Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 7429 |
| ensemblid | ENSG00000127831.11 |
| hgncid | 12690 |
| symbol | VIL1 |
| name | villin 1 |
| refseq_nuc | NM_007127.3 |
| refseq_prot | NP_009058.2 |
| ensembl_nuc | ENST00000248444.10 |
| ensembl_prot | ENSP00000248444.5 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 218419123 |
| end | 218453295 |
| strand | + |
| ver | v1.2 |
| region | chr2:218419123-218453295 |
| region5000 | chr2:218414123-218458295 |
| regionname0 | VIL1_chr2_218419123_218453295 |
| regionname5000 | VIL1_chr2_218414123_218458295 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 827 | 313 | 72 | 51 | 126 | 16 | 46 | 98 | VIL1_chr2_218414123_218458295 | VIL1 | MTKLS others(822): Show |
chr2 | 218414123 | 218458295 |
| a0002 | 0/0 | 827 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | MTKLS others(822): Show |
chr2 | 218414123 | 218458295 |
| a0003 | 0/0 | 827 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | MTKLS others(822): Show |
chr2 | 218414123 | 218458295 |
| a0004 | 0/0 | 827 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | MTKLS others(822): Show |
chr2 | 218414123 | 218458295 |
| a0005 | 0/0 | 827 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | MTKLS others(822): Show |
chr2 | 218414123 | 218458295 |
| a0006 | 0/0 | 827 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | MTKLS others(822): Show |
chr2 | 218414123 | 218458295 |
| a0007 | 0/0 | 827 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | MTKLS others(822): Show |
chr2 | 218414123 | 218458295 |
| a0008 | 0/0 | 827 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | MTKLS others(822): Show |
chr2 | 218414123 | 218458295 |
| a0009 | 0/0 | 827 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | VIL1_chr2_218414123_218458295 | VIL1 | MTKLS others(822): Show |
chr2 | 218414123 | 218458295 |
| a0010 | 0/0 | 827 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | VIL1_chr2_218414123_218458295 | VIL1 | MTKLS others(822): Show |
chr2 | 218414123 | 218458295 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2481 | 306 | 68 | 50 | 125 | 16 | 45 | VIL1_chr2_218414123_218458295 | VIL1 | ATGAC others(2476): Show |
chr2 | 218414123 | 218458295 | ||
| a0001c0005 | 0/0 | 2481 | 4 | 4 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | ATGAC others(2476): Show |
chr2 | 218414123 | 218458295 | ||
| a0001c0012 | 0/0 | 2481 | 1 | 0 | 1 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | ATGAC others(2476): Show |
chr2 | 218414123 | 218458295 | ||
| a0001c0013 | 0/0 | 2481 | 1 | 0 | 0 | 0 | 0 | 1 | VIL1_chr2_218414123_218458295 | VIL1 | ATGAC others(2476): Show |
chr2 | 218414123 | 218458295 | ||
| a0001c0014 | 0/0 | 2481 | 1 | 0 | 0 | 1 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | ATGAC others(2476): Show |
chr2 | 218414123 | 218458295 | ||
| a0002c0002 | 0/0 | 2481 | 6 | 6 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | ATGAC others(2476): Show |
chr2 | 218414123 | 218458295 | ||
| a0003c0003 | 0/0 | 2481 | 5 | 5 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | ATGAC others(2476): Show |
chr2 | 218414123 | 218458295 | ||
| a0004c0004 | 0/0 | 2481 | 5 | 5 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | ATGAC others(2476): Show |
chr2 | 218414123 | 218458295 | ||
| a0005c0006 | 0/0 | 2481 | 2 | 2 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | ATGAC others(2476): Show |
chr2 | 218414123 | 218458295 | ||
| a0006c0008 | 0/0 | 2481 | 1 | 0 | 1 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | ATGAC others(2476): Show |
chr2 | 218414123 | 218458295 | ||
| a0007c0007 | 0/0 | 2481 | 1 | 1 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | ATGAC others(2476): Show |
chr2 | 218414123 | 218458295 | ||
| a0008c0009 | 0/0 | 2481 | 1 | 1 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | ATGAC others(2476): Show |
chr2 | 218414123 | 218458295 | ||
| a0009c0011 | 0/0 | 2481 | 1 | 0 | 0 | 1 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | ATGAC others(2476): Show |
chr2 | 218414123 | 218458295 | ||
| a0010c0010 | 0/0 | 2481 | 1 | 0 | 0 | 1 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | ATGAC others(2476): Show |
chr2 | 218414123 | 218458295 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 6508 | 128 | 4 | 25 | 67 | 6 | 25 | VIL1_chr2_218414123_218458295 | VIL1 | ACAAT others(6503): Show |
chr2 | 218414123 | 218458295 |
| a0001c0001t0002 | 0/0 | 6508 | 51 | 22 | 1 | 24 | 0 | 4 | VIL1_chr2_218414123_218458295 | VIL1 | ACAAT others(6503): Show |
chr2 | 218414123 | 218458295 |
| a0001c0001t0003 | 0/0 | 6508 | 57 | 11 | 13 | 19 | 4 | 10 | VIL1_chr2_218414123_218458295 | VIL1 | ACAAT others(6503): Show |
chr2 | 218414123 | 218458295 |
| a0001c0001t0004 | 0/0 | 6508 | 17 | 0 | 8 | 0 | 6 | 3 | VIL1_chr2_218414123_218458295 | VIL1 | ACAAT others(6503): Show |
chr2 | 218414123 | 218458295 |
| a0001c0001t0005 | 0/0 | 6508 | 11 | 9 | 2 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | ACAAT others(6503): Show |
chr2 | 218414123 | 218458295 |
| a0001c0001t0006 | 0/0 | 6505 | 9 | 9 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | ACAAT others(6500): Show |
chr2 | 218414123 | 218458295 |
| a0001c0001t0007 | 0/0 | 6508 | 10 | 0 | 0 | 10 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | ACAAT others(6503): Show |
chr2 | 218414123 | 218458295 |
| a0001c0001t0008 | 1/0 | 6500 | 6 | 5 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | ACAAT others(6495): Show |
chr2 | 218414123 | 218458295 |
| a0001c0001t0009 | 0/0 | 6508 | 3 | 3 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | ACAAT others(6503): Show |
chr2 | 218414123 | 218458295 |
| a0001c0001t0011 | 0/0 | 6505 | 2 | 2 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | ACAAT others(6500): Show |
chr2 | 218414123 | 218458295 |
| a0001c0001t0013 | 0/0 | 6508 | 1 | 0 | 0 | 1 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | ACAAT others(6503): Show |
chr2 | 218414123 | 218458295 |
| a0001c0001t0014 | 0/0 | 6508 | 1 | 0 | 0 | 0 | 0 | 1 | VIL1_chr2_218414123_218458295 | VIL1 | ACAAT others(6503): Show |
chr2 | 218414123 | 218458295 |
| a0001c0001t0015 | 0/0 | 6508 | 1 | 0 | 0 | 1 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | ACAAT others(6503): Show |
chr2 | 218414123 | 218458295 |
| a0001c0001t0016 | 0/0 | 6508 | 1 | 0 | 0 | 1 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | ACAAT others(6503): Show |
chr2 | 218414123 | 218458295 |
| a0001c0001t0017 | 0/0 | 6508 | 1 | 1 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | ACAAT others(6503): Show |
chr2 | 218414123 | 218458295 |
| a0001c0001t0018 | 0/0 | 6508 | 1 | 0 | 0 | 0 | 0 | 1 | VIL1_chr2_218414123_218458295 | VIL1 | ACAAT others(6503): Show |
chr2 | 218414123 | 218458295 |
| a0001c0001t0019 | 0/0 | 6508 | 1 | 1 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | ACAAT others(6503): Show |
chr2 | 218414123 | 218458295 |
| a0001c0001t0020 | 0/0 | 6500 | 1 | 0 | 1 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | ACAAT others(6495): Show |
chr2 | 218414123 | 218458295 |
| a0001c0001t0021 | 0/0 | 6508 | 1 | 0 | 0 | 1 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | ACAAT others(6503): Show |
chr2 | 218414123 | 218458295 |
| a0001c0001t0022 | 0/0 | 6508 | 1 | 0 | 0 | 1 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | ACAAT others(6503): Show |
chr2 | 218414123 | 218458295 |
| a0001c0001t0023 | 0/0 | 6508 | 1 | 1 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | ACAAT others(6503): Show |
chr2 | 218414123 | 218458295 |
| a0001c0001t0024 | 0/0 | 6508 | 1 | 0 | 0 | 0 | 0 | 1 | VIL1_chr2_218414123_218458295 | VIL1 | ACAAT others(6503): Show |
chr2 | 218414123 | 218458295 |
| a0001c0005t0002 | 0/0 | 6508 | 4 | 4 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | ACAAT others(6503): Show |
chr2 | 218414123 | 218458295 |
| a0001c0012t0003 | 0/0 | 6508 | 1 | 0 | 1 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | ACAAT others(6503): Show |
chr2 | 218414123 | 218458295 |
| a0001c0013t0004 | 0/0 | 6508 | 1 | 0 | 0 | 0 | 0 | 1 | VIL1_chr2_218414123_218458295 | VIL1 | ACAAT others(6503): Show |
chr2 | 218414123 | 218458295 |
| a0001c0014t0001 | 0/0 | 6508 | 1 | 0 | 0 | 1 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | ACAAT others(6503): Show |
chr2 | 218414123 | 218458295 |
| a0002c0002t0005 | 0/0 | 6508 | 6 | 6 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | ACAAT others(6503): Show |
chr2 | 218414123 | 218458295 |
| a0003c0003t0010 | 0/0 | 6507 | 3 | 3 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | ACAAT others(6502): Show |
chr2 | 218414123 | 218458295 |
| a0003c0003t0012 | 0/0 | 6507 | 2 | 2 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | ACAAT others(6502): Show |
chr2 | 218414123 | 218458295 |
| a0004c0004t0002 | 0/0 | 6508 | 5 | 5 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | ACAAT others(6503): Show |
chr2 | 218414123 | 218458295 |
| a0005c0006t0002 | 0/0 | 6508 | 2 | 2 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | ACAAT others(6503): Show |
chr2 | 218414123 | 218458295 |
| a0006c0008t0001 | 0/0 | 6508 | 1 | 0 | 1 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | ACAAT others(6503): Show |
chr2 | 218414123 | 218458295 |
| a0007c0007t0002 | 0/0 | 6508 | 1 | 1 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | ACAAT others(6503): Show |
chr2 | 218414123 | 218458295 |
| a0008c0009t0006 | 0/0 | 6505 | 1 | 1 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | ACAAT others(6500): Show |
chr2 | 218414123 | 218458295 |
| a0009c0011t0003 | 0/0 | 6508 | 1 | 0 | 0 | 1 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | ACAAT others(6503): Show |
chr2 | 218414123 | 218458295 |
| a0010c0010t0001 | 0/0 | 6508 | 1 | 0 | 0 | 1 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | ACAAT others(6503): Show |
chr2 | 218414123 | 218458295 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 33 | 0 | 5 | 22 | 3 | 3 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0001g0025 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0001g0160 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0002g0003 | 0/0 | 7 | 0 | 0 | 6 | 0 | 1 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0002g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0002g0007 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0002g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0002g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0002g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0002g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0002g0034 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0002g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0002g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0003g0002 | 0/0 | 8 | 1 | 2 | 3 | 1 | 1 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0003g0004 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0003g0006 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0003g0008 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0003g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0003g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0003g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0003g0033 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0003g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0003g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0003g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0004g0002 | 0/0 | 6 | 0 | 1 | 0 | 3 | 2 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0004g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0004g0018 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0004g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0004g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0004g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0004g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0004g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0004g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0005g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0005g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0005g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0005g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0005g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0005g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0005g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0005g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0005g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0005g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0006g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0006g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0006g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0006g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0006g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0006g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0006g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0006g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0007g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0007g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0007g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0007g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0007g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0007g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0007g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0008g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0008g0043 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0008g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0008g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0008g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0009g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0009g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0011g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0013g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0014g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0015g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0016g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0017g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0018g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0019g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0020g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0021g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0022g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0023g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0001t0024g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0005t0002g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0005t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0005t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0012t0003g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0013t0004g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0001c0014t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0002c0002t0005g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0002c0002t0005g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0002c0002t0005g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0002c0002t0005g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0002c0002t0005g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0002c0002t0005g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0003c0003t0010g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0003c0003t0010g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0003c0003t0010g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0003c0003t0012g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0003c0003t0012g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0004c0004t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0004c0004t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0004c0004t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0004c0004t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0004c0004t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0005c0006t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0005c0006t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0006c0008t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0007c0007t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0008c0009t0006g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0009c0011t0003g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| a0010c0010t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0141 | EUR | GBR | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG00099 | hp2 | a0001 | c0001 | t0004 | g0090 | EUR | GBR | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG00140 | hp1 | a0001 | c0001 | t0004 | g0018 | EUR | GBR | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0156 | EUR | GBR | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0162 | EUR | FIN | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG00323 | hp1 | a0001 | c0001 | t0003 | g0002 | EUR | FIN | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG00408 | hp2 | a0001 | c0001 | t0022 | g0001 | EAS | CHS | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | CHS | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0128 | EAS | CHS | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | CHS | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | CHS | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0095 | AMR | PUR | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG00733 | hp1 | a0001 | c0001 | t0004 | g0019 | AMR | PUR | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0082 | AMR | PUR | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0166 | AMR | PUR | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG00741 | hp2 | a0001 | c0001 | t0020 | g0146 | AMR | PUR | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG01069 | hp1 | a0001 | c0001 | t0004 | g0002 | AMR | PUR | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG01069 | hp2 | a0001 | c0012 | t0003 | g0002 | AMR | PUR | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG01070 | hp1 | a0001 | c0001 | t0004 | g0080 | AMR | PUR | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG01081 | hp2 | a0001 | c0001 | t0004 | g0004 | AMR | PUR | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG01099 | hp2 | a0001 | c0001 | t0004 | g0087 | AMR | PUR | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG01109 | hp1 | a0001 | c0001 | t0005 | g0176 | AMR | PUR | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG01109 | hp2 | a0001 | c0001 | t0004 | g0004 | AMR | PUR | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG01175 | hp1 | a0006 | c0008 | t0001 | g0119 | AMR | PUR | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0053 | AMR | PUR | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0094 | AMR | PUR | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG01243 | hp1 | a0001 | c0001 | t0004 | g0019 | AMR | PUR | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG01243 | hp2 | a0001 | c0001 | t0005 | g0049 | AMR | PUR | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG01255 | hp1 | a0001 | c0001 | t0004 | g0052 | AMR | CLM | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0182 | AMR | CLM | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | CLM | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | CLM | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | CLM | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG01261 | hp2 | a0001 | c0001 | t0003 | g0183 | AMR | CLM | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0006 | AMR | CLM | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG01516 | hp1 | a0001 | c0001 | t0004 | g0018 | EUR | IBS | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0033 | EUR | IBS | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG01517 | hp1 | a0001 | c0001 | t0003 | g0033 | EUR | IBS | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG01517 | hp2 | a0001 | c0001 | t0004 | g0002 | EUR | IBS | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0037 | AFR | ACB | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG01884 | hp2 | a0002 | c0002 | t0005 | g0204 | AFR | ACB | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG01943 | hp2 | a0001 | c0001 | t0003 | g0089 | AMR | PEL | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0034 | AMR | PEL | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG01975 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | PEL | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG01993 | hp1 | a0001 | c0001 | t0003 | g0083 | AMR | PEL | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | KHV | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | KHV | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG02055 | hp1 | a0002 | c0002 | t0005 | g0074 | AFR | ACB | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0048 | AFR | ACB | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG02056 | hp1 | a0001 | c0014 | t0001 | g0026 | EAS | KHV | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | KHV | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | KHV | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG02080 | hp2 | a0001 | c0001 | t0003 | g0098 | EAS | KHV | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | KHV | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | KHV | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG02145 | hp1 | a0001 | c0001 | t0005 | g0050 | AFR | ACB | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0021 | AFR | ACB | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CDX | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0008 | AFR | ACB | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0064 | AFR | ACB | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0065 | AFR | ACB | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG02280 | hp2 | a0001 | c0001 | t0005 | g0203 | AFR | ACB | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0186 | AFR | ACB | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG02451 | hp2 | a0007 | c0007 | t0002 | g0190 | AFR | ACB | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG02523 | hp1 | a0001 | c0001 | t0015 | g0137 | EAS | KHV | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | KHV | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG02572 | hp1 | a0002 | c0002 | t0005 | g0073 | AFR | GWD | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0107 | AFR | GWD | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0006 | SAS | PJL | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0158 | SAS | PJL | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG02615 | hp2 | a0001 | c0001 | t0006 | g0218 | AFR | GWD | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG02622 | hp2 | a0001 | c0001 | t0006 | g0220 | AFR | GWD | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG02630 | hp1 | a0001 | c0001 | t0006 | g0069 | AFR | GWD | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG02630 | hp2 | a0001 | c0001 | t0008 | g0102 | AFR | GWD | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG02647 | hp1 | a0001 | c0001 | t0005 | g0077 | AFR | GWD | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0201 | AFR | GWD | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG02683 | hp2 | a0001 | c0013 | t0004 | g0002 | SAS | PJL | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG02717 | hp1 | a0003 | c0003 | t0010 | g0013 | AFR | GWD | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG02717 | hp2 | a0008 | c0009 | t0006 | g0216 | AFR | GWD | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | GWD | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG02723 | hp2 | a0001 | c0005 | t0002 | g0014 | AFR | GWD | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG02735 | hp1 | a0001 | c0001 | t0004 | g0100 | SAS | PJL | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG02735 | hp2 | a0001 | c0001 | t0024 | g0165 | SAS | PJL | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG02809 | hp1 | a0001 | c0001 | t0008 | g0194 | AFR | GWD | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG02809 | hp2 | a0001 | c0001 | t0008 | g0036 | AFR | GWD | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG02818 | hp1 | a0002 | c0002 | t0005 | g0075 | AFR | GWD | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0108 | AFR | GWD | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG02886 | hp1 | a0003 | c0003 | t0012 | g0013 | AFR | GWD | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0035 | AFR | GWD | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG02896 | hp1 | a0001 | c0001 | t0005 | g0219 | AFR | GWD | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG02896 | hp2 | a0001 | c0005 | t0002 | g0014 | AFR | GWD | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG02897 | hp1 | a0001 | c0001 | t0005 | g0211 | AFR | GWD | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG02897 | hp2 | a0001 | c0001 | t0009 | g0009 | AFR | GWD | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | ESN | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | ESN | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG02965 | hp1 | a0005 | c0006 | t0002 | g0103 | AFR | ESN | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0215 | AFR | ESN | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG02970 | hp1 | a0001 | c0001 | t0005 | g0017 | AFR | ESN | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0021 | AFR | ESN | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG02976 | hp1 | a0001 | c0001 | t0017 | g0178 | AFR | ESN | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG02976 | hp2 | a0003 | c0003 | t0012 | g0040 | AFR | ESN | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG03017 | hp1 | a0001 | c0001 | t0003 | g0081 | SAS | PJL | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0181 | SAS | PJL | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG03041 | hp1 | a0001 | c0001 | t0011 | g0038 | AFR | GWD | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG03041 | hp2 | a0003 | c0003 | t0010 | g0042 | AFR | GWD | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG03098 | hp1 | a0001 | c0005 | t0002 | g0066 | AFR | MSL | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG03098 | hp2 | a0003 | c0003 | t0010 | g0041 | AFR | MSL | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0144 | AFR | ESN | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0037 | AFR | ESN | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | ESN | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | ESN | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG03195 | hp1 | a0001 | c0001 | t0006 | g0015 | AFR | ESN | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0034 | AFR | ESN | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG03209 | hp1 | a0001 | c0001 | t0006 | g0015 | AFR | MSL | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0008 | AFR | MSL | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG03225 | hp1 | a0001 | c0001 | t0005 | g0071 | AFR | MSL | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG03225 | hp2 | a0001 | c0001 | t0005 | g0017 | AFR | MSL | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0101 | SAS | PJL | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0035 | AFR | MSL | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG03453 | hp2 | a0002 | c0002 | t0005 | g0076 | AFR | MSL | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG03486 | hp1 | a0001 | c0001 | t0008 | g0036 | AFR | MSL | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG03486 | hp2 | a0001 | c0005 | t0002 | g0106 | AFR | MSL | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0093 | SAS | PJL | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | ESN | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG03516 | hp2 | a0004 | c0004 | t0002 | g0205 | AFR | ESN | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG03540 | hp1 | a0001 | c0001 | t0009 | g0202 | AFR | GWD | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | GWD | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG03579 | hp1 | a0001 | c0001 | t0011 | g0038 | AFR | MSL | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG03579 | hp2 | a0005 | c0006 | t0002 | g0104 | AFR | MSL | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0191 | SAS | PJL | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG03669 | hp1 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0187 | SAS | STU | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0175 | SAS | STU | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0092 | SAS | PJL | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | BEB | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0060 | SAS | BEB | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0096 | SAS | BEB | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | BEB | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0004 | SAS | BEB | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | BEB | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0062 | SAS | BEB | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG04115 | hp1 | a0001 | c0001 | t0018 | g0006 | SAS | STU | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG04115 | hp2 | a0001 | c0001 | t0003 | g0091 | SAS | STU | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG04184 | hp1 | a0001 | c0001 | t0004 | g0002 | SAS | BEB | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | BEB | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG04199 | hp1 | a0001 | c0001 | t0014 | g0117 | SAS | STU | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | STU | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | STU | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0184 | SAS | STU | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA18522 | hp1 | a0001 | c0001 | t0005 | g0212 | AFR | YRI | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | YRI | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | CHB | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CHB | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA18939 | hp1 | a0001 | c0001 | t0007 | g0173 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA18943 | hp2 | a0009 | c0011 | t0003 | g0004 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA18944 | hp1 | a0010 | c0010 | t0001 | g0135 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA18950 | hp1 | a0001 | c0001 | t0003 | g0085 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA18953 | hp2 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA18959 | hp1 | a0001 | c0001 | t0016 | g0001 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA18961 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA18964 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA18964 | hp2 | a0001 | c0001 | t0013 | g0109 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA18968 | hp2 | a0001 | c0001 | t0007 | g0003 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA18971 | hp1 | a0001 | c0001 | t0007 | g0003 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA18977 | hp2 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA18978 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA18984 | hp2 | a0001 | c0001 | t0003 | g0088 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA18988 | hp1 | a0001 | c0001 | t0003 | g0051 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA18998 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA19005 | hp2 | a0001 | c0001 | t0003 | g0086 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA19012 | hp2 | a0001 | c0001 | t0007 | g0174 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA19030 | hp1 | a0004 | c0004 | t0002 | g0195 | AFR | LWK | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA19030 | hp2 | a0001 | c0001 | t0006 | g0217 | AFR | LWK | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA19043 | hp1 | a0002 | c0002 | t0005 | g0072 | AFR | LWK | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0008 | AFR | LWK | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA19062 | hp1 | a0001 | c0001 | t0007 | g0003 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA19063 | hp2 | a0001 | c0001 | t0003 | g0044 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA19064 | hp1 | a0001 | c0001 | t0007 | g0163 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA19074 | hp2 | a0001 | c0001 | t0003 | g0197 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA19076 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA19077 | hp1 | a0001 | c0001 | t0007 | g0179 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA19078 | hp2 | a0001 | c0001 | t0003 | g0084 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA19079 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA19081 | hp1 | a0001 | c0001 | t0007 | g0005 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA19087 | hp2 | a0001 | c0001 | t0003 | g0099 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA19089 | hp2 | a0001 | c0001 | t0007 | g0177 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA19090 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA19091 | hp1 | a0001 | c0001 | t0007 | g0003 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA19091 | hp2 | a0001 | c0001 | t0021 | g0001 | EAS | JPT | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA19240 | hp1 | a0001 | c0001 | t0008 | g0200 | AFR | YRI | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA19240 | hp2 | a0004 | c0004 | t0002 | g0068 | AFR | YRI | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA20129 | hp1 | a0004 | c0004 | t0002 | g0067 | AFR | ASW | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | ASW | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA20752 | hp2 | a0001 | c0001 | t0004 | g0002 | EUR | TSI | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA20805 | hp1 | a0001 | c0001 | t0004 | g0002 | EUR | TSI | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0154 | EUR | TSI | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0169 | SAS | GIH | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA20905 | hp2 | a0001 | c0001 | t0004 | g0002 | SAS | GIH | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG01123 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | CLM | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | CLM | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG02109 | hp1 | a0001 | c0001 | t0003 | g0022 | AFR | ACB | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG02109 | hp2 | a0001 | c0001 | t0019 | g0206 | AFR | ACB | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG02486 | hp1 | a0001 | c0001 | t0006 | g0070 | AFR | ACB | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0008 | AFR | ACB | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0143 | AFR | ACB | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG02559 | hp2 | a0001 | c0001 | t0006 | g0214 | AFR | ACB | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG03471 | hp1 | a0001 | c0001 | t0023 | g0196 | AFR | MSL | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0022 | AFR | MSL | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG06807 | hp1 | a0004 | c0004 | t0002 | g0207 | AFR | USA | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| HG06807 | hp2 | a0001 | c0001 | t0006 | g0213 | AFR | USA | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0002 | AFR | USA | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA20300 | hp2 | a0001 | c0001 | t0009 | g0009 | AFR | USA | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0145 | AFR | LWK | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | LWK | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0160 | REF | REF | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0008 | g0043 | REF | REF | VIL1_chr2_218414123_218458295 | VIL1 | chr2 | 218414123 | 218458295 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:218423794 | G | A | 1 | a0007 | 1 | HG02451.hp2 | missense_variant | MODERATE | c.16G>A | p.Ala6Thr | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 2/20 | 73/6500 | 16/2484 | 6/827 | chr2 | 218423794 | |||
| chr2:218429420 | G | A | 1 | a0002 | 6 | HG01884.hp2 HG02055.hp1 HG02572.hp1 others(3): Show |
missense_variant | MODERATE | c.703G>A | p.Glu235Lys | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 7/20 | 760/6500 | 703/2484 | 235/827 | chr2 | 218429420 | |||
| chr2:218429466 | A | C | 1 | a0005 | 2 | HG02965.hp1 HG03579.hp2 |
missense_variant | MODERATE | c.749A>C | p.Lys250Thr | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 7/20 | 806/6500 | 749/2484 | 250/827 | chr2 | 218429466 | |||
| chr2:218429478 | A | G | 1 | a0004 | 5 | HG03516.hp2 HG06807.hp1 NA19030.hp1 others(2): Show |
missense_variant | MODERATE | c.761A>G | p.Lys254Arg | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 7/20 | 818/6500 | 761/2484 | 254/827 | chr2 | 218429478 | |||
| chr2:218429598 | G | C | 1 | a0003 | 5 | HG02717.hp1 HG02886.hp1 HG02976.hp2 others(2): Show |
missense_variant&splice_region_variant | MODERATE | c.772G>C | p.Val258Leu | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 8/20 | 829/6500 | 772/2484 | 258/827 | chr2 | 218429598 | |||
| chr2:218432892 | A | G | 1 | a0009 | 1 | NA18943.hp2 | missense_variant | MODERATE | c.1441A>G | p.Met481Val | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 13/20 | 1498/6500 | 1441/2484 | 481/827 | chr2 | 218432892 | |||
| chr2:218434638 | A | G | 1 | a0010 | 1 | NA18944.hp1 | missense_variant | MODERATE | c.1613A>G | p.Asn538Ser | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 14/20 | 1670/6500 | 1613/2484 | 538/827 | chr2 | 218434638 | |||
| chr2:218434667 | C | A | 1 | a0006 | 1 | HG01175.hp1 | missense_variant | MODERATE | c.1642C>A | p.Leu548Ile | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 14/20 | 1699/6500 | 1642/2484 | 548/827 | chr2 | 218434667 | |||
| chr2:218435307 | C | T | 1 | a0008 | 1 | HG02717.hp2 | missense_variant | MODERATE | c.1699C>T | p.Arg567Trp | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 15/20 | 1756/6500 | 1699/2484 | 567/827 | chr2 | 218435307 | |||
| chr2:218435387 | C | A | 1 | a0003 | 5 | HG02717.hp1 HG02886.hp1 HG02976.hp2 others(2): Show |
missense_variant | MODERATE | c.1779C>A | p.Asn593Lys | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 15/20 | 1836/6500 | 1779/2484 | 593/827 | chr2 | 218435387 | |||
| chr2:218436543 | C | T | 1 | a0003 | 5 | HG02717.hp1 HG02886.hp1 HG02976.hp2 others(2): Show |
missense_variant | MODERATE | c.1888C>T | p.Arg630Cys | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 16/20 | 1945/6500 | 1888/2484 | 630/827 | chr2 | 218436543 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:218429609 | C | T | 1 | a0001c0014 | 1 | HG02056.hp1 | synonymous_variant | LOW | c.783C>T | p.Ser261Ser | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 8/20 | 840/6500 | 783/2484 | 261/827 | chr2 | 218429609 | |||
| chr2:218429887 | C | T | 1 | a0001c0013 | 1 | HG02683.hp2 | synonymous_variant | LOW | c.888C>T | p.Tyr296Tyr | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 9/20 | 945/6500 | 888/2484 | 296/827 | chr2 | 218429887 | |||
| chr2:218432114 | C | T | 1 | a0001c0012 | 1 | HG01069.hp2 | synonymous_variant | LOW | c.1272C>T | p.Gly424Gly | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 12/20 | 1329/6500 | 1272/2484 | 424/827 | chr2 | 218432114 | |||
| chr2:218437171 | C | T | 1 | a0001c0005 | 4 | HG02723.hp2 HG02896.hp2 HG03098.hp1 others(1): Show |
synonymous_variant | LOW | c.2019C>T | p.Ala673Ala | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 17/20 | 2076/6500 | 2019/2484 | 673/827 | chr2 | 218437171 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:218449377 | T | C | 1 | a0001c0001t0013 | 1 | NA18964.hp2 | 3_prime_UTR_variant | MODIFIER | c.*41T>C | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 20/20 | 41 | chr2 | 218449377 | ||||||
| chr2:218449612 | C | G | 1 | a0001c0001t0024 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*276C>G | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 20/20 | 276 | chr2 | 218449612 | ||||||
| chr2:218449755 | C | T | 1 | a0001c0001t0023 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*419C>T | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 20/20 | 419 | chr2 | 218449755 | ||||||
| chr2:218449850 | A | T | 2 | a0001c0001t0004 a0001c0013t0004 |
18 | HG00099.hp2 HG00140.hp1 HG00733.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*514A>T | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 20/20 | 514 | chr2 | 218449850 | ||||||
| chr2:218450048 | C | A | 1 | a0001c0001t0014 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*712C>A | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 20/20 | 712 | chr2 | 218450048 | ||||||
| chr2:218450334 | G | A | 2 | a0001c0001t0005 a0002c0002t0005 |
17 | HG01109.hp1 HG01243.hp2 HG01884.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*998G>A | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 20/20 | 998 | chr2 | 218450334 | ||||||
| chr2:218450739 | T | C | 1 | a0001c0001t0009 | 3 | HG02897.hp2 HG03540.hp1 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1403T>C | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 20/20 | 1403 | chr2 | 218450739 | ||||||
| chr2:218450769 | T | A | 1 | a0001c0001t0011 | 2 | HG03041.hp1 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1433T>A | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 20/20 | 1433 | chr2 | 218450769 | ||||||
| chr2:218451010 | A | G | 1 | a0003c0003t0012 | 2 | HG02886.hp1 HG02976.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1674A>G | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 20/20 | 1674 | chr2 | 218451010 | ||||||
| chr2:218451237 | C | G | 1 | a0001c0001t0022 | 1 | HG00408.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1901C>G | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 20/20 | 1901 | chr2 | 218451237 | ||||||
| chr2:218451427 | A | G | 1 | a0001c0001t0021 | 1 | NA19091.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2091A>G | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 20/20 | 2091 | chr2 | 218451427 | ||||||
| chr2:218451572 | T | TTATACAA others(1): Show |
34 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(31): Show |
328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
3_prime_UTR_variant | MODIFIER | c.*2240_*2241insCAAC others(4): Show |
VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 20/20 | 2241 | INFO_REALIGN_3_PRIME | chr2 | 218451572 | |||||
| chr2:218451580 | G | A | 11 | a0001c0001t0001 a0001c0001t0013 a0001c0001t0014 others(8): Show |
137 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(134): Show |
3_prime_UTR_variant | MODIFIER | c.*2244G>A | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 20/20 | 2244 | chr2 | 218451580 | ||||||
| chr2:218451698 | T | C | 35 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(32): Show |
329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
3_prime_UTR_variant | MODIFIER | c.*2362T>C | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 20/20 | 2362 | chr2 | 218451698 | ||||||
| chr2:218451864 | C | G | 1 | a0001c0001t0007 | 10 | NA18939.hp1 NA18968.hp2 NA18971.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2528C>G | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 20/20 | 2528 | chr2 | 218451864 | ||||||
| chr2:218451930 | T | G | 1 | a0001c0001t0017 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2594T>G | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 20/20 | 2594 | chr2 | 218451930 | ||||||
| chr2:218452166 | C | T | 1 | a0001c0001t0016 | 1 | NA18959.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2830C>T | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 20/20 | 2830 | chr2 | 218452166 | ||||||
| chr2:218452186 | A | G | 1 | a0001c0001t0019 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2850A>G | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 20/20 | 2850 | chr2 | 218452186 | ||||||
| chr2:218452525 | T | C | 7 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0018 others(4): Show |
79 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*3189T>C | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 20/20 | 3189 | chr2 | 218452525 | ||||||
| chr2:218452853 | G | A | 3 | a0001c0001t0006 a0001c0001t0011 a0008c0009t0006 |
12 | HG02486.hp1 HG02559.hp2 HG02615.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*3517G>A | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 20/20 | 3517 | chr2 | 218452853 | ||||||
| chr2:218453016 | AC | A | 2 | a0003c0003t0010 a0003c0003t0012 |
5 | HG02717.hp1 HG02886.hp1 HG02976.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3682delC | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 20/20 | 3682 | INFO_REALIGN_3_PRIME | chr2 | 218453016 | |||||
| chr2:218453248 | GTTT | G | 3 | a0001c0001t0006 a0001c0001t0011 a0008c0009t0006 |
12 | HG02486.hp1 HG02559.hp2 HG02615.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*3918_*3920delTTT | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 20/20 | 3918 | INFO_REALIGN_3_PRIME | chr2 | 218453248 | |||||
| chr2:218453268 | C | T | 2 | a0001c0001t0015 a0001c0001t0018 |
2 | HG02523.hp1 HG04115.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3932C>T | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 20/20 | 3932 | chr2 | 218453268 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:218419197 | G | T | 11 | a0001c0001t0002g0215 a0001c0001t0005g0211 a0001c0001t0005g0212 others(8): Show |
12 | HG02559.hp2 HG02615.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.-12+29G>T | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 1/19 | chr2 | 218419197 | |||||||
| chr2:218419272 | C | T | 3 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0210 |
3 | NA18951.hp2 NA18967.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.-12+104C>T | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 1/19 | chr2 | 218419272 | |||||||
| chr2:218419435 | C | T | 3 | a0001c0001t0019g0206 a0004c0004t0002g0205 a0004c0004t0002g0207 |
3 | HG02109.hp2 HG03516.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-12+267C>T | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 1/19 | chr2 | 218419435 | |||||||
| chr2:218419483 | G | A | 1 | a0001c0001t0001g0039 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-12+315G>A | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 1/19 | chr2 | 218419483 | |||||||
| chr2:218419492 | G | A | 45 | a0001c0001t0001g0097 a0001c0001t0002g0186 a0001c0001t0003g0002 others(42): Show |
72 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.-12+324G>A | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 1/19 | chr2 | 218419492 | |||||||
| chr2:218419843 | A | G | 227 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(224): Show |
329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.-12+675A>G | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 1/19 | chr2 | 218419843 | |||||||
| chr2:218420245 | C | T | 1 | a0002c0002t0005g0204 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-12+1077C>T | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 1/19 | chr2 | 218420245 | |||||||
| chr2:218420297 | C | T | 1 | a0001c0001t0005g0203 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-12+1129C>T | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 1/19 | chr2 | 218420297 | |||||||
| chr2:218420301 | C | CA | 4 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0002g0047 others(1): Show |
4 | NA18957.hp1 NA18966.hp1 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.-12+1133_-12+1134i others(3): Show |
VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 1/19 | chr2 | 218420301 | |||||||
| chr2:218420428 | C | CA | 186 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(183): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.-12+1279dupA | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | 218420428 | ||||||
| chr2:218420428 | C | CAA | 13 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0056 others(10): Show |
13 | HG01175.hp2 HG01243.hp2 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.-12+1278_-12+1279d others(4): Show |
VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | 218420428 | ||||||
| chr2:218420453 | GA | G | 14 | a0001c0001t0002g0215 a0001c0001t0005g0211 a0001c0001t0005g0212 others(11): Show |
15 | HG02109.hp2 HG02559.hp2 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.-12+1292delA | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | 218420453 | ||||||
| chr2:218420578 | GT | G | 173 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(170): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.-12+1424delT | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | 218420578 | ||||||
| chr2:218420580 | T | G | 16 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0002g0215 others(13): Show |
17 | HG02109.hp2 HG02559.hp2 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.-12+1412T>G | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 1/19 | chr2 | 218420580 | |||||||
| chr2:218420581 | T | G | 1 | a0001c0001t0008g0194 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-12+1413T>G | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 1/19 | chr2 | 218420581 | |||||||
| chr2:218420582 | T | G | 1 | a0001c0001t0001g0063 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-12+1414T>G | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 1/19 | chr2 | 218420582 | |||||||
| chr2:218420589 | T | G | 28 | a0001c0001t0001g0078 a0001c0001t0002g0007 a0001c0001t0002g0016 others(25): Show |
36 | HG01074.hp1 HG01243.hp2 HG01884.hp2 others(33): Show |
intron_variant | MODIFIER | c.-12+1421T>G | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 1/19 | chr2 | 218420589 | |||||||
| chr2:218420592 | T | G | 33 | a0001c0001t0001g0060 a0001c0001t0001g0164 a0001c0001t0001g0167 others(30): Show |
47 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.-12+1424T>G | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 1/19 | chr2 | 218420592 | |||||||
| chr2:218420593 | G | GT | 7 | a0001c0001t0002g0059 a0001c0001t0002g0186 a0001c0001t0003g0033 others(4): Show |
8 | HG00741.hp1 HG01517.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.-12+1435dupT | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | 218420593 | ||||||
| chr2:218420593 | G | T | 33 | a0001c0001t0001g0060 a0001c0001t0001g0164 a0001c0001t0001g0167 others(30): Show |
47 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.-12+1425G>T | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 1/19 | chr2 | 218420593 | |||||||
| chr2:218420594 | T | G | 1 | a0001c0001t0001g0161 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-12+1426T>G | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 1/19 | chr2 | 218420594 | |||||||
| chr2:218420599 | T | G | 1 | a0001c0001t0004g0018 | 2 | HG00140.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.-12+1431T>G | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 1/19 | chr2 | 218420599 | |||||||
| chr2:218420828 | G | A | 1 | a0001c0001t0002g0064 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-12+1660G>A | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 1/19 | chr2 | 218420828 | |||||||
| chr2:218420863 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-12+1695G>A | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 1/19 | chr2 | 218420863 | |||||||
| chr2:218421002 | G | A | 1 | a0001c0001t0002g0035 | 2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-12+1834G>A | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 1/19 | chr2 | 218421002 | |||||||
| chr2:218421174 | G | A | 1 | a0001c0001t0008g0036 | 2 | HG02809.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-12+2006G>A | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 1/19 | chr2 | 218421174 | |||||||
| chr2:218421196 | G | T | 1 | a0001c0001t0001g0193 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-12+2028G>T | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 1/19 | chr2 | 218421196 | |||||||
| chr2:218421293 | G | A | 1 | a0001c0001t0002g0065 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-12+2125G>A | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 1/19 | chr2 | 218421293 | |||||||
| chr2:218421725 | G | C | 4 | a0001c0001t0001g0001 a0001c0001t0001g0138 a0001c0001t0001g0139 others(1): Show |
7 | HG00408.hp2 NA18952.hp2 NA18966.hp2 others(4): Show |
intron_variant | MODIFIER | c.-11-2043G>C | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 1/19 | chr2 | 218421725 | |||||||
| chr2:218421809 | A | G | 2 | a0001c0001t0002g0034 a0001c0001t0023g0196 |
3 | HG01975.hp1 HG03195.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-11-1959A>G | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 1/19 | chr2 | 218421809 | |||||||
| chr2:218421818 | G | C | 39 | a0001c0001t0001g0097 a0001c0001t0003g0002 a0001c0001t0003g0004 others(36): Show |
61 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.-11-1950G>C | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 1/19 | chr2 | 218421818 | |||||||
| chr2:218421979 | C | T | 2 | a0001c0001t0003g0053 a0001c0001t0003g0101 |
2 | HG01175.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.-11-1789C>T | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 1/19 | chr2 | 218421979 | |||||||
| chr2:218422151 | G | A | 218 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(215): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.-11-1617G>A | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 1/19 | chr2 | 218422151 | |||||||
| chr2:218422268 | A | G | 1 | a0001c0001t0001g0192 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-11-1500A>G | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 1/19 | chr2 | 218422268 | |||||||
| chr2:218422330 | C | T | 1 | a0001c0001t0001g0046 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-11-1438C>T | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 1/19 | chr2 | 218422330 | |||||||
| chr2:218422553 | C | A | 112 | a0001c0001t0001g0060 a0001c0001t0001g0097 a0001c0001t0001g0164 others(109): Show |
164 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.-11-1215C>A | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 1/19 | chr2 | 218422553 | |||||||
| chr2:218422647 | A | G | 45 | a0001c0001t0001g0097 a0001c0001t0002g0186 a0001c0001t0003g0002 others(42): Show |
72 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.-11-1121A>G | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 1/19 | chr2 | 218422647 | |||||||
| chr2:218422689 | T | C | 1 | a0001c0001t0003g0162 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-11-1079T>C | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 1/19 | chr2 | 218422689 | |||||||
| chr2:218423287 | C | T | 5 | a0001c0001t0002g0009 a0001c0001t0002g0037 a0001c0001t0002g0201 others(2): Show |
8 | HG01884.hp1 HG02647.hp2 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.-11-481C>T | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 1/19 | chr2 | 218423287 | |||||||
| chr2:218423295 | T | C | 26 | a0001c0001t0002g0007 a0001c0001t0002g0016 a0001c0001t0002g0048 others(23): Show |
33 | HG01243.hp2 HG01884.hp2 HG02055.hp1 others(30): Show |
intron_variant | MODIFIER | c.-11-473T>C | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 1/19 | chr2 | 218423295 | |||||||
| chr2:218423317 | C | G | 1 | a0001c0001t0006g0220 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-11-451C>G | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 1/19 | chr2 | 218423317 | |||||||
| chr2:218423381 | C | T | 1 | a0001c0001t0005g0077 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-11-387C>T | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 1/19 | chr2 | 218423381 | |||||||
| chr2:218423414 | A | G | 218 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(215): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.-11-354A>G | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 1/19 | chr2 | 218423414 | |||||||
| chr2:218423464 | G | T | 4 | a0001c0001t0002g0035 a0001c0001t0008g0036 a0001c0001t0008g0194 others(1): Show |
6 | HG02809.hp1 HG02809.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.-11-304G>T | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 1/19 | chr2 | 218423464 | |||||||
| chr2:218423556 | T | C | 1 | a0001c0001t0002g0035 | 2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-11-212T>C | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 1/19 | chr2 | 218423556 | |||||||
| chr2:218423596 | G | A | 11 | a0001c0001t0002g0215 a0001c0001t0005g0211 a0001c0001t0005g0212 others(8): Show |
12 | HG02559.hp2 HG02615.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.-11-172G>A | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 1/19 | chr2 | 218423596 | |||||||
| chr2:218423659 | A | G | 216 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(213): Show |
312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.-11-109A>G | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 1/19 | chr2 | 218423659 | |||||||
| chr2:218424036 | C | T | 1 | a0001c0001t0001g0191 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.75+183C>T | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 2/19 | chr2 | 218424036 | |||||||
| chr2:218424104 | T | C | 5 | a0001c0001t0002g0009 a0001c0001t0002g0037 a0001c0001t0002g0201 others(2): Show |
8 | HG01884.hp1 HG02647.hp2 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.76-173T>C | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 2/19 | chr2 | 218424104 | |||||||
| chr2:218424176 | C | T | 47 | a0001c0001t0001g0045 a0001c0001t0001g0097 a0001c0001t0001g0159 others(44): Show |
74 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.76-101C>T | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 2/19 | chr2 | 218424176 | |||||||
| chr2:218424218 | C | T | 1 | a0001c0001t0001g0158 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.76-59C>T | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 2/19 | chr2 | 218424218 | |||||||
| chr2:218424663 | A | T | 4 | a0002c0002t0005g0073 a0002c0002t0005g0074 a0002c0002t0005g0075 others(1): Show |
4 | HG02055.hp1 HG02572.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.150+312A>T | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 3/19 | chr2 | 218424663 | |||||||
| chr2:218424666 | AT | A | 13 | a0001c0001t0002g0007 a0001c0001t0002g0016 a0001c0001t0002g0048 others(10): Show |
19 | HG02055.hp2 HG02258.hp2 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.150+322delT | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr2 | 218424666 | ||||||
| chr2:218424750 | G | A | 1 | a0001c0001t0008g0102 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.150+399G>A | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 3/19 | chr2 | 218424750 | |||||||
| chr2:218424798 | A | G | 1 | a0001c0001t0002g0185 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.150+447A>G | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 3/19 | chr2 | 218424798 | |||||||
| chr2:218424813 | C | T | 6 | a0001c0001t0002g0016 a0001c0001t0002g0048 a0001c0001t0002g0064 others(3): Show |
8 | HG02055.hp2 HG02258.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.150+462C>T | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 3/19 | chr2 | 218424813 | |||||||
| chr2:218424920 | A | G | 103 | a0001c0001t0001g0060 a0001c0001t0001g0097 a0001c0001t0001g0164 others(100): Show |
156 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.150+569A>G | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 3/19 | chr2 | 218424920 | |||||||
| chr2:218424942 | G | A | 1 | a0001c0005t0002g0014 | 2 | HG02723.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.150+591G>A | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 3/19 | chr2 | 218424942 | |||||||
| chr2:218424976 | A | G | 3 | a0001c0001t0008g0036 a0001c0001t0008g0194 a0001c0001t0008g0200 |
4 | HG02809.hp1 HG02809.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.150+625A>G | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 3/19 | chr2 | 218424976 | |||||||
| chr2:218425227 | T | A | 1 | a0001c0001t0013g0109 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.151-388T>A | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 3/19 | chr2 | 218425227 | |||||||
| chr2:218425229 | T | C | 231 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(228): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.151-386T>C | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 3/19 | chr2 | 218425229 | |||||||
| chr2:218425953 | C | T | 49 | a0001c0001t0001g0097 a0001c0001t0002g0009 a0001c0001t0002g0037 others(46): Show |
79 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.347+142C>T | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 4/19 | chr2 | 218425953 | |||||||
| chr2:218425998 | C | T | 1 | a0001c0001t0004g0100 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.347+187C>T | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 4/19 | chr2 | 218425998 | |||||||
| chr2:218426168 | C | A | 1 | a0001c0001t0003g0081 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.347+357C>A | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 4/19 | chr2 | 218426168 | |||||||
| chr2:218426169 | C | A | 1 | a0001c0001t0003g0081 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.347+358C>A | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 4/19 | chr2 | 218426169 | |||||||
| chr2:218426262 | T | C | 5 | a0001c0001t0003g0008 a0001c0001t0003g0021 a0001c0001t0003g0022 others(2): Show |
10 | HG02109.hp1 HG02145.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.347+451T>C | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 4/19 | chr2 | 218426262 | |||||||
| chr2:218426295 | C | T | 1 | a0002c0002t0005g0204 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.347+484C>T | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 4/19 | chr2 | 218426295 | |||||||
| chr2:218426308 | A | G | 1 | a0001c0001t0001g0157 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.347+497A>G | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 4/19 | chr2 | 218426308 | |||||||
| chr2:218426358 | G | A | 23 | a0001c0001t0002g0215 a0001c0001t0005g0017 a0001c0001t0005g0049 others(20): Show |
25 | HG01243.hp2 HG01884.hp2 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.347+547G>A | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 4/19 | chr2 | 218426358 | |||||||
| chr2:218426472 | A | G | 231 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(228): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.347+661A>G | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 4/19 | chr2 | 218426472 | |||||||
| chr2:218426758 | C | T | 2 | a0001c0001t0001g0155 a0001c0001t0001g0156 |
2 | HG00140.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.347+947C>T | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 4/19 | chr2 | 218426758 | |||||||
| chr2:218426763 | G | A | 2 | a0001c0001t0001g0011 a0001c0001t0001g0110 |
4 | HG00733.hp2 HG00735.hp2 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.347+952G>A | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 4/19 | chr2 | 218426763 | |||||||
| chr2:218426824 | A | G | 1 | a0001c0001t0001g0154 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.347+1013A>G | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 4/19 | chr2 | 218426824 | |||||||
| chr2:218426925 | A | G | 4 | a0001c0001t0003g0033 a0001c0001t0003g0182 a0001c0001t0003g0183 others(1): Show |
5 | HG01256.hp1 HG01261.hp2 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.348-1040A>G | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 4/19 | chr2 | 218426925 | |||||||
| chr2:218426937 | C | T | 12 | a0001c0001t0001g0031 a0001c0001t0001g0057 a0001c0001t0001g0058 others(9): Show |
13 | HG00544.hp1 HG01123.hp2 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.348-1028C>T | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 4/19 | chr2 | 218426937 | |||||||
| chr2:218427056 | G | T | 1 | a0001c0001t0002g0181 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.348-909G>T | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 4/19 | chr2 | 218427056 | |||||||
| chr2:218427179 | A | C | 1 | a0001c0005t0002g0106 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.348-786A>C | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 4/19 | chr2 | 218427179 | |||||||
| chr2:218427218 | C | A | 7 | a0001c0001t0005g0017 a0001c0001t0005g0049 a0001c0001t0005g0050 others(4): Show |
8 | HG01243.hp2 HG02145.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.348-747C>A | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 4/19 | chr2 | 218427218 | |||||||
| chr2:218427301 | C | T | 1 | a0001c0001t0001g0198 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.348-664C>T | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 4/19 | chr2 | 218427301 | |||||||
| chr2:218427326 | CT | C | 199 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(196): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.348-624delT | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr2 | 218427326 | ||||||
| chr2:218427326 | CTT | C | 19 | a0001c0001t0001g0023 a0001c0001t0001g0164 a0001c0001t0002g0009 others(16): Show |
26 | HG01256.hp1 HG01884.hp1 HG01975.hp1 others(23): Show |
intron_variant | MODIFIER | c.348-625_348-624del others(2): Show |
VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr2 | 218427326 | ||||||
| chr2:218427514 | T | C | 1 | a0001c0005t0002g0106 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.348-451T>C | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 4/19 | chr2 | 218427514 | |||||||
| chr2:218427525 | C | G | 1 | a0001c0001t0008g0102 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.348-440C>G | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 4/19 | chr2 | 218427525 | |||||||
| chr2:218427563 | T | C | 7 | a0001c0001t0002g0007 a0001c0001t0002g0016 a0001c0001t0002g0048 others(4): Show |
12 | HG02055.hp2 HG02258.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.348-402T>C | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 4/19 | chr2 | 218427563 | |||||||
| chr2:218427633 | A | G | 1 | a0001c0001t0002g0180 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.348-332A>G | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 4/19 | chr2 | 218427633 | |||||||
| chr2:218427716 | C | T | 1 | a0001c0001t0001g0153 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.348-249C>T | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 4/19 | chr2 | 218427716 | |||||||
| chr2:218427872 | C | T | 35 | a0001c0001t0001g0164 a0001c0001t0001g0171 a0001c0001t0001g0172 others(32): Show |
52 | HG00558.hp1 HG00621.hp1 HG01109.hp1 others(49): Show |
intron_variant | MODIFIER | c.348-93C>T | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 4/19 | chr2 | 218427872 | |||||||
| chr2:218427873 | G | A | 1 | a0001c0001t0024g0165 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.348-92G>A | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 4/19 | chr2 | 218427873 | |||||||
| chr2:218428363 | C | G | 1 | a0001c0001t0003g0098 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.567+26C>G | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 6/19 | chr2 | 218428363 | |||||||
| chr2:218428482 | G | A | 2 | a0001c0001t0006g0015 a0001c0001t0006g0069 |
3 | HG02630.hp1 HG03195.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.567+145G>A | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 6/19 | chr2 | 218428482 | |||||||
| chr2:218428603 | C | T | 91 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(88): Show |
135 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.567+266C>T | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 6/19 | chr2 | 218428603 | |||||||
| chr2:218428677 | A | AT | 9 | a0001c0001t0002g0009 a0001c0001t0002g0034 a0001c0001t0002g0035 others(6): Show |
14 | HG01884.hp1 HG01975.hp1 HG02647.hp2 others(11): Show |
intron_variant | MODIFIER | c.567+350dupT | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr2 | 218428677 | ||||||
| chr2:218428786 | T | C | 210 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(207): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.567+449T>C | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 6/19 | chr2 | 218428786 | |||||||
| chr2:218428830 | C | T | 1 | a0001c0001t0001g0029 | 2 | HG02738.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.568-455C>T | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 6/19 | chr2 | 218428830 | |||||||
| chr2:218428996 | C | T | 1 | a0001c0001t0001g0152 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.568-289C>T | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 6/19 | chr2 | 218428996 | |||||||
| chr2:218429124 | T | C | 5 | a0001c0001t0002g0007 a0001c0001t0002g0016 a0001c0001t0002g0048 others(2): Show |
9 | HG02055.hp2 HG02258.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.568-161T>C | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 6/19 | chr2 | 218429124 | |||||||
| chr2:218429535 | A | C | 68 | a0001c0001t0002g0009 a0001c0001t0002g0034 a0001c0001t0002g0035 others(65): Show |
102 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.770+48A>C | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 7/19 | chr2 | 218429535 | |||||||
| chr2:218429564 | C | T | 1 | a0001c0001t0003g0096 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.771-33C>T | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 7/19 | chr2 | 218429564 | |||||||
| chr2:218429698 | C | T | 1 | a0001c0001t0002g0186 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.849+23C>T | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 8/19 | chr2 | 218429698 | |||||||
| chr2:218429731 | G | A | 5 | a0003c0003t0010g0013 a0003c0003t0010g0041 a0003c0003t0010g0042 others(2): Show |
5 | HG02717.hp1 HG02886.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.849+56G>A | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 8/19 | chr2 | 218429731 | |||||||
| chr2:218429777 | CT | C | 2 | a0001c0001t0003g0021 a0001c0001t0003g0022 |
4 | HG02109.hp1 HG02145.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.850-66delT | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr2 | 218429777 | ||||||
| chr2:218429962 | G | A | 1 | a0001c0001t0003g0082 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.948+15G>A | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 9/19 | chr2 | 218429962 | |||||||
| chr2:218430015 | G | C | 15 | a0001c0001t0005g0017 a0001c0001t0005g0049 a0001c0001t0005g0050 others(12): Show |
16 | HG01243.hp2 HG01884.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.948+68G>C | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 9/19 | chr2 | 218430015 | |||||||
| chr2:218430371 | A | G | 1 | a0001c0001t0002g0007 | 4 | HG02723.hp1 HG03139.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.949-354A>G | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 9/19 | chr2 | 218430371 | |||||||
| chr2:218430420 | C | T | 2 | a0005c0006t0002g0103 a0005c0006t0002g0104 |
2 | HG02965.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.949-305C>T | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 9/19 | chr2 | 218430420 | |||||||
| chr2:218430524 | G | A | 1 | a0001c0001t0001g0024 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.949-201G>A | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 9/19 | chr2 | 218430524 | |||||||
| chr2:218430526 | C | T | 66 | a0001c0001t0002g0009 a0001c0001t0002g0034 a0001c0001t0002g0035 others(63): Show |
99 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.949-199C>T | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 9/19 | chr2 | 218430526 | |||||||
| chr2:218430995 | G | A | 2 | a0001c0001t0002g0007 a0001c0001t0002g0065 |
5 | HG02280.hp1 HG02723.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1102+117G>A | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 10/19 | chr2 | 218430995 | |||||||
| chr2:218431112 | G | A | 91 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(88): Show |
135 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.1102+234G>A | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 10/19 | chr2 | 218431112 | |||||||
| chr2:218431351 | CA | C | 107 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(104): Show |
152 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.1103-484delA | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr2 | 218431351 | ||||||
| chr2:218431351 | CAA | C | 18 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0140 others(15): Show |
26 | HG00099.hp1 HG01167.hp1 HG01255.hp2 others(23): Show |
intron_variant | MODIFIER | c.1103-485_1103-484d others(4): Show |
VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr2 | 218431351 | ||||||
| chr2:218431351 | CAAA | C | 60 | a0001c0001t0002g0009 a0001c0001t0002g0035 a0001c0001t0002g0186 others(57): Show |
92 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.1103-486_1103-484d others(5): Show |
VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr2 | 218431351 | ||||||
| chr2:218431372 | A | G | 1 | a0001c0001t0001g0198 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1103-485A>G | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 10/19 | chr2 | 218431372 | |||||||
| chr2:218431743 | C | T | 2 | a0001c0001t0001g0138 a0001c0001t0001g0139 |
2 | NA18974.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.1103-114C>T | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 10/19 | chr2 | 218431743 | |||||||
| chr2:218431783 | C | T | 15 | a0001c0001t0005g0017 a0001c0001t0005g0049 a0001c0001t0005g0050 others(12): Show |
16 | HG01243.hp2 HG01884.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.1103-74C>T | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 10/19 | chr2 | 218431783 | |||||||
| chr2:218431822 | G | A | 66 | a0001c0001t0002g0009 a0001c0001t0002g0034 a0001c0001t0002g0035 others(63): Show |
99 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.1103-35G>A | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 10/19 | chr2 | 218431822 | |||||||
| chr2:218432219 | G | A | 2 | a0001c0001t0001g0061 a0001c0001t0001g0062 |
2 | HG03710.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1341+36G>A | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 12/19 | chr2 | 218432219 | |||||||
| chr2:218432463 | G | A | 16 | a0001c0001t0002g0016 a0001c0001t0002g0037 a0001c0001t0002g0048 others(13): Show |
20 | HG01884.hp1 HG02055.hp2 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.1341+280G>A | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 12/19 | chr2 | 218432463 | |||||||
| chr2:218432518 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1342-275G>A | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 12/19 | chr2 | 218432518 | |||||||
| chr2:218432604 | G | T | 1 | a0001c0001t0005g0176 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1342-189G>T | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 12/19 | chr2 | 218432604 | |||||||
| chr2:218433013 | A | T | 1 | a0001c0001t0002g0175 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1500+62A>T | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 13/19 | chr2 | 218433013 | |||||||
| chr2:218433070 | G | A | 1 | a0002c0002t0005g0072 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1500+119G>A | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 13/19 | chr2 | 218433070 | |||||||
| chr2:218433195 | G | C | 1 | a0001c0001t0002g0199 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1500+244G>C | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 13/19 | chr2 | 218433195 | |||||||
| chr2:218433195 | G | T | 81 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(78): Show |
124 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.1500+244G>T | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 13/19 | chr2 | 218433195 | |||||||
| chr2:218433325 | C | T | 6 | a0001c0001t0002g0009 a0001c0001t0002g0034 a0001c0001t0002g0035 others(3): Show |
10 | HG01975.hp1 HG02886.hp2 HG02897.hp2 others(7): Show |
intron_variant | MODIFIER | c.1500+374C>T | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 13/19 | chr2 | 218433325 | |||||||
| chr2:218433396 | A | T | 231 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(228): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.1500+445A>T | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 13/19 | chr2 | 218433396 | |||||||
| chr2:218433413 | C | T | 1 | a0001c0005t0002g0014 | 2 | HG02723.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.1500+462C>T | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 13/19 | chr2 | 218433413 | |||||||
| chr2:218433420 | G | T | 1 | a0001c0001t0005g0212 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1500+469G>T | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 13/19 | chr2 | 218433420 | |||||||
| chr2:218433503 | TGAGGTGG others(162): Show |
T | 1 | a0001c0001t0014g0117 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1500+579_1500+747d others(2): Show |
VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr2 | 218433503 | ||||||
| chr2:218433693 | G | C | 66 | a0001c0001t0002g0009 a0001c0001t0002g0034 a0001c0001t0002g0035 others(63): Show |
99 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.1500+742G>C | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 13/19 | chr2 | 218433693 | |||||||
| chr2:218433893 | G | A | 6 | a0001c0001t0001g0012 a0001c0001t0001g0079 a0001c0001t0001g0113 others(3): Show |
8 | HG00099.hp1 HG01099.hp1 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.1501-633G>A | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 13/19 | chr2 | 218433893 | |||||||
| chr2:218433901 | GA | G | 5 | a0001c0001t0002g0016 a0001c0001t0002g0037 a0001c0001t0002g0048 others(2): Show |
7 | HG01884.hp1 HG02055.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1501-612delA | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr2 | 218433901 | ||||||
| chr2:218433972 | G | A | 66 | a0001c0001t0002g0009 a0001c0001t0002g0034 a0001c0001t0002g0035 others(63): Show |
99 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.1501-554G>A | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 13/19 | chr2 | 218433972 | |||||||
| chr2:218434053 | C | T | 1 | a0001c0001t0015g0137 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1501-473C>T | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 13/19 | chr2 | 218434053 | |||||||
| chr2:218434193 | G | A | 4 | a0001c0001t0008g0036 a0001c0001t0008g0102 a0001c0001t0008g0194 others(1): Show |
5 | HG02630.hp2 HG02809.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1501-333G>A | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 13/19 | chr2 | 218434193 | |||||||
| chr2:218434197 | C | CA | 6 | a0001c0001t0001g0111 a0001c0001t0001g0120 a0001c0001t0001g0121 others(3): Show |
9 | HG01261.hp1 HG02280.hp1 HG02602.hp2 others(6): Show |
intron_variant | MODIFIER | c.1501-314dupA | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr2 | 218434197 | ||||||
| chr2:218434197 | C | CAAAAAAA others(3): Show |
8 | a0001c0001t0003g0008 a0001c0001t0003g0021 a0001c0001t0003g0022 others(5): Show |
13 | HG00642.hp1 HG01192.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1501-323_1501-314d others(12): Show |
VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr2 | 218434197 | ||||||
| chr2:218434197 | C | CAAAAAAA others(4): Show |
37 | a0001c0001t0002g0035 a0001c0001t0003g0002 a0001c0001t0003g0006 others(34): Show |
56 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(53): Show |
intron_variant | MODIFIER | c.1501-324_1501-314d others(13): Show |
VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr2 | 218434197 | ||||||
| chr2:218434197 | C | CAAAAAAA others(5): Show |
15 | a0001c0001t0002g0034 a0001c0001t0003g0004 a0001c0001t0003g0053 others(12): Show |
22 | HG00733.hp1 HG00735.hp1 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.1501-325_1501-314d others(14): Show |
VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr2 | 218434197 | ||||||
| chr2:218434197 | C | CAAAAAAA others(6): Show |
3 | a0001c0001t0002g0009 a0001c0001t0008g0200 a0001c0001t0009g0009 |
5 | HG02897.hp2 HG02922.hp1 NA19240.hp1 others(2): Show |
intron_variant | MODIFIER | c.1501-326_1501-314d others(15): Show |
VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr2 | 218434197 | ||||||
| chr2:218434197 | C | CAAAAAAA others(7): Show |
1 | a0001c0001t0009g0202 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1501-327_1501-314d others(16): Show |
VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr2 | 218434197 | ||||||
| chr2:218434398 | G | C | 1 | a0001c0001t0001g0147 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1501-128G>C | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 13/19 | chr2 | 218434398 | |||||||
| chr2:218434832 | G | A | 1 | a0001c0001t0001g0114 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1680+127G>A | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 14/19 | chr2 | 218434832 | |||||||
| chr2:218435094 | ACT | A | 66 | a0001c0001t0002g0009 a0001c0001t0002g0034 a0001c0001t0002g0035 others(63): Show |
99 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.1681-190_1681-189d others(4): Show |
VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr2 | 218435094 | ||||||
| chr2:218435098 | T | C | 1 | a0004c0004t0002g0205 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1681-191T>C | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 14/19 | chr2 | 218435098 | |||||||
| chr2:218435265 | T | C | 1 | a0001c0001t0002g0181 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1681-24T>C | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 14/19 | chr2 | 218435265 | |||||||
| chr2:218435486 | A | G | 1 | a0001c0001t0002g0201 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1826+52A>G | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 15/19 | chr2 | 218435486 | |||||||
| chr2:218435502 | C | T | 4 | a0001c0001t0008g0036 a0001c0001t0008g0102 a0001c0001t0008g0194 others(1): Show |
5 | HG02630.hp2 HG02809.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1826+68C>T | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 15/19 | chr2 | 218435502 | |||||||
| chr2:218435504 | C | T | 1 | a0002c0002t0005g0204 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1826+70C>T | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 15/19 | chr2 | 218435504 | |||||||
| chr2:218435538 | T | C | 3 | a0001c0001t0008g0036 a0001c0001t0008g0194 a0001c0001t0008g0200 |
4 | HG02809.hp1 HG02809.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1826+104T>C | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 15/19 | chr2 | 218435538 | |||||||
| chr2:218435754 | T | C | 1 | a0001c0001t0004g0087 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1826+320T>C | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 15/19 | chr2 | 218435754 | |||||||
| chr2:218436000 | G | A | 91 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(88): Show |
135 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.1827-482G>A | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 15/19 | chr2 | 218436000 | |||||||
| chr2:218436079 | T | G | 5 | a0001c0001t0003g0008 a0001c0001t0003g0021 a0001c0001t0003g0022 others(2): Show |
10 | HG02109.hp1 HG02145.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1827-403T>G | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 15/19 | chr2 | 218436079 | |||||||
| chr2:218436132 | A | C | 210 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(207): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.1827-350A>C | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 15/19 | chr2 | 218436132 | |||||||
| chr2:218436716 | T | C | 1 | a0001c0001t0002g0186 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1971+90T>C | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 16/19 | chr2 | 218436716 | |||||||
| chr2:218436818 | G | A | 1 | a0001c0001t0001g0122 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1971+192G>A | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 16/19 | chr2 | 218436818 | |||||||
| chr2:218436881 | A | C | 5 | a0003c0003t0010g0013 a0003c0003t0010g0041 a0003c0003t0010g0042 others(2): Show |
5 | HG02717.hp1 HG02886.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1972-243A>C | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 16/19 | chr2 | 218436881 | |||||||
| chr2:218436939 | A | G | 1 | a0001c0001t0001g0136 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1972-185A>G | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 16/19 | chr2 | 218436939 | |||||||
| chr2:218437082 | G | A | 1 | a0001c0001t0001g0111 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1972-42G>A | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 16/19 | chr2 | 218437082 | |||||||
| chr2:218437083 | A | G | 1 | a0001c0001t0001g0111 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1972-41A>G | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 16/19 | chr2 | 218437083 | |||||||
| chr2:218437387 | G | A | 1 | a0001c0001t0008g0102 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2160+75G>A | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 17/19 | chr2 | 218437387 | |||||||
| chr2:218437514 | A | T | 1 | a0010c0010t0001g0135 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.2160+202A>T | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 17/19 | chr2 | 218437514 | |||||||
| chr2:218437680 | G | C | 2 | a0001c0001t0002g0034 a0001c0001t0023g0196 |
3 | HG01975.hp1 HG03195.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2160+368G>C | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 17/19 | chr2 | 218437680 | |||||||
| chr2:218437729 | C | T | 225 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(222): Show |
327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.2160+417C>T | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 17/19 | chr2 | 218437729 | |||||||
| chr2:218437743 | G | A | 66 | a0001c0001t0002g0009 a0001c0001t0002g0034 a0001c0001t0002g0035 others(63): Show |
99 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.2160+431G>A | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 17/19 | chr2 | 218437743 | |||||||
| chr2:218437783 | T | C | 1 | a0001c0001t0001g0123 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.2160+471T>C | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 17/19 | chr2 | 218437783 | |||||||
| chr2:218437900 | G | A | 2 | a0001c0001t0002g0007 a0001c0001t0002g0065 |
5 | HG02280.hp1 HG02723.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2160+588G>A | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 17/19 | chr2 | 218437900 | |||||||
| chr2:218437919 | G | T | 1 | a0004c0004t0002g0195 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2160+607G>T | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 17/19 | chr2 | 218437919 | |||||||
| chr2:218438077 | A | C | 1 | a0001c0001t0002g0034 | 2 | HG01975.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2161-581A>C | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 17/19 | chr2 | 218438077 | |||||||
| chr2:218438167 | C | CTCAT | 65 | a0001c0001t0002g0009 a0001c0001t0002g0034 a0001c0001t0002g0035 others(62): Show |
98 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.2161-471_2161-468d others(6): Show |
VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr2 | 218438167 | ||||||
| chr2:218438247 | C | T | 3 | a0001c0001t0001g0030 a0001c0001t0001g0188 a0001c0001t0020g0146 |
4 | HG00642.hp2 HG00741.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.2161-411C>T | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 17/19 | chr2 | 218438247 | |||||||
| chr2:218438284 | G | A | 1 | a0001c0001t0004g0087 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2161-374G>A | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 17/19 | chr2 | 218438284 | |||||||
| chr2:218438532 | T | C | 2 | a0001c0001t0001g0124 a0001c0001t0001g0125 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.2161-126T>C | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 17/19 | chr2 | 218438532 | |||||||
| chr2:218438797 | G | A | 1 | a0001c0005t0002g0106 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2229+71G>A | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 18/19 | chr2 | 218438797 | |||||||
| chr2:218438836 | A | G | 1 | a0006c0008t0001g0119 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2229+110A>G | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 18/19 | chr2 | 218438836 | |||||||
| chr2:218438846 | C | G | 4 | a0001c0001t0002g0034 a0001c0001t0023g0196 a0004c0004t0002g0205 others(1): Show |
5 | HG01975.hp1 HG03195.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.2229+120C>G | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 18/19 | chr2 | 218438846 | |||||||
| chr2:218438926 | A | AT | 87 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(84): Show |
134 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.2229+222dupT | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr2 | 218438926 | ||||||
| chr2:218438926 | A | ATT | 41 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0060 others(38): Show |
58 | HG00558.hp1 HG00621.hp1 HG00733.hp2 others(55): Show |
intron_variant | MODIFIER | c.2229+221_2229+222d others(4): Show |
VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr2 | 218438926 | ||||||
| chr2:218438926 | A | ATTT | 6 | a0001c0001t0001g0025 a0001c0001t0001g0140 a0001c0001t0002g0180 others(3): Show |
7 | HG01257.hp2 HG01258.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.2229+220_2229+222d others(5): Show |
VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr2 | 218438926 | ||||||
| chr2:218438926 | AT | A | 60 | a0001c0001t0002g0009 a0001c0001t0002g0034 a0001c0001t0002g0035 others(57): Show |
93 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.2229+222delT | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr2 | 218438926 | ||||||
| chr2:218439352 | A | G | 2 | a0001c0001t0003g0081 a0001c0001t0003g0091 |
2 | HG03017.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.2229+626A>G | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 18/19 | chr2 | 218439352 | |||||||
| chr2:218439388 | T | C | 1 | a0001c0001t0008g0102 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2229+662T>C | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 18/19 | chr2 | 218439388 | |||||||
| chr2:218439407 | G | A | 15 | a0001c0001t0005g0017 a0001c0001t0005g0049 a0001c0001t0005g0050 others(12): Show |
16 | HG01243.hp2 HG01884.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.2229+681G>A | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 18/19 | chr2 | 218439407 | |||||||
| chr2:218439639 | G | A | 5 | a0003c0003t0010g0013 a0003c0003t0010g0041 a0003c0003t0010g0042 others(2): Show |
5 | HG02717.hp1 HG02886.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.2229+913G>A | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 18/19 | chr2 | 218439639 | |||||||
| chr2:218439687 | C | T | 1 | a0001c0001t0003g0022 | 2 | HG02109.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2229+961C>T | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 18/19 | chr2 | 218439687 | |||||||
| chr2:218439720 | G | A | 1 | a0002c0002t0005g0073 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2229+994G>A | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 18/19 | chr2 | 218439720 | |||||||
| chr2:218439816 | C | CA | 55 | a0001c0001t0001g0026 a0001c0001t0001g0046 a0001c0001t0001g0057 others(52): Show |
66 | HG00558.hp2 HG00642.hp1 HG01123.hp2 others(63): Show |
intron_variant | MODIFIER | c.2230-885dupA | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr2 | 218439816 | ||||||
| chr2:218439816 | C | CAA | 31 | a0001c0001t0001g0127 a0001c0001t0001g0157 a0001c0001t0001g0164 others(28): Show |
44 | HG00558.hp1 HG02027.hp2 HG02074.hp1 others(41): Show |
intron_variant | MODIFIER | c.2230-886_2230-885d others(4): Show |
VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr2 | 218439816 | ||||||
| chr2:218439816 | C | CAAA | 11 | a0001c0001t0002g0005 a0001c0001t0002g0105 a0001c0001t0002g0180 others(8): Show |
15 | HG00621.hp1 HG01109.hp1 HG03098.hp1 others(12): Show |
intron_variant | MODIFIER | c.2230-887_2230-885d others(5): Show |
VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr2 | 218439816 | ||||||
| chr2:218439838 | C | A | 9 | a0001c0001t0005g0017 a0001c0001t0005g0049 a0001c0001t0005g0050 others(6): Show |
10 | HG01243.hp2 HG02145.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.2230-884C>A | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 18/19 | chr2 | 218439838 | |||||||
| chr2:218439945 | A | G | 3 | a0001c0001t0003g0083 a0001c0001t0003g0095 a0001c0001t0003g0096 |
3 | HG00642.hp1 HG01993.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.2230-777A>G | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 18/19 | chr2 | 218439945 | |||||||
| chr2:218440128 | C | A | 66 | a0001c0001t0002g0009 a0001c0001t0002g0034 a0001c0001t0002g0035 others(63): Show |
99 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.2230-594C>A | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 18/19 | chr2 | 218440128 | |||||||
| chr2:218440134 | A | G | 6 | a0001c0001t0002g0009 a0001c0001t0002g0034 a0001c0001t0002g0035 others(3): Show |
10 | HG01975.hp1 HG02886.hp2 HG02897.hp2 others(7): Show |
intron_variant | MODIFIER | c.2230-588A>G | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 18/19 | chr2 | 218440134 | |||||||
| chr2:218440200 | T | G | 1 | a0001c0001t0005g0049 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2230-522T>G | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 18/19 | chr2 | 218440200 | |||||||
| chr2:218440331 | G | A | 1 | a0001c0001t0001g0127 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.2230-391G>A | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 18/19 | chr2 | 218440331 | |||||||
| chr2:218440472 | G | A | 32 | a0001c0001t0001g0164 a0001c0001t0001g0171 a0001c0001t0001g0172 others(29): Show |
48 | HG00558.hp1 HG00621.hp1 HG01109.hp1 others(45): Show |
intron_variant | MODIFIER | c.2230-250G>A | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 18/19 | chr2 | 218440472 | |||||||
| chr2:218440533 | G | T | 1 | a0001c0001t0002g0048 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2230-189G>T | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 18/19 | chr2 | 218440533 | |||||||
| chr2:218440681 | G | C | 91 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(88): Show |
135 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.2230-41G>C | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 18/19 | chr2 | 218440681 | |||||||
| chr2:218440868 | T | C | 1 | a0001c0001t0001g0129 | 1 | HG01070.hp2 | splice_region_variant&intron_variant | LOW | c.2370+6T>C | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | chr2 | 218440868 | |||||||
| chr2:218441111 | G | A | 5 | a0001c0001t0005g0017 a0001c0001t0005g0049 a0001c0001t0005g0077 others(2): Show |
6 | HG01243.hp2 HG02280.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.2370+249G>A | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | chr2 | 218441111 | |||||||
| chr2:218441286 | G | A | 5 | a0003c0003t0010g0013 a0003c0003t0010g0041 a0003c0003t0010g0042 others(2): Show |
5 | HG02717.hp1 HG02886.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.2370+424G>A | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | chr2 | 218441286 | |||||||
| chr2:218441313 | C | CA | 11 | a0001c0001t0002g0215 a0001c0001t0006g0015 a0001c0001t0006g0069 others(8): Show |
13 | HG02486.hp1 HG02559.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.2370+451_2370+452i others(3): Show |
VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | chr2 | 218441313 | |||||||
| chr2:218441974 | T | C | 2 | a0001c0001t0001g0011 a0001c0001t0001g0110 |
4 | HG00733.hp2 HG00735.hp2 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.2370+1112T>C | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | chr2 | 218441974 | |||||||
| chr2:218441979 | C | A | 3 | a0001c0001t0001g0030 a0001c0001t0001g0188 a0001c0001t0020g0146 |
4 | HG00642.hp2 HG00741.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.2370+1117C>A | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | chr2 | 218441979 | |||||||
| chr2:218441993 | G | GATA | 42 | a0001c0001t0001g0164 a0001c0001t0001g0171 a0001c0001t0001g0172 others(39): Show |
64 | HG00558.hp1 HG00621.hp1 HG01109.hp1 others(61): Show |
intron_variant | MODIFIER | c.2370+1146_2370+114 others(7): Show |
VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr2 | 218441993 | ||||||
| chr2:218442140 | A | T | 1 | a0001c0001t0002g0199 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.2370+1278A>T | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | chr2 | 218442140 | |||||||
| chr2:218442176 | T | C | 1 | a0004c0004t0002g0067 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2370+1314T>C | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | chr2 | 218442176 | |||||||
| chr2:218442283 | G | A | 231 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(228): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.2370+1421G>A | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | chr2 | 218442283 | |||||||
| chr2:218442790 | T | C | 11 | a0001c0001t0002g0215 a0001c0001t0006g0015 a0001c0001t0006g0069 others(8): Show |
13 | HG02486.hp1 HG02559.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.2370+1928T>C | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | chr2 | 218442790 | |||||||
| chr2:218442984 | C | A | 1 | a0001c0001t0001g0130 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2370+2122C>A | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | chr2 | 218442984 | |||||||
| chr2:218442985 | C | A | 1 | a0001c0001t0001g0130 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2370+2123C>A | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | chr2 | 218442985 | |||||||
| chr2:218442986 | C | A | 1 | a0001c0001t0001g0130 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2370+2124C>A | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | chr2 | 218442986 | |||||||
| chr2:218442987 | T | A | 1 | a0001c0001t0001g0130 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2370+2125T>A | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | chr2 | 218442987 | |||||||
| chr2:218442991 | T | A | 1 | a0001c0001t0001g0130 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2370+2129T>A | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | chr2 | 218442991 | |||||||
| chr2:218442992 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2370+2130G>A | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | chr2 | 218442992 | |||||||
| chr2:218442994 | T | A | 1 | a0001c0001t0001g0130 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2370+2132T>A | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | chr2 | 218442994 | |||||||
| chr2:218442995 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2370+2133G>A | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | chr2 | 218442995 | |||||||
| chr2:218442997 | C | A | 1 | a0001c0001t0001g0130 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2370+2135C>A | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | chr2 | 218442997 | |||||||
| chr2:218443000 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2370+2138G>A | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | chr2 | 218443000 | |||||||
| chr2:218443001 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2370+2139C>T | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | chr2 | 218443001 | |||||||
| chr2:218443002 | T | A | 1 | a0001c0001t0001g0130 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2370+2140T>A | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | chr2 | 218443002 | |||||||
| chr2:218443006 | C | A | 1 | a0001c0001t0001g0130 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2370+2144C>A | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | chr2 | 218443006 | |||||||
| chr2:218443007 | C | A | 1 | a0001c0001t0001g0130 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2370+2145C>A | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | chr2 | 218443007 | |||||||
| chr2:218443008 | C | A | 1 | a0001c0001t0001g0130 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2370+2146C>A | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | chr2 | 218443008 | |||||||
| chr2:218443010 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2370+2148G>A | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | chr2 | 218443010 | |||||||
| chr2:218443011 | C | A | 1 | a0001c0001t0001g0130 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2370+2149C>A | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | chr2 | 218443011 | |||||||
| chr2:218443012 | C | A | 1 | a0001c0001t0001g0130 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2370+2150C>A | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | chr2 | 218443012 | |||||||
| chr2:218443013 | C | A | 1 | a0001c0001t0001g0130 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2370+2151C>A | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | chr2 | 218443013 | |||||||
| chr2:218443014 | T | A | 1 | a0001c0001t0001g0130 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2370+2152T>A | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | chr2 | 218443014 | |||||||
| chr2:218443015 | T | A | 1 | a0001c0001t0001g0130 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2370+2153T>A | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | chr2 | 218443015 | |||||||
| chr2:218443017 | G | T | 1 | a0001c0001t0001g0130 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2370+2155G>T | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | chr2 | 218443017 | |||||||
| chr2:218443020 | C | A | 1 | a0001c0001t0001g0130 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2370+2158C>A | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | chr2 | 218443020 | |||||||
| chr2:218443021 | A | G | 7 | a0001c0001t0002g0007 a0001c0001t0002g0016 a0001c0001t0002g0037 others(4): Show |
12 | HG01884.hp1 HG02055.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.2370+2159A>G | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | chr2 | 218443021 | |||||||
| chr2:218443027 | C | A | 1 | a0001c0001t0001g0130 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2370+2165C>A | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | chr2 | 218443027 | |||||||
| chr2:218443029 | C | A | 1 | a0001c0001t0001g0130 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2370+2167C>A | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | chr2 | 218443029 | |||||||
| chr2:218443030 | T | A | 1 | a0001c0001t0001g0130 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2370+2168T>A | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | chr2 | 218443030 | |||||||
| chr2:218443031 | A | G | 1 | a0001c0001t0001g0130 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2370+2169A>G | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | chr2 | 218443031 | |||||||
| chr2:218443032 | C | G | 1 | a0001c0001t0001g0130 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2370+2170C>G | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | chr2 | 218443032 | |||||||
| chr2:218443036 | T | A | 1 | a0001c0001t0001g0130 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2370+2174T>A | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | chr2 | 218443036 | |||||||
| chr2:218443039 | A | G | 1 | a0001c0001t0001g0130 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2370+2177A>G | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | chr2 | 218443039 | |||||||
| chr2:218443042 | C | A | 1 | a0001c0001t0001g0130 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2370+2180C>A | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | chr2 | 218443042 | |||||||
| chr2:218443043 | T | G | 1 | a0001c0001t0001g0130 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2370+2181T>G | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | chr2 | 218443043 | |||||||
| chr2:218443044 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2370+2182G>A | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | chr2 | 218443044 | |||||||
| chr2:218443046 | T | C | 1 | a0001c0001t0001g0130 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2370+2184T>C | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | chr2 | 218443046 | |||||||
| chr2:218443048 | T | C | 1 | a0001c0001t0001g0130 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2370+2186T>C | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | chr2 | 218443048 | |||||||
| chr2:218443050 | A | C | 1 | a0001c0001t0001g0130 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2370+2188A>C | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | chr2 | 218443050 | |||||||
| chr2:218443051 | T | A | 1 | a0001c0001t0001g0130 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2370+2189T>A | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | chr2 | 218443051 | |||||||
| chr2:218443052 | T | C | 1 | a0001c0001t0001g0130 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2370+2190T>C | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | chr2 | 218443052 | |||||||
| chr2:218443054 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2370+2192C>T | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | chr2 | 218443054 | |||||||
| chr2:218443055 | C | G | 1 | a0001c0001t0001g0130 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2370+2193C>G | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | chr2 | 218443055 | |||||||
| chr2:218443075 | C | T | 1 | a0001c0001t0015g0137 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2370+2213C>T | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | chr2 | 218443075 | |||||||
| chr2:218443202 | C | CT | 204 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(201): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.2370+2354dupT | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr2 | 218443202 | ||||||
| chr2:218443202 | C | CTT | 7 | a0001c0001t0011g0038 a0001c0001t0019g0206 a0004c0004t0002g0067 others(4): Show |
8 | HG02109.hp2 HG03041.hp1 HG03516.hp2 others(5): Show |
intron_variant | MODIFIER | c.2370+2353_2370+235 others(6): Show |
VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr2 | 218443202 | ||||||
| chr2:218443261 | C | T | 1 | a0001c0001t0001g0150 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.2370+2399C>T | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | chr2 | 218443261 | |||||||
| chr2:218443272 | C | T | 1 | a0001c0001t0004g0090 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2370+2410C>T | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | chr2 | 218443272 | |||||||
| chr2:218443342 | C | T | 22 | a0001c0001t0002g0007 a0001c0001t0002g0016 a0001c0001t0002g0037 others(19): Show |
28 | HG01243.hp2 HG01884.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.2370+2480C>T | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | chr2 | 218443342 | |||||||
| chr2:218443421 | C | T | 94 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(91): Show |
138 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.2370+2559C>T | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | chr2 | 218443421 | |||||||
| chr2:218443741 | G | A | 15 | a0001c0001t0005g0017 a0001c0001t0005g0049 a0001c0001t0005g0050 others(12): Show |
16 | HG01243.hp2 HG01884.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.2370+2879G>A | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | chr2 | 218443741 | |||||||
| chr2:218443845 | C | T | 1 | a0001c0001t0019g0206 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2370+2983C>T | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | chr2 | 218443845 | |||||||
| chr2:218443931 | A | G | 1 | a0001c0001t0001g0134 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2370+3069A>G | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | chr2 | 218443931 | |||||||
| chr2:218443941 | C | T | 1 | a0007c0007t0002g0190 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2370+3079C>T | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | chr2 | 218443941 | |||||||
| chr2:218444510 | C | T | 93 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(90): Show |
137 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.2370+3648C>T | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | chr2 | 218444510 | |||||||
| chr2:218444573 | C | T | 1 | a0001c0001t0005g0212 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2370+3711C>T | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | chr2 | 218444573 | |||||||
| chr2:218444580 | C | T | 11 | a0001c0001t0002g0215 a0001c0001t0006g0015 a0001c0001t0006g0069 others(8): Show |
13 | HG02486.hp1 HG02559.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.2370+3718C>T | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | chr2 | 218444580 | |||||||
| chr2:218444699 | G | A | 5 | a0003c0003t0010g0013 a0003c0003t0010g0041 a0003c0003t0010g0042 others(2): Show |
5 | HG02717.hp1 HG02886.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.2370+3837G>A | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | chr2 | 218444699 | |||||||
| chr2:218444873 | C | A | 1 | a0001c0001t0008g0194 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2370+4011C>A | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | chr2 | 218444873 | |||||||
| chr2:218445014 | G | C | 1 | a0001c0001t0001g0024 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.2370+4152G>C | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | chr2 | 218445014 | |||||||
| chr2:218445085 | T | C | 1 | a0001c0001t0002g0007 | 4 | HG02723.hp1 HG03139.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2371-4138T>C | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | chr2 | 218445085 | |||||||
| chr2:218445129 | T | C | 1 | a0001c0001t0001g0054 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2371-4094T>C | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | chr2 | 218445129 | |||||||
| chr2:218445758 | T | C | 8 | a0001c0001t0001g0025 a0001c0001t0001g0054 a0001c0001t0001g0055 others(5): Show |
9 | HG01257.hp2 HG01258.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.2371-3465T>C | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | chr2 | 218445758 | |||||||
| chr2:218445760 | A | C | 166 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(163): Show |
234 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(231): Show |
intron_variant | MODIFIER | c.2371-3463A>C | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | chr2 | 218445760 | |||||||
| chr2:218445768 | T | C | 5 | a0001c0001t0006g0070 a0001c0001t0006g0213 a0001c0001t0006g0218 others(2): Show |
5 | HG02486.hp1 HG02615.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.2371-3455T>C | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | chr2 | 218445768 | |||||||
| chr2:218446220 | G | C | 1 | a0001c0001t0007g0177 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.2371-3003G>C | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | chr2 | 218446220 | |||||||
| chr2:218446432 | A | C | 1 | a0001c0001t0002g0181 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2371-2791A>C | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | chr2 | 218446432 | |||||||
| chr2:218446635 | C | T | 1 | a0001c0001t0001g0024 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.2371-2588C>T | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | chr2 | 218446635 | |||||||
| chr2:218446656 | A | C | 2 | a0001c0001t0001g0130 a0001c0001t0001g0133 |
2 | HG02015.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.2371-2567A>C | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | chr2 | 218446656 | |||||||
| chr2:218446760 | C | CT | 54 | a0001c0001t0002g0009 a0001c0001t0002g0034 a0001c0001t0002g0186 others(51): Show |
79 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.2371-2442dupT | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr2 | 218446760 | ||||||
| chr2:218446760 | C | CTT | 6 | a0001c0001t0002g0035 a0001c0001t0004g0019 a0001c0001t0006g0217 others(3): Show |
8 | HG00733.hp1 HG01243.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.2371-2443_2371-244 others(6): Show |
VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr2 | 218446760 | ||||||
| chr2:218446760 | C | CTTT | 34 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0010 others(31): Show |
52 | HG00558.hp1 HG00621.hp1 HG02027.hp2 others(49): Show |
intron_variant | MODIFIER | c.2371-2444_2371-244 others(7): Show |
VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr2 | 218446760 | ||||||
| chr2:218446760 | C | CTTTT | 8 | a0001c0001t0002g0007 a0001c0001t0002g0016 a0001c0001t0002g0037 others(5): Show |
13 | HG01884.hp1 HG02074.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.2371-2445_2371-244 others(8): Show |
VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr2 | 218446760 | ||||||
| chr2:218446760 | C | CTTTTT | 18 | a0001c0001t0002g0048 a0001c0001t0002g0065 a0001c0001t0002g0144 others(15): Show |
19 | HG01109.hp1 HG01243.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.2371-2446_2371-244 others(9): Show |
VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr2 | 218446760 | ||||||
| chr2:218446760 | CTTTTTTT | C | 91 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(88): Show |
135 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.2371-2448_2371-244 others(11): Show |
VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr2 | 218446760 | ||||||
| chr2:218446787 | A | G | 1 | a0001c0001t0013g0109 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.2371-2436A>G | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | chr2 | 218446787 | |||||||
| chr2:218446792 | C | T | 93 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(90): Show |
137 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.2371-2431C>T | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | chr2 | 218446792 | |||||||
| chr2:218446887 | C | T | 1 | a0001c0001t0023g0196 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2371-2336C>T | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | chr2 | 218446887 | |||||||
| chr2:218446888 | G | A | 1 | a0001c0001t0002g0035 | 2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2371-2335G>A | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | chr2 | 218446888 | |||||||
| chr2:218446983 | C | T | 17 | a0001c0001t0006g0015 a0001c0001t0006g0069 a0001c0001t0006g0070 others(14): Show |
19 | HG02109.hp2 HG02451.hp2 HG02486.hp1 others(16): Show |
intron_variant | MODIFIER | c.2371-2240C>T | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | chr2 | 218446983 | |||||||
| chr2:218447053 | C | T | 1 | a0004c0004t0002g0067 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2371-2170C>T | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | chr2 | 218447053 | |||||||
| chr2:218447115 | C | T | 16 | a0001c0001t0005g0017 a0001c0001t0005g0049 a0001c0001t0005g0050 others(13): Show |
17 | HG01109.hp1 HG01243.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.2371-2108C>T | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | chr2 | 218447115 | |||||||
| chr2:218447210 | G | A | 28 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0010 others(25): Show |
44 | HG00558.hp1 HG00621.hp1 HG02027.hp2 others(41): Show |
intron_variant | MODIFIER | c.2371-2013G>A | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | chr2 | 218447210 | |||||||
| chr2:218447383 | T | C | 28 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0010 others(25): Show |
44 | HG00558.hp1 HG00621.hp1 HG02027.hp2 others(41): Show |
intron_variant | MODIFIER | c.2371-1840T>C | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | chr2 | 218447383 | |||||||
| chr2:218447462 | C | T | 5 | a0004c0004t0002g0067 a0004c0004t0002g0068 a0004c0004t0002g0195 others(2): Show |
5 | HG03516.hp2 HG06807.hp1 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.2371-1761C>T | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | chr2 | 218447462 | |||||||
| chr2:218447492 | A | C | 1 | a0001c0001t0001g0132 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2371-1731A>C | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | chr2 | 218447492 | |||||||
| chr2:218447740 | G | GT | 27 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0010 others(24): Show |
43 | HG00558.hp1 HG00621.hp1 HG02027.hp2 others(40): Show |
intron_variant | MODIFIER | c.2371-1473dupT | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr2 | 218447740 | ||||||
| chr2:218447746 | T | C | 51 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0006 others(48): Show |
79 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.2371-1477T>C | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | chr2 | 218447746 | |||||||
| chr2:218448032 | GGTGGACT others(74): Show |
G | 1 | a0001c0001t0003g0089 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2371-1189_2371-110 others(85): Show |
VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr2 | 218448032 | ||||||
| chr2:218448292 | T | C | 1 | a0001c0001t0004g0052 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2371-931T>C | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | chr2 | 218448292 | |||||||
| chr2:218448631 | T | C | 46 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0006 others(43): Show |
69 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(66): Show |
intron_variant | MODIFIER | c.2371-592T>C | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | chr2 | 218448631 | |||||||
| chr2:218448786 | C | G | 1 | a0001c0001t0005g0176 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2371-437C>G | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | chr2 | 218448786 | |||||||
| chr2:218448802 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2371-421C>T | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | chr2 | 218448802 | |||||||
| chr2:218448867 | T | C | 1 | a0001c0001t0001g0193 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2371-356T>C | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | chr2 | 218448867 | |||||||
| chr2:218448873 | C | T | 5 | a0003c0003t0010g0013 a0003c0003t0010g0041 a0003c0003t0010g0042 others(2): Show |
5 | HG02717.hp1 HG02886.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.2371-350C>T | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | chr2 | 218448873 | |||||||
| chr2:218449005 | G | GA | 92 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(89): Show |
136 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.2371-205dupA | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr2 | 218449005 | ||||||
| chr2:218449005 | GA | G | 56 | a0001c0001t0002g0186 a0001c0001t0003g0002 a0001c0001t0003g0004 others(53): Show |
84 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.2371-205delA | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr2 | 218449005 | ||||||
| chr2:218449081 | C | T | 1 | a0001c0001t0002g0186 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2371-142C>T | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | chr2 | 218449081 | |||||||
| chr2:218449168 | G | A | 1 | a0001c0001t0002g0035 | 2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2371-55G>A | VIL1 | ENSG00000127831.11 | transcript | ENST00000248444.10 | protein_coding | 19/19 | chr2 | 218449168 |