Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 79805 |
| ensemblid | ENSG00000143494.16 |
| hgncid | 25723 |
| symbol | VASH2 |
| name | vasohibin 2 |
| refseq_nuc | NM_001301056.2 |
| refseq_prot | NP_001287985.1 |
| ensembl_nuc | ENST00000517399.3 |
| ensembl_prot | ENSP00000428324.1 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 212950541 |
| end | 212991585 |
| strand | + |
| ver | v1.2 |
| region | chr1:212950541-212991585 |
| region5000 | chr1:212945541-212996585 |
| regionname0 | VASH2_chr1_212950541_212991585 |
| regionname5000 | VASH2_chr1_212945541_212996585 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 355 | 371 | 96 | 59 | 172 | 14 | 28 | 134 | VASH2_chr1_212945541_212996585 | VASH2 | MTGSA others(350): Show |
chr1 | 212945541 | 212996585 |
| a0002 | 0/0 | 355 | 4 | 0 | 2 | 0 | 0 | 2 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | MTGSA others(350): Show |
chr1 | 212945541 | 212996585 |
| a0003 | 0/0 | 355 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | MTGSA others(350): Show |
chr1 | 212945541 | 212996585 |
| a0004 | 0/0 | 355 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | MTGSA others(350): Show |
chr1 | 212945541 | 212996585 |
| a0005 | 0/0 | 355 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | MTGSA others(350): Show |
chr1 | 212945541 | 212996585 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1065 | 368 | 95 | 59 | 170 | 14 | 28 | VASH2_chr1_212945541_212996585 | VASH2 | ATGAC others(1060): Show |
chr1 | 212945541 | 212996585 | ||
| a0001c0005 | 0/0 | 1065 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | ATGAC others(1060): Show |
chr1 | 212945541 | 212996585 | ||
| a0001c0006 | 0/0 | 1065 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | ATGAC others(1060): Show |
chr1 | 212945541 | 212996585 | ||
| a0001c0008 | 0/0 | 1065 | 1 | 1 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | ATGAC others(1060): Show |
chr1 | 212945541 | 212996585 | ||
| a0002c0002 | 0/0 | 1065 | 4 | 0 | 2 | 0 | 0 | 2 | VASH2_chr1_212945541_212996585 | VASH2 | ATGAC others(1060): Show |
chr1 | 212945541 | 212996585 | ||
| a0003c0007 | 0/0 | 1065 | 1 | 0 | 1 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | ATGAC others(1060): Show |
chr1 | 212945541 | 212996585 | ||
| a0004c0003 | 0/0 | 1065 | 1 | 0 | 1 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | ATGAC others(1060): Show |
chr1 | 212945541 | 212996585 | ||
| a0005c0004 | 0/0 | 1065 | 1 | 0 | 1 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | ATGAC others(1060): Show |
chr1 | 212945541 | 212996585 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 4477 | 85 | 2 | 18 | 53 | 4 | 7 | VASH2_chr1_212945541_212996585 | VASH2 | ATTCG others(4472): Show |
chr1 | 212945541 | 212996585 |
| a0001c0001t0002 | 0/0 | 4477 | 66 | 1 | 6 | 45 | 5 | 9 | VASH2_chr1_212945541_212996585 | VASH2 | ATTCG others(4472): Show |
chr1 | 212945541 | 212996585 |
| a0001c0001t0003 | 0/0 | 4477 | 60 | 33 | 9 | 18 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | ATTCG others(4472): Show |
chr1 | 212945541 | 212996585 |
| a0001c0001t0004 | 0/0 | 4477 | 37 | 1 | 10 | 18 | 2 | 6 | VASH2_chr1_212945541_212996585 | VASH2 | ATTCG others(4472): Show |
chr1 | 212945541 | 212996585 |
| a0001c0001t0005 | 0/0 | 4477 | 10 | 9 | 1 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | ATTCG others(4472): Show |
chr1 | 212945541 | 212996585 |
| a0001c0001t0006 | 0/0 | 4477 | 7 | 0 | 2 | 3 | 2 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | ATTCG others(4472): Show |
chr1 | 212945541 | 212996585 |
| a0001c0001t0007 | 0/0 | 4477 | 8 | 3 | 1 | 3 | 0 | 1 | VASH2_chr1_212945541_212996585 | VASH2 | ATTCG others(4472): Show |
chr1 | 212945541 | 212996585 |
| a0001c0001t0008 | 1/0 | 4473 | 7 | 6 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | ATTCG others(4468): Show |
chr1 | 212945541 | 212996585 |
| a0001c0001t0009 | 0/0 | 4477 | 7 | 7 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | ATTCG others(4472): Show |
chr1 | 212945541 | 212996585 |
| a0001c0001t0010 | 0/0 | 4477 | 4 | 4 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | ATTCG others(4472): Show |
chr1 | 212945541 | 212996585 |
| a0001c0001t0011 | 0/0 | 4477 | 4 | 0 | 0 | 4 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | ATTCG others(4472): Show |
chr1 | 212945541 | 212996585 |
| a0001c0001t0012 | 0/0 | 4477 | 4 | 0 | 0 | 4 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | ATTCG others(4472): Show |
chr1 | 212945541 | 212996585 |
| a0001c0001t0013 | 0/0 | 4477 | 4 | 4 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | ATTCG others(4472): Show |
chr1 | 212945541 | 212996585 |
| a0001c0001t0014 | 0/0 | 4476 | 3 | 0 | 1 | 2 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | ATTCG others(4471): Show |
chr1 | 212945541 | 212996585 |
| a0001c0001t0015 | 0/0 | 4477 | 3 | 0 | 0 | 3 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | ATTCG others(4472): Show |
chr1 | 212945541 | 212996585 |
| a0001c0001t0016 | 0/0 | 4477 | 3 | 0 | 0 | 3 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | ATTCG others(4472): Show |
chr1 | 212945541 | 212996585 |
| a0001c0001t0017 | 0/0 | 4477 | 3 | 3 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | ATTCG others(4472): Show |
chr1 | 212945541 | 212996585 |
| a0001c0001t0018 | 0/0 | 4477 | 3 | 0 | 3 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | ATTCG others(4472): Show |
chr1 | 212945541 | 212996585 |
| a0001c0001t0019 | 0/0 | 4477 | 2 | 1 | 1 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | ATTCG others(4472): Show |
chr1 | 212945541 | 212996585 |
| a0001c0001t0020 | 0/0 | 4477 | 2 | 0 | 0 | 2 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | ATTCG others(4472): Show |
chr1 | 212945541 | 212996585 |
| a0001c0001t0021 | 0/0 | 4477 | 2 | 0 | 0 | 2 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | ATTCG others(4472): Show |
chr1 | 212945541 | 212996585 |
| a0001c0001t0022 | 0/0 | 4477 | 2 | 2 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | ATTCG others(4472): Show |
chr1 | 212945541 | 212996585 |
| a0001c0001t0023 | 0/0 | 4476 | 2 | 1 | 0 | 0 | 0 | 1 | VASH2_chr1_212945541_212996585 | VASH2 | ATTCG others(4471): Show |
chr1 | 212945541 | 212996585 |
| a0001c0001t0024 | 0/0 | 4477 | 2 | 0 | 0 | 0 | 1 | 1 | VASH2_chr1_212945541_212996585 | VASH2 | ATTCG others(4472): Show |
chr1 | 212945541 | 212996585 |
| a0001c0001t0025 | 0/0 | 4477 | 2 | 0 | 2 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | ATTCG others(4472): Show |
chr1 | 212945541 | 212996585 |
| a0001c0001t0026 | 0/0 | 4476 | 2 | 0 | 0 | 2 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | ATTCG others(4471): Show |
chr1 | 212945541 | 212996585 |
| a0001c0001t0027 | 0/0 | 4477 | 2 | 2 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | ATTCG others(4472): Show |
chr1 | 212945541 | 212996585 |
| a0001c0001t0028 | 0/0 | 4477 | 2 | 0 | 0 | 2 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | ATTCG others(4472): Show |
chr1 | 212945541 | 212996585 |
| a0001c0001t0029 | 0/0 | 4477 | 2 | 1 | 0 | 0 | 0 | 1 | VASH2_chr1_212945541_212996585 | VASH2 | ATTCG others(4472): Show |
chr1 | 212945541 | 212996585 |
| a0001c0001t0031 | 0/0 | 4477 | 2 | 2 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | ATTCG others(4472): Show |
chr1 | 212945541 | 212996585 |
| a0001c0001t0032 | 0/0 | 4477 | 2 | 2 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | ATTCG others(4472): Show |
chr1 | 212945541 | 212996585 |
| a0001c0001t0033 | 0/0 | 4477 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | ATTCG others(4472): Show |
chr1 | 212945541 | 212996585 |
| a0001c0001t0034 | 0/0 | 4477 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | ATTCG others(4472): Show |
chr1 | 212945541 | 212996585 |
| a0001c0001t0035 | 0/0 | 4477 | 1 | 0 | 1 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | ATTCG others(4472): Show |
chr1 | 212945541 | 212996585 |
| a0001c0001t0036 | 0/0 | 4445 | 1 | 0 | 0 | 0 | 0 | 1 | VASH2_chr1_212945541_212996585 | VASH2 | ATTCG others(4440): Show |
chr1 | 212945541 | 212996585 |
| a0001c0001t0037 | 0/0 | 4477 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | ATTCG others(4472): Show |
chr1 | 212945541 | 212996585 |
| a0001c0001t0038 | 0/0 | 4477 | 1 | 1 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | ATTCG others(4472): Show |
chr1 | 212945541 | 212996585 |
| a0001c0001t0039 | 0/0 | 4477 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | ATTCG others(4472): Show |
chr1 | 212945541 | 212996585 |
| a0001c0001t0040 | 0/0 | 4477 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | ATTCG others(4472): Show |
chr1 | 212945541 | 212996585 |
| a0001c0001t0041 | 0/0 | 4476 | 1 | 0 | 1 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | ATTCG others(4471): Show |
chr1 | 212945541 | 212996585 |
| a0001c0001t0042 | 0/0 | 4477 | 1 | 0 | 1 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | ATTCG others(4472): Show |
chr1 | 212945541 | 212996585 |
| a0001c0001t0043 | 0/0 | 4476 | 1 | 0 | 1 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | ATTCG others(4471): Show |
chr1 | 212945541 | 212996585 |
| a0001c0001t0044 | 0/0 | 4477 | 1 | 1 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | ATTCG others(4472): Show |
chr1 | 212945541 | 212996585 |
| a0001c0001t0045 | 0/0 | 4477 | 1 | 1 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | ATTCG others(4472): Show |
chr1 | 212945541 | 212996585 |
| a0001c0001t0046 | 0/0 | 4476 | 1 | 1 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | ATTCG others(4471): Show |
chr1 | 212945541 | 212996585 |
| a0001c0001t0047 | 0/0 | 4476 | 1 | 1 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | ATTCG others(4471): Show |
chr1 | 212945541 | 212996585 |
| a0001c0001t0048 | 0/0 | 4477 | 1 | 1 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | ATTCG others(4472): Show |
chr1 | 212945541 | 212996585 |
| a0001c0001t0049 | 0/0 | 4477 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | ATTCG others(4472): Show |
chr1 | 212945541 | 212996585 |
| a0001c0001t0050 | 0/0 | 4477 | 1 | 1 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | ATTCG others(4472): Show |
chr1 | 212945541 | 212996585 |
| a0001c0001t0051 | 0/0 | 4477 | 1 | 0 | 1 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | ATTCG others(4472): Show |
chr1 | 212945541 | 212996585 |
| a0001c0001t0052 | 0/0 | 4473 | 1 | 1 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | ATTCG others(4468): Show |
chr1 | 212945541 | 212996585 |
| a0001c0001t0053 | 0/0 | 4477 | 1 | 0 | 0 | 0 | 0 | 1 | VASH2_chr1_212945541_212996585 | VASH2 | ATTCG others(4472): Show |
chr1 | 212945541 | 212996585 |
| a0001c0001t0054 | 0/0 | 4477 | 1 | 1 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | ATTCG others(4472): Show |
chr1 | 212945541 | 212996585 |
| a0001c0001t0055 | 0/0 | 4477 | 1 | 1 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | ATTCG others(4472): Show |
chr1 | 212945541 | 212996585 |
| a0001c0001t0056 | 0/0 | 4477 | 1 | 1 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | ATTCG others(4472): Show |
chr1 | 212945541 | 212996585 |
| a0001c0005t0001 | 0/0 | 4477 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | ATTCG others(4472): Show |
chr1 | 212945541 | 212996585 |
| a0001c0006t0002 | 0/0 | 4477 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | ATTCG others(4472): Show |
chr1 | 212945541 | 212996585 |
| a0001c0008t0003 | 0/0 | 4477 | 1 | 1 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | ATTCG others(4472): Show |
chr1 | 212945541 | 212996585 |
| a0002c0002t0005 | 0/0 | 4477 | 2 | 0 | 0 | 0 | 0 | 2 | VASH2_chr1_212945541_212996585 | VASH2 | ATTCG others(4472): Show |
chr1 | 212945541 | 212996585 |
| a0002c0002t0030 | 0/0 | 4476 | 2 | 0 | 2 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | ATTCG others(4471): Show |
chr1 | 212945541 | 212996585 |
| a0003c0007t0001 | 0/0 | 4477 | 1 | 0 | 1 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | ATTCG others(4472): Show |
chr1 | 212945541 | 212996585 |
| a0004c0003t0006 | 0/0 | 4477 | 1 | 0 | 1 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | ATTCG others(4472): Show |
chr1 | 212945541 | 212996585 |
| a0005c0004t0005 | 0/0 | 4477 | 1 | 0 | 1 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | ATTCG others(4472): Show |
chr1 | 212945541 | 212996585 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 9 | 1 | 0 | 8 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0001g0004 | 0/0 | 8 | 0 | 2 | 6 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0001g0006 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0001g0007 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0001g0008 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 0 | 3 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0001g0179 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0002g0001 | 0/0 | 10 | 0 | 0 | 6 | 0 | 4 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0002g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0002g0011 | 0/0 | 3 | 0 | 0 | 0 | 3 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0002g0012 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0002g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0002g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0002g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0003g0003 | 0/0 | 9 | 0 | 2 | 7 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0003g0010 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0003g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0003g0016 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0003g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0003g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0003g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0003g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0003g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0003g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0003g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0003g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0003g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0003g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0003g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0003g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0003g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0003g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0003g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0003g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0003g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0003g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0003g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0003g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0003g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0003g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0003g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0003g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0003g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0003g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0003g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0003g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0003g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0004g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0004g0026 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0004g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0004g0028 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0004g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0004g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0004g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0004g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0004g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0004g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0004g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0004g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0004g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0004g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0004g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0004g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0004g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0004g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0004g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0004g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0004g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0004g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0004g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0004g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0004g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0004g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0004g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0004g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0004g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0004g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0004g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0005g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0005g0040 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0005g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0005g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0005g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0005g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0005g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0005g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0006g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0006g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0006g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0006g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0006g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0006g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0007g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0007g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0007g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0007g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0007g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0007g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0007g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0007g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0008g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0008g0162 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0008g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0008g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0008g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0008g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0009g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0009g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0009g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0009g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0009g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0009g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0009g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0010g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0010g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0010g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0010g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0011g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0012g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0012g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0012g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0012g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0013g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0013g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0014g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0014g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0015g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0015g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0016g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0016g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0016g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0017g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0017g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0017g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0018g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0018g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0018g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0019g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0019g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0020g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0020g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0021g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0022g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0022g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0023g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0023g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0024g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0024g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0025g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0025g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0026g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0026g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0027g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0027g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0028g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0028g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0029g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0029g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0031g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0031g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0032g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0033g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0034g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0035g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0036g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0037g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0038g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0039g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0040g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0041g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0042g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0043g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0044g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0045g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0046g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0047g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0048g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0049g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0050g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0051g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0052g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0053g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0054g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0055g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0001t0056g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0005t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0006t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0001c0008t0003g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0002c0002t0005g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0002c0002t0005g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0002c0002t0030g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0003c0007t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0004c0003t0006g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| a0005c0004t0005g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0006 | g0056 | EUR | GBR | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG00099 | hp2 | a0001 | c0001 | t0004 | g0153 | EUR | GBR | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0068 | EUR | GBR | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0009 | EUR | GBR | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG00323 | hp1 | a0001 | c0001 | t0024 | g0076 | EUR | FIN | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0011 | EUR | FIN | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | CHS | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG00408 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | CHS | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG00423 | hp1 | a0001 | c0001 | t0012 | g0094 | EAS | CHS | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | CHS | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG00438 | hp1 | a0001 | c0001 | t0004 | g0028 | EAS | CHS | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG00438 | hp2 | a0001 | c0001 | t0004 | g0026 | EAS | CHS | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0117 | EAS | CHS | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | CHS | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG00558 | hp2 | a0001 | c0001 | t0033 | g0267 | EAS | CHS | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0221 | EAS | CHS | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG00597 | hp2 | a0001 | c0001 | t0007 | g0092 | EAS | CHS | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG00609 | hp1 | a0001 | c0001 | t0003 | g0218 | EAS | CHS | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG00609 | hp2 | a0001 | c0001 | t0004 | g0033 | EAS | CHS | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG00621 | hp1 | a0001 | c0001 | t0021 | g0045 | EAS | CHS | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | CHS | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG00639 | hp1 | a0001 | c0001 | t0004 | g0026 | AMR | PUR | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0234 | AMR | PUR | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG00642 | hp1 | a0003 | c0007 | t0001 | g0009 | AMR | PUR | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0275 | AMR | PUR | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG00738 | hp1 | a0001 | c0001 | t0042 | g0167 | AMR | PUR | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0022 | AMR | PUR | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG00741 | hp1 | a0001 | c0001 | t0019 | g0188 | AMR | PUR | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0022 | AMR | PUR | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG01069 | hp1 | a0001 | c0001 | t0014 | g0266 | AMR | PUR | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG01069 | hp2 | a0001 | c0001 | t0025 | g0125 | AMR | PUR | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG01070 | hp1 | a0001 | c0001 | t0004 | g0027 | AMR | PUR | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG01070 | hp2 | a0002 | c0002 | t0030 | g0041 | AMR | PUR | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG01071 | hp1 | a0002 | c0002 | t0030 | g0041 | AMR | PUR | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG01071 | hp2 | a0001 | c0001 | t0025 | g0124 | AMR | PUR | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG01074 | hp2 | a0001 | c0001 | t0043 | g0190 | AMR | PUR | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG01081 | hp1 | a0001 | c0001 | t0006 | g0018 | AMR | PUR | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG01099 | hp1 | a0004 | c0003 | t0006 | g0119 | AMR | PUR | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG01099 | hp2 | a0001 | c0001 | t0006 | g0018 | AMR | PUR | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG01109 | hp1 | a0001 | c0001 | t0051 | g0256 | AMR | PUR | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG01109 | hp2 | a0001 | c0001 | t0005 | g0040 | AMR | PUR | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | PUR | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG01167 | hp2 | a0005 | c0004 | t0005 | g0253 | AMR | PUR | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG01175 | hp1 | a0001 | c0001 | t0004 | g0132 | AMR | PUR | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0183 | AMR | PUR | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0010 | AMR | PUR | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG01243 | hp2 | a0001 | c0001 | t0035 | g0070 | AMR | PUR | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG01257 | hp1 | a0001 | c0001 | t0004 | g0168 | AMR | CLM | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG01258 | hp1 | a0001 | c0001 | t0007 | g0107 | AMR | CLM | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | CLM | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG01346 | hp1 | a0001 | c0001 | t0004 | g0165 | AMR | CLM | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG01358 | hp2 | a0001 | c0001 | t0003 | g0016 | AMR | CLM | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG01433 | hp1 | a0001 | c0001 | t0004 | g0166 | AMR | CLM | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG01496 | hp1 | a0001 | c0001 | t0041 | g0121 | AMR | CLM | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG01496 | hp2 | a0001 | c0001 | t0004 | g0027 | AMR | CLM | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG01515 | hp1 | a0001 | c0001 | t0004 | g0193 | EUR | IBS | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0009 | EUR | IBS | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0030 | EUR | IBS | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0011 | EUR | IBS | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | IBS | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0011 | EUR | IBS | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG01884 | hp1 | a0001 | c0001 | t0009 | g0139 | AFR | ACB | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG01884 | hp2 | a0001 | c0001 | t0005 | g0238 | AFR | ACB | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG01891 | hp1 | a0001 | c0001 | t0052 | g0242 | AFR | ACB | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0137 | AFR | ACB | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PEL | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG01943 | hp2 | a0001 | c0001 | t0004 | g0194 | AMR | PEL | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG01952 | hp2 | a0001 | c0001 | t0003 | g0016 | AMR | PEL | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | PEL | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG01981 | hp1 | a0001 | c0001 | t0004 | g0172 | AMR | PEL | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG01981 | hp2 | a0001 | c0001 | t0018 | g0152 | AMR | PEL | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG01993 | hp1 | a0001 | c0001 | t0018 | g0058 | AMR | PEL | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG02004 | hp1 | a0001 | c0001 | t0004 | g0148 | AMR | PEL | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG02004 | hp2 | a0001 | c0001 | t0003 | g0231 | AMR | PEL | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG02040 | hp1 | a0001 | c0001 | t0015 | g0036 | EAS | KHV | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0147 | AFR | ACB | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG02055 | hp2 | a0001 | c0001 | t0009 | g0049 | AFR | ACB | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG02056 | hp1 | a0001 | c0001 | t0015 | g0036 | EAS | KHV | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | KHV | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | KHV | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | KHV | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | KHV | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | KHV | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG02080 | hp2 | a0001 | c0001 | t0003 | g0016 | EAS | KHV | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0219 | EAS | KHV | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | KHV | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG02129 | hp1 | a0001 | c0001 | t0026 | g0226 | EAS | KHV | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG02129 | hp2 | a0001 | c0001 | t0012 | g0063 | EAS | KHV | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG02132 | hp1 | a0001 | c0001 | t0004 | g0055 | EAS | KHV | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG02145 | hp1 | a0001 | c0001 | t0048 | g0118 | AFR | ACB | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG02145 | hp2 | a0001 | c0001 | t0017 | g0141 | AFR | ACB | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0102 | AMR | PEL | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG02165 | hp1 | a0001 | c0001 | t0004 | g0159 | EAS | CDX | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG02165 | hp2 | a0001 | c0001 | t0021 | g0045 | EAS | CDX | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0128 | AFR | ACB | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG02257 | hp2 | a0001 | c0001 | t0047 | g0035 | AFR | ACB | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG02258 | hp1 | a0001 | c0001 | t0005 | g0246 | AFR | ACB | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG02258 | hp2 | a0001 | c0001 | t0013 | g0017 | AFR | ACB | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PEL | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG02280 | hp1 | a0001 | c0001 | t0008 | g0043 | AFR | ACB | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG02280 | hp2 | a0001 | c0001 | t0013 | g0017 | AFR | ACB | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG02300 | hp1 | a0001 | c0001 | t0018 | g0059 | AMR | PEL | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG02451 | hp1 | a0001 | c0001 | t0027 | g0262 | AFR | ACB | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG02451 | hp2 | a0001 | c0001 | t0007 | g0086 | AFR | ACB | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG02523 | hp2 | a0001 | c0001 | t0004 | g0223 | EAS | KHV | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG02572 | hp1 | a0001 | c0001 | t0008 | g0170 | AFR | GWD | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG02572 | hp2 | a0001 | c0001 | t0010 | g0274 | AFR | GWD | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0012 | SAS | PJL | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0228 | SAS | PJL | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG02622 | hp1 | a0001 | c0001 | t0013 | g0017 | AFR | GWD | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG02622 | hp2 | a0001 | c0001 | t0010 | g0270 | AFR | GWD | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0140 | AFR | GWD | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG02630 | hp2 | a0001 | c0001 | t0005 | g0039 | AFR | GWD | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0212 | AFR | GWD | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG02647 | hp2 | a0001 | c0001 | t0009 | g0169 | AFR | GWD | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG02698 | hp1 | a0001 | c0001 | t0029 | g0248 | SAS | PJL | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG02698 | hp2 | a0001 | c0001 | t0004 | g0182 | SAS | PJL | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG02717 | hp1 | a0001 | c0001 | t0009 | g0263 | AFR | GWD | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG02717 | hp2 | a0001 | c0001 | t0019 | g0161 | AFR | GWD | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG02723 | hp1 | a0001 | c0001 | t0032 | g0042 | AFR | GWD | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0015 | AFR | GWD | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG02738 | hp1 | a0001 | c0001 | t0053 | g0244 | SAS | PJL | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG02738 | hp2 | a0001 | c0001 | t0004 | g0131 | SAS | PJL | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG02809 | hp1 | a0001 | c0001 | t0031 | g0237 | AFR | GWD | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG02809 | hp2 | a0001 | c0001 | t0050 | g0254 | AFR | GWD | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG02886 | hp1 | a0001 | c0001 | t0031 | g0252 | AFR | GWD | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG02886 | hp2 | a0001 | c0001 | t0005 | g0039 | AFR | GWD | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG02895 | hp1 | a0001 | c0001 | t0046 | g0025 | AFR | GWD | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG02895 | hp2 | a0001 | c0001 | t0003 | g0210 | AFR | GWD | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0035 | AFR | GWD | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0191 | AFR | GWD | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0192 | AFR | GWD | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG02897 | hp2 | a0001 | c0001 | t0017 | g0025 | AFR | GWD | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0127 | AFR | ESN | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0010 | AFR | ESN | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG02965 | hp1 | a0001 | c0001 | t0009 | g0047 | AFR | ESN | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0136 | AFR | ESN | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG02970 | hp1 | a0001 | c0001 | t0027 | g0146 | AFR | ESN | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0158 | AFR | ESN | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG02976 | hp1 | a0001 | c0001 | t0013 | g0247 | AFR | ESN | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0208 | AFR | ESN | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0010 | AFR | GWD | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG03041 | hp2 | a0001 | c0001 | t0008 | g0259 | AFR | GWD | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG03098 | hp1 | a0001 | c0001 | t0008 | g0043 | AFR | MSL | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0143 | AFR | MSL | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0260 | AFR | ESN | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG03130 | hp2 | a0001 | c0001 | t0005 | g0255 | AFR | ESN | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG03139 | hp1 | a0001 | c0001 | t0005 | g0239 | AFR | ESN | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG03139 | hp2 | a0001 | c0001 | t0005 | g0249 | AFR | ESN | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0211 | AFR | ESN | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG03195 | hp2 | a0001 | c0001 | t0010 | g0273 | AFR | ESN | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG03209 | hp1 | a0001 | c0001 | t0056 | g0250 | AFR | MSL | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG03209 | hp2 | a0001 | c0001 | t0004 | g0130 | AFR | MSL | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0015 | AFR | MSL | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0213 | AFR | MSL | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0010 | AFR | MSL | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG03453 | hp2 | a0001 | c0008 | t0003 | g0048 | AFR | MSL | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG03486 | hp1 | a0001 | c0001 | t0008 | g0257 | AFR | MSL | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0138 | AFR | MSL | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG03490 | hp1 | a0001 | c0001 | t0023 | g0060 | SAS | PJL | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0232 | SAS | PJL | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0054 | SAS | PJL | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0114 | SAS | PJL | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0233 | SAS | PJL | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0115 | SAS | PJL | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG03516 | hp1 | a0001 | c0001 | t0007 | g0085 | AFR | ESN | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG03516 | hp2 | a0001 | c0001 | t0054 | g0258 | AFR | ESN | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0157 | AFR | GWD | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG03540 | hp2 | a0001 | c0001 | t0038 | g0046 | AFR | GWD | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0204 | AFR | MSL | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0145 | AFR | MSL | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG03710 | hp2 | a0001 | c0001 | t0004 | g0173 | SAS | PJL | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG03831 | hp1 | a0001 | c0001 | t0004 | g0028 | SAS | BEB | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | BEB | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | BEB | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0178 | SAS | BEB | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG03942 | hp1 | a0001 | c0001 | t0024 | g0097 | SAS | BEB | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG03942 | hp2 | a0001 | c0001 | t0004 | g0053 | SAS | BEB | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | BEB | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | BEB | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG04199 | hp1 | a0001 | c0001 | t0007 | g0062 | SAS | STU | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG04199 | hp2 | a0002 | c0002 | t0005 | g0251 | SAS | STU | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG04204 | hp1 | a0001 | c0001 | t0004 | g0174 | SAS | STU | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG04204 | hp2 | a0001 | c0001 | t0036 | g0001 | SAS | STU | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG04228 | hp1 | a0002 | c0002 | t0005 | g0245 | SAS | STU | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0087 | SAS | STU | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA18522 | hp1 | a0001 | c0001 | t0055 | g0241 | AFR | YRI | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0126 | AFR | YRI | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | CHB | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHB | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA18906 | hp1 | a0001 | c0001 | t0044 | g0261 | AFR | YRI | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA18906 | hp2 | a0001 | c0001 | t0045 | g0207 | AFR | YRI | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA18940 | hp2 | a0001 | c0001 | t0016 | g0195 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA18941 | hp1 | a0001 | c0001 | t0003 | g0215 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA18941 | hp2 | a0001 | c0001 | t0015 | g0160 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA18944 | hp1 | a0001 | c0001 | t0040 | g0198 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA18947 | hp1 | a0001 | c0001 | t0007 | g0061 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA18950 | hp1 | a0001 | c0001 | t0004 | g0150 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA18952 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA18952 | hp2 | a0001 | c0001 | t0004 | g0144 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA18953 | hp2 | a0001 | c0001 | t0028 | g0104 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA18956 | hp1 | a0001 | c0001 | t0016 | g0196 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA18956 | hp2 | a0001 | c0001 | t0014 | g0044 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA18960 | hp1 | a0001 | c0001 | t0003 | g0224 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA18961 | hp2 | a0001 | c0001 | t0004 | g0014 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA18964 | hp2 | a0001 | c0001 | t0034 | g0268 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA18969 | hp1 | a0001 | c0001 | t0039 | g0123 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA18969 | hp2 | a0001 | c0001 | t0004 | g0014 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA18970 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA18970 | hp2 | a0001 | c0001 | t0004 | g0205 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA18972 | hp1 | a0001 | c0001 | t0003 | g0220 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA18977 | hp1 | a0001 | c0001 | t0004 | g0230 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA18978 | hp2 | a0001 | c0001 | t0037 | g0072 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA18981 | hp1 | a0001 | c0001 | t0011 | g0005 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA18983 | hp1 | a0001 | c0001 | t0011 | g0005 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA18983 | hp2 | a0001 | c0005 | t0001 | g0002 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA18985 | hp2 | a0001 | c0001 | t0028 | g0113 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA18986 | hp2 | a0001 | c0001 | t0004 | g0149 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA18993 | hp1 | a0001 | c0006 | t0002 | g0112 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA18995 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA18998 | hp2 | a0001 | c0001 | t0003 | g0037 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA19002 | hp1 | a0001 | c0001 | t0026 | g0227 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA19002 | hp2 | a0001 | c0001 | t0006 | g0096 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA19004 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA19005 | hp1 | a0001 | c0001 | t0003 | g0037 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA19005 | hp2 | a0001 | c0001 | t0004 | g0185 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA19006 | hp1 | a0001 | c0001 | t0016 | g0197 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA19007 | hp2 | a0001 | c0001 | t0004 | g0033 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA19010 | hp2 | a0001 | c0001 | t0006 | g0103 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA19012 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0101 | AFR | LWK | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA19030 | hp2 | a0001 | c0001 | t0022 | g0272 | AFR | LWK | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0235 | AFR | LWK | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA19043 | hp2 | a0001 | c0001 | t0010 | g0269 | AFR | LWK | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA19057 | hp2 | a0001 | c0001 | t0012 | g0088 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA19058 | hp1 | a0001 | c0001 | t0003 | g0217 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA19063 | hp1 | a0001 | c0001 | t0011 | g0005 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA19065 | hp1 | a0001 | c0001 | t0012 | g0001 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA19065 | hp2 | a0001 | c0001 | t0014 | g0044 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA19068 | hp2 | a0001 | c0001 | t0004 | g0014 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA19074 | hp2 | a0001 | c0001 | t0011 | g0005 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA19075 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA19079 | hp2 | a0001 | c0001 | t0006 | g0067 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA19080 | hp2 | a0001 | c0001 | t0007 | g0110 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA19084 | hp2 | a0001 | c0001 | t0004 | g0203 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA19089 | hp1 | a0001 | c0001 | t0049 | g0020 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA19090 | hp1 | a0001 | c0001 | t0020 | g0264 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA19091 | hp1 | a0001 | c0001 | t0003 | g0216 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA19091 | hp2 | a0001 | c0001 | t0004 | g0186 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0015 | AFR | YRI | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA19240 | hp2 | a0001 | c0001 | t0005 | g0040 | AFR | YRI | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA20129 | hp1 | a0001 | c0001 | t0022 | g0271 | AFR | ASW | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA20129 | hp2 | a0001 | c0001 | t0005 | g0240 | AFR | ASW | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA20752 | hp1 | a0001 | c0001 | t0006 | g0089 | EUR | TSI | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0066 | EUR | TSI | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0073 | SAS | GIH | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0176 | SAS | GIH | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0105 | AMR | CLM | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG02109 | hp1 | a0001 | c0001 | t0008 | g0276 | AFR | ACB | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0209 | AFR | ACB | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG02486 | hp1 | a0001 | c0001 | t0017 | g0129 | AFR | ACB | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG02486 | hp2 | a0001 | c0001 | t0029 | g0243 | AFR | ACB | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0135 | AFR | ACB | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG02559 | hp2 | a0001 | c0001 | t0032 | g0042 | AFR | ACB | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG03471 | hp2 | a0001 | c0001 | t0009 | g0171 | AFR | MSL | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0154 | AFR | USA | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0050 | AFR | USA | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA18955 | hp1 | a0001 | c0001 | t0020 | g0265 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA20300 | hp1 | a0001 | c0001 | t0007 | g0098 | AFR | USA | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA20300 | hp2 | a0001 | c0001 | t0023 | g0120 | AFR | USA | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA21309 | hp1 | a0001 | c0001 | t0009 | g0122 | AFR | LWK | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| NA21309 | hp2 | a0001 | c0001 | t0003 | g0236 | AFR | LWK | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0179 | REF | REF | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0008 | g0162 | REF | REF | VASH2_chr1_212945541_212996585 | VASH2 | chr1 | 212945541 | 212996585 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:212961241 | A | C | 1 | a0003 | 1 | HG00642.hp1 | missense_variant | MODERATE | c.352A>C | p.Met118Leu | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 3/8 | 756/4473 | 352/1068 | 118/355 | chr1 | 212961241 | |||
| chr1:212972705 | G | C | 1 | a0004 | 1 | HG01099.hp1 | missense_variant | MODERATE | c.623G>C | p.Gly208Ala | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 6/8 | 1027/4473 | 623/1068 | 208/355 | chr1 | 212972705 | |||
| chr1:212974058 | G | A | 1 | a0002 | 4 | HG01070.hp2 HG01071.hp1 HG04199.hp2 others(1): Show |
missense_variant | MODERATE | c.983G>A | p.Arg328Gln | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/8 | 1387/4473 | 983/1068 | 328/355 | chr1 | 212974058 | |||
| chr1:212974061 | G | A | 1 | a0005 | 1 | HG01167.hp2 | missense_variant | MODERATE | c.986G>A | p.Arg329Gln | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/8 | 1390/4473 | 986/1068 | 329/355 | chr1 | 212974061 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:212951575 | C | T | 1 | a0001c0008 | 1 | HG03453.hp2 | synonymous_variant | LOW | c.33C>T | p.Cys11Cys | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/8 | 437/4473 | 33/1068 | 11/355 | chr1 | 212951575 | |||
| chr1:212988533 | G | A | 1 | a0001c0005 | 1 | NA18983.hp2 | synonymous_variant | LOW | c.1017G>A | p.Lys339Lys | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 8/8 | 1421/4473 | 1017/1068 | 339/355 | chr1 | 212988533 | |||
| chr1:212988539 | T | C | 1 | a0001c0006 | 1 | NA18993.hp1 | synonymous_variant | LOW | c.1023T>C | p.Ala341Ala | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 8/8 | 1427/4473 | 1023/1068 | 341/355 | chr1 | 212988539 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:212950564 | G | C | 1 | a0001c0001t0019 | 2 | HG00741.hp1 HG02717.hp2 |
5_prime_UTR_variant | MODIFIER | c.-381G>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 1/8 | 979 | chr1 | 212950564 | ||||||
| chr1:212950705 | G | A | 5 | a0001c0001t0014 a0001c0001t0020 a0001c0001t0021 others(2): Show |
9 | HG00558.hp2 HG00621.hp1 HG01069.hp1 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-240G>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 1/8 | 838 | chr1 | 212950705 | ||||||
| chr1:212951347 | G | A | 2 | a0001c0001t0010 a0001c0001t0022 |
6 | HG02572.hp2 HG02622.hp2 HG03195.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-196G>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/8 | 196 | chr1 | 212951347 | ||||||
| chr1:212951423 | A | G | 15 | a0001c0001t0005 a0001c0001t0013 a0001c0001t0029 others(12): Show |
32 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(29): Show |
5_prime_UTR_variant | MODIFIER | c.-120A>G | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/8 | 120 | chr1 | 212951423 | ||||||
| chr1:212951475 | C | G | 5 | a0001c0001t0014 a0001c0001t0020 a0001c0001t0021 others(2): Show |
9 | HG00558.hp2 HG00621.hp1 HG01069.hp1 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-68C>G | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/8 | 68 | chr1 | 212951475 | ||||||
| chr1:212951482 | C | T | 1 | a0001c0001t0049 | 1 | NA19089.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-61C>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/8 | chr1 | 212951482 | |||||||
| chr1:212951487 | C | T | 1 | a0001c0001t0048 | 1 | HG02145.hp1 | 5_prime_UTR_variant | MODIFIER | c.-56C>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/8 | 56 | chr1 | 212951487 | ||||||
| chr1:212951526 | C | T | 2 | a0001c0001t0012 a0001c0001t0028 |
6 | HG00423.hp1 HG02129.hp2 NA18953.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-17C>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/8 | 17 | chr1 | 212951526 | ||||||
| chr1:212951529 | G | A | 15 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0007 others(12): Show |
102 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(99): Show |
5_prime_UTR_variant | MODIFIER | c.-14G>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/8 | 14 | chr1 | 212951529 | ||||||
| chr1:212988646 | T | C | 1 | a0001c0001t0048 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*62T>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 8/8 | 62 | chr1 | 212988646 | ||||||
| chr1:212988711 | A | G | 3 | a0001c0001t0009 a0001c0001t0032 a0001c0001t0056 |
10 | HG01884.hp1 HG02055.hp2 HG02559.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*127A>G | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 8/8 | 127 | chr1 | 212988711 | ||||||
| chr1:212988804 | G | A | 16 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0013 others(13): Show |
114 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(111): Show |
3_prime_UTR_variant | MODIFIER | c.*220G>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 8/8 | 220 | chr1 | 212988804 | ||||||
| chr1:212988812 | C | T | 1 | a0001c0001t0021 | 2 | HG00621.hp1 HG02165.hp2 |
3_prime_UTR_variant | MODIFIER | c.*228C>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 8/8 | 228 | chr1 | 212988812 | ||||||
| chr1:212988839 | G | A | 1 | a0001c0001t0022 | 2 | NA19030.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*255G>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 8/8 | 255 | chr1 | 212988839 | ||||||
| chr1:212988909 | T | C | 1 | a0001c0001t0025 | 2 | HG01069.hp2 HG01071.hp2 |
3_prime_UTR_variant | MODIFIER | c.*325T>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 8/8 | 325 | chr1 | 212988909 | ||||||
| chr1:212988983 | C | T | 1 | a0001c0001t0055 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*399C>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 8/8 | 399 | chr1 | 212988983 | ||||||
| chr1:212989125 | T | G | 6 | a0001c0001t0014 a0001c0001t0023 a0001c0001t0026 others(3): Show |
11 | HG00738.hp1 HG01069.hp1 HG01070.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*541T>G | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 8/8 | 541 | chr1 | 212989125 | ||||||
| chr1:212989293 | T | C | 2 | a0001c0001t0011 a0001c0001t0016 |
7 | NA18940.hp2 NA18956.hp1 NA18981.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*709T>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 8/8 | 709 | chr1 | 212989293 | ||||||
| chr1:212989401 | G | A | 1 | a0001c0001t0044 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*817G>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 8/8 | 817 | chr1 | 212989401 | ||||||
| chr1:212989472 | G | C | 1 | a0001c0001t0015 | 3 | HG02040.hp1 HG02056.hp1 NA18941.hp2 |
3_prime_UTR_variant | MODIFIER | c.*888G>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 8/8 | 888 | chr1 | 212989472 | ||||||
| chr1:212989756 | G | A | 2 | a0001c0001t0038 a0001c0001t0050 |
2 | HG02809.hp2 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1172G>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 8/8 | 1172 | chr1 | 212989756 | ||||||
| chr1:212989776 | A | C | 1 | a0001c0001t0054 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1192A>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 8/8 | 1192 | chr1 | 212989776 | ||||||
| chr1:212990062 | TA | T | 8 | a0001c0001t0014 a0001c0001t0023 a0001c0001t0026 others(5): Show |
13 | HG01069.hp1 HG01070.hp2 HG01071.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1491delA | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 8/8 | 1491 | INFO_REALIGN_3_PRIME | chr1 | 212990062 | |||||
| chr1:212990081 | T | C | 3 | a0001c0001t0017 a0001c0001t0046 a0001c0001t0051 |
5 | HG01109.hp1 HG02145.hp2 HG02486.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1497T>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 8/8 | 1497 | chr1 | 212990081 | ||||||
| chr1:212990178 | T | C | 1 | a0001c0001t0045 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1594T>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 8/8 | 1594 | chr1 | 212990178 | ||||||
| chr1:212990306 | A | G | 1 | a0001c0001t0027 | 2 | HG02451.hp1 HG02970.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1722A>G | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 8/8 | 1722 | chr1 | 212990306 | ||||||
| chr1:212990710 | G | C | 1 | a0001c0001t0031 | 2 | HG02809.hp1 HG02886.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2126G>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 8/8 | 2126 | chr1 | 212990710 | ||||||
| chr1:212990741 | A | G | 17 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0011 others(14): Show |
130 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(127): Show |
3_prime_UTR_variant | MODIFIER | c.*2157A>G | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 8/8 | 2157 | chr1 | 212990741 | ||||||
| chr1:212990951 | C | A | 1 | a0001c0001t0056 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2367C>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 8/8 | 2367 | chr1 | 212990951 | ||||||
| chr1:212991008 | T | C | 1 | a0001c0001t0039 | 1 | NA18969.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2424T>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 8/8 | 2424 | chr1 | 212991008 | ||||||
| chr1:212991024 | C | A | 1 | a0001c0001t0035 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2440C>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 8/8 | 2440 | chr1 | 212991024 | ||||||
| chr1:212991070 | A | G | 1 | a0001c0001t0037 | 1 | NA18978.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2486A>G | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 8/8 | 2486 | chr1 | 212991070 | ||||||
| chr1:212991140 | T | C | 1 | a0001c0001t0043 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2556T>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 8/8 | 2556 | chr1 | 212991140 | ||||||
| chr1:212991158 | G | A | 1 | a0001c0001t0031 | 2 | HG02809.hp1 HG02886.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2574G>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 8/8 | 2574 | chr1 | 212991158 | ||||||
| chr1:212991158 | GGAGATAT others(21): Show |
G | 1 | a0001c0001t0036 | 1 | HG04204.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2577_*2604delGATA others(24): Show |
VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 8/8 | 2577 | INFO_REALIGN_3_PRIME | chr1 | 212991158 | |||||
| chr1:212991160 | A | AAAGT | 60 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(57): Show |
368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
3_prime_UTR_variant | MODIFIER | c.*2576_*2577insAAGT | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 8/8 | 2577 | chr1 | 212991160 | ||||||
| chr1:212991576 | G | A | 14 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0015 others(11): Show |
112 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(109): Show |
3_prime_UTR_variant | MODIFIER | c.*2992G>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 8/8 | 2992 | chr1 | 212991576 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:212950875 | G | C | 5 | a0001c0001t0003g0050 a0001c0001t0009g0047 a0001c0001t0009g0049 others(2): Show |
5 | HG02055.hp2 HG02965.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.-205+135G>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 1/7 | chr1 | 212950875 | |||||||
| chr1:212950935 | G | T | 2 | a0001c0001t0003g0275 a0001c0001t0008g0276 |
2 | HG00642.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.-205+195G>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 1/7 | chr1 | 212950935 | |||||||
| chr1:212950949 | C | A | 1 | a0001c0001t0001g0051 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-205+209C>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 1/7 | chr1 | 212950949 | |||||||
| chr1:212950961 | A | G | 56 | a0001c0001t0001g0260 a0001c0001t0003g0050 a0001c0001t0003g0234 others(53): Show |
65 | HG00558.hp2 HG00621.hp1 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.-205+221A>G | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 1/7 | chr1 | 212950961 | |||||||
| chr1:212950990 | G | C | 3 | a0001c0001t0003g0234 a0001c0001t0003g0235 a0001c0001t0003g0236 |
3 | HG00639.hp2 NA19043.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-205+250G>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 1/7 | chr1 | 212950990 | |||||||
| chr1:212951086 | T | C | 37 | a0001c0001t0003g0050 a0001c0001t0003g0234 a0001c0001t0003g0235 others(34): Show |
43 | HG00639.hp2 HG00642.hp2 HG01070.hp2 others(40): Show |
intron_variant | MODIFIER | c.-204-253T>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 1/7 | chr1 | 212951086 | |||||||
| chr1:212951109 | G | A | 9 | a0001c0001t0005g0039 a0001c0001t0005g0040 a0001c0001t0005g0238 others(6): Show |
11 | HG01109.hp2 HG01884.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.-204-230G>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 1/7 | chr1 | 212951109 | |||||||
| chr1:212951144 | T | C | 84 | a0001c0001t0001g0054 a0001c0001t0001g0057 a0001c0001t0002g0001 others(81): Show |
108 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.-204-195T>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 1/7 | chr1 | 212951144 | |||||||
| chr1:212951845 | G | A | 1 | a0001c0001t0041g0121 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.276+27G>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212951845 | |||||||
| chr1:212951878 | T | C | 1 | a0001c0001t0009g0122 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.276+60T>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212951878 | |||||||
| chr1:212951913 | A | G | 1 | a0001c0001t0023g0120 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.276+95A>G | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212951913 | |||||||
| chr1:212952328 | G | GT | 6 | a0001c0001t0010g0269 a0001c0001t0010g0270 a0001c0001t0010g0273 others(3): Show |
6 | HG02572.hp2 HG02622.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.276+518dupT | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | 212952328 | ||||||
| chr1:212952349 | G | T | 4 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0003g0275 others(1): Show |
4 | HG00642.hp2 HG02109.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.276+531G>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212952349 | |||||||
| chr1:212952357 | G | T | 147 | a0001c0001t0001g0038 a0001c0001t0001g0214 a0001c0001t0001g0222 others(144): Show |
191 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.276+539G>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212952357 | |||||||
| chr1:212952358 | T | C | 1 | a0001c0001t0009g0263 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.276+540T>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212952358 | |||||||
| chr1:212952359 | G | T | 9 | a0001c0001t0005g0039 a0001c0001t0005g0040 a0001c0001t0005g0238 others(6): Show |
11 | HG01109.hp2 HG01884.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.276+541G>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212952359 | |||||||
| chr1:212952723 | T | C | 1 | a0001c0001t0039g0123 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.276+905T>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212952723 | |||||||
| chr1:212952811 | T | G | 55 | a0001c0001t0001g0260 a0001c0001t0003g0050 a0001c0001t0003g0234 others(52): Show |
63 | HG00558.hp2 HG00639.hp2 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.276+993T>G | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212952811 | |||||||
| chr1:212952813 | C | T | 1 | a0001c0001t0003g0231 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.276+995C>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212952813 | |||||||
| chr1:212952952 | A | C | 1 | a0004c0003t0006g0119 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.276+1134A>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212952952 | |||||||
| chr1:212953053 | G | A | 2 | a0001c0001t0003g0234 a0001c0001t0003g0236 |
2 | HG00639.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.276+1235G>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212953053 | |||||||
| chr1:212953199 | T | C | 83 | a0001c0001t0001g0054 a0001c0001t0001g0057 a0001c0001t0002g0001 others(80): Show |
108 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.276+1381T>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212953199 | |||||||
| chr1:212953209 | C | G | 1 | a0001c0001t0004g0230 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.276+1391C>G | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212953209 | |||||||
| chr1:212953223 | G | A | 80 | a0001c0001t0001g0054 a0001c0001t0002g0001 a0001c0001t0002g0005 others(77): Show |
105 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.276+1405G>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212953223 | |||||||
| chr1:212953230 | C | CG | 37 | a0001c0001t0001g0009 a0001c0001t0001g0038 a0001c0001t0001g0133 others(34): Show |
52 | HG00140.hp2 HG00408.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.276+1421dupG | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | 212953230 | ||||||
| chr1:212953230 | C | CGG | 17 | a0001c0001t0001g0214 a0001c0001t0003g0126 a0001c0001t0003g0127 others(14): Show |
19 | HG01069.hp2 HG01071.hp2 HG02071.hp2 others(16): Show |
intron_variant | MODIFIER | c.276+1420_276+1421d others(4): Show |
VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | 212953230 | ||||||
| chr1:212953235 | G | GC | 82 | a0001c0001t0001g0054 a0001c0001t0001g0057 a0001c0001t0002g0001 others(79): Show |
107 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.276+1417_276+1418i others(3): Show |
VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212953235 | |||||||
| chr1:212953242 | C | T | 1 | a0001c0001t0002g0117 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.276+1424C>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212953242 | |||||||
| chr1:212953252 | G | T | 1 | a0001c0001t0054g0258 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.276+1434G>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212953252 | |||||||
| chr1:212953390 | C | T | 1 | a0001c0001t0008g0257 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.276+1572C>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212953390 | |||||||
| chr1:212953535 | C | T | 10 | a0001c0001t0003g0010 a0001c0001t0003g0015 a0001c0001t0003g0137 others(7): Show |
15 | HG01243.hp1 HG01891.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.276+1717C>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212953535 | |||||||
| chr1:212953705 | A | G | 1 | a0001c0001t0002g0116 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.276+1887A>G | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212953705 | |||||||
| chr1:212953747 | A | C | 9 | a0001c0001t0003g0010 a0001c0001t0003g0015 a0001c0001t0003g0137 others(6): Show |
14 | HG01243.hp1 HG01891.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.276+1929A>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212953747 | |||||||
| chr1:212953759 | G | A | 30 | a0001c0001t0003g0234 a0001c0001t0003g0235 a0001c0001t0003g0236 others(27): Show |
36 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.276+1941G>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212953759 | |||||||
| chr1:212953770 | G | C | 6 | a0001c0001t0001g0260 a0001c0001t0003g0234 a0001c0001t0003g0235 others(3): Show |
7 | HG00639.hp2 HG02280.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.276+1952G>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212953770 | |||||||
| chr1:212953800 | A | G | 2 | a0001c0001t0003g0275 a0001c0001t0008g0276 |
2 | HG00642.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.276+1982A>G | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212953800 | |||||||
| chr1:212953812 | C | T | 1 | a0001c0001t0010g0274 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.276+1994C>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212953812 | |||||||
| chr1:212953922 | A | G | 4 | a0001c0001t0005g0255 a0001c0001t0032g0042 a0001c0001t0050g0254 others(1): Show |
5 | HG01109.hp1 HG02559.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.276+2104A>G | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212953922 | |||||||
| chr1:212953936 | G | A | 5 | a0001c0001t0003g0050 a0001c0001t0009g0047 a0001c0001t0009g0049 others(2): Show |
5 | HG02055.hp2 HG02965.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.276+2118G>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212953936 | |||||||
| chr1:212953938 | C | G | 1 | a0001c0001t0003g0236 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.276+2120C>G | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212953938 | |||||||
| chr1:212954010 | G | A | 2 | a0001c0001t0003g0208 a0001c0001t0003g0209 |
2 | HG02109.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.276+2192G>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212954010 | |||||||
| chr1:212954262 | C | T | 2 | a0001c0001t0013g0017 a0001c0001t0013g0247 |
4 | HG02258.hp2 HG02280.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.276+2444C>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212954262 | |||||||
| chr1:212954489 | C | T | 2 | a0001c0001t0002g0114 a0001c0001t0002g0115 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.276+2671C>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212954489 | |||||||
| chr1:212954513 | C | T | 1 | a0001c0001t0048g0118 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.276+2695C>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212954513 | |||||||
| chr1:212954639 | C | T | 1 | a0001c0001t0054g0258 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.276+2821C>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212954639 | |||||||
| chr1:212954670 | G | A | 2 | a0001c0001t0023g0060 a0001c0001t0023g0120 |
2 | HG03490.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.276+2852G>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212954670 | |||||||
| chr1:212954709 | C | T | 1 | a0001c0001t0010g0274 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.276+2891C>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212954709 | |||||||
| chr1:212954779 | T | C | 182 | a0001c0001t0001g0038 a0001c0001t0001g0057 a0001c0001t0001g0142 others(179): Show |
232 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(229): Show |
intron_variant | MODIFIER | c.276+2961T>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212954779 | |||||||
| chr1:212954789 | C | T | 1 | a0001c0001t0028g0113 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.276+2971C>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212954789 | |||||||
| chr1:212954871 | C | G | 2 | a0001c0001t0001g0206 a0001c0001t0004g0205 |
2 | NA18970.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.276+3053C>G | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212954871 | |||||||
| chr1:212954897 | C | G | 43 | a0001c0001t0001g0038 a0001c0001t0001g0214 a0001c0001t0001g0222 others(40): Show |
60 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(57): Show |
intron_variant | MODIFIER | c.276+3079C>G | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212954897 | |||||||
| chr1:212954907 | T | G | 7 | a0001c0001t0010g0269 a0001c0001t0010g0270 a0001c0001t0010g0273 others(4): Show |
7 | HG02572.hp2 HG02622.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.276+3089T>G | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212954907 | |||||||
| chr1:212955221 | G | A | 7 | a0001c0001t0003g0138 a0001c0001t0003g0140 a0001c0001t0003g0234 others(4): Show |
7 | HG00639.hp2 HG01884.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.276+3403G>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212955221 | |||||||
| chr1:212955264 | G | A | 1 | a0001c0001t0050g0254 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.276+3446G>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212955264 | |||||||
| chr1:212955332 | C | T | 6 | a0001c0001t0002g0024 a0001c0001t0002g0108 a0001c0001t0002g0109 others(3): Show |
7 | NA18948.hp1 NA18955.hp2 NA18985.hp1 others(4): Show |
intron_variant | MODIFIER | c.276+3514C>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212955332 | |||||||
| chr1:212955396 | C | T | 4 | a0001c0001t0005g0246 a0001c0001t0008g0257 a0001c0001t0031g0252 others(1): Show |
4 | HG01167.hp2 HG02258.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.276+3578C>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212955396 | |||||||
| chr1:212955477 | A | G | 1 | a0001c0001t0015g0036 | 2 | HG02040.hp1 HG02056.hp1 |
intron_variant | MODIFIER | c.276+3659A>G | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212955477 | |||||||
| chr1:212955499 | G | A | 1 | a0001c0001t0004g0148 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.276+3681G>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212955499 | |||||||
| chr1:212955511 | C | T | 7 | a0001c0001t0001g0034 a0001c0001t0001g0202 a0001c0001t0001g0229 others(4): Show |
8 | HG02257.hp2 HG02896.hp1 HG03579.hp1 others(5): Show |
intron_variant | MODIFIER | c.276+3693C>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212955511 | |||||||
| chr1:212955529 | G | A | 1 | a0001c0001t0045g0207 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.276+3711G>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212955529 | |||||||
| chr1:212955578 | C | T | 1 | a0001c0001t0001g0228 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.276+3760C>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212955578 | |||||||
| chr1:212955708 | T | C | 2 | a0001c0001t0003g0275 a0001c0001t0031g0237 |
2 | HG00642.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.276+3890T>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212955708 | |||||||
| chr1:212955735 | C | T | 6 | a0001c0001t0003g0050 a0001c0001t0009g0122 a0001c0001t0010g0273 others(3): Show |
6 | HG01891.hp1 HG02486.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.276+3917C>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212955735 | |||||||
| chr1:212955809 | C | A | 7 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0142 others(4): Show |
18 | HG01081.hp2 HG01123.hp1 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.276+3991C>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212955809 | |||||||
| chr1:212955809 | C | T | 3 | a0001c0001t0003g0050 a0001c0001t0010g0273 a0001c0001t0050g0254 |
3 | HG02809.hp2 HG03195.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.276+3991C>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212955809 | |||||||
| chr1:212956036 | T | C | 1 | a0001c0001t0004g0153 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.276+4218T>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212956036 | |||||||
| chr1:212956037 | A | G | 2 | a0001c0001t0003g0275 a0001c0001t0031g0237 |
2 | HG00642.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.276+4219A>G | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212956037 | |||||||
| chr1:212956045 | C | G | 6 | a0001c0001t0001g0006 a0001c0001t0001g0051 a0001c0001t0001g0199 others(3): Show |
11 | HG02083.hp2 HG02132.hp1 HG02132.hp2 others(8): Show |
intron_variant | MODIFIER | c.276+4227C>G | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212956045 | |||||||
| chr1:212956081 | T | C | 6 | a0001c0001t0001g0006 a0001c0001t0001g0051 a0001c0001t0001g0199 others(3): Show |
11 | HG02083.hp2 HG02132.hp1 HG02132.hp2 others(8): Show |
intron_variant | MODIFIER | c.276+4263T>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212956081 | |||||||
| chr1:212956321 | C | T | 94 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0011 others(91): Show |
124 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.276+4503C>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212956321 | |||||||
| chr1:212956332 | CT | C | 7 | a0001c0001t0003g0050 a0001c0001t0005g0255 a0001c0001t0009g0122 others(4): Show |
7 | HG01891.hp1 HG02486.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.276+4515delT | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212956332 | |||||||
| chr1:212956466 | A | C | 1 | a0001c0001t0004g0193 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.276+4648A>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212956466 | |||||||
| chr1:212956467 | G | A | 1 | a0001c0001t0004g0193 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.276+4649G>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212956467 | |||||||
| chr1:212956573 | C | A | 1 | a0001c0001t0002g0065 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.277-4593C>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212956573 | |||||||
| chr1:212956576 | C | T | 13 | a0001c0001t0003g0035 a0001c0001t0003g0135 a0001c0001t0003g0136 others(10): Show |
16 | HG01070.hp2 HG01071.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.277-4590C>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212956576 | |||||||
| chr1:212956579 | T | A | 3 | a0001c0001t0001g0009 a0001c0001t0006g0056 a0003c0007t0001g0009 |
5 | HG00099.hp1 HG00140.hp2 HG00642.hp1 others(2): Show |
intron_variant | MODIFIER | c.277-4587T>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212956579 | |||||||
| chr1:212956742 | G | C | 1 | a0001c0001t0007g0061 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.277-4424G>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212956742 | |||||||
| chr1:212956837 | C | A | 1 | a0001c0001t0008g0276 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.277-4329C>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212956837 | |||||||
| chr1:212956870 | T | C | 1 | a0001c0001t0002g0066 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.277-4296T>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212956870 | |||||||
| chr1:212956926 | A | C | 2 | a0001c0001t0003g0191 a0001c0001t0003g0192 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.277-4240A>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212956926 | |||||||
| chr1:212956974 | G | A | 1 | a0001c0001t0045g0207 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.277-4192G>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212956974 | |||||||
| chr1:212957209 | C | T | 3 | a0001c0001t0023g0060 a0001c0001t0023g0120 a0001c0001t0043g0190 |
3 | HG01074.hp2 HG03490.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.277-3957C>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212957209 | |||||||
| chr1:212957218 | G | A | 4 | a0001c0001t0003g0154 a0001c0001t0005g0255 a0001c0001t0029g0243 others(1): Show |
4 | HG01891.hp1 HG02486.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.277-3948G>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212957218 | |||||||
| chr1:212957284 | A | G | 1 | a0001c0001t0017g0129 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.277-3882A>G | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212957284 | |||||||
| chr1:212957314 | C | T | 1 | a0001c0001t0009g0049 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.277-3852C>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212957314 | |||||||
| chr1:212957374 | A | T | 1 | a0001c0001t0001g0189 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.277-3792A>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212957374 | |||||||
| chr1:212957414 | T | C | 75 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0038 others(72): Show |
108 | HG00140.hp1 HG00408.hp2 HG00597.hp1 others(105): Show |
intron_variant | MODIFIER | c.277-3752T>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212957414 | |||||||
| chr1:212957558 | A | G | 43 | a0001c0001t0001g0038 a0001c0001t0001g0214 a0001c0001t0001g0222 others(40): Show |
57 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.277-3608A>G | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212957558 | |||||||
| chr1:212957617 | C | CT | 21 | a0001c0001t0001g0051 a0001c0001t0002g0023 a0001c0001t0002g0052 others(18): Show |
27 | HG01123.hp2 HG01167.hp2 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.277-3531dupT | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | 212957617 | ||||||
| chr1:212957617 | C | CTT | 13 | a0001c0001t0002g0068 a0001c0001t0003g0143 a0001c0001t0003g0234 others(10): Show |
16 | HG00140.hp1 HG00639.hp2 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.277-3532_277-3531d others(4): Show |
VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | 212957617 | ||||||
| chr1:212957617 | CT | C | 49 | a0001c0001t0001g0038 a0001c0001t0001g0214 a0001c0001t0001g0222 others(46): Show |
64 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.277-3531delT | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | 212957617 | ||||||
| chr1:212957755 | C | T | 1 | a0001c0001t0038g0046 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.277-3411C>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212957755 | |||||||
| chr1:212957763 | A | G | 10 | a0001c0001t0003g0127 a0001c0001t0003g0128 a0001c0001t0003g0147 others(7): Show |
10 | HG02055.hp1 HG02257.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.277-3403A>G | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212957763 | |||||||
| chr1:212957772 | A | G | 1 | a0001c0001t0003g0235 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.277-3394A>G | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212957772 | |||||||
| chr1:212957786 | T | C | 1 | a0001c0001t0050g0254 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.277-3380T>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212957786 | |||||||
| chr1:212957810 | G | A | 1 | a0001c0001t0054g0258 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.277-3356G>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212957810 | |||||||
| chr1:212957881 | T | C | 1 | a0001c0001t0045g0207 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.277-3285T>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212957881 | |||||||
| chr1:212957946 | C | T | 10 | a0001c0001t0003g0010 a0001c0001t0003g0015 a0001c0001t0003g0138 others(7): Show |
15 | HG01167.hp2 HG01243.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.277-3220C>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212957946 | |||||||
| chr1:212957992 | G | A | 2 | a0001c0001t0001g0232 a0001c0001t0001g0233 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.277-3174G>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212957992 | |||||||
| chr1:212958002 | G | C | 3 | a0001c0001t0003g0037 a0001c0001t0003g0215 a0001c0001t0003g0216 |
4 | NA18941.hp1 NA18998.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.277-3164G>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212958002 | |||||||
| chr1:212958135 | C | T | 1 | a0001c0001t0019g0188 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.277-3031C>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212958135 | |||||||
| chr1:212958223 | C | G | 10 | a0001c0001t0003g0127 a0001c0001t0003g0128 a0001c0001t0003g0147 others(7): Show |
10 | HG02055.hp1 HG02257.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.277-2943C>G | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212958223 | |||||||
| chr1:212958351 | G | T | 1 | a0001c0001t0001g0187 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.277-2815G>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212958351 | |||||||
| chr1:212958546 | A | C | 4 | a0001c0001t0003g0050 a0001c0001t0009g0139 a0001c0001t0010g0273 others(1): Show |
5 | HG01884.hp1 HG02559.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.277-2620A>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212958546 | |||||||
| chr1:212958659 | A | G | 95 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0038 others(92): Show |
128 | HG00140.hp1 HG00408.hp2 HG00597.hp1 others(125): Show |
intron_variant | MODIFIER | c.277-2507A>G | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212958659 | |||||||
| chr1:212958769 | G | A | 5 | a0001c0001t0003g0127 a0001c0001t0003g0128 a0001c0001t0003g0147 others(2): Show |
5 | HG02055.hp1 HG02257.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.277-2397G>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212958769 | |||||||
| chr1:212958859 | G | A | 1 | a0001c0001t0035g0070 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.277-2307G>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212958859 | |||||||
| chr1:212958881 | TTTTC | T | 10 | a0001c0001t0014g0044 a0001c0001t0014g0266 a0001c0001t0020g0265 others(7): Show |
11 | HG00558.hp2 HG01069.hp1 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.277-2265_277-2262d others(6): Show |
VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | 212958881 | ||||||
| chr1:212959001 | T | C | 1 | a0001c0001t0009g0122 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.277-2165T>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212959001 | |||||||
| chr1:212959156 | C | T | 1 | a0001c0001t0009g0122 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.277-2010C>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212959156 | |||||||
| chr1:212959207 | A | T | 2 | a0001c0001t0004g0185 a0001c0001t0004g0186 |
2 | NA19005.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.277-1959A>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212959207 | |||||||
| chr1:212959266 | C | CTG | 84 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(81): Show |
116 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(113): Show |
intron_variant | MODIFIER | c.277-1882_277-1881d others(4): Show |
VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | 212959266 | ||||||
| chr1:212959266 | CTG | C | 3 | a0001c0001t0003g0275 a0001c0001t0009g0047 a0001c0001t0031g0237 |
3 | HG00642.hp2 HG02809.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.277-1882_277-1881d others(4): Show |
VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | 212959266 | ||||||
| chr1:212959441 | G | T | 6 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0184 others(3): Show |
11 | HG01074.hp1 HG01099.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.277-1725G>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212959441 | |||||||
| chr1:212959447 | T | TCA | 3 | a0001c0001t0001g0260 a0001c0001t0008g0043 a0001c0001t0008g0259 |
4 | HG02280.hp1 HG03041.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.277-1698_277-1697d others(4): Show |
VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | 212959447 | ||||||
| chr1:212959447 | TCA | T | 98 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0142 others(95): Show |
138 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.277-1698_277-1697d others(4): Show |
VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | 212959447 | ||||||
| chr1:212959447 | TCACA | T | 2 | a0001c0001t0002g0071 a0002c0002t0030g0041 |
3 | HG01070.hp2 HG01071.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.277-1700_277-1697d others(6): Show |
VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | 212959447 | ||||||
| chr1:212959447 | TCACACA | T | 99 | a0001c0001t0001g0038 a0001c0001t0001g0214 a0001c0001t0001g0222 others(96): Show |
120 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(117): Show |
intron_variant | MODIFIER | c.277-1702_277-1697d others(8): Show |
VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | 212959447 | ||||||
| chr1:212959481 | G | C | 1 | a0001c0001t0004g0194 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.277-1685G>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212959481 | |||||||
| chr1:212959501 | C | G | 1 | a0001c0001t0050g0254 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.277-1665C>G | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212959501 | |||||||
| chr1:212959516 | C | T | 3 | a0001c0001t0014g0044 a0001c0001t0026g0227 a0001c0001t0034g0268 |
4 | NA18956.hp2 NA18964.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.277-1650C>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212959516 | |||||||
| chr1:212959580 | A | G | 2 | a0001c0001t0002g0114 a0001c0001t0002g0115 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.277-1586A>G | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212959580 | |||||||
| chr1:212959697 | C | T | 18 | a0001c0001t0003g0010 a0001c0001t0003g0015 a0001c0001t0003g0138 others(15): Show |
23 | HG00639.hp2 HG01243.hp1 HG01258.hp1 others(20): Show |
intron_variant | MODIFIER | c.277-1469C>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212959697 | |||||||
| chr1:212959795 | C | T | 5 | a0001c0001t0010g0269 a0001c0001t0010g0270 a0001c0001t0022g0271 others(2): Show |
5 | HG02622.hp2 NA18906.hp1 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.277-1371C>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212959795 | |||||||
| chr1:212959796 | G | A | 57 | a0001c0001t0001g0038 a0001c0001t0001g0214 a0001c0001t0001g0222 others(54): Show |
72 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.277-1370G>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212959796 | |||||||
| chr1:212960072 | C | T | 10 | a0001c0001t0014g0044 a0001c0001t0014g0266 a0001c0001t0020g0265 others(7): Show |
11 | HG00558.hp2 HG01069.hp1 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.277-1094C>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212960072 | |||||||
| chr1:212960269 | C | T | 1 | a0001c0001t0009g0049 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.277-897C>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212960269 | |||||||
| chr1:212960323 | G | T | 2 | a0001c0001t0003g0157 a0001c0001t0003g0158 |
2 | HG02970.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.277-843G>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212960323 | |||||||
| chr1:212960510 | G | A | 1 | a0001c0001t0037g0072 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.277-656G>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212960510 | |||||||
| chr1:212960636 | C | G | 43 | a0001c0001t0001g0038 a0001c0001t0001g0214 a0001c0001t0001g0222 others(40): Show |
57 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.277-530C>G | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212960636 | |||||||
| chr1:212960643 | G | A | 8 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0142 others(5): Show |
19 | HG01081.hp2 HG01123.hp1 HG01261.hp2 others(16): Show |
intron_variant | MODIFIER | c.277-523G>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212960643 | |||||||
| chr1:212960685 | C | T | 11 | a0001c0001t0003g0050 a0001c0001t0003g0140 a0001c0001t0005g0240 others(8): Show |
12 | HG01109.hp1 HG01167.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.277-481C>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212960685 | |||||||
| chr1:212960714 | A | G | 7 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0142 others(4): Show |
18 | HG01081.hp2 HG01123.hp1 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.277-452A>G | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212960714 | |||||||
| chr1:212960811 | C | T | 3 | a0001c0001t0003g0154 a0001c0001t0029g0243 a0001c0001t0052g0242 |
3 | HG01891.hp1 HG02486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.277-355C>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212960811 | |||||||
| chr1:212960835 | G | A | 8 | a0001c0001t0003g0127 a0001c0001t0003g0128 a0001c0001t0003g0147 others(5): Show |
8 | HG02055.hp1 HG02257.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.277-331G>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212960835 | |||||||
| chr1:212960872 | A | G | 1 | a0001c0001t0009g0122 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.277-294A>G | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212960872 | |||||||
| chr1:212960880 | T | C | 3 | a0001c0001t0003g0154 a0001c0001t0029g0243 a0001c0001t0052g0242 |
3 | HG01891.hp1 HG02486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.277-286T>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212960880 | |||||||
| chr1:212961065 | G | T | 3 | a0001c0001t0002g0012 a0001c0001t0002g0101 a0001c0001t0035g0070 |
5 | HG01167.hp1 HG01243.hp2 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.277-101G>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212961065 | |||||||
| chr1:212961068 | C | T | 1 | a0001c0001t0004g0205 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.277-98C>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 2/7 | chr1 | 212961068 | |||||||
| chr1:212961309 | C | T | 21 | a0001c0001t0003g0050 a0001c0001t0003g0140 a0001c0001t0005g0240 others(18): Show |
23 | HG00558.hp2 HG01069.hp1 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.365+55C>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 3/7 | chr1 | 212961309 | |||||||
| chr1:212961416 | C | T | 1 | a0001c0001t0044g0261 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.365+162C>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 3/7 | chr1 | 212961416 | |||||||
| chr1:212961540 | A | G | 1 | a0001c0001t0004g0182 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.365+286A>G | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 3/7 | chr1 | 212961540 | |||||||
| chr1:212961565 | T | G | 10 | a0001c0001t0003g0127 a0001c0001t0003g0128 a0001c0001t0003g0147 others(7): Show |
10 | HG02055.hp1 HG02257.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.365+311T>G | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 3/7 | chr1 | 212961565 | |||||||
| chr1:212961623 | C | G | 197 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0038 others(194): Show |
261 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(258): Show |
intron_variant | MODIFIER | c.365+369C>G | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 3/7 | chr1 | 212961623 | |||||||
| chr1:212961667 | T | C | 132 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0142 others(129): Show |
177 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.365+413T>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 3/7 | chr1 | 212961667 | |||||||
| chr1:212961704 | G | A | 1 | a0001c0001t0056g0250 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.365+450G>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 3/7 | chr1 | 212961704 | |||||||
| chr1:212961760 | A | T | 4 | a0001c0001t0002g0068 a0002c0002t0005g0245 a0002c0002t0005g0251 others(1): Show |
5 | HG00140.hp1 HG01070.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.365+506A>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 3/7 | chr1 | 212961760 | |||||||
| chr1:212961815 | C | G | 3 | a0001c0001t0003g0126 a0001c0001t0025g0124 a0001c0001t0025g0125 |
3 | HG01069.hp2 HG01071.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.365+561C>G | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 3/7 | chr1 | 212961815 | |||||||
| chr1:212961851 | C | T | 2 | a0001c0001t0009g0047 a0001c0001t0031g0237 |
2 | HG02809.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.365+597C>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 3/7 | chr1 | 212961851 | |||||||
| chr1:212961858 | C | T | 22 | a0001c0001t0003g0050 a0001c0001t0003g0140 a0001c0001t0005g0240 others(19): Show |
24 | HG00558.hp2 HG01069.hp1 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.365+604C>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 3/7 | chr1 | 212961858 | |||||||
| chr1:212961881 | T | C | 6 | a0001c0001t0002g0068 a0001c0001t0005g0249 a0001c0001t0055g0241 others(3): Show |
7 | HG00140.hp1 HG01070.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.365+627T>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 3/7 | chr1 | 212961881 | |||||||
| chr1:212961935 | C | T | 1 | a0001c0001t0001g0181 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.365+681C>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 3/7 | chr1 | 212961935 | |||||||
| chr1:212962042 | C | A | 21 | a0001c0001t0003g0050 a0001c0001t0003g0140 a0001c0001t0005g0240 others(18): Show |
23 | HG00558.hp2 HG01069.hp1 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.365+788C>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 3/7 | chr1 | 212962042 | |||||||
| chr1:212962101 | C | T | 1 | a0001c0001t0001g0201 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.365+847C>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 3/7 | chr1 | 212962101 | |||||||
| chr1:212962317 | A | C | 1 | a0001c0001t0001g0181 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.365+1063A>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 3/7 | chr1 | 212962317 | |||||||
| chr1:212962344 | G | A | 1 | a0001c0001t0003g0235 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.365+1090G>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 3/7 | chr1 | 212962344 | |||||||
| chr1:212962407 | C | T | 1 | a0001c0001t0002g0100 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.365+1153C>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 3/7 | chr1 | 212962407 | |||||||
| chr1:212962600 | T | C | 6 | a0001c0001t0003g0143 a0001c0001t0005g0246 a0001c0001t0013g0017 others(3): Show |
8 | HG02258.hp1 HG02258.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.365+1346T>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 3/7 | chr1 | 212962600 | |||||||
| chr1:212962684 | C | T | 3 | a0001c0001t0002g0114 a0001c0001t0002g0115 a0001c0001t0038g0046 |
3 | HG03491.hp2 HG03492.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.365+1430C>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 3/7 | chr1 | 212962684 | |||||||
| chr1:212962758 | G | A | 3 | a0001c0001t0023g0060 a0001c0001t0023g0120 a0001c0001t0043g0190 |
3 | HG01074.hp2 HG03490.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.365+1504G>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 3/7 | chr1 | 212962758 | |||||||
| chr1:212962787 | G | A | 1 | a0001c0001t0009g0049 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.365+1533G>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 3/7 | chr1 | 212962787 | |||||||
| chr1:212962806 | C | G | 209 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0038 others(206): Show |
273 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(270): Show |
intron_variant | MODIFIER | c.365+1552C>G | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 3/7 | chr1 | 212962806 | |||||||
| chr1:212962816 | T | C | 2 | a0001c0001t0005g0249 a0001c0001t0055g0241 |
2 | HG03139.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.365+1562T>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 3/7 | chr1 | 212962816 | |||||||
| chr1:212962904 | G | A | 2 | a0001c0001t0025g0124 a0001c0001t0025g0125 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.365+1650G>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 3/7 | chr1 | 212962904 | |||||||
| chr1:212962961 | G | A | 1 | a0001c0001t0002g0073 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.365+1707G>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 3/7 | chr1 | 212962961 | |||||||
| chr1:212962977 | C | CTT | 42 | a0001c0001t0001g0038 a0001c0001t0001g0214 a0001c0001t0001g0222 others(39): Show |
56 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.365+1734_365+1735d others(4): Show |
VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 212962977 | ||||||
| chr1:212962977 | C | CTTT | 19 | a0001c0001t0003g0140 a0001c0001t0003g0235 a0001c0001t0005g0240 others(16): Show |
21 | HG00558.hp2 HG01069.hp1 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.365+1733_365+1735d others(5): Show |
VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 212962977 | ||||||
| chr1:212962977 | CT | C | 20 | a0001c0001t0001g0004 a0001c0001t0001g0142 a0001c0001t0001g0155 others(17): Show |
29 | HG00323.hp1 HG01123.hp1 HG01358.hp1 others(26): Show |
intron_variant | MODIFIER | c.365+1735delT | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 212962977 | ||||||
| chr1:212962977 | CTT | C | 16 | a0001c0001t0003g0010 a0001c0001t0003g0015 a0001c0001t0003g0138 others(13): Show |
21 | HG00639.hp2 HG01243.hp1 HG01258.hp1 others(18): Show |
intron_variant | MODIFIER | c.365+1734_365+1735d others(4): Show |
VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 212962977 | ||||||
| chr1:212963018 | A | G | 1 | a0001c0001t0048g0118 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.365+1764A>G | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 3/7 | chr1 | 212963018 | |||||||
| chr1:212963021 | G | T | 10 | a0001c0001t0014g0044 a0001c0001t0014g0266 a0001c0001t0020g0265 others(7): Show |
11 | HG00558.hp2 HG01069.hp1 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.365+1767G>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 3/7 | chr1 | 212963021 | |||||||
| chr1:212963246 | G | A | 4 | a0001c0001t0004g0027 a0001c0001t0004g0165 a0001c0001t0004g0166 others(1): Show |
5 | HG01070.hp1 HG01346.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.365+1992G>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 3/7 | chr1 | 212963246 | |||||||
| chr1:212963309 | C | T | 1 | a0001c0001t0002g0116 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.365+2055C>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 3/7 | chr1 | 212963309 | |||||||
| chr1:212963310 | G | A | 9 | a0001c0001t0003g0126 a0001c0001t0003g0127 a0001c0001t0003g0128 others(6): Show |
9 | HG02055.hp1 HG02257.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.365+2056G>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 3/7 | chr1 | 212963310 | |||||||
| chr1:212963502 | G | T | 3 | a0001c0001t0002g0023 a0001c0001t0002g0099 a0001c0001t0002g0106 |
4 | NA18944.hp2 NA18988.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.366-2220G>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 3/7 | chr1 | 212963502 | |||||||
| chr1:212963503 | C | T | 14 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0142 others(11): Show |
27 | HG01081.hp2 HG01123.hp1 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.366-2219C>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 3/7 | chr1 | 212963503 | |||||||
| chr1:212963504 | G | A | 1 | a0001c0001t0002g0077 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.366-2218G>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 3/7 | chr1 | 212963504 | |||||||
| chr1:212963528 | C | T | 3 | a0001c0001t0022g0271 a0001c0001t0022g0272 a0001c0001t0050g0254 |
3 | HG02809.hp2 NA19030.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.366-2194C>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 3/7 | chr1 | 212963528 | |||||||
| chr1:212963558 | A | AC | 3 | a0001c0001t0022g0271 a0001c0001t0022g0272 a0001c0001t0050g0254 |
3 | HG02809.hp2 NA19030.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.366-2162dupC | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 212963558 | ||||||
| chr1:212963563 | C | CAAGAGTA others(313): Show |
7 | a0001c0001t0003g0126 a0001c0001t0003g0127 a0001c0001t0003g0128 others(4): Show |
7 | HG02257.hp1 HG02622.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.366-2143_366-2142i others(322): Show |
VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 212963563 | ||||||
| chr1:212963563 | C | CAAGAGTA others(314): Show |
2 | a0001c0001t0003g0147 a0001c0001t0010g0274 |
2 | HG02055.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.366-2143_366-2142i others(323): Show |
VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 212963563 | ||||||
| chr1:212963563 | C | CAAGAGTA others(311): Show |
1 | a0001c0001t0002g0068 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.366-2143_366-2142i others(320): Show |
VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 212963563 | ||||||
| chr1:212963563 | C | CAAGAGTA others(312): Show |
3 | a0002c0002t0005g0245 a0002c0002t0005g0251 a0002c0002t0030g0041 |
4 | HG01070.hp2 HG01071.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.366-2143_366-2142i others(321): Show |
VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 212963563 | ||||||
| chr1:212963563 | C | CAAGAGTA others(313): Show |
4 | a0001c0001t0003g0275 a0001c0001t0009g0047 a0001c0001t0031g0237 others(1): Show |
4 | HG00642.hp2 HG02145.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.366-2143_366-2142i others(322): Show |
VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 212963563 | ||||||
| chr1:212963652 | C | T | 1 | a0001c0001t0007g0098 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.366-2070C>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 3/7 | chr1 | 212963652 | |||||||
| chr1:212963775 | T | A | 62 | a0001c0001t0001g0038 a0001c0001t0001g0214 a0001c0001t0001g0222 others(59): Show |
78 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(75): Show |
intron_variant | MODIFIER | c.366-1947T>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 3/7 | chr1 | 212963775 | |||||||
| chr1:212963880 | T | C | 3 | a0001c0001t0009g0263 a0001c0001t0025g0124 a0001c0001t0025g0125 |
3 | HG01069.hp2 HG01071.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.366-1842T>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 3/7 | chr1 | 212963880 | |||||||
| chr1:212963917 | T | C | 1 | a0001c0001t0003g0140 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.366-1805T>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 3/7 | chr1 | 212963917 | |||||||
| chr1:212963936 | ATCACT | A | 7 | a0001c0001t0002g0068 a0001c0001t0013g0017 a0001c0001t0013g0247 others(4): Show |
10 | HG00140.hp1 HG01070.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.366-1781_366-1777d others(7): Show |
VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 212963936 | ||||||
| chr1:212963963 | C | A | 1 | a0001c0001t0005g0238 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.366-1759C>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 3/7 | chr1 | 212963963 | |||||||
| chr1:212964199 | G | C | 9 | a0001c0001t0003g0126 a0001c0001t0003g0127 a0001c0001t0003g0128 others(6): Show |
9 | HG02055.hp1 HG02257.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.366-1523G>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 3/7 | chr1 | 212964199 | |||||||
| chr1:212964319 | G | A | 1 | a0001c0001t0003g0010 | 4 | HG01243.hp1 HG02922.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.366-1403G>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 3/7 | chr1 | 212964319 | |||||||
| chr1:212964347 | C | G | 6 | a0001c0001t0014g0044 a0001c0001t0014g0266 a0001c0001t0020g0265 others(3): Show |
7 | HG00558.hp2 HG01069.hp1 HG02129.hp1 others(4): Show |
intron_variant | MODIFIER | c.366-1375C>G | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 3/7 | chr1 | 212964347 | |||||||
| chr1:212964354 | C | G | 1 | a0001c0001t0003g0235 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.366-1368C>G | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 3/7 | chr1 | 212964354 | |||||||
| chr1:212964481 | C | T | 9 | a0001c0001t0003g0126 a0001c0001t0003g0127 a0001c0001t0003g0128 others(6): Show |
9 | HG02055.hp1 HG02257.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.366-1241C>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 3/7 | chr1 | 212964481 | |||||||
| chr1:212964714 | CAG | C | 9 | a0001c0001t0014g0044 a0001c0001t0014g0266 a0001c0001t0020g0265 others(6): Show |
10 | HG00558.hp2 HG01069.hp1 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.366-1005_366-1004d others(4): Show |
VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 212964714 | ||||||
| chr1:212964733 | C | A | 197 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0038 others(194): Show |
261 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(258): Show |
intron_variant | MODIFIER | c.366-989C>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 3/7 | chr1 | 212964733 | |||||||
| chr1:212964759 | C | T | 1 | a0001c0001t0009g0122 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.366-963C>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 3/7 | chr1 | 212964759 | |||||||
| chr1:212964922 | G | GT | 19 | a0001c0001t0001g0180 a0001c0001t0002g0022 a0001c0001t0002g0095 others(16): Show |
21 | HG00558.hp2 HG00738.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.366-783dupT | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 212964922 | ||||||
| chr1:212964936 | T | C | 1 | a0001c0001t0008g0276 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.366-786T>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 3/7 | chr1 | 212964936 | |||||||
| chr1:212964950 | T | C | 1 | a0001c0001t0001g0184 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.366-772T>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 3/7 | chr1 | 212964950 | |||||||
| chr1:212965016 | A | C | 6 | a0001c0001t0003g0143 a0001c0001t0005g0246 a0001c0001t0013g0017 others(3): Show |
8 | HG02258.hp1 HG02258.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.366-706A>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 3/7 | chr1 | 212965016 | |||||||
| chr1:212965068 | A | G | 1 | a0001c0001t0002g0011 | 3 | HG00323.hp2 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.366-654A>G | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 3/7 | chr1 | 212965068 | |||||||
| chr1:212965384 | A | C | 1 | a0001c0001t0029g0243 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.366-338A>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 3/7 | chr1 | 212965384 | |||||||
| chr1:212965573 | GCTA | G | 9 | a0001c0001t0014g0044 a0001c0001t0014g0266 a0001c0001t0020g0265 others(6): Show |
10 | HG00558.hp2 HG01069.hp1 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.366-142_366-140del others(3): Show |
VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 212965573 | ||||||
| chr1:212965621 | C | T | 4 | a0001c0001t0009g0263 a0001c0001t0025g0124 a0001c0001t0025g0125 others(1): Show |
4 | HG01069.hp2 HG01071.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.366-101C>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 3/7 | chr1 | 212965621 | |||||||
| chr1:212965628 | A | C | 10 | a0001c0001t0003g0126 a0001c0001t0003g0127 a0001c0001t0003g0128 others(7): Show |
10 | HG02055.hp1 HG02257.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.366-94A>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 3/7 | chr1 | 212965628 | |||||||
| chr1:212965651 | A | G | 1 | a0001c0001t0045g0207 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.366-71A>G | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 3/7 | chr1 | 212965651 | |||||||
| chr1:212965678 | C | G | 1 | a0001c0001t0004g0166 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.366-44C>G | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 3/7 | chr1 | 212965678 | |||||||
| chr1:212965860 | G | A | 9 | a0001c0001t0014g0044 a0001c0001t0014g0266 a0001c0001t0020g0265 others(6): Show |
10 | HG00558.hp2 HG01069.hp1 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.422+82G>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 4/7 | chr1 | 212965860 | |||||||
| chr1:212965992 | T | C | 9 | a0001c0001t0003g0010 a0001c0001t0003g0015 a0001c0001t0003g0138 others(6): Show |
14 | HG01243.hp1 HG02109.hp2 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.422+214T>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 4/7 | chr1 | 212965992 | |||||||
| chr1:212966079 | A | G | 9 | a0001c0001t0003g0010 a0001c0001t0003g0015 a0001c0001t0003g0138 others(6): Show |
14 | HG01243.hp1 HG02109.hp2 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.423-192A>G | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 4/7 | chr1 | 212966079 | |||||||
| chr1:212966081 | G | A | 2 | a0001c0001t0029g0243 a0001c0001t0052g0242 |
2 | HG01891.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.423-190G>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 4/7 | chr1 | 212966081 | |||||||
| chr1:212966093 | C | T | 2 | a0001c0001t0005g0246 a0001c0001t0031g0252 |
2 | HG02258.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.423-178C>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 4/7 | chr1 | 212966093 | |||||||
| chr1:212966160 | G | A | 3 | a0002c0002t0005g0245 a0002c0002t0005g0251 a0002c0002t0030g0041 |
4 | HG01070.hp2 HG01071.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.423-111G>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 4/7 | chr1 | 212966160 | |||||||
| chr1:212966219 | G | A | 2 | a0001c0001t0003g0275 a0001c0001t0031g0237 |
2 | HG00642.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.423-52G>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 4/7 | chr1 | 212966219 | |||||||
| chr1:212966382 | A | C | 8 | a0001c0001t0003g0035 a0001c0001t0003g0135 a0001c0001t0003g0136 others(5): Show |
8 | HG02257.hp2 HG02451.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.497+37A>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 5/7 | chr1 | 212966382 | |||||||
| chr1:212966399 | TG | T | 9 | a0001c0001t0014g0044 a0001c0001t0014g0266 a0001c0001t0020g0265 others(6): Show |
10 | HG00558.hp2 HG01069.hp1 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.497+58delG | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 212966399 | ||||||
| chr1:212966406 | T | G | 185 | a0001c0001t0001g0038 a0001c0001t0001g0054 a0001c0001t0001g0057 others(182): Show |
236 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(233): Show |
intron_variant | MODIFIER | c.497+61T>G | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 5/7 | chr1 | 212966406 | |||||||
| chr1:212966480 | T | A | 9 | a0001c0001t0014g0044 a0001c0001t0014g0266 a0001c0001t0020g0265 others(6): Show |
10 | HG00558.hp2 HG01069.hp1 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.497+135T>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 5/7 | chr1 | 212966480 | |||||||
| chr1:212966551 | G | A | 1 | a0001c0001t0004g0205 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.497+206G>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 5/7 | chr1 | 212966551 | |||||||
| chr1:212966713 | G | A | 3 | a0001c0001t0001g0034 a0001c0001t0001g0202 a0001c0001t0001g0229 |
4 | NA18975.hp1 NA18978.hp1 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.497+368G>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 5/7 | chr1 | 212966713 | |||||||
| chr1:212966724 | A | G | 6 | a0001c0001t0003g0143 a0001c0001t0005g0246 a0001c0001t0013g0017 others(3): Show |
8 | HG02258.hp1 HG02258.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.497+379A>G | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 5/7 | chr1 | 212966724 | |||||||
| chr1:212966897 | T | TTTTGTTT others(1): Show |
9 | a0001c0001t0014g0044 a0001c0001t0014g0266 a0001c0001t0020g0265 others(6): Show |
10 | HG00558.hp2 HG01069.hp1 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.497+562_497+569dup others(8): Show |
VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 212966897 | ||||||
| chr1:212967009 | T | G | 1 | a0001c0001t0008g0257 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.497+664T>G | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 5/7 | chr1 | 212967009 | |||||||
| chr1:212967020 | G | A | 90 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0011 others(87): Show |
119 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.497+675G>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 5/7 | chr1 | 212967020 | |||||||
| chr1:212967020 | G | C | 3 | a0002c0002t0005g0245 a0002c0002t0005g0251 a0002c0002t0030g0041 |
4 | HG01070.hp2 HG01071.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.497+675G>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 5/7 | chr1 | 212967020 | |||||||
| chr1:212967045 | C | T | 9 | a0001c0001t0014g0044 a0001c0001t0014g0266 a0001c0001t0020g0265 others(6): Show |
10 | HG00558.hp2 HG01069.hp1 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.497+700C>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 5/7 | chr1 | 212967045 | |||||||
| chr1:212967056 | A | C | 110 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0011 others(107): Show |
140 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.497+711A>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 5/7 | chr1 | 212967056 | |||||||
| chr1:212967082 | C | T | 1 | a0001c0001t0004g0153 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.497+737C>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 5/7 | chr1 | 212967082 | |||||||
| chr1:212967327 | C | T | 198 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0038 others(195): Show |
262 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(259): Show |
intron_variant | MODIFIER | c.497+982C>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 5/7 | chr1 | 212967327 | |||||||
| chr1:212967460 | A | G | 1 | a0001c0001t0001g0225 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.497+1115A>G | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 5/7 | chr1 | 212967460 | |||||||
| chr1:212967489 | A | G | 2 | a0001c0001t0014g0044 a0001c0001t0026g0227 |
3 | NA18956.hp2 NA19002.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.497+1144A>G | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 5/7 | chr1 | 212967489 | |||||||
| chr1:212967800 | G | C | 1 | a0001c0001t0045g0207 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.497+1455G>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 5/7 | chr1 | 212967800 | |||||||
| chr1:212967812 | A | G | 12 | a0001c0001t0014g0044 a0001c0001t0014g0266 a0001c0001t0020g0265 others(9): Show |
13 | HG00558.hp2 HG01069.hp1 HG01074.hp2 others(10): Show |
intron_variant | MODIFIER | c.497+1467A>G | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 5/7 | chr1 | 212967812 | |||||||
| chr1:212968142 | A | G | 4 | a0001c0001t0004g0027 a0001c0001t0004g0165 a0001c0001t0004g0166 others(1): Show |
5 | HG01070.hp1 HG01346.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.497+1797A>G | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 5/7 | chr1 | 212968142 | |||||||
| chr1:212968346 | A | G | 1 | a0001c0001t0001g0032 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.497+2001A>G | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 5/7 | chr1 | 212968346 | |||||||
| chr1:212968610 | C | T | 1 | a0001c0006t0002g0112 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.497+2265C>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 5/7 | chr1 | 212968610 | |||||||
| chr1:212968906 | G | A | 1 | a0001c0001t0042g0167 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.497+2561G>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 5/7 | chr1 | 212968906 | |||||||
| chr1:212969020 | A | G | 1 | a0001c0001t0027g0146 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.497+2675A>G | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 5/7 | chr1 | 212969020 | |||||||
| chr1:212969114 | A | G | 81 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(78): Show |
111 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.497+2769A>G | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 5/7 | chr1 | 212969114 | |||||||
| chr1:212969194 | C | CT | 14 | a0001c0001t0007g0098 a0001c0001t0009g0171 a0001c0001t0014g0044 others(11): Show |
15 | HG00558.hp2 HG01069.hp1 HG01074.hp2 others(12): Show |
intron_variant | MODIFIER | c.497+2865dupT | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 212969194 | ||||||
| chr1:212969194 | CT | C | 97 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(94): Show |
140 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.497+2865delT | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 212969194 | ||||||
| chr1:212969253 | C | T | 91 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(88): Show |
134 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.497+2908C>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 5/7 | chr1 | 212969253 | |||||||
| chr1:212969362 | A | AT | 90 | a0001c0001t0001g0057 a0001c0001t0002g0001 a0001c0001t0002g0005 others(87): Show |
119 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.497+3024dupT | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 212969362 | ||||||
| chr1:212969418 | A | G | 12 | a0001c0001t0014g0044 a0001c0001t0014g0266 a0001c0001t0020g0265 others(9): Show |
13 | HG00558.hp2 HG01069.hp1 HG01074.hp2 others(10): Show |
intron_variant | MODIFIER | c.497+3073A>G | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 5/7 | chr1 | 212969418 | |||||||
| chr1:212969515 | G | A | 91 | a0001c0001t0001g0057 a0001c0001t0002g0001 a0001c0001t0002g0005 others(88): Show |
120 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.498-3065G>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 5/7 | chr1 | 212969515 | |||||||
| chr1:212969672 | G | C | 1 | a0001c0001t0006g0103 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.498-2908G>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 5/7 | chr1 | 212969672 | |||||||
| chr1:212969760 | T | C | 1 | a0001c0001t0027g0262 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.498-2820T>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 5/7 | chr1 | 212969760 | |||||||
| chr1:212969852 | G | A | 8 | a0001c0001t0003g0010 a0001c0001t0003g0015 a0001c0001t0003g0138 others(5): Show |
13 | HG01243.hp1 HG02109.hp2 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.498-2728G>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 5/7 | chr1 | 212969852 | |||||||
| chr1:212969875 | T | C | 1 | a0001c0001t0048g0118 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.498-2705T>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 5/7 | chr1 | 212969875 | |||||||
| chr1:212970074 | T | C | 41 | a0001c0001t0001g0038 a0001c0001t0001g0214 a0001c0001t0001g0222 others(38): Show |
56 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.498-2506T>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 5/7 | chr1 | 212970074 | |||||||
| chr1:212970230 | A | G | 2 | a0001c0001t0001g0232 a0001c0001t0001g0233 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.498-2350A>G | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 5/7 | chr1 | 212970230 | |||||||
| chr1:212970476 | A | G | 12 | a0001c0001t0014g0044 a0001c0001t0014g0266 a0001c0001t0020g0265 others(9): Show |
13 | HG00558.hp2 HG01069.hp1 HG01074.hp2 others(10): Show |
intron_variant | MODIFIER | c.498-2104A>G | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 5/7 | chr1 | 212970476 | |||||||
| chr1:212970497 | G | C | 9 | a0001c0001t0003g0010 a0001c0001t0003g0015 a0001c0001t0003g0138 others(6): Show |
14 | HG01243.hp1 HG02109.hp2 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.498-2083G>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 5/7 | chr1 | 212970497 | |||||||
| chr1:212970529 | A | ACCATTTT others(338): Show |
1 | a0001c0001t0025g0124 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.498-2034_498-2033i others(347): Show |
VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 212970529 | ||||||
| chr1:212970529 | A | ACCATTTT others(339): Show |
1 | a0001c0001t0025g0125 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.498-2034_498-2033i others(348): Show |
VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 212970529 | ||||||
| chr1:212970529 | A | ACCATTTT others(348): Show |
1 | a0001c0001t0009g0263 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.498-2034_498-2033i others(357): Show |
VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 212970529 | ||||||
| chr1:212970555 | A | C | 15 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0142 others(12): Show |
28 | HG01081.hp2 HG01123.hp1 HG01261.hp2 others(25): Show |
intron_variant | MODIFIER | c.498-2025A>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 5/7 | chr1 | 212970555 | |||||||
| chr1:212970854 | C | T | 1 | a0001c0001t0012g0094 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.498-1726C>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 5/7 | chr1 | 212970854 | |||||||
| chr1:212970860 | A | T | 1 | a0001c0001t0027g0146 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.498-1720A>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 5/7 | chr1 | 212970860 | |||||||
| chr1:212970898 | G | GAAAA | 12 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0142 others(9): Show |
23 | HG01081.hp2 HG01123.hp1 HG01261.hp2 others(20): Show |
intron_variant | MODIFIER | c.498-1675_498-1672d others(6): Show |
VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 212970898 | ||||||
| chr1:212970898 | G | GAAAAA | 7 | a0001c0001t0003g0143 a0001c0001t0005g0246 a0001c0001t0009g0122 others(4): Show |
9 | HG02258.hp1 HG02258.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.498-1676_498-1672d others(7): Show |
VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 212970898 | ||||||
| chr1:212971087 | T | G | 6 | a0001c0001t0002g0005 a0001c0001t0002g0074 a0001c0001t0011g0005 others(3): Show |
11 | NA18940.hp2 NA18956.hp1 NA18965.hp1 others(8): Show |
intron_variant | MODIFIER | c.498-1493T>G | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 5/7 | chr1 | 212971087 | |||||||
| chr1:212971107 | A | C | 6 | a0001c0001t0003g0143 a0001c0001t0005g0246 a0001c0001t0013g0017 others(3): Show |
8 | HG02258.hp1 HG02258.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.498-1473A>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 5/7 | chr1 | 212971107 | |||||||
| chr1:212971206 | T | C | 3 | a0002c0002t0005g0245 a0002c0002t0005g0251 a0002c0002t0030g0041 |
4 | HG01070.hp2 HG01071.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.498-1374T>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 5/7 | chr1 | 212971206 | |||||||
| chr1:212971232 | T | C | 74 | a0001c0001t0001g0038 a0001c0001t0001g0214 a0001c0001t0001g0222 others(71): Show |
90 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(87): Show |
intron_variant | MODIFIER | c.498-1348T>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 5/7 | chr1 | 212971232 | |||||||
| chr1:212971309 | C | G | 7 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0142 others(4): Show |
18 | HG01081.hp2 HG01123.hp1 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.498-1271C>G | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 5/7 | chr1 | 212971309 | |||||||
| chr1:212971509 | G | A | 90 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0011 others(87): Show |
119 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.498-1071G>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 5/7 | chr1 | 212971509 | |||||||
| chr1:212971585 | G | A | 2 | a0001c0001t0029g0243 a0001c0001t0052g0242 |
2 | HG01891.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.498-995G>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 5/7 | chr1 | 212971585 | |||||||
| chr1:212971878 | G | A | 1 | a0001c0001t0009g0122 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.498-702G>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 5/7 | chr1 | 212971878 | |||||||
| chr1:212971933 | G | A | 3 | a0002c0002t0005g0245 a0002c0002t0005g0251 a0002c0002t0030g0041 |
4 | HG01070.hp2 HG01071.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.498-647G>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 5/7 | chr1 | 212971933 | |||||||
| chr1:212972022 | G | C | 90 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0011 others(87): Show |
119 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.498-558G>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 5/7 | chr1 | 212972022 | |||||||
| chr1:212972062 | G | C | 28 | a0001c0001t0003g0035 a0001c0001t0003g0050 a0001c0001t0003g0126 others(25): Show |
28 | HG01069.hp2 HG01071.hp2 HG01167.hp2 others(25): Show |
intron_variant | MODIFIER | c.498-518G>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 5/7 | chr1 | 212972062 | |||||||
| chr1:212972094 | A | G | 3 | a0002c0002t0005g0245 a0002c0002t0005g0251 a0002c0002t0030g0041 |
4 | HG01070.hp2 HG01071.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.498-486A>G | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 5/7 | chr1 | 212972094 | |||||||
| chr1:212972119 | A | G | 1 | a0001c0001t0003g0224 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.498-461A>G | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 5/7 | chr1 | 212972119 | |||||||
| chr1:212972136 | G | T | 9 | a0001c0001t0014g0044 a0001c0001t0014g0266 a0001c0001t0020g0265 others(6): Show |
10 | HG00558.hp2 HG01069.hp1 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.498-444G>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 5/7 | chr1 | 212972136 | |||||||
| chr1:212972180 | T | A | 90 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0011 others(87): Show |
119 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.498-400T>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 5/7 | chr1 | 212972180 | |||||||
| chr1:212972194 | G | A | 1 | a0001c0001t0002g0079 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.498-386G>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 5/7 | chr1 | 212972194 | |||||||
| chr1:212972398 | G | T | 1 | a0001c0001t0004g0230 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.498-182G>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 5/7 | chr1 | 212972398 | |||||||
| chr1:212972399 | T | G | 1 | a0001c0001t0003g0236 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.498-181T>G | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 5/7 | chr1 | 212972399 | |||||||
| chr1:212972526 | C | T | 1 | a0001c0001t0009g0049 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.498-54C>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 5/7 | chr1 | 212972526 | |||||||
| chr1:212973496 | G | A | 9 | a0001c0001t0014g0044 a0001c0001t0014g0266 a0001c0001t0020g0265 others(6): Show |
10 | HG00558.hp2 HG01069.hp1 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.880-459G>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 6/7 | chr1 | 212973496 | |||||||
| chr1:212973602 | A | G | 205 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0038 others(202): Show |
269 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(266): Show |
intron_variant | MODIFIER | c.880-353A>G | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 6/7 | chr1 | 212973602 | |||||||
| chr1:212973610 | G | T | 37 | a0001c0001t0003g0035 a0001c0001t0003g0050 a0001c0001t0003g0126 others(34): Show |
38 | HG00558.hp2 HG01069.hp1 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.880-345G>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 6/7 | chr1 | 212973610 | |||||||
| chr1:212973715 | G | A | 9 | a0001c0001t0014g0044 a0001c0001t0014g0266 a0001c0001t0020g0265 others(6): Show |
10 | HG00558.hp2 HG01069.hp1 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.880-240G>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 6/7 | chr1 | 212973715 | |||||||
| chr1:212973813 | T | TTTTTTAG others(44): Show |
1 | a0001c0001t0002g0106 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.880-111_880-110ins others(51): Show |
VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 212973813 | ||||||
| chr1:212973903 | G | T | 1 | a0001c0001t0002g0106 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.880-52G>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 6/7 | chr1 | 212973903 | |||||||
| chr1:212974133 | G | C | 1 | a0001c0001t0002g0106 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.995+63G>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212974133 | |||||||
| chr1:212974135 | C | G | 1 | a0001c0001t0002g0106 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.995+65C>G | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212974135 | |||||||
| chr1:212974239 | G | T | 36 | a0001c0001t0003g0035 a0001c0001t0003g0050 a0001c0001t0003g0126 others(33): Show |
37 | HG00558.hp2 HG01069.hp1 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.995+169G>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212974239 | |||||||
| chr1:212974285 | C | T | 1 | a0001c0001t0010g0273 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.995+215C>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212974285 | |||||||
| chr1:212974522 | A | G | 1 | a0001c0001t0024g0076 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.995+452A>G | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212974522 | |||||||
| chr1:212974531 | C | T | 14 | a0001c0001t0003g0035 a0001c0001t0003g0050 a0001c0001t0003g0135 others(11): Show |
14 | HG01167.hp2 HG02145.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.995+461C>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212974531 | |||||||
| chr1:212974556 | C | T | 1 | a0001c0001t0019g0188 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.995+486C>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212974556 | |||||||
| chr1:212974755 | A | G | 2 | a0001c0001t0002g0069 a0001c0001t0002g0093 |
2 | NA18990.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.995+685A>G | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212974755 | |||||||
| chr1:212974817 | C | G | 1 | a0001c0001t0004g0150 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.995+747C>G | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212974817 | |||||||
| chr1:212974839 | A | G | 1 | a0001c0001t0012g0063 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.995+769A>G | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212974839 | |||||||
| chr1:212974884 | C | G | 3 | a0002c0002t0005g0245 a0002c0002t0005g0251 a0002c0002t0030g0041 |
4 | HG01070.hp2 HG01071.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.995+814C>G | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212974884 | |||||||
| chr1:212974884 | C | T | 1 | a0001c0001t0003g0137 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.995+814C>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212974884 | |||||||
| chr1:212974906 | C | T | 1 | a0001c0001t0002g0106 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.995+836C>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212974906 | |||||||
| chr1:212975153 | TG | T | 39 | a0001c0001t0003g0035 a0001c0001t0003g0050 a0001c0001t0003g0126 others(36): Show |
40 | HG00558.hp2 HG01069.hp1 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.995+1087delG | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 212975153 | ||||||
| chr1:212975223 | A | AAGAAC | 4 | a0001c0001t0008g0043 a0001c0001t0008g0259 a0001c0001t0029g0243 others(1): Show |
5 | HG01891.hp1 HG02280.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.995+1156_995+1160d others(7): Show |
VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 212975223 | ||||||
| chr1:212975331 | T | C | 9 | a0001c0001t0014g0044 a0001c0001t0014g0266 a0001c0001t0020g0265 others(6): Show |
10 | HG00558.hp2 HG01069.hp1 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.995+1261T>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212975331 | |||||||
| chr1:212975397 | G | C | 1 | a0001c0001t0003g0140 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.995+1327G>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212975397 | |||||||
| chr1:212975441 | G | C | 1 | a0001c0001t0002g0106 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.995+1371G>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212975441 | |||||||
| chr1:212975442 | C | G | 1 | a0001c0001t0002g0106 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.995+1372C>G | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212975442 | |||||||
| chr1:212975442 | C | T | 3 | a0002c0002t0005g0245 a0002c0002t0005g0251 a0002c0002t0030g0041 |
4 | HG01070.hp2 HG01071.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.995+1372C>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212975442 | |||||||
| chr1:212975521 | G | A | 1 | a0001c0001t0003g0183 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.995+1451G>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212975521 | |||||||
| chr1:212975541 | C | T | 3 | a0002c0002t0005g0245 a0002c0002t0005g0251 a0002c0002t0030g0041 |
4 | HG01070.hp2 HG01071.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.995+1471C>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212975541 | |||||||
| chr1:212975547 | C | A | 8 | a0001c0001t0003g0010 a0001c0001t0003g0015 a0001c0001t0003g0138 others(5): Show |
13 | HG01243.hp1 HG02109.hp2 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.995+1477C>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212975547 | |||||||
| chr1:212975800 | T | C | 1 | a0001c0001t0008g0259 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.995+1730T>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212975800 | |||||||
| chr1:212975869 | A | T | 12 | a0001c0001t0003g0126 a0001c0001t0003g0127 a0001c0001t0003g0128 others(9): Show |
12 | HG02055.hp1 HG02257.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.995+1799A>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212975869 | |||||||
| chr1:212975976 | A | G | 14 | a0001c0001t0003g0035 a0001c0001t0003g0050 a0001c0001t0003g0135 others(11): Show |
14 | HG01167.hp2 HG02145.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.995+1906A>G | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212975976 | |||||||
| chr1:212976005 | C | T | 16 | a0001c0001t0002g0023 a0001c0001t0002g0024 a0001c0001t0002g0079 others(13): Show |
19 | HG00597.hp2 HG00621.hp1 HG02165.hp2 others(16): Show |
intron_variant | MODIFIER | c.995+1935C>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212976005 | |||||||
| chr1:212976006 | G | A | 2 | a0001c0001t0005g0240 a0001c0001t0005g0246 |
2 | HG02258.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.995+1936G>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212976006 | |||||||
| chr1:212976139 | T | C | 2 | a0001c0001t0002g0080 a0001c0001t0034g0268 |
2 | NA18964.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.995+2069T>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212976139 | |||||||
| chr1:212976188 | G | A | 3 | a0002c0002t0005g0245 a0002c0002t0005g0251 a0002c0002t0030g0041 |
4 | HG01070.hp2 HG01071.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.995+2118G>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212976188 | |||||||
| chr1:212976299 | G | A | 1 | a0001c0001t0045g0207 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.995+2229G>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212976299 | |||||||
| chr1:212976353 | C | A | 44 | a0001c0001t0003g0035 a0001c0001t0003g0050 a0001c0001t0003g0126 others(41): Show |
45 | HG00558.hp2 HG01069.hp1 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.995+2283C>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212976353 | |||||||
| chr1:212976394 | A | G | 1 | a0001c0001t0003g0212 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.995+2324A>G | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212976394 | |||||||
| chr1:212976522 | G | A | 1 | a0001c0001t0003g0218 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.995+2452G>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212976522 | |||||||
| chr1:212976568 | T | TA | 105 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0032 others(102): Show |
135 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(132): Show |
intron_variant | MODIFIER | c.995+2510dupA | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 212976568 | ||||||
| chr1:212976568 | T | TAA | 123 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0142 others(120): Show |
167 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.995+2509_995+2510d others(4): Show |
VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 212976568 | ||||||
| chr1:212976711 | A | G | 1 | a0001c0001t0012g0063 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.995+2641A>G | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212976711 | |||||||
| chr1:212976744 | G | GGT | 46 | a0001c0001t0002g0084 a0001c0001t0003g0035 a0001c0001t0003g0050 others(43): Show |
47 | HG00558.hp2 HG01069.hp1 HG01069.hp2 others(44): Show |
intron_variant | MODIFIER | c.995+2677_995+2678d others(4): Show |
VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 212976744 | ||||||
| chr1:212976755 | A | G | 1 | a0001c0001t0001g0054 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.995+2685A>G | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212976755 | |||||||
| chr1:212976848 | T | C | 10 | a0001c0001t0002g0084 a0001c0001t0014g0044 a0001c0001t0014g0266 others(7): Show |
11 | HG00558.hp2 HG01069.hp1 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.995+2778T>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212976848 | |||||||
| chr1:212976954 | G | T | 10 | a0001c0001t0002g0021 a0001c0001t0002g0052 a0001c0001t0002g0069 others(7): Show |
13 | HG00423.hp1 NA18950.hp2 NA18953.hp1 others(10): Show |
intron_variant | MODIFIER | c.995+2884G>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212976954 | |||||||
| chr1:212977014 | C | T | 14 | a0001c0001t0001g0038 a0001c0001t0003g0003 a0001c0001t0003g0016 others(11): Show |
26 | HG00408.hp2 HG01192.hp1 HG01192.hp2 others(23): Show |
intron_variant | MODIFIER | c.995+2944C>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212977014 | |||||||
| chr1:212977079 | A | G | 279 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(276): Show |
373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.995+3009A>G | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212977079 | |||||||
| chr1:212977105 | A | G | 3 | a0001c0001t0002g0020 a0001c0001t0002g0082 a0001c0001t0049g0020 |
3 | NA19067.hp1 NA19068.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.995+3035A>G | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212977105 | |||||||
| chr1:212977183 | GGCCA | G | 3 | a0001c0001t0003g0137 a0001c0001t0007g0085 a0001c0001t0007g0086 |
3 | HG01891.hp2 HG02451.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.995+3115_995+3118d others(6): Show |
VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 212977183 | ||||||
| chr1:212977187 | A | AG | 216 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(213): Show |
282 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(279): Show |
intron_variant | MODIFIER | c.995+3118dupG | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 212977187 | ||||||
| chr1:212977278 | C | A | 1 | a0001c0001t0003g0213 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.995+3208C>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212977278 | |||||||
| chr1:212977450 | G | A | 87 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0038 others(84): Show |
115 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(112): Show |
intron_variant | MODIFIER | c.995+3380G>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212977450 | |||||||
| chr1:212977627 | C | T | 15 | a0001c0001t0003g0035 a0001c0001t0003g0050 a0001c0001t0003g0135 others(12): Show |
15 | HG01167.hp2 HG02145.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.995+3557C>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212977627 | |||||||
| chr1:212977838 | T | G | 1 | a0001c0001t0007g0085 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.995+3768T>G | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212977838 | |||||||
| chr1:212977855 | C | T | 3 | a0001c0001t0009g0263 a0001c0001t0025g0124 a0001c0001t0025g0125 |
3 | HG01069.hp2 HG01071.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.995+3785C>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212977855 | |||||||
| chr1:212978012 | T | C | 1 | a0001c0001t0045g0207 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.995+3942T>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212978012 | |||||||
| chr1:212978188 | C | T | 1 | a0001c0001t0003g0136 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.995+4118C>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212978188 | |||||||
| chr1:212978238 | T | G | 211 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0038 others(208): Show |
277 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(274): Show |
intron_variant | MODIFIER | c.995+4168T>G | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212978238 | |||||||
| chr1:212978244 | C | T | 96 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0011 others(93): Show |
126 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.995+4174C>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212978244 | |||||||
| chr1:212978352 | C | T | 74 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0038 others(71): Show |
100 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(97): Show |
intron_variant | MODIFIER | c.995+4282C>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212978352 | |||||||
| chr1:212978364 | C | T | 1 | a0001c0001t0004g0174 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.995+4294C>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212978364 | |||||||
| chr1:212978473 | G | A | 3 | a0002c0002t0005g0245 a0002c0002t0005g0251 a0002c0002t0030g0041 |
4 | HG01070.hp2 HG01071.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.995+4403G>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212978473 | |||||||
| chr1:212978719 | T | A | 1 | a0001c0001t0001g0176 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.995+4649T>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212978719 | |||||||
| chr1:212978725 | C | G | 3 | a0001c0001t0002g0080 a0001c0001t0004g0159 a0001c0001t0034g0268 |
3 | HG02165.hp1 NA18964.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.995+4655C>G | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212978725 | |||||||
| chr1:212978749 | C | T | 1 | a0001c0001t0004g0174 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.995+4679C>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212978749 | |||||||
| chr1:212978808 | A | G | 1 | a0001c0001t0018g0059 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.995+4738A>G | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212978808 | |||||||
| chr1:212978820 | G | T | 18 | a0001c0001t0003g0035 a0001c0001t0003g0050 a0001c0001t0003g0135 others(15): Show |
18 | HG01069.hp2 HG01071.hp2 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.995+4750G>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212978820 | |||||||
| chr1:212979026 | TAGG | T | 2 | a0001c0001t0004g0033 a0001c0001t0004g0144 |
3 | HG00609.hp2 NA18952.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.995+4962_995+4964d others(5): Show |
VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 212979026 | ||||||
| chr1:212979049 | C | T | 106 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0011 others(103): Show |
139 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.995+4979C>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212979049 | |||||||
| chr1:212979062 | TAAG | T | 129 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0011 others(126): Show |
167 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.995+5000_995+5002d others(5): Show |
VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 212979062 | ||||||
| chr1:212979136 | C | T | 1 | a0001c0001t0002g0084 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.995+5066C>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212979136 | |||||||
| chr1:212979162 | G | A | 5 | a0001c0001t0010g0269 a0001c0001t0010g0270 a0001c0001t0017g0025 others(2): Show |
5 | HG02622.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.995+5092G>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212979162 | |||||||
| chr1:212979261 | T | C | 1 | a0001c0001t0045g0207 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.995+5191T>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212979261 | |||||||
| chr1:212979479 | G | A | 2 | a0001c0001t0001g0133 a0001c0001t0045g0207 |
2 | NA18906.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.995+5409G>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212979479 | |||||||
| chr1:212979591 | T | C | 2 | a0001c0001t0005g0249 a0001c0001t0055g0241 |
2 | HG03139.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.995+5521T>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212979591 | |||||||
| chr1:212979658 | A | G | 3 | a0001c0001t0009g0263 a0001c0001t0025g0124 a0001c0001t0025g0125 |
3 | HG01069.hp2 HG01071.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.995+5588A>G | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212979658 | |||||||
| chr1:212979697 | G | A | 1 | a0001c0001t0010g0269 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.995+5627G>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212979697 | |||||||
| chr1:212979759 | G | A | 9 | a0001c0001t0003g0010 a0001c0001t0003g0015 a0001c0001t0003g0138 others(6): Show |
14 | HG01243.hp1 HG02109.hp2 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.995+5689G>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212979759 | |||||||
| chr1:212979865 | G | GATTCATG others(10): Show |
1 | a0001c0001t0054g0258 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.995+5796_995+5812d others(19): Show |
VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 212979865 | ||||||
| chr1:212980023 | G | A | 9 | a0001c0001t0003g0157 a0001c0001t0003g0158 a0001c0001t0005g0239 others(6): Show |
10 | HG01884.hp1 HG02055.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.995+5953G>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212980023 | |||||||
| chr1:212980034 | A | C | 12 | a0001c0001t0003g0126 a0001c0001t0003g0127 a0001c0001t0003g0128 others(9): Show |
12 | HG02055.hp1 HG02257.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.995+5964A>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212980034 | |||||||
| chr1:212980062 | C | T | 21 | a0001c0001t0002g0084 a0001c0001t0003g0126 a0001c0001t0003g0127 others(18): Show |
22 | HG00558.hp2 HG01069.hp1 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.995+5992C>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212980062 | |||||||
| chr1:212980120 | A | G | 10 | a0001c0001t0003g0010 a0001c0001t0003g0015 a0001c0001t0003g0138 others(7): Show |
15 | HG01243.hp1 HG02109.hp2 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.995+6050A>G | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212980120 | |||||||
| chr1:212980317 | G | T | 266 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(263): Show |
358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.995+6247G>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212980317 | |||||||
| chr1:212980746 | G | A | 4 | a0001c0001t0022g0271 a0001c0001t0022g0272 a0001c0001t0038g0046 others(1): Show |
4 | HG02809.hp2 HG03540.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.995+6676G>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212980746 | |||||||
| chr1:212980862 | C | T | 2 | a0001c0001t0001g0176 a0001c0001t0001g0178 |
2 | HG03834.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.995+6792C>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212980862 | |||||||
| chr1:212980872 | G | A | 1 | a0001c0001t0019g0188 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.995+6802G>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212980872 | |||||||
| chr1:212981010 | G | T | 1 | a0001c0001t0004g0144 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.995+6940G>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212981010 | |||||||
| chr1:212981027 | G | T | 10 | a0001c0001t0003g0191 a0001c0001t0003g0192 a0001c0001t0003g0234 others(7): Show |
10 | HG00639.hp2 HG01258.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.995+6957G>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212981027 | |||||||
| chr1:212981089 | G | A | 1 | a0001c0001t0007g0061 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.995+7019G>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212981089 | |||||||
| chr1:212981117 | T | A | 3 | a0001c0001t0001g0029 a0001c0001t0001g0180 a0001c0001t0001g0199 |
4 | NA18946.hp1 NA18947.hp2 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.995+7047T>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212981117 | |||||||
| chr1:212981188 | G | A | 1 | a0001c0001t0002g0081 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.995+7118G>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212981188 | |||||||
| chr1:212981212 | G | A | 1 | a0001c0001t0004g0165 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.995+7142G>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212981212 | |||||||
| chr1:212981341 | A | T | 2 | a0001c0001t0003g0234 a0001c0001t0007g0107 |
2 | HG00639.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.996-7171A>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212981341 | |||||||
| chr1:212981347 | G | A | 9 | a0001c0001t0003g0191 a0001c0001t0003g0192 a0001c0001t0003g0234 others(6): Show |
9 | HG00639.hp2 HG01258.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.996-7165G>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212981347 | |||||||
| chr1:212981481 | T | C | 1 | a0001c0001t0003g0143 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.996-7031T>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212981481 | |||||||
| chr1:212981493 | G | T | 1 | a0005c0004t0005g0253 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.996-7019G>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212981493 | |||||||
| chr1:212981699 | G | GGTGA | 3 | a0001c0001t0001g0031 a0001c0001t0001g0134 a0001c0001t0020g0265 |
4 | HG00408.hp1 HG00423.hp2 NA18939.hp2 others(1): Show |
intron_variant | MODIFIER | c.996-6811_996-6808d others(6): Show |
VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 212981699 | ||||||
| chr1:212981712 | C | T | 14 | a0001c0001t0003g0191 a0001c0001t0003g0192 a0001c0001t0003g0234 others(11): Show |
14 | HG00639.hp2 HG01258.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.996-6800C>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212981712 | |||||||
| chr1:212981722 | A | G | 8 | a0001c0001t0014g0044 a0001c0001t0014g0266 a0001c0001t0023g0120 others(5): Show |
10 | HG00558.hp2 HG01069.hp1 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.996-6790A>G | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212981722 | |||||||
| chr1:212982086 | C | T | 17 | a0001c0001t0003g0003 a0001c0001t0003g0016 a0001c0001t0003g0037 others(14): Show |
28 | HG00408.hp2 HG00597.hp1 HG00597.hp2 others(25): Show |
intron_variant | MODIFIER | c.996-6426C>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212982086 | |||||||
| chr1:212982171 | G | A | 1 | a0001c0001t0003g0126 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.996-6341G>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212982171 | |||||||
| chr1:212982212 | G | A | 1 | a0001c0001t0003g0211 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.996-6300G>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212982212 | |||||||
| chr1:212982224 | G | T | 95 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0011 others(92): Show |
125 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.996-6288G>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212982224 | |||||||
| chr1:212982321 | G | A | 1 | a0001c0001t0004g0028 | 2 | HG00438.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.996-6191G>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212982321 | |||||||
| chr1:212982350 | A | T | 2 | a0001c0001t0001g0260 a0001c0001t0029g0243 |
2 | HG02486.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.996-6162A>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212982350 | |||||||
| chr1:212982390 | G | C | 3 | a0001c0001t0003g0157 a0001c0001t0003g0158 a0001c0001t0005g0239 |
3 | HG02970.hp2 HG03139.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.996-6122G>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212982390 | |||||||
| chr1:212982525 | G | T | 10 | a0001c0001t0014g0044 a0001c0001t0014g0266 a0001c0001t0023g0060 others(7): Show |
12 | HG00558.hp2 HG01069.hp1 HG01070.hp2 others(9): Show |
intron_variant | MODIFIER | c.996-5987G>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212982525 | |||||||
| chr1:212982656 | CCTA | C | 19 | a0001c0001t0003g0010 a0001c0001t0003g0015 a0001c0001t0003g0126 others(16): Show |
24 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.996-5853_996-5851d others(5): Show |
VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 212982656 | ||||||
| chr1:212982670 | A | G | 10 | a0001c0001t0014g0044 a0001c0001t0014g0266 a0001c0001t0023g0060 others(7): Show |
12 | HG00558.hp2 HG01069.hp1 HG01070.hp2 others(9): Show |
intron_variant | MODIFIER | c.996-5842A>G | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212982670 | |||||||
| chr1:212982790 | C | T | 1 | a0001c0001t0029g0248 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.996-5722C>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212982790 | |||||||
| chr1:212982833 | C | T | 1 | a0001c0001t0045g0207 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.996-5679C>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212982833 | |||||||
| chr1:212982956 | G | A | 27 | a0001c0001t0003g0003 a0001c0001t0003g0016 a0001c0001t0003g0037 others(24): Show |
40 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.996-5556G>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212982956 | |||||||
| chr1:212983076 | A | C | 27 | a0001c0001t0003g0003 a0001c0001t0003g0016 a0001c0001t0003g0037 others(24): Show |
40 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.996-5436A>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212983076 | |||||||
| chr1:212983120 | C | T | 1 | a0001c0001t0045g0207 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.996-5392C>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212983120 | |||||||
| chr1:212983253 | T | C | 1 | a0001c0001t0029g0243 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.996-5259T>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212983253 | |||||||
| chr1:212983507 | G | A | 1 | a0001c0001t0003g0143 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.996-5005G>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212983507 | |||||||
| chr1:212983512 | G | A | 17 | a0001c0001t0003g0003 a0001c0001t0003g0016 a0001c0001t0003g0037 others(14): Show |
28 | HG00408.hp2 HG00597.hp1 HG00597.hp2 others(25): Show |
intron_variant | MODIFIER | c.996-5000G>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212983512 | |||||||
| chr1:212983566 | G | A | 1 | a0001c0001t0031g0252 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.996-4946G>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212983566 | |||||||
| chr1:212983797 | G | A | 3 | a0001c0001t0008g0043 a0001c0001t0008g0259 a0001c0001t0052g0242 |
4 | HG01891.hp1 HG02280.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.996-4715G>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212983797 | |||||||
| chr1:212983853 | T | G | 27 | a0001c0001t0003g0003 a0001c0001t0003g0016 a0001c0001t0003g0037 others(24): Show |
40 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.996-4659T>G | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212983853 | |||||||
| chr1:212984034 | T | G | 17 | a0001c0001t0003g0003 a0001c0001t0003g0016 a0001c0001t0003g0037 others(14): Show |
28 | HG00408.hp2 HG00597.hp1 HG00597.hp2 others(25): Show |
intron_variant | MODIFIER | c.996-4478T>G | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212984034 | |||||||
| chr1:212984412 | G | A | 2 | a0001c0001t0014g0044 a0001c0001t0026g0227 |
3 | NA18956.hp2 NA19002.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.996-4100G>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212984412 | |||||||
| chr1:212984452 | G | C | 7 | a0001c0001t0008g0276 a0001c0001t0009g0047 a0001c0001t0009g0122 others(4): Show |
8 | HG01884.hp1 HG02109.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.996-4060G>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212984452 | |||||||
| chr1:212984549 | G | A | 278 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(275): Show |
371 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(368): Show |
intron_variant | MODIFIER | c.996-3963G>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212984549 | |||||||
| chr1:212984681 | C | G | 17 | a0001c0001t0003g0003 a0001c0001t0003g0016 a0001c0001t0003g0037 others(14): Show |
28 | HG00408.hp2 HG00597.hp1 HG00597.hp2 others(25): Show |
intron_variant | MODIFIER | c.996-3831C>G | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212984681 | |||||||
| chr1:212985122 | A | G | 1 | a0001c0001t0003g0217 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.996-3390A>G | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212985122 | |||||||
| chr1:212985177 | A | G | 1 | a0001c0001t0003g0216 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.996-3335A>G | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212985177 | |||||||
| chr1:212985198 | C | CT | 30 | a0001c0001t0001g0030 a0001c0001t0002g0019 a0001c0001t0002g0024 others(27): Show |
35 | HG00621.hp2 HG01109.hp2 HG01123.hp2 others(32): Show |
intron_variant | MODIFIER | c.996-3291dupT | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 212985198 | ||||||
| chr1:212985198 | C | CTT | 13 | a0001c0001t0003g0003 a0001c0001t0003g0183 a0001c0001t0003g0215 others(10): Show |
21 | HG00408.hp2 HG00609.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.996-3292_996-3291d others(4): Show |
VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 212985198 | ||||||
| chr1:212985198 | C | CTTT | 7 | a0001c0001t0003g0016 a0001c0001t0003g0037 a0001c0001t0003g0143 others(4): Show |
10 | HG00597.hp1 HG00597.hp2 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.996-3293_996-3291d others(5): Show |
VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 212985198 | ||||||
| chr1:212985198 | CT | C | 20 | a0001c0001t0003g0010 a0001c0001t0003g0015 a0001c0001t0003g0126 others(17): Show |
25 | HG00642.hp2 HG01243.hp1 HG02257.hp1 others(22): Show |
intron_variant | MODIFIER | c.996-3291delT | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 212985198 | ||||||
| chr1:212985198 | CTTTTTTT | C | 64 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(61): Show |
103 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.996-3297_996-3291d others(9): Show |
VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 212985198 | ||||||
| chr1:212985403 | C | T | 53 | a0001c0001t0003g0010 a0001c0001t0003g0015 a0001c0001t0003g0035 others(50): Show |
59 | HG00639.hp2 HG00642.hp2 HG01243.hp1 others(56): Show |
intron_variant | MODIFIER | c.996-3109C>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212985403 | |||||||
| chr1:212985419 | C | CT | 13 | a0001c0001t0003g0145 a0001c0001t0004g0166 a0001c0001t0014g0044 others(10): Show |
15 | HG00558.hp2 HG00738.hp1 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.996-3077dupT | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 212985419 | ||||||
| chr1:212985419 | CT | C | 17 | a0001c0001t0001g0175 a0001c0001t0001g0177 a0001c0001t0002g0114 others(14): Show |
17 | HG00642.hp2 HG02055.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.996-3077delT | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 212985419 | ||||||
| chr1:212985419 | CTT | C | 16 | a0001c0001t0003g0003 a0001c0001t0003g0016 a0001c0001t0003g0037 others(13): Show |
27 | HG00408.hp2 HG00597.hp1 HG00597.hp2 others(24): Show |
intron_variant | MODIFIER | c.996-3078_996-3077d others(4): Show |
VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 212985419 | ||||||
| chr1:212985520 | A | C | 2 | a0001c0001t0022g0271 a0001c0001t0022g0272 |
2 | NA19030.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.996-2992A>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212985520 | |||||||
| chr1:212985752 | G | A | 17 | a0001c0001t0003g0003 a0001c0001t0003g0016 a0001c0001t0003g0037 others(14): Show |
28 | HG00408.hp2 HG00597.hp1 HG00597.hp2 others(25): Show |
intron_variant | MODIFIER | c.996-2760G>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212985752 | |||||||
| chr1:212985976 | C | T | 1 | a0002c0002t0005g0251 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.996-2536C>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212985976 | |||||||
| chr1:212986077 | A | G | 1 | a0001c0001t0045g0207 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.996-2435A>G | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212986077 | |||||||
| chr1:212986144 | T | C | 1 | a0001c0001t0045g0207 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.996-2368T>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212986144 | |||||||
| chr1:212986192 | T | C | 10 | a0001c0001t0014g0044 a0001c0001t0014g0266 a0001c0001t0023g0060 others(7): Show |
12 | HG00738.hp1 HG01069.hp1 HG01070.hp2 others(9): Show |
intron_variant | MODIFIER | c.996-2320T>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212986192 | |||||||
| chr1:212986213 | A | C | 1 | a0001c0001t0002g0111 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.996-2299A>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212986213 | |||||||
| chr1:212986280 | T | A | 7 | a0001c0001t0003g0236 a0001c0001t0005g0039 a0001c0001t0005g0040 others(4): Show |
9 | HG01109.hp2 HG01884.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.996-2232T>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212986280 | |||||||
| chr1:212986414 | AGGAGACA others(4): Show |
A | 3 | a0001c0001t0003g0050 a0001c0001t0010g0273 a0005c0004t0005g0253 |
3 | HG01167.hp2 HG03195.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.996-2093_996-2083d others(13): Show |
VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 212986414 | ||||||
| chr1:212986463 | A | C | 1 | a0001c0001t0004g0186 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.996-2049A>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212986463 | |||||||
| chr1:212986487 | G | A | 1 | a0001c0001t0002g0022 | 2 | HG00738.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.996-2025G>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212986487 | |||||||
| chr1:212986662 | T | C | 1 | a0001c0001t0043g0190 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.996-1850T>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212986662 | |||||||
| chr1:212986742 | A | AG | 134 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(131): Show |
191 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.996-1769dupG | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 212986742 | ||||||
| chr1:212986792 | A | C | 3 | a0001c0001t0003g0157 a0001c0001t0003g0158 a0001c0001t0005g0239 |
3 | HG02970.hp2 HG03139.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.996-1720A>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212986792 | |||||||
| chr1:212986803 | T | C | 17 | a0001c0001t0003g0035 a0001c0001t0003g0135 a0001c0001t0003g0136 others(14): Show |
17 | HG00639.hp2 HG01258.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.996-1709T>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212986803 | |||||||
| chr1:212986864 | G | A | 4 | a0001c0001t0003g0275 a0001c0001t0005g0249 a0001c0001t0010g0269 others(1): Show |
4 | HG00642.hp2 HG03139.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.996-1648G>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212986864 | |||||||
| chr1:212986906 | G | A | 1 | a0001c0001t0045g0207 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.996-1606G>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212986906 | |||||||
| chr1:212987031 | C | CAGAG | 18 | a0001c0001t0003g0003 a0001c0001t0003g0016 a0001c0001t0003g0037 others(15): Show |
29 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(26): Show |
intron_variant | MODIFIER | c.996-1459_996-1456d others(6): Show |
VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 212987031 | ||||||
| chr1:212987031 | CAGAG | C | 22 | a0001c0001t0003g0035 a0001c0001t0003g0135 a0001c0001t0003g0136 others(19): Show |
22 | HG00099.hp2 HG00639.hp2 HG01175.hp1 others(19): Show |
intron_variant | MODIFIER | c.996-1459_996-1456d others(6): Show |
VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 212987031 | ||||||
| chr1:212987066 | G | T | 1 | a0001c0001t0001g0187 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.996-1446G>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212987066 | |||||||
| chr1:212987258 | C | CT | 47 | a0001c0001t0003g0003 a0001c0001t0003g0010 a0001c0001t0003g0015 others(44): Show |
64 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.996-1239dupT | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 212987258 | ||||||
| chr1:212987484 | G | A | 159 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(156): Show |
220 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(217): Show |
intron_variant | MODIFIER | c.996-1028G>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212987484 | |||||||
| chr1:212987561 | C | T | 7 | a0001c0001t0003g0236 a0001c0001t0005g0039 a0001c0001t0005g0040 others(4): Show |
9 | HG01109.hp2 HG01884.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.996-951C>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212987561 | |||||||
| chr1:212987563 | A | C | 1 | a0001c0001t0001g0030 | 2 | HG01516.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.996-949A>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212987563 | |||||||
| chr1:212987660 | T | C | 1 | a0001c0001t0027g0262 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.996-852T>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212987660 | |||||||
| chr1:212987683 | AC | A | 19 | a0001c0001t0003g0003 a0001c0001t0003g0016 a0001c0001t0003g0037 others(16): Show |
30 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(27): Show |
intron_variant | MODIFIER | c.996-828delC | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212987683 | |||||||
| chr1:212987720 | C | T | 1 | a0001c0001t0004g0150 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.996-792C>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212987720 | |||||||
| chr1:212987814 | T | C | 3 | a0001c0001t0014g0266 a0001c0001t0042g0167 a0002c0002t0030g0041 |
4 | HG00738.hp1 HG01069.hp1 HG01070.hp2 others(1): Show |
intron_variant | MODIFIER | c.996-698T>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212987814 | |||||||
| chr1:212987821 | C | T | 2 | a0001c0001t0022g0271 a0001c0001t0022g0272 |
2 | NA19030.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.996-691C>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212987821 | |||||||
| chr1:212987829 | T | C | 99 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0011 others(96): Show |
129 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.996-683T>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212987829 | |||||||
| chr1:212987992 | C | A | 2 | a0001c0001t0025g0124 a0001c0001t0025g0125 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.996-520C>A | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212987992 | |||||||
| chr1:212988166 | C | T | 19 | a0001c0001t0003g0003 a0001c0001t0003g0016 a0001c0001t0003g0037 others(16): Show |
30 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(27): Show |
intron_variant | MODIFIER | c.996-346C>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212988166 | |||||||
| chr1:212988246 | C | T | 1 | a0001c0001t0002g0074 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.996-266C>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212988246 | |||||||
| chr1:212988294 | C | T | 19 | a0001c0001t0003g0003 a0001c0001t0003g0016 a0001c0001t0003g0037 others(16): Show |
30 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(27): Show |
intron_variant | MODIFIER | c.996-218C>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212988294 | |||||||
| chr1:212988309 | G | T | 2 | a0001c0001t0013g0017 a0001c0001t0013g0247 |
4 | HG02258.hp2 HG02280.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.996-203G>T | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212988309 | |||||||
| chr1:212988367 | A | C | 1 | a0001c0001t0031g0237 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.996-145A>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212988367 | |||||||
| chr1:212988489 | A | G | 9 | a0001c0001t0014g0044 a0001c0001t0014g0266 a0001c0001t0023g0060 others(6): Show |
11 | HG00738.hp1 HG01069.hp1 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.996-23A>G | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212988489 | |||||||
| chr1:212988492 | T | C | 3 | a0001c0001t0023g0060 a0001c0001t0023g0120 a0001c0001t0043g0190 |
3 | HG01074.hp2 HG03490.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.996-20T>C | VASH2 | ENSG00000143494.16 | transcript | ENST00000517399.3 | protein_coding | 7/7 | chr1 | 212988492 |