | T | 2 | a0001c0001t0068 a0001c0002t0082 |
2 | HG02572.hp1 HG02818.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3474A>T | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 2/2 | 3474 | chr11 | 76407232 | ||||||
| chr11:76407239 | A | ATTGTTTT others(14): Show |
1 | a0001c0001t0036 | 1 | NA19006.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3482_*3502dupTTGT others(17): Show |
GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 2/2 | 3503 | INFO_REALIGN_3_PRIME | chr11 | 76407239 | |||||
| chr11:76407275 | G | A | 2 | a0001c0001t0019 a0001c0001t0048 |
4 | HG02717.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3517G>A | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 2/2 | 3517 | chr11 | 76407275 | ||||||
| chr11:76407306 | A | G | 74 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(71): Show |
337 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(334): Show |
3_prime_UTR_variant | MODIFIER | c.*3548A>G | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 2/2 | 3548 | chr11 | 76407306 | ||||||
| chr11:76407317 | C | T | 13 | a0001c0001t0006 a0001c0001t0009 a0001c0001t0016 others(10): Show |
33 | HG00323.hp2 HG01243.hp1 HG02015.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*3559C>T | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 2/2 | 3559 | chr11 | 76407317 | ||||||
| chr11:76407406 | T | G | 46 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0006 others(43): Show |
182 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(179): Show |
3_prime_UTR_variant | MODIFIER | c.*3648T>G | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 2/2 | 3648 | chr11 | 76407406 | ||||||
| chr11:76407423 | A | G | 1 | a0001c0001t0035 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3665A>G | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 2/2 | 3665 | chr11 | 76407423 | ||||||
| chr11:76407449 | T | C | 46 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0006 others(43): Show |
182 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(179): Show |
3_prime_UTR_variant | MODIFIER | c.*3691T>C | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 2/2 | 3691 | chr11 | 76407449 | ||||||
| chr11:76407532 | G | A | 4 | a0001c0001t0010 a0001c0001t0052 a0001c0001t0062 others(1): Show |
11 | HG01261.hp1 HG01358.hp1 HG01433.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3774G>A | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 2/2 | 3774 | chr11 | 76407532 | ||||||
| chr11:76407539 | T | C | 1 | a0001c0001t0017 | 3 | HG02056.hp2 NA18952.hp1 NA19066.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3781T>C | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 2/2 | 3781 | chr11 | 76407539 | ||||||
| chr11:76407556 | G | A | 1 | a0001c0001t0051 | 1 | HG01175.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3798G>A | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 2/2 | 3798 | chr11 | 76407556 | ||||||
| chr11:76407557 | G | A | 1 | a0001c0001t0051 | 1 | HG01175.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3799G>A | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 2/2 | 3799 | chr11 | 76407557 | ||||||
| chr11:76407566 | G | A | 1 | a0001c0001t0051 | 1 | HG01175.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3808G>A | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 2/2 | 3808 | chr11 | 76407566 | ||||||
| chr11:76407576 | C | CA | 15 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0015 others(12): Show |
78 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*3845dupA | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 2/2 | 3846 | INFO_REALIGN_3_PRIME | chr11 | 76407576 | |||||
| chr11:76407576 | C | CAA | 4 | a0001c0001t0013 a0001c0001t0049 a0001c0001t0051 others(1): Show |
8 | HG01175.hp1 HG03831.hp2 NA18964.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3844_*3845dupAA | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 2/2 | 3846 | INFO_REALIGN_3_PRIME | chr11 | 76407576 | |||||
| chr11:76407576 | CA | C | 5 | a0001c0001t0011 a0001c0001t0061 a0001c0001t0064 others(2): Show |
11 | HG02040.hp1 HG02572.hp1 HG02976.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3845delA | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 2/2 | 3845 | INFO_REALIGN_3_PRIME | chr11 | 76407576 | |||||
| chr11:76407576 | CAA | C | 4 | a0001c0001t0010 a0001c0001t0052 a0001c0001t0062 others(1): Show |
11 | HG01261.hp1 HG01358.hp1 HG01433.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3844_*3845delAA | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 2/2 | 3844 | INFO_REALIGN_3_PRIME | chr11 | 76407576 | |||||
| chr11:76407576 | CAAA | C | 4 | a0001c0001t0007 a0001c0001t0027 a0001c0001t0028 others(1): Show |
13 | HG00597.hp1 HG00673.hp2 HG02922.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*3843_*3845delAAA | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 2/2 | 3843 | INFO_REALIGN_3_PRIME | chr11 | 76407576 | |||||
| chr11:76407576 | CAAAAAA | C | 4 | a0001c0001t0018 a0001c0001t0065 a0001c0001t0071 others(1): Show |
6 | HG02717.hp1 HG03579.hp1 HG04228.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3840_*3845delAAAA others(2): Show |
GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 2/2 | 3840 | INFO_REALIGN_3_PRIME | chr11 | 76407576 | |||||
| chr11:76407576 | CAAAAAAA | C | 18 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0017 others(15): Show |
113 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*3839_*3845delAAAA others(3): Show |
GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 2/2 | 3839 | INFO_REALIGN_3_PRIME | chr11 | 76407576 | |||||
| chr11:76407579 | A | C | 1 | a0001c0001t0064 | 1 | HG03710.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3821A>C | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 2/2 | 3821 | chr11 | 76407579 | ||||||
| chr11:76407580 | A | C | 4 | a0001c0001t0010 a0001c0001t0052 a0001c0001t0062 others(1): Show |
11 | HG01261.hp1 HG01358.hp1 HG01433.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3822A>C | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 2/2 | 3822 | chr11 | 76407580 | ||||||
| chr11:76407581 | A | C | 4 | a0001c0001t0007 a0001c0001t0027 a0001c0001t0028 others(1): Show |
13 | HG00597.hp1 HG00673.hp2 HG02922.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*3823A>C | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 2/2 | 3823 | chr11 | 76407581 | ||||||
| chr11:76407582 | A | C | 1 | a0001c0001t0066 | 1 | NA19056.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3824A>C | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 2/2 | 3824 | chr11 | 76407582 | ||||||
| chr11:76407584 | A | C | 4 | a0001c0001t0018 a0001c0001t0065 a0001c0001t0071 others(1): Show |
6 | HG02717.hp1 HG03579.hp1 HG04228.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3826A>C | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 2/2 | 3826 | chr11 | 76407584 | ||||||
| chr11:76407585 | A | C | 18 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0017 others(15): Show |
113 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*3827A>C | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 2/2 | 3827 | chr11 | 76407585 | ||||||
| chr11:76407640 | G | A | 10 | a0001c0001t0007 a0001c0001t0010 a0001c0001t0027 others(7): Show |
26 | HG00597.hp1 HG00673.hp2 HG01261.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*3882G>A | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 2/2 | 3882 | chr11 | 76407640 | ||||||
| chr11:76407641 | ATTTCTTA others(6): Show |
A | 2 | a0001c0001t0028 a0001c0001t0030 |
2 | HG02922.hp2 HG02970.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3895_*3907delTCTT others(9): Show |
GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 2/2 | 3895 | INFO_REALIGN_3_PRIME | chr11 | 76407641 | |||||
| chr11:76407694 | T | C | 6 | a0001c0001t0010 a0001c0001t0028 a0001c0001t0030 others(3): Show |
13 | HG01261.hp1 HG01358.hp1 HG01433.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*3936T>C | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 2/2 | 3936 | chr11 | 76407694 | ||||||
| chr11:76407703 | C | T | 7 | a0001c0001t0010 a0001c0001t0028 a0001c0001t0030 others(4): Show |
14 | HG01261.hp1 HG01358.hp1 HG01433.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*3945C>T | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 2/2 | 3945 | chr11 | 76407703 | ||||||
| chr11:76407942 | T | TA | 60 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(57): Show |
316 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(313): Show |
3_prime_UTR_variant | MODIFIER | c.*4188dupA | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 2/2 | 4189 | INFO_REALIGN_3_PRIME | chr11 | 76407942 | |||||
| chr11:76407947 | C | A | 62 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(59): Show |
318 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(315): Show |
3_prime_UTR_variant | MODIFIER | c.*4189C>A | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 2/2 | 4189 | chr11 | 76407947 | ||||||
| chr11:76408051 | T | A | 10 | a0001c0001t0006 a0001c0001t0009 a0001c0001t0014 others(7): Show |
33 | HG00323.hp2 HG01243.hp1 HG02015.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*4293T>A | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 2/2 | 4293 | chr11 | 76408051 | ||||||
| chr11:76408065 | A | T | 1 | a0001c0001t0035 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4307A>T | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 2/2 | 4307 | chr11 | 76408065 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:76382355 | C | G | 2 | a0001c0001t0012g0012 a0001c0001t0033g0012 |
6 | HG00544.hp1 HG01975.hp1 HG01993.hp2 others(3): Show |
intron_variant | MODIFIER | c.465+62C>G | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76382355 | |||||||
| chr11:76382363 | C | T | 1 | a0001c0001t0002g0164 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.465+70C>T | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76382363 | |||||||
| chr11:76382375 | C | T | 2 | a0001c0002t0077g0163 a0001c0002t0080g0162 |
2 | HG02622.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.465+82C>T | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76382375 | |||||||
| chr11:76382936 | T | C | 13 | a0001c0001t0028g0025 a0001c0001t0029g0025 a0001c0001t0030g0044 others(10): Show |
13 | HG02622.hp1 HG02647.hp2 HG02818.hp1 others(10): Show |
intron_variant | MODIFIER | c.465+643T>C | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76382936 | |||||||
| chr11:76382975 | G | A | 34 | a0001c0001t0001g0015 a0001c0001t0001g0059 a0001c0001t0002g0005 others(31): Show |
55 | HG00609.hp1 HG00642.hp2 HG01106.hp1 others(52): Show |
intron_variant | MODIFIER | c.465+682G>A | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76382975 | |||||||
| chr11:76383166 | C | T | 1 | a0001c0001t0003g0161 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.465+873C>T | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76383166 | |||||||
| chr11:76383236 | A | G | 1 | a0001c0001t0001g0160 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.465+943A>G | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76383236 | |||||||
| chr11:76383285 | G | C | 1 | a0001c0001t0023g0067 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.465+992G>C | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76383285 | |||||||
| chr11:76383449 | C | T | 1 | a0001c0001t0030g0044 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.465+1156C>T | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76383449 | |||||||
| chr11:76383669 | C | T | 1 | a0001c0001t0002g0159 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.465+1376C>T | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76383669 | |||||||
| chr11:76383778 | A | C | 192 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(189): Show |
339 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(336): Show |
intron_variant | MODIFIER | c.465+1485A>C | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76383778 | |||||||
| chr11:76383779 | A | C | 191 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(188): Show |
338 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(335): Show |
intron_variant | MODIFIER | c.465+1486A>C | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76383779 | |||||||
| chr11:76383780 | A | C | 86 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0015 others(83): Show |
143 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(140): Show |
intron_variant | MODIFIER | c.465+1487A>C | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76383780 | |||||||
| chr11:76383781 | A | C | 31 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0016 others(28): Show |
51 | HG00280.hp2 HG00733.hp2 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.465+1488A>C | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76383781 | |||||||
| chr11:76383782 | A | C | 1 | a0001c0001t0052g0158 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.465+1489A>C | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76383782 | |||||||
| chr11:76383906 | A | G | 18 | a0001c0001t0001g0003 a0001c0001t0001g0023 a0001c0001t0001g0132 others(15): Show |
35 | HG00408.hp1 HG00673.hp2 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.465+1613A>G | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76383906 | |||||||
| chr11:76384104 | A | G | 1 | a0001c0001t0005g0019 | 3 | HG01884.hp1 HG02258.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.465+1811A>G | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76384104 | |||||||
| chr11:76384360 | C | T | 1 | a0001c0001t0005g0129 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.465+2067C>T | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76384360 | |||||||
| chr11:76384408 | C | T | 1 | a0001c0001t0002g0033 | 2 | HG00558.hp2 HG00597.hp2 |
intron_variant | MODIFIER | c.465+2115C>T | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76384408 | |||||||
| chr11:76384575 | G | C | 1 | a0001c0001t0003g0149 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.465+2282G>C | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76384575 | |||||||
| chr11:76384667 | C | T | 1 | a0001c0002t0078g0040 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.465+2374C>T | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76384667 | |||||||
| chr11:76384710 | A | G | 1 | a0001c0001t0002g0128 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.465+2417A>G | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76384710 | |||||||
| chr11:76384730 | T | A | 1 | a0001c0001t0001g0020 | 3 | HG01109.hp2 HG01257.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.465+2437T>A | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76384730 | |||||||
| chr11:76384731 | C | A | 1 | a0001c0001t0001g0020 | 3 | HG01109.hp2 HG01257.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.465+2438C>A | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76384731 | |||||||
| chr11:76384851 | A | C | 2 | a0001c0001t0061g0065 a0001c0001t0063g0064 |
2 | HG02723.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.465+2558A>C | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76384851 | |||||||
| chr11:76385025 | T | C | 1 | a0001c0001t0002g0081 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.465+2732T>C | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76385025 | |||||||
| chr11:76385026 | C | G | 194 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(191): Show |
340 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(337): Show |
intron_variant | MODIFIER | c.465+2733C>G | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76385026 | |||||||
| chr11:76385120 | A | G | 1 | a0001c0001t0002g0127 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.465+2827A>G | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76385120 | |||||||
| chr11:76385789 | T | G | 4 | a0001c0001t0025g0142 a0001c0001t0025g0143 a0001c0001t0030g0044 others(1): Show |
4 | HG02257.hp2 HG02970.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.465+3496T>G | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76385789 | |||||||
| chr11:76386055 | A | T | 1 | a0001c0001t0001g0037 | 2 | HG01346.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.465+3762A>T | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76386055 | |||||||
| chr11:76386075 | C | T | 2 | a0001c0001t0028g0025 a0001c0001t0029g0025 |
2 | HG02922.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.465+3782C>T | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76386075 | |||||||
| chr11:76386105 | G | A | 2 | a0001c0001t0028g0025 a0001c0001t0029g0025 |
2 | HG02922.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.465+3812G>A | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76386105 | |||||||
| chr11:76386183 | T | G | 1 | a0001c0001t0001g0150 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.465+3890T>G | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76386183 | |||||||
| chr11:76386632 | T | C | 8 | a0001c0001t0007g0087 a0001c0001t0010g0011 a0001c0001t0010g0045 others(5): Show |
12 | HG01261.hp1 HG01358.hp1 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.465+4339T>C | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76386632 | |||||||
| chr11:76386898 | A | G | 1 | a0001c0002t0079g0043 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.465+4605A>G | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76386898 | |||||||
| chr11:76387201 | C | T | 3 | a0001c0002t0073g0017 a0001c0002t0074g0017 a0001c0002t0075g0017 |
3 | HG02896.hp1 HG02976.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.465+4908C>T | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76387201 | |||||||
| chr11:76387206 | C | T | 1 | a0001c0001t0003g0126 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.465+4913C>T | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76387206 | |||||||
| chr11:76387292 | C | T | 4 | a0001c0001t0004g0010 a0001c0001t0004g0076 a0001c0001t0013g0010 others(1): Show |
7 | NA18747.hp1 NA18942.hp1 NA18957.hp2 others(4): Show |
intron_variant | MODIFIER | c.465+4999C>T | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76387292 | |||||||
| chr11:76387333 | G | A | 1 | a0001c0001t0010g0151 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.465+5040G>A | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76387333 | |||||||
| chr11:76387386 | T | C | 192 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(189): Show |
338 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(335): Show |
intron_variant | MODIFIER | c.465+5093T>C | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76387386 | |||||||
| chr11:76387448 | T | C | 1 | a0001c0001t0058g0078 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.465+5155T>C | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76387448 | |||||||
| chr11:76387483 | G | A | 1 | a0001c0001t0001g0020 | 3 | HG01109.hp2 HG01257.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.465+5190G>A | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76387483 | |||||||
| chr11:76388017 | T | C | 1 | a0001c0001t0009g0046 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.465+5724T>C | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76388017 | |||||||
| chr11:76388327 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.465+6034C>T | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76388327 | |||||||
| chr11:76388343 | G | T | 1 | a0001c0001t0001g0124 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.465+6050G>T | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76388343 | |||||||
| chr11:76388399 | G | A | 1 | a0001c0001t0030g0044 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.465+6106G>A | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76388399 | |||||||
| chr11:76388468 | A | C | 194 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(191): Show |
340 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(337): Show |
intron_variant | MODIFIER | c.465+6175A>C | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76388468 | |||||||
| chr11:76388470 | T | G | 194 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(191): Show |
340 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(337): Show |
intron_variant | MODIFIER | c.465+6177T>G | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76388470 | |||||||
| chr11:76388483 | T | C | 194 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(191): Show |
340 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(337): Show |
intron_variant | MODIFIER | c.465+6190T>C | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76388483 | |||||||
| chr11:76388825 | A | T | 194 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(191): Show |
340 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(337): Show |
intron_variant | MODIFIER | c.465+6532A>T | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76388825 | |||||||
| chr11:76389117 | C | T | 1 | a0001c0001t0008g0157 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.465+6824C>T | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76389117 | |||||||
| chr11:76389153 | G | A | 192 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(189): Show |
338 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(335): Show |
intron_variant | MODIFIER | c.465+6860G>A | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76389153 | |||||||
| chr11:76389355 | A | G | 10 | a0001c0001t0001g0009 a0001c0001t0003g0009 a0001c0001t0003g0062 others(7): Show |
14 | HG00639.hp2 HG01074.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.465+7062A>G | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76389355 | |||||||
| chr11:76389468 | GC | G | 49 | a0001c0001t0001g0110 a0001c0001t0001g0118 a0001c0001t0001g0141 others(46): Show |
94 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.465+7176delC | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76389468 | |||||||
| chr11:76389546 | A | G | 3 | a0001c0002t0073g0017 a0001c0002t0074g0017 a0001c0002t0075g0017 |
3 | HG02896.hp1 HG02976.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.465+7253A>G | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76389546 | |||||||
| chr11:76389575 | C | G | 218 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(215): Show |
379 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(376): Show |
intron_variant | MODIFIER | c.465+7282C>G | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76389575 | |||||||
| chr11:76389845 | A | G | 1 | a0001c0001t0004g0074 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.465+7552A>G | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76389845 | |||||||
| chr11:76389880 | T | G | 17 | a0001c0001t0007g0013 a0001c0001t0007g0026 a0001c0001t0007g0069 others(14): Show |
23 | HG00597.hp1 HG01261.hp1 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.465+7587T>G | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76389880 | |||||||
| chr11:76389992 | T | A | 1 | a0001c0001t0059g0077 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.465+7699T>A | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76389992 | |||||||
| chr11:76390006 | A | G | 1 | a0001c0001t0059g0077 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.465+7713A>G | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76390006 | |||||||
| chr11:76390012 | A | G | 2 | a0001c0001t0002g0106 a0001c0001t0002g0123 |
2 | HG00673.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.465+7719A>G | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76390012 | |||||||
| chr11:76390039 | T | G | 1 | a0001c0001t0011g0130 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.465+7746T>G | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76390039 | |||||||
| chr11:76390069 | G | T | 1 | a0001c0001t0007g0084 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.465+7776G>T | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76390069 | |||||||
| chr11:76390202 | A | G | 1 | a0001c0001t0018g0122 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.465+7909A>G | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76390202 | |||||||
| chr11:76390212 | A | C | 1 | a0001c0001t0032g0105 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.465+7919A>C | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76390212 | |||||||
| chr11:76390423 | A | G | 1 | a0001c0001t0002g0121 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.465+8130A>G | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76390423 | |||||||
| chr11:76390459 | G | A | 1 | a0001c0001t0003g0131 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.465+8166G>A | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76390459 | |||||||
| chr11:76390530 | G | A | 1 | a0001c0001t0001g0020 | 3 | HG01109.hp2 HG01257.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.465+8237G>A | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76390530 | |||||||
| chr11:76390562 | A | G | 1 | a0001c0001t0009g0061 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.465+8269A>G | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76390562 | |||||||
| chr11:76390631 | C | A | 1 | a0001c0001t0007g0069 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.465+8338C>A | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76390631 | |||||||
| chr11:76390632 | G | A | 12 | a0001c0001t0020g0027 a0001c0001t0032g0105 a0001c0001t0035g0085 others(9): Show |
13 | HG02559.hp2 HG02572.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.465+8339G>A | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76390632 | |||||||
| chr11:76390659 | T | TA | 13 | a0001c0001t0020g0027 a0001c0001t0032g0105 a0001c0001t0035g0085 others(10): Show |
14 | HG02559.hp2 HG02572.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.465+8373dupA | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr11 | 76390659 | ||||||
| chr11:76390669 | C | T | 1 | a0001c0001t0004g0073 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.465+8376C>T | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76390669 | |||||||
| chr11:76390676 | A | G | 3 | a0001c0001t0028g0025 a0001c0001t0029g0025 a0001c0001t0030g0044 |
3 | HG02922.hp2 HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.465+8383A>G | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76390676 | |||||||
| chr11:76390826 | TA | T | 84 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(81): Show |
147 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(144): Show |
intron_variant | MODIFIER | c.465+8549delA | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr11 | 76390826 | ||||||
| chr11:76390905 | A | AGTGTATA others(60): Show |
1 | a0001c0001t0010g0152 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.465+8658_465+8724d others(69): Show |
GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr11 | 76390905 | ||||||
| chr11:76390905 | AGTGTATA others(60): Show |
A | 1 | a0001c0001t0013g0070 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.465+8658_465+8724d others(69): Show |
GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr11 | 76390905 | ||||||
| chr11:76391085 | G | C | 87 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(84): Show |
151 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(148): Show |
intron_variant | MODIFIER | c.465+8792G>C | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76391085 | |||||||
| chr11:76391138 | G | A | 1 | a0001c0001t0002g0107 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.465+8845G>A | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76391138 | |||||||
| chr11:76391139 | C | A | 1 | a0001c0001t0001g0096 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.465+8846C>A | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76391139 | |||||||
| chr11:76391234 | G | T | 9 | a0001c0001t0020g0027 a0001c0001t0035g0085 a0001c0001t0058g0078 others(6): Show |
10 | HG02572.hp1 HG02630.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.465+8941G>T | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76391234 | |||||||
| chr11:76391298 | T | C | 1 | a0001c0001t0001g0150 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.465+9005T>C | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76391298 | |||||||
| chr11:76391478 | A | G | 2 | a0001c0001t0022g0057 a0001c0001t0083g0058 |
2 | HG00642.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.465+9185A>G | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76391478 | |||||||
| chr11:76391528 | G | A | 1 | a0001c0001t0001g0132 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.465+9235G>A | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76391528 | |||||||
| chr11:76391536 | T | C | 1 | a0001c0001t0058g0078 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.465+9243T>C | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76391536 | |||||||
| chr11:76391682 | G | A | 1 | a0001c0001t0002g0108 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.465+9389G>A | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76391682 | |||||||
| chr11:76391698 | A | C | 1 | a0001c0001t0002g0022 | 3 | HG00438.hp2 HG00621.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.465+9405A>C | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76391698 | |||||||
| chr11:76391724 | T | C | 149 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(146): Show |
248 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(245): Show |
intron_variant | MODIFIER | c.465+9431T>C | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76391724 | |||||||
| chr11:76391860 | A | G | 2 | a0001c0001t0028g0025 a0001c0001t0029g0025 |
2 | HG02922.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.465+9567A>G | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76391860 | |||||||
| chr11:76391969 | A | C | 52 | a0001c0001t0001g0118 a0001c0001t0002g0001 a0001c0001t0002g0005 others(49): Show |
102 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.465+9676A>C | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76391969 | |||||||
| chr11:76392007 | C | T | 3 | a0001c0001t0028g0025 a0001c0001t0029g0025 a0001c0001t0030g0044 |
3 | HG02922.hp2 HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.465+9714C>T | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76392007 | |||||||
| chr11:76392090 | G | A | 17 | a0001c0001t0007g0013 a0001c0001t0007g0026 a0001c0001t0007g0069 others(14): Show |
23 | HG00597.hp1 HG00673.hp2 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.465+9797G>A | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76392090 | |||||||
| chr11:76392093 | G | A | 85 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(82): Show |
149 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(146): Show |
intron_variant | MODIFIER | c.465+9800G>A | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76392093 | |||||||
| chr11:76392189 | C | A | 64 | a0001c0001t0001g0110 a0001c0001t0003g0051 a0001c0001t0003g0054 others(61): Show |
99 | HG00323.hp2 HG00544.hp1 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.465+9896C>A | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76392189 | |||||||
| chr11:76392293 | C | G | 1 | a0001c0001t0031g0146 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.465+10000C>G | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76392293 | |||||||
| chr11:76392318 | A | G | 1 | a0001c0001t0058g0078 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.465+10025A>G | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76392318 | |||||||
| chr11:76392401 | G | T | 44 | a0001c0001t0001g0110 a0001c0001t0003g0051 a0001c0001t0003g0054 others(41): Show |
73 | HG00323.hp2 HG00544.hp1 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.465+10108G>T | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76392401 | |||||||
| chr11:76392441 | T | C | 2 | a0001c0001t0009g0049 a0001c0001t0009g0050 |
2 | HG02451.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.465+10148T>C | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76392441 | |||||||
| chr11:76392453 | G | T | 3 | a0001c0001t0001g0096 a0001c0001t0001g0104 a0001c0001t0003g0103 |
3 | HG01255.hp1 HG01515.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.465+10160G>T | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76392453 | |||||||
| chr11:76392519 | G | C | 1 | a0001c0001t0001g0037 | 2 | HG01346.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.465+10226G>C | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76392519 | |||||||
| chr11:76392522 | C | T | 2 | a0001c0001t0028g0025 a0001c0001t0029g0025 |
2 | HG02922.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.465+10229C>T | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76392522 | |||||||
| chr11:76392818 | T | C | 3 | a0001c0001t0028g0025 a0001c0001t0029g0025 a0001c0001t0030g0044 |
3 | HG02922.hp2 HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.465+10525T>C | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76392818 | |||||||
| chr11:76392971 | T | G | 1 | a0001c0001t0002g0134 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.465+10678T>G | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76392971 | |||||||
| chr11:76393041 | C | T | 60 | a0001c0001t0001g0110 a0001c0001t0003g0051 a0001c0001t0003g0054 others(57): Show |
95 | HG00323.hp2 HG00544.hp1 HG00597.hp1 others(92): Show |
intron_variant | MODIFIER | c.466-10619C>T | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76393041 | |||||||
| chr11:76393043 | C | T | 1 | a0001c0001t0001g0102 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.466-10617C>T | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76393043 | |||||||
| chr11:76393284 | C | T | 1 | a0001c0001t0002g0119 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.466-10376C>T | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76393284 | |||||||
| chr11:76393312 | A | T | 85 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(82): Show |
149 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(146): Show |
intron_variant | MODIFIER | c.466-10348A>T | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76393312 | |||||||
| chr11:76393475 | T | C | 52 | a0001c0001t0001g0118 a0001c0001t0002g0001 a0001c0001t0002g0005 others(49): Show |
102 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.466-10185T>C | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76393475 | |||||||
| chr11:76393597 | C | A | 11 | a0001c0001t0007g0013 a0001c0001t0007g0026 a0001c0001t0007g0069 others(8): Show |
13 | HG00597.hp1 HG00673.hp2 NA18948.hp2 others(10): Show |
intron_variant | MODIFIER | c.466-10063C>A | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76393597 | |||||||
| chr11:76393781 | A | G | 5 | a0001c0001t0020g0027 a0001c0001t0059g0077 a0001c0002t0077g0163 others(2): Show |
6 | HG02630.hp2 HG02647.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.466-9879A>G | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76393781 | |||||||
| chr11:76393888 | G | GTTATTA | 3 | a0001c0001t0001g0023 a0001c0001t0001g0135 a0001c0001t0032g0105 |
5 | HG02559.hp2 NA18942.hp2 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.466-9751_466-9746d others(8): Show |
GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr11 | 76393888 | ||||||
| chr11:76393888 | GTTA | G | 58 | a0001c0001t0003g0054 a0001c0001t0005g0008 a0001c0001t0005g0018 others(55): Show |
92 | HG00323.hp2 HG00544.hp1 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.466-9748_466-9746d others(5): Show |
GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr11 | 76393888 | ||||||
| chr11:76393891 | A | G | 1 | a0001c0001t0003g0004 | 2 | HG00733.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.466-9769A>G | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76393891 | |||||||
| chr11:76394109 | G | A | 1 | a0001c0001t0003g0038 | 2 | HG00280.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.466-9551G>A | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76394109 | |||||||
| chr11:76394176 | G | A | 3 | a0001c0001t0028g0025 a0001c0001t0029g0025 a0001c0001t0030g0044 |
3 | HG02922.hp2 HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.466-9484G>A | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76394176 | |||||||
| chr11:76394187 | C | T | 4 | a0001c0001t0032g0105 a0001c0002t0073g0017 a0001c0002t0074g0017 others(1): Show |
4 | HG02559.hp2 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.466-9473C>T | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76394187 | |||||||
| chr11:76394620 | T | C | 1 | a0001c0001t0001g0097 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.466-9040T>C | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76394620 | |||||||
| chr11:76394694 | T | G | 53 | a0001c0001t0001g0118 a0001c0001t0002g0001 a0001c0001t0002g0005 others(50): Show |
104 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.466-8966T>G | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76394694 | |||||||
| chr11:76394724 | A | G | 6 | a0001c0001t0010g0011 a0001c0001t0010g0045 a0001c0001t0010g0151 others(3): Show |
10 | HG01261.hp1 HG01358.hp1 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.466-8936A>G | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76394724 | |||||||
| chr11:76394798 | A | G | 31 | a0001c0001t0003g0051 a0001c0001t0003g0054 a0001c0001t0005g0008 others(28): Show |
58 | HG00323.hp2 HG00544.hp1 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.466-8862A>G | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76394798 | |||||||
| chr11:76394815 | A | T | 3 | a0001c0001t0028g0025 a0001c0001t0029g0025 a0001c0001t0030g0044 |
3 | HG02922.hp2 HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.466-8845A>T | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76394815 | |||||||
| chr11:76394834 | T | C | 110 | a0001c0001t0001g0118 a0001c0001t0002g0001 a0001c0001t0002g0005 others(107): Show |
195 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(192): Show |
intron_variant | MODIFIER | c.466-8826T>C | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76394834 | |||||||
| chr11:76395052 | GA | G | 31 | a0001c0001t0003g0051 a0001c0001t0003g0054 a0001c0001t0005g0008 others(28): Show |
58 | HG00323.hp2 HG00544.hp1 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.466-8606delA | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr11 | 76395052 | ||||||
| chr11:76395306 | A | G | 3 | a0001c0001t0025g0142 a0001c0001t0025g0143 a0001c0001t0058g0078 |
3 | HG02257.hp2 HG03540.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.466-8354A>G | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76395306 | |||||||
| chr11:76395350 | A | G | 31 | a0001c0001t0003g0051 a0001c0001t0003g0054 a0001c0001t0005g0008 others(28): Show |
58 | HG00323.hp2 HG00544.hp1 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.466-8310A>G | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76395350 | |||||||
| chr11:76395765 | A | C | 1 | a0001c0001t0014g0089 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.466-7895A>C | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76395765 | |||||||
| chr11:76395931 | G | A | 3 | a0001c0001t0025g0142 a0001c0001t0025g0143 a0001c0001t0058g0078 |
3 | HG02257.hp2 HG03540.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.466-7729G>A | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76395931 | |||||||
| chr11:76396014 | A | G | 1 | a0001c0001t0001g0101 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.466-7646A>G | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76396014 | |||||||
| chr11:76396313 | A | T | 2 | a0001c0001t0001g0118 a0001c0001t0003g0100 |
2 | HG00741.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.466-7347A>T | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76396313 | |||||||
| chr11:76396400 | C | T | 87 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(84): Show |
151 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(148): Show |
intron_variant | MODIFIER | c.466-7260C>T | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76396400 | |||||||
| chr11:76396402 | C | T | 1 | a0001c0002t0080g0162 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.466-7258C>T | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76396402 | |||||||
| chr11:76396410 | G | C | 1 | a0001c0001t0001g0098 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.466-7250G>C | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76396410 | |||||||
| chr11:76396433 | GC | G | 18 | a0001c0001t0003g0140 a0001c0001t0007g0013 a0001c0001t0007g0026 others(15): Show |
24 | HG00597.hp1 HG00673.hp2 HG01261.hp1 others(21): Show |
intron_variant | MODIFIER | c.466-7222delC | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr11 | 76396433 | ||||||
| chr11:76396460 | G | T | 1 | a0001c0001t0001g0059 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.466-7200G>T | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76396460 | |||||||
| chr11:76396562 | ACCTTGGC others(3792): Show |
A | 1 | a0001c0001t0035g0085 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.466-7094_466-3296d others(2): Show |
GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr11 | 76396562 | ||||||
| chr11:76396608 | C | A | 105 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0022 others(102): Show |
190 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.466-7052C>A | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76396608 | |||||||
| chr11:76396664 | C | A | 1 | a0001c0001t0072g0003 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.466-6996C>A | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76396664 | |||||||
| chr11:76396676 | G | A | 1 | a0001c0001t0002g0001 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.466-6984G>A | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76396676 | |||||||
| chr11:76396714 | A | G | 1 | a0001c0001t0003g0100 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.466-6946A>G | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76396714 | |||||||
| chr11:76397002 | C | CT | 70 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(67): Show |
96 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.466-6638dupT | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr11 | 76397002 | ||||||
| chr11:76397002 | C | CTT | 39 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0015 others(36): Show |
70 | HG00408.hp1 HG00735.hp1 HG00738.hp1 others(67): Show |
intron_variant | MODIFIER | c.466-6639_466-6638d others(4): Show |
GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr11 | 76397002 | ||||||
| chr11:76397002 | CT | C | 14 | a0001c0001t0004g0010 a0001c0001t0005g0091 a0001c0001t0005g0129 others(11): Show |
18 | HG00323.hp2 HG00558.hp1 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.466-6638delT | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr11 | 76397002 | ||||||
| chr11:76397150 | C | T | 1 | a0001c0001t0002g0001 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.466-6510C>T | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76397150 | |||||||
| chr11:76397167 | C | A | 1 | a0001c0002t0079g0043 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.466-6493C>A | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76397167 | |||||||
| chr11:76397292 | A | T | 1 | a0001c0001t0003g0136 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.466-6368A>T | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76397292 | |||||||
| chr11:76397295 | C | T | 1 | a0001c0001t0003g0136 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.466-6365C>T | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76397295 | |||||||
| chr11:76397298 | A | C | 1 | a0001c0001t0003g0136 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.466-6362A>C | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76397298 | |||||||
| chr11:76397299 | G | A | 1 | a0001c0001t0003g0136 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.466-6361G>A | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76397299 | |||||||
| chr11:76397311 | C | T | 1 | a0001c0001t0003g0136 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.466-6349C>T | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76397311 | |||||||
| chr11:76397313 | T | C | 1 | a0001c0001t0003g0136 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.466-6347T>C | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76397313 | |||||||
| chr11:76397316 | T | C | 1 | a0001c0001t0003g0136 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.466-6344T>C | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76397316 | |||||||
| chr11:76397318 | T | G | 1 | a0001c0001t0003g0136 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.466-6342T>G | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76397318 | |||||||
| chr11:76397319 | G | C | 1 | a0001c0001t0003g0136 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.466-6341G>C | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76397319 | |||||||
| chr11:76397324 | AATAACAT others(3): Show |
A | 52 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0022 others(49): Show |
103 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.466-6333_466-6324d others(12): Show |
GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr11 | 76397324 | ||||||
| chr11:76397338 | G | T | 1 | a0001c0001t0003g0136 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.466-6322G>T | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76397338 | |||||||
| chr11:76397630 | C | T | 1 | a0001c0001t0041g0095 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.466-6030C>T | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76397630 | |||||||
| chr11:76397752 | G | A | 89 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(86): Show |
153 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(150): Show |
intron_variant | MODIFIER | c.466-5908G>A | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76397752 | |||||||
| chr11:76397807 | G | T | 4 | a0001c0001t0032g0105 a0001c0002t0073g0017 a0001c0002t0074g0017 others(1): Show |
4 | HG02559.hp2 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.466-5853G>T | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76397807 | |||||||
| chr11:76397863 | A | G | 1 | a0001c0001t0007g0084 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.466-5797A>G | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76397863 | |||||||
| chr11:76397892 | T | C | 3 | a0001c0001t0001g0016 a0001c0001t0003g0004 a0001c0001t0003g0016 |
3 | HG01070.hp1 HG01071.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.466-5768T>C | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76397892 | |||||||
| chr11:76398134 | C | CA | 98 | a0001c0001t0001g0035 a0001c0001t0002g0001 a0001c0001t0002g0005 others(95): Show |
172 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.466-5510dupA | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr11 | 76398134 | ||||||
| chr11:76398134 | C | CAA | 8 | a0001c0001t0002g0081 a0001c0001t0002g0128 a0001c0001t0005g0018 others(5): Show |
8 | HG02818.hp1 HG02976.hp1 NA18939.hp2 others(5): Show |
intron_variant | MODIFIER | c.466-5511_466-5510d others(4): Show |
GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr11 | 76398134 | ||||||
| chr11:76398376 | A | G | 33 | a0001c0001t0005g0008 a0001c0001t0005g0018 a0001c0001t0005g0019 others(30): Show |
61 | HG00323.hp2 HG00544.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.466-5284A>G | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76398376 | |||||||
| chr11:76398469 | G | A | 1 | a0001c0001t0018g0001 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.466-5191G>A | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76398469 | |||||||
| chr11:76398478 | A | T | 1 | a0001c0001t0016g0007 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.466-5182A>T | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76398478 | |||||||
| chr11:76398506 | T | C | 52 | a0001c0001t0005g0008 a0001c0001t0005g0018 a0001c0001t0005g0019 others(49): Show |
86 | HG00323.hp2 HG00544.hp1 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.466-5154T>C | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76398506 | |||||||
| chr11:76398664 | T | A | 3 | a0001c0001t0020g0027 a0001c0001t0059g0077 a0001c0002t0077g0163 |
4 | HG02630.hp2 HG03130.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.466-4996T>A | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76398664 | |||||||
| chr11:76398930 | A | C | 1 | a0001c0001t0005g0008 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.466-4730A>C | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76398930 | |||||||
| chr11:76398949 | A | G | 1 | a0001c0001t0009g0046 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.466-4711A>G | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76398949 | |||||||
| chr11:76399094 | A | AATTGT | 5 | a0001c0001t0010g0011 a0001c0001t0010g0045 a0001c0001t0010g0151 others(2): Show |
8 | HG01261.hp1 HG01358.hp1 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.466-4552_466-4548d others(7): Show |
GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr11 | 76399094 | ||||||
| chr11:76399094 | A | AATTGTAT others(3): Show |
13 | a0001c0001t0007g0013 a0001c0001t0007g0026 a0001c0001t0007g0069 others(10): Show |
14 | HG00597.hp1 HG00673.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.466-4557_466-4548d others(12): Show |
GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr11 | 76399094 | ||||||
| chr11:76399108 | G | GTATTGTA others(8): Show |
1 | a0001c0001t0007g0013 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.466-4548_466-4547i others(17): Show |
GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr11 | 76399108 | ||||||
| chr11:76399108 | G | GTATTT | 2 | a0001c0001t0020g0027 a0001c0002t0077g0163 |
3 | HG03130.hp1 HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.466-4536_466-4532d others(7): Show |
GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr11 | 76399108 | ||||||
| chr11:76399113 | T | G | 99 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(96): Show |
166 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(163): Show |
intron_variant | MODIFIER | c.466-4547T>G | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76399113 | |||||||
| chr11:76399118 | T | G | 10 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0097 others(7): Show |
12 | HG01261.hp2 HG02129.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.466-4542T>G | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76399118 | |||||||
| chr11:76399129 | C | T | 19 | a0001c0001t0007g0013 a0001c0001t0007g0026 a0001c0001t0007g0069 others(16): Show |
26 | HG00597.hp1 HG00673.hp2 HG01261.hp1 others(23): Show |
intron_variant | MODIFIER | c.466-4531C>T | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76399129 | |||||||
| chr11:76399243 | G | A | 3 | a0001c0001t0010g0011 a0001c0001t0010g0151 a0001c0001t0064g0011 |
7 | HG01261.hp1 HG01358.hp1 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.466-4417G>A | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76399243 | |||||||
| chr11:76399285 | G | A | 51 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0022 others(48): Show |
102 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.466-4375G>A | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76399285 | |||||||
| chr11:76399290 | T | A | 17 | a0001c0001t0007g0013 a0001c0001t0007g0026 a0001c0001t0007g0069 others(14): Show |
23 | HG00597.hp1 HG00673.hp2 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.466-4370T>A | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76399290 | |||||||
| chr11:76399525 | T | A | 17 | a0001c0001t0007g0013 a0001c0001t0007g0026 a0001c0001t0007g0069 others(14): Show |
23 | HG00597.hp1 HG00673.hp2 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.466-4135T>A | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76399525 | |||||||
| chr11:76399647 | T | C | 1 | a0001c0001t0006g0007 | 3 | NA18955.hp1 NA18992.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.466-4013T>C | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76399647 | |||||||
| chr11:76399672 | G | A | 2 | a0001c0001t0001g0102 a0001c0001t0003g0002 |
3 | HG03017.hp1 HG03654.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.466-3988G>A | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76399672 | |||||||
| chr11:76399786 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.466-3874C>T | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76399786 | |||||||
| chr11:76399888 | T | G | 1 | a0001c0002t0078g0040 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.466-3772T>G | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76399888 | |||||||
| chr11:76399904 | T | C | 17 | a0001c0001t0007g0013 a0001c0001t0007g0026 a0001c0001t0007g0069 others(14): Show |
23 | HG00597.hp1 HG00673.hp2 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.466-3756T>C | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76399904 | |||||||
| chr11:76399994 | T | G | 1 | a0001c0001t0005g0019 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.466-3666T>G | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76399994 | |||||||
| chr11:76400006 | T | TAC | 25 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0015 others(22): Show |
32 | HG00099.hp2 HG00558.hp1 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.466-3611_466-3610d others(4): Show |
GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr11 | 76400006 | ||||||
| chr11:76400006 | T | TACAC | 28 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0098 others(25): Show |
34 | HG00408.hp1 HG00738.hp1 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.466-3613_466-3610d others(6): Show |
GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr11 | 76400006 | ||||||
| chr11:76400006 | T | TACACAC | 24 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(21): Show |
34 | HG00733.hp2 HG00741.hp1 HG01074.hp1 others(31): Show |
intron_variant | MODIFIER | c.466-3615_466-3610d others(8): Show |
GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr11 | 76400006 | ||||||
| chr11:76400006 | T | TACACACA others(1): Show |
19 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0021 others(16): Show |
26 | HG00280.hp2 HG01192.hp1 HG01255.hp2 others(23): Show |
intron_variant | MODIFIER | c.466-3617_466-3610d others(10): Show |
GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr11 | 76400006 | ||||||
| chr11:76400006 | T | TACACACA others(3): Show |
10 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0104 others(7): Show |
12 | HG01070.hp1 HG01071.hp2 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.466-3619_466-3610d others(12): Show |
GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr11 | 76400006 | ||||||
| chr11:76400006 | T | TACACACA others(5): Show |
6 | a0001c0001t0001g0099 a0001c0001t0001g0110 a0001c0001t0002g0134 others(3): Show |
7 | HG00738.hp2 HG01167.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.466-3621_466-3610d others(14): Show |
GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr11 | 76400006 | ||||||
| chr11:76400006 | TAC | T | 28 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0020 others(25): Show |
43 | HG00544.hp2 HG00597.hp2 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.466-3611_466-3610d others(4): Show |
GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr11 | 76400006 | ||||||
| chr11:76400006 | TACAC | T | 25 | a0001c0001t0001g0037 a0001c0001t0002g0005 a0001c0001t0002g0022 others(22): Show |
29 | HG00099.hp1 HG00438.hp2 HG01346.hp1 others(26): Show |
intron_variant | MODIFIER | c.466-3613_466-3610d others(6): Show |
GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr11 | 76400006 | ||||||
| chr11:76400006 | TACACAC | T | 11 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0002g0033 others(8): Show |
12 | HG00558.hp2 HG01109.hp1 HG01975.hp2 others(9): Show |
intron_variant | MODIFIER | c.466-3615_466-3610d others(8): Show |
GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr11 | 76400006 | ||||||
| chr11:76400006 | TACACACA others(1): Show |
T | 23 | a0001c0001t0003g0014 a0001c0001t0003g0120 a0001c0001t0006g0007 others(20): Show |
40 | HG00323.hp2 HG00544.hp1 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.466-3617_466-3610d others(10): Show |
GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr11 | 76400006 | ||||||
| chr11:76400006 | TACACACA others(7): Show |
T | 1 | a0001c0001t0002g0094 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.466-3623_466-3610d others(16): Show |
GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr11 | 76400006 | ||||||
| chr11:76400006 | TACACACA others(9): Show |
T | 1 | a0001c0001t0004g0072 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.466-3625_466-3610d others(18): Show |
GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr11 | 76400006 | ||||||
| chr11:76400038 | C | CACAT | 9 | a0001c0001t0001g0009 a0001c0001t0003g0009 a0001c0001t0003g0062 others(6): Show |
12 | HG00639.hp2 HG01074.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.466-3619_466-3618i others(6): Show |
GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr11 | 76400038 | ||||||
| chr11:76400112 | C | CT | 18 | a0001c0001t0001g0139 a0001c0001t0007g0013 a0001c0001t0007g0026 others(15): Show |
24 | HG00597.hp1 HG00673.hp2 HG01261.hp1 others(21): Show |
intron_variant | MODIFIER | c.466-3538dupT | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr11 | 76400112 | ||||||
| chr11:76400139 | T | G | 1 | a0001c0001t0048g0004 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.466-3521T>G | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76400139 | |||||||
| chr11:76400398 | G | A | 1 | a0001c0001t0002g0111 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.466-3262G>A | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76400398 | |||||||
| chr11:76400418 | TTTTG | T | 18 | a0001c0001t0007g0013 a0001c0001t0007g0026 a0001c0001t0007g0069 others(15): Show |
24 | HG00597.hp1 HG00673.hp2 HG01261.hp1 others(21): Show |
intron_variant | MODIFIER | c.466-3230_466-3227d others(6): Show |
GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr11 | 76400418 | ||||||
| chr11:76400434 | T | G | 3 | a0001c0001t0020g0027 a0001c0001t0059g0077 a0001c0002t0077g0163 |
4 | HG02630.hp2 HG03130.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.466-3226T>G | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76400434 | |||||||
| chr11:76400460 | G | A | 30 | a0001c0001t0005g0008 a0001c0001t0005g0018 a0001c0001t0005g0019 others(27): Show |
57 | HG00323.hp2 HG00544.hp1 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.466-3200G>A | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76400460 | |||||||
| chr11:76400639 | T | C | 106 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0022 others(103): Show |
191 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.466-3021T>C | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76400639 | |||||||
| chr11:76400643 | C | T | 32 | a0001c0001t0005g0008 a0001c0001t0005g0018 a0001c0001t0005g0019 others(29): Show |
59 | HG00323.hp2 HG00544.hp1 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.466-3017C>T | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76400643 | |||||||
| chr11:76400645 | C | T | 18 | a0001c0001t0007g0013 a0001c0001t0007g0026 a0001c0001t0007g0069 others(15): Show |
24 | HG00597.hp1 HG00673.hp2 HG01261.hp1 others(21): Show |
intron_variant | MODIFIER | c.466-3015C>T | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76400645 | |||||||
| chr11:76400662 | C | G | 1 | a0001c0001t0020g0027 | 2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.466-2998C>G | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76400662 | |||||||
| chr11:76400715 | C | T | 1 | a0001c0001t0003g0051 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.466-2945C>T | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76400715 | |||||||
| chr11:76400770 | CT | C | 2 | a0001c0001t0001g0028 a0001c0001t0001g0097 |
3 | HG02559.hp1 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.466-2885delT | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr11 | 76400770 | ||||||
| chr11:76400803 | C | T | 1 | a0001c0001t0035g0085 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.466-2857C>T | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76400803 | |||||||
| chr11:76400848 | C | T | 1 | a0001c0001t0001g0154 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.466-2812C>T | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76400848 | |||||||
| chr11:76400885 | C | G | 1 | a0001c0001t0009g0050 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.466-2775C>G | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76400885 | |||||||
| chr11:76401039 | A | AT | 16 | a0001c0001t0006g0007 a0001c0001t0006g0034 a0001c0001t0009g0109 others(13): Show |
33 | HG00323.hp2 HG00544.hp1 HG01975.hp1 others(30): Show |
intron_variant | MODIFIER | c.466-2620dupT | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr11 | 76401039 | ||||||
| chr11:76401039 | A | T | 20 | a0001c0001t0005g0008 a0001c0001t0005g0018 a0001c0001t0005g0019 others(17): Show |
32 | HG00609.hp1 HG01106.hp1 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.466-2621A>T | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76401039 | |||||||
| chr11:76401041 | A | T | 171 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(168): Show |
314 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(311): Show |
intron_variant | MODIFIER | c.466-2619A>T | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76401041 | |||||||
| chr11:76401103 | G | A | 1 | a0001c0001t0062g0047 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.466-2557G>A | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76401103 | |||||||
| chr11:76401179 | C | T | 17 | a0001c0001t0007g0013 a0001c0001t0007g0026 a0001c0001t0007g0069 others(14): Show |
23 | HG00597.hp1 HG00673.hp2 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.466-2481C>T | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76401179 | |||||||
| chr11:76401283 | C | T | 1 | a0001c0001t0035g0085 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.466-2377C>T | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76401283 | |||||||
| chr11:76401408 | T | C | 1 | a0001c0001t0062g0047 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.466-2252T>C | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76401408 | |||||||
| chr11:76401495 | C | T | 1 | a0001c0001t0083g0058 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.466-2165C>T | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76401495 | |||||||
| chr11:76401500 | G | A | 1 | a0001c0001t0035g0085 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.466-2160G>A | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76401500 | |||||||
| chr11:76401512 | G | A | 2 | a0001c0001t0002g0113 a0001c0001t0002g0127 |
2 | HG02523.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.466-2148G>A | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76401512 | |||||||
| chr11:76401668 | G | T | 46 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0022 others(43): Show |
96 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.466-1992G>T | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76401668 | |||||||
| chr11:76401761 | G | A | 1 | a0001c0001t0003g0120 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.466-1899G>A | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76401761 | |||||||
| chr11:76401773 | C | CA | 70 | a0001c0001t0001g0020 a0001c0001t0001g0029 a0001c0001t0001g0135 others(67): Show |
129 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.466-1869dupA | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr11 | 76401773 | ||||||
| chr11:76401773 | C | CAA | 29 | a0001c0001t0002g0106 a0001c0001t0002g0114 a0001c0001t0002g0123 others(26): Show |
54 | HG00544.hp1 HG00609.hp1 HG00673.hp1 others(51): Show |
intron_variant | MODIFIER | c.466-1870_466-1869d others(4): Show |
GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr11 | 76401773 | ||||||
| chr11:76401773 | C | CAAA | 6 | a0001c0001t0005g0018 a0001c0001t0005g0024 a0001c0001t0005g0090 others(3): Show |
8 | HG02155.hp2 HG02717.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.466-1871_466-1869d others(5): Show |
GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr11 | 76401773 | ||||||
| chr11:76401773 | CA | C | 5 | a0001c0001t0001g0016 a0001c0001t0001g0139 a0001c0001t0003g0016 others(2): Show |
7 | HG01070.hp1 HG01070.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.466-1869delA | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr11 | 76401773 | ||||||
| chr11:76401829 | G | A | 1 | a0001c0001t0002g0055 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.466-1831G>A | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76401829 | |||||||
| chr11:76401912 | C | T | 3 | a0001c0001t0025g0142 a0001c0001t0025g0143 a0001c0001t0058g0078 |
3 | HG02257.hp2 HG03540.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.466-1748C>T | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76401912 | |||||||
| chr11:76401918 | A | T | 1 | a0001c0001t0061g0065 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.466-1742A>T | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76401918 | |||||||
| chr11:76401972 | G | T | 1 | a0001c0001t0026g0030 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.466-1688G>T | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76401972 | |||||||
| chr11:76402107 | C | A | 1 | a0001c0001t0025g0142 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.466-1553C>A | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76402107 | |||||||
| chr11:76402140 | G | A | 1 | a0001c0001t0007g0087 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.466-1520G>A | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76402140 | |||||||
| chr11:76402178 | C | T | 1 | a0001c0001t0002g0164 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.466-1482C>T | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76402178 | |||||||
| chr11:76402369 | A | G | 1 | a0001c0001t0007g0083 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.466-1291A>G | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76402369 | |||||||
| chr11:76402411 | G | C | 1 | a0001c0001t0003g0136 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.466-1249G>C | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76402411 | |||||||
| chr11:76402552 | C | CA | 10 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0002g0081 others(7): Show |
10 | HG00642.hp2 HG01167.hp1 HG01515.hp2 others(7): Show |
intron_variant | MODIFIER | c.466-1094dupA | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr11 | 76402552 | ||||||
| chr11:76402552 | C | CAA | 43 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0022 others(40): Show |
93 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.466-1095_466-1094d others(4): Show |
GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr11 | 76402552 | ||||||
| chr11:76402619 | G | A | 17 | a0001c0001t0007g0013 a0001c0001t0007g0026 a0001c0001t0007g0069 others(14): Show |
23 | HG00597.hp1 HG00673.hp2 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.466-1041G>A | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76402619 | |||||||
| chr11:76402851 | A | G | 51 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0022 others(48): Show |
102 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.466-809A>G | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76402851 | |||||||
| chr11:76402941 | T | A | 30 | a0001c0001t0005g0008 a0001c0001t0005g0018 a0001c0001t0005g0019 others(27): Show |
57 | HG00323.hp2 HG00544.hp1 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.466-719T>A | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76402941 | |||||||
| chr11:76402959 | TA | T | 37 | a0001c0001t0002g0001 a0001c0001t0002g0022 a0001c0001t0002g0032 others(34): Show |
78 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(75): Show |
intron_variant | MODIFIER | c.466-700delA | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76402959 | |||||||
| chr11:76402977 | T | G | 37 | a0001c0001t0002g0001 a0001c0001t0002g0022 a0001c0001t0002g0032 others(34): Show |
78 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(75): Show |
intron_variant | MODIFIER | c.466-683T>G | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76402977 | |||||||
| chr11:76402991 | A | T | 4 | a0001c0001t0002g0036 a0001c0001t0002g0116 a0001c0001t0002g0121 others(1): Show |
4 | NA18970.hp1 NA18987.hp1 NA19086.hp1 others(1): Show |
intron_variant | MODIFIER | c.466-669A>T | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76402991 | |||||||
| chr11:76403009 | G | A | 1 | a0001c0002t0079g0043 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.466-651G>A | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76403009 | |||||||
| chr11:76403092 | G | T | 202 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(199): Show |
351 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(348): Show |
intron_variant | MODIFIER | c.466-568G>T | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76403092 | |||||||
| chr11:76403096 | C | T | 1 | a0001c0001t0001g0155 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.466-564C>T | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76403096 | |||||||
| chr11:76403189 | G | A | 1 | a0001c0001t0001g0138 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.466-471G>A | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76403189 | |||||||
| chr11:76403239 | C | T | 1 | a0001c0001t0002g0115 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.466-421C>T | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76403239 | |||||||
| chr11:76403242 | G | A | 51 | a0001c0001t0001g0145 a0001c0001t0005g0008 a0001c0001t0005g0018 others(48): Show |
84 | HG00323.hp2 HG00544.hp1 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.466-418G>A | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76403242 | |||||||
| chr11:76403279 | G | T | 32 | a0001c0001t0005g0008 a0001c0001t0005g0018 a0001c0001t0005g0019 others(29): Show |
59 | HG00323.hp2 HG00544.hp1 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.466-381G>T | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76403279 | |||||||
| chr11:76403306 | G | C | 1 | a0001c0001t0035g0085 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.466-354G>C | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76403306 | |||||||
| chr11:76403334 | C | T | 54 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0022 others(51): Show |
105 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.466-326C>T | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76403334 | |||||||
| chr11:76403335 | G | A | 1 | a0001c0001t0009g0109 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.466-325G>A | GVQW3 | ENSG00000179240.13 | transcript | ENST00000529331.2 | protein_coding | 1/1 | chr11 | 76403335 |