Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 50853 |
| ensemblid | ENSG00000136059.16 |
| hgncid | 30906 |
| symbol | VILL |
| name | villin like |
| refseq_nuc | NM_015873.4 |
| refseq_prot | NP_056957.3 |
| ensembl_nuc | ENST00000383759.7 |
| ensembl_prot | ENSP00000373266.2 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 37990786 |
| end | 38007185 |
| strand | + |
| ver | v1.2 |
| region | chr3:37990786-38007185 |
| region5000 | chr3:37985786-38012185 |
| regionname0 | VILL_chr3_37990786_38007185 |
| regionname5000 | VILL_chr3_37985786_38012185 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 856 | 225 | 39 | 49 | 101 | 8 | 26 | 71 | VILL_chr3_37985786_38012185 | VILL | MDISK others(851): Show |
chr3 | 37985786 | 38012185 |
| a0002 | 0/0 | 856 | 61 | 30 | 9 | 8 | 2 | 12 | 4 | VILL_chr3_37985786_38012185 | VILL | MDISK others(851): Show |
chr3 | 37985786 | 38012185 |
| a0003 | 0/0 | 857 | 29 | 5 | 3 | 20 | 0 | 1 | 13 | VILL_chr3_37985786_38012185 | VILL | MDISK others(852): Show |
chr3 | 37985786 | 38012185 |
| a0004 | 0/0 | 856 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | MDISK others(851): Show |
chr3 | 37985786 | 38012185 |
| a0005 | 0/0 | 856 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | MDISK others(851): Show |
chr3 | 37985786 | 38012185 |
| a0006 | 0/0 | 856 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | MDISK others(851): Show |
chr3 | 37985786 | 38012185 |
| a0007 | 0/0 | 856 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | VILL_chr3_37985786_38012185 | VILL | MDISK others(851): Show |
chr3 | 37985786 | 38012185 |
| a0008 | 0/0 | 856 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | MDISK others(851): Show |
chr3 | 37985786 | 38012185 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2568 | 218 | 38 | 47 | 98 | 8 | 25 | VILL_chr3_37985786_38012185 | VILL | ATGGA others(2563): Show |
chr3 | 37985786 | 38012185 | ||
| a0001c0011 | 0/0 | 2568 | 2 | 0 | 0 | 2 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | ATGGA others(2563): Show |
chr3 | 37985786 | 38012185 | ||
| a0001c0015 | 0/0 | 2568 | 1 | 1 | 0 | 0 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | ATGGA others(2563): Show |
chr3 | 37985786 | 38012185 | ||
| a0001c0016 | 0/0 | 2568 | 1 | 0 | 1 | 0 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | ATGGA others(2563): Show |
chr3 | 37985786 | 38012185 | ||
| a0001c0017 | 0/0 | 2568 | 1 | 0 | 0 | 1 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | ATGGA others(2563): Show |
chr3 | 37985786 | 38012185 | ||
| a0001c0020 | 0/0 | 2568 | 1 | 0 | 0 | 0 | 0 | 1 | VILL_chr3_37985786_38012185 | VILL | ATGGA others(2563): Show |
chr3 | 37985786 | 38012185 | ||
| a0001c0021 | 0/0 | 2568 | 1 | 0 | 1 | 0 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | ATGGA others(2563): Show |
chr3 | 37985786 | 38012185 | ||
| a0002c0002 | 0/0 | 2568 | 26 | 3 | 6 | 8 | 2 | 7 | VILL_chr3_37985786_38012185 | VILL | ATGGA others(2563): Show |
chr3 | 37985786 | 38012185 | ||
| a0002c0004 | 0/0 | 2568 | 20 | 17 | 3 | 0 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | ATGGA others(2563): Show |
chr3 | 37985786 | 38012185 | ||
| a0002c0005 | 0/0 | 2568 | 5 | 5 | 0 | 0 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | ATGGA others(2563): Show |
chr3 | 37985786 | 38012185 | ||
| a0002c0006 | 0/0 | 2568 | 5 | 0 | 0 | 0 | 0 | 5 | VILL_chr3_37985786_38012185 | VILL | ATGGA others(2563): Show |
chr3 | 37985786 | 38012185 | ||
| a0002c0008 | 0/0 | 2568 | 4 | 4 | 0 | 0 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | ATGGA others(2563): Show |
chr3 | 37985786 | 38012185 | ||
| a0002c0013 | 0/0 | 2568 | 1 | 1 | 0 | 0 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | ATGGA others(2563): Show |
chr3 | 37985786 | 38012185 | ||
| a0003c0003 | 0/0 | 2571 | 25 | 5 | 1 | 18 | 0 | 1 | VILL_chr3_37985786_38012185 | VILL | ATGGA others(2566): Show |
chr3 | 37985786 | 38012185 | ||
| a0003c0009 | 0/0 | 2571 | 3 | 0 | 2 | 1 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | ATGGA others(2566): Show |
chr3 | 37985786 | 38012185 | ||
| a0003c0019 | 0/0 | 2571 | 1 | 0 | 0 | 1 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | ATGGA others(2566): Show |
chr3 | 37985786 | 38012185 | ||
| a0004c0007 | 0/0 | 2568 | 4 | 3 | 1 | 0 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | ATGGA others(2563): Show |
chr3 | 37985786 | 38012185 | ||
| a0005c0010 | 0/0 | 2568 | 2 | 0 | 2 | 0 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | ATGGA others(2563): Show |
chr3 | 37985786 | 38012185 | ||
| a0006c0012 | 0/0 | 2568 | 1 | 1 | 0 | 0 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | ATGGA others(2563): Show |
chr3 | 37985786 | 38012185 | ||
| a0007c0014 | 0/0 | 2568 | 1 | 0 | 0 | 0 | 0 | 1 | VILL_chr3_37985786_38012185 | VILL | ATGGA others(2563): Show |
chr3 | 37985786 | 38012185 | ||
| a0008c0018 | 0/0 | 2568 | 1 | 0 | 0 | 1 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | ATGGA others(2563): Show |
chr3 | 37985786 | 38012185 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2831 | 218 | 38 | 47 | 98 | 8 | 25 | VILL_chr3_37985786_38012185 | VILL | ACTGC others(2826): Show |
chr3 | 37985786 | 38012185 |
| a0001c0011t0001 | 0/0 | 2831 | 2 | 0 | 0 | 2 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | ACTGC others(2826): Show |
chr3 | 37985786 | 38012185 |
| a0001c0015t0001 | 0/0 | 2831 | 1 | 1 | 0 | 0 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | ACTGC others(2826): Show |
chr3 | 37985786 | 38012185 |
| a0001c0016t0001 | 0/0 | 2831 | 1 | 0 | 1 | 0 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | ACTGC others(2826): Show |
chr3 | 37985786 | 38012185 |
| a0001c0017t0001 | 0/0 | 2831 | 1 | 0 | 0 | 1 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | ACTGC others(2826): Show |
chr3 | 37985786 | 38012185 |
| a0001c0020t0001 | 0/0 | 2831 | 1 | 0 | 0 | 0 | 0 | 1 | VILL_chr3_37985786_38012185 | VILL | ACTGC others(2826): Show |
chr3 | 37985786 | 38012185 |
| a0001c0021t0001 | 0/0 | 2831 | 1 | 0 | 1 | 0 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | ACTGC others(2826): Show |
chr3 | 37985786 | 38012185 |
| a0002c0002t0001 | 0/0 | 2831 | 26 | 3 | 6 | 8 | 2 | 7 | VILL_chr3_37985786_38012185 | VILL | ACTGC others(2826): Show |
chr3 | 37985786 | 38012185 |
| a0002c0004t0001 | 0/0 | 2831 | 20 | 17 | 3 | 0 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | ACTGC others(2826): Show |
chr3 | 37985786 | 38012185 |
| a0002c0005t0001 | 0/0 | 2831 | 5 | 5 | 0 | 0 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | ACTGC others(2826): Show |
chr3 | 37985786 | 38012185 |
| a0002c0006t0001 | 0/0 | 2831 | 5 | 0 | 0 | 0 | 0 | 5 | VILL_chr3_37985786_38012185 | VILL | ACTGC others(2826): Show |
chr3 | 37985786 | 38012185 |
| a0002c0008t0001 | 0/0 | 2831 | 4 | 4 | 0 | 0 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | ACTGC others(2826): Show |
chr3 | 37985786 | 38012185 |
| a0002c0013t0001 | 0/0 | 2831 | 1 | 1 | 0 | 0 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | ACTGC others(2826): Show |
chr3 | 37985786 | 38012185 |
| a0003c0003t0001 | 0/0 | 2834 | 25 | 5 | 1 | 18 | 0 | 1 | VILL_chr3_37985786_38012185 | VILL | ACTGC others(2829): Show |
chr3 | 37985786 | 38012185 |
| a0003c0009t0001 | 0/0 | 2834 | 3 | 0 | 2 | 1 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | ACTGC others(2829): Show |
chr3 | 37985786 | 38012185 |
| a0003c0019t0001 | 0/0 | 2834 | 1 | 0 | 0 | 1 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | ACTGC others(2829): Show |
chr3 | 37985786 | 38012185 |
| a0004c0007t0001 | 0/0 | 2831 | 4 | 3 | 1 | 0 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | ACTGC others(2826): Show |
chr3 | 37985786 | 38012185 |
| a0005c0010t0001 | 0/0 | 2831 | 2 | 0 | 2 | 0 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | ACTGC others(2826): Show |
chr3 | 37985786 | 38012185 |
| a0006c0012t0001 | 0/0 | 2831 | 1 | 1 | 0 | 0 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | ACTGC others(2826): Show |
chr3 | 37985786 | 38012185 |
| a0007c0014t0001 | 0/0 | 2831 | 1 | 0 | 0 | 0 | 0 | 1 | VILL_chr3_37985786_38012185 | VILL | ACTGC others(2826): Show |
chr3 | 37985786 | 38012185 |
| a0008c0018t0001 | 0/0 | 2831 | 1 | 0 | 0 | 1 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | ACTGC others(2826): Show |
chr3 | 37985786 | 38012185 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 82 | 14 | 15 | 39 | 4 | 10 | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| a0001c0001t0001g0002 | 0/0 | 53 | 0 | 19 | 26 | 1 | 7 | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| a0001c0001t0001g0004 | 0/0 | 11 | 0 | 4 | 6 | 0 | 1 | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| a0001c0001t0001g0007 | 0/0 | 7 | 6 | 1 | 0 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| a0001c0001t0001g0008 | 0/0 | 6 | 5 | 1 | 0 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| a0001c0001t0001g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| a0001c0001t0001g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| a0001c0001t0001g0029 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| a0001c0001t0001g0046 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| a0001c0011t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| a0001c0015t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| a0001c0016t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| a0001c0017t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| a0001c0020t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| a0001c0021t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| a0002c0002t0001g0005 | 0/0 | 13 | 0 | 1 | 7 | 0 | 5 | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| a0002c0002t0001g0019 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| a0002c0002t0001g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| a0002c0002t0001g0032 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| a0002c0002t0001g0033 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| a0002c0002t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| a0002c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| a0002c0002t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| a0002c0004t0001g0006 | 0/0 | 7 | 5 | 2 | 0 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| a0002c0004t0001g0009 | 0/0 | 6 | 5 | 1 | 0 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| a0002c0004t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| a0002c0004t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| a0002c0004t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| a0002c0004t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| a0002c0004t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| a0002c0004t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| a0002c0005t0001g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| a0002c0005t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| a0002c0006t0001g0010 | 0/0 | 5 | 0 | 0 | 0 | 0 | 5 | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| a0002c0008t0001g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| a0002c0008t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| a0002c0013t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| a0003c0003t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| a0003c0003t0001g0003 | 0/0 | 15 | 0 | 1 | 13 | 0 | 1 | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| a0003c0003t0001g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| a0003c0003t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| a0003c0003t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| a0003c0003t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| a0003c0003t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| a0003c0003t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| a0003c0009t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| a0003c0009t0001g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| a0003c0009t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| a0003c0019t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| a0004c0007t0001g0013 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| a0005c0010t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| a0006c0012t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| a0007c0014t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| a0008c0018t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0043 | EUR | GBR | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | CHS | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG00423 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | CHS | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG00544 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | CHS | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG00597 | hp1 | a0003 | c0003 | t0001 | g0003 | EAS | CHS | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG00673 | hp2 | a0003 | c0003 | t0001 | g0001 | EAS | CHS | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG00741 | hp2 | a0002 | c0002 | t0001 | g0078 | AMR | PUR | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG01070 | hp2 | a0005 | c0010 | t0001 | g0004 | AMR | PUR | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG01071 | hp1 | a0005 | c0010 | t0001 | g0004 | AMR | PUR | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG01074 | hp2 | a0001 | c0016 | t0001 | g0001 | AMR | PUR | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG01081 | hp2 | a0002 | c0002 | t0001 | g0005 | AMR | PUR | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG01109 | hp2 | a0002 | c0004 | t0001 | g0009 | AMR | PUR | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG01167 | hp1 | a0002 | c0004 | t0001 | g0006 | AMR | PUR | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG01169 | hp2 | a0002 | c0004 | t0001 | g0006 | AMR | PUR | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG01192 | hp1 | a0004 | c0007 | t0001 | g0013 | AMR | PUR | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG01243 | hp2 | a0001 | c0021 | t0001 | g0001 | AMR | PUR | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG01358 | hp1 | a0003 | c0003 | t0001 | g0003 | AMR | CLM | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG01358 | hp2 | a0003 | c0009 | t0001 | g0003 | AMR | CLM | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | CLM | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG01515 | hp2 | a0002 | c0002 | t0001 | g0032 | EUR | IBS | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0027 | EUR | IBS | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0027 | EUR | IBS | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG01517 | hp2 | a0002 | c0002 | t0001 | g0032 | EUR | IBS | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG01884 | hp1 | a0002 | c0008 | t0001 | g0018 | AFR | ACB | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG01891 | hp2 | a0002 | c0004 | t0001 | g0072 | AFR | ACB | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG01934 | hp2 | a0002 | c0002 | t0001 | g0076 | AMR | PEL | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG01943 | hp2 | a0002 | c0002 | t0001 | g0019 | AMR | PEL | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG01975 | hp1 | a0002 | c0002 | t0001 | g0019 | AMR | PEL | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG01993 | hp1 | a0002 | c0002 | t0001 | g0019 | AMR | PEL | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | KHV | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG02040 | hp2 | a0003 | c0003 | t0001 | g0055 | EAS | KHV | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG02055 | hp1 | a0002 | c0004 | t0001 | g0009 | AFR | ACB | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG02055 | hp2 | a0002 | c0013 | t0001 | g0071 | AFR | ACB | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG02071 | hp1 | a0003 | c0003 | t0001 | g0003 | EAS | KHV | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG02074 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | KHV | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | KHV | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG02132 | hp2 | a0003 | c0003 | t0001 | g0003 | EAS | KHV | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | KHV | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG02155 | hp2 | a0003 | c0003 | t0001 | g0079 | EAS | CDX | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG02165 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | CDX | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | ACB | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | ACB | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG02273 | hp1 | a0003 | c0009 | t0001 | g0040 | AMR | PEL | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | ACB | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PEL | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG02523 | hp1 | a0003 | c0019 | t0001 | g0003 | EAS | KHV | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG02572 | hp1 | a0006 | c0012 | t0001 | g0074 | AFR | GWD | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG02602 | hp2 | a0002 | c0006 | t0001 | g0010 | SAS | PJL | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG02622 | hp1 | a0002 | c0005 | t0001 | g0012 | AFR | GWD | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG02622 | hp2 | a0002 | c0004 | t0001 | g0006 | AFR | GWD | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG02630 | hp1 | a0002 | c0004 | t0001 | g0068 | AFR | GWD | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0054 | SAS | PJL | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG02698 | hp1 | a0002 | c0006 | t0001 | g0010 | SAS | PJL | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG02698 | hp2 | a0002 | c0002 | t0001 | g0005 | SAS | PJL | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG02717 | hp2 | a0003 | c0003 | t0001 | g0026 | AFR | GWD | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG02723 | hp1 | a0002 | c0004 | t0001 | g0006 | AFR | GWD | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG02723 | hp2 | a0002 | c0008 | t0001 | g0018 | AFR | GWD | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG02735 | hp1 | a0001 | c0020 | t0001 | g0001 | SAS | PJL | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG02809 | hp1 | a0003 | c0003 | t0001 | g0017 | AFR | GWD | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG02818 | hp1 | a0002 | c0002 | t0001 | g0020 | AFR | GWD | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG02818 | hp2 | a0001 | c0015 | t0001 | g0036 | AFR | GWD | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | GWD | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG02895 | hp1 | a0004 | c0007 | t0001 | g0013 | AFR | GWD | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG02896 | hp1 | a0004 | c0007 | t0001 | g0013 | AFR | GWD | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG02896 | hp2 | a0002 | c0004 | t0001 | g0030 | AFR | GWD | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG02897 | hp1 | a0002 | c0004 | t0001 | g0030 | AFR | GWD | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG02922 | hp1 | a0002 | c0004 | t0001 | g0009 | AFR | ESN | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG02965 | hp2 | a0002 | c0005 | t0001 | g0012 | AFR | ESN | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG02970 | hp1 | a0002 | c0004 | t0001 | g0006 | AFR | ESN | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | ESN | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG02976 | hp1 | a0002 | c0004 | t0001 | g0009 | AFR | ESN | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG02976 | hp2 | a0002 | c0004 | t0001 | g0006 | AFR | ESN | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG03041 | hp2 | a0002 | c0005 | t0001 | g0012 | AFR | GWD | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG03098 | hp1 | a0003 | c0003 | t0001 | g0017 | AFR | MSL | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG03130 | hp1 | a0002 | c0002 | t0001 | g0020 | AFR | ESN | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG03130 | hp2 | a0002 | c0005 | t0001 | g0012 | AFR | ESN | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG03139 | hp2 | a0002 | c0004 | t0001 | g0069 | AFR | ESN | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | MSL | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG03225 | hp2 | a0002 | c0004 | t0001 | g0009 | AFR | MSL | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG03239 | hp2 | a0002 | c0006 | t0001 | g0010 | SAS | PJL | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | MSL | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG03486 | hp2 | a0002 | c0004 | t0001 | g0009 | AFR | MSL | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG03491 | hp1 | a0002 | c0002 | t0001 | g0005 | SAS | PJL | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG03491 | hp2 | a0002 | c0002 | t0001 | g0033 | SAS | PJL | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG03492 | hp2 | a0002 | c0002 | t0001 | g0033 | SAS | PJL | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG03540 | hp1 | a0002 | c0008 | t0001 | g0018 | AFR | GWD | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG03579 | hp1 | a0002 | c0008 | t0001 | g0070 | AFR | MSL | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG03579 | hp2 | a0004 | c0007 | t0001 | g0013 | AFR | MSL | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG03704 | hp1 | a0002 | c0006 | t0001 | g0010 | SAS | PJL | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG03704 | hp2 | a0002 | c0002 | t0001 | g0005 | SAS | PJL | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0044 | SAS | PJL | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG03834 | hp1 | a0003 | c0003 | t0001 | g0003 | SAS | BEB | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0041 | SAS | STU | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | STU | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG04199 | hp2 | a0002 | c0006 | t0001 | g0010 | SAS | STU | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG04204 | hp1 | a0002 | c0002 | t0001 | g0005 | SAS | STU | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | STU | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG04228 | hp2 | a0007 | c0014 | t0001 | g0064 | SAS | STU | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA18522 | hp1 | a0002 | c0004 | t0001 | g0006 | AFR | YRI | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA18522 | hp2 | a0002 | c0005 | t0001 | g0065 | AFR | YRI | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA18612 | hp2 | a0008 | c0018 | t0001 | g0002 | EAS | CHB | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA18943 | hp1 | a0002 | c0002 | t0001 | g0077 | EAS | JPT | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA18952 | hp2 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA18956 | hp2 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA18959 | hp1 | a0003 | c0009 | t0001 | g0001 | EAS | JPT | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA18961 | hp1 | a0001 | c0011 | t0001 | g0001 | EAS | JPT | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA18961 | hp2 | a0003 | c0003 | t0001 | g0053 | EAS | JPT | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA18963 | hp1 | a0003 | c0003 | t0001 | g0056 | EAS | JPT | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA18964 | hp1 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA18967 | hp2 | a0001 | c0017 | t0001 | g0011 | EAS | JPT | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA18969 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA18970 | hp1 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA18982 | hp2 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA18985 | hp1 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA18989 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA18997 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA19003 | hp2 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA19043 | hp1 | a0002 | c0004 | t0001 | g0073 | AFR | LWK | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | LWK | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA19060 | hp1 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA19067 | hp2 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA19082 | hp2 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA19091 | hp1 | a0001 | c0011 | t0001 | g0001 | EAS | JPT | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ASW | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA20129 | hp2 | a0002 | c0002 | t0001 | g0020 | AFR | ASW | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA20905 | hp1 | a0002 | c0002 | t0001 | g0005 | SAS | GIH | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG02486 | hp1 | a0003 | c0003 | t0001 | g0017 | AFR | ACB | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| HG03471 | hp2 | a0003 | c0003 | t0001 | g0026 | AFR | MSL | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| NA20300 | hp2 | a0002 | c0004 | t0001 | g0067 | AFR | USA | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0046 | REF | REF | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0029 | REF | REF | VILL_chr3_37985786_38012185 | VILL | chr3 | 37985786 | 38012185 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:37998943 | A | ACAC | 1 | a0003 | 29 | HG00597.hp1 HG00673.hp2 HG01358.hp1 others(26): Show |
disruptive_inframe_insertion | MODERATE | c.977_979dupCCA | p.Thr326dup | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 10/20 | 1110/2831 | 980/2571 | 327/856 | INFO_REALIGN_3_PRIME | chr3 | 37998943 | ||
| chr3:38001456 | G | T | 1 | a0008 | 1 | NA18612.hp2 | missense_variant&splice_region_variant | MODERATE | c.1183G>T | p.Val395Leu | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 12/20 | 1313/2831 | 1183/2571 | 395/856 | chr3 | 38001456 | |||
| chr3:38002522 | A | G | 1 | a0003 | 1 | HG02523.hp1 | missense_variant | MODERATE | c.1606A>G | p.Ser536Gly | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 14/20 | 1736/2831 | 1606/2571 | 536/856 | chr3 | 38002522 | |||
| chr3:38002552 | G | A | 1 | a0007 | 1 | HG04228.hp2 | missense_variant | MODERATE | c.1636G>A | p.Val546Ile | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 14/20 | 1766/2831 | 1636/2571 | 546/856 | chr3 | 38002552 | |||
| chr3:38004279 | C | G | 1 | a0003 | 3 | HG01358.hp2 HG02273.hp1 NA18959.hp1 |
missense_variant | MODERATE | c.1830C>G | p.Phe610Leu | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 16/20 | 1960/2831 | 1830/2571 | 610/856 | chr3 | 38004279 | |||
| chr3:38004294 | T | A | 1 | a0007 | 1 | HG04228.hp2 | missense_variant | MODERATE | c.1845T>A | p.Phe615Leu | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 16/20 | 1975/2831 | 1845/2571 | 615/856 | chr3 | 38004294 | |||
| chr3:38004304 | A | C | 1 | a0005 | 2 | HG01070.hp2 HG01071.hp1 |
missense_variant | MODERATE | c.1855A>C | p.Ser619Arg | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 16/20 | 1985/2831 | 1855/2571 | 619/856 | chr3 | 38004304 | |||
| chr3:38006463 | G | C | 4 | a0002 a0004 a0006 others(1): Show |
67 | HG00423.hp2 HG00544.hp1 HG00741.hp2 others(64): Show |
missense_variant | MODERATE | c.2220G>C | p.Leu740Phe | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 19/20 | 2350/2831 | 2220/2571 | 740/856 | chr3 | 38006463 | |||
| chr3:38006667 | C | A | 1 | a0006 | 1 | HG02572.hp1 | missense_variant | MODERATE | c.2424C>A | p.Asp808Glu | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 19/20 | 2554/2831 | 2424/2571 | 808/856 | chr3 | 38006667 | |||
| chr3:38006990 | G | A | 1 | a0004 | 4 | HG01192.hp1 HG02895.hp1 HG02896.hp1 others(1): Show |
missense_variant | MODERATE | c.2506G>A | p.Glu836Lys | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 20/20 | 2636/2831 | 2506/2571 | 836/856 | chr3 | 38006990 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:37995793 | C | T | 1 | a0001c0021 | 1 | HG01243.hp2 | synonymous_variant | LOW | c.396C>T | p.Phe132Phe | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 5/20 | 526/2831 | 396/2571 | 132/856 | chr3 | 37995793 | |||
| chr3:37997128 | C | T | 1 | a0001c0020 | 1 | HG02735.hp1 | synonymous_variant | LOW | c.502C>T | p.Leu168Leu | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 6/20 | 632/2831 | 502/2571 | 168/856 | chr3 | 37997128 | |||
| chr3:37997491 | T | C | 10 | a0001c0015 a0002c0002 a0002c0004 others(7): Show |
68 | HG00423.hp2 HG00544.hp1 HG00741.hp2 others(65): Show |
synonymous_variant | LOW | c.570T>C | p.Ala190Ala | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 7/20 | 700/2831 | 570/2571 | 190/856 | chr3 | 37997491 | |||
| chr3:37997572 | G | A | 2 | a0002c0004 a0006c0012 |
21 | HG01109.hp2 HG01167.hp1 HG01169.hp2 others(18): Show |
synonymous_variant | LOW | c.651G>A | p.Pro217Pro | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 7/20 | 781/2831 | 651/2571 | 217/856 | chr3 | 37997572 | |||
| chr3:37999046 | G | A | 1 | a0002c0013 | 1 | HG02055.hp2 | synonymous_variant | LOW | c.1077G>A | p.Gly359Gly | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 10/20 | 1207/2831 | 1077/2571 | 359/856 | chr3 | 37999046 | |||
| chr3:38001827 | C | T | 1 | a0001c0017 | 1 | NA18967.hp2 | synonymous_variant | LOW | c.1446C>T | p.Leu482Leu | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 13/20 | 1576/2831 | 1446/2571 | 482/856 | chr3 | 38001827 | |||
| chr3:38002413 | T | C | 6 | a0001c0015 a0002c0002 a0002c0004 others(3): Show |
54 | HG00423.hp2 HG00544.hp1 HG00741.hp2 others(51): Show |
synonymous_variant | LOW | c.1497T>C | p.His499His | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 14/20 | 1627/2831 | 1497/2571 | 499/856 | chr3 | 38002413 | |||
| chr3:38004289 | C | T | 1 | a0001c0011 | 2 | NA18961.hp1 NA19091.hp1 |
synonymous_variant | LOW | c.1840C>T | p.Leu614Leu | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 16/20 | 1970/2831 | 1840/2571 | 614/856 | chr3 | 38004289 | |||
| chr3:38005836 | G | A | 1 | a0002c0006 | 5 | HG02602.hp2 HG02698.hp1 HG03239.hp2 others(2): Show |
synonymous_variant | LOW | c.1995G>A | p.Ala665Ala | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 17/20 | 2125/2831 | 1995/2571 | 665/856 | chr3 | 38005836 | |||
| chr3:38006189 | G | A | 1 | a0002c0002 | 26 | HG00423.hp2 HG00544.hp1 HG00741.hp2 others(23): Show |
synonymous_variant | LOW | c.2142G>A | p.Pro714Pro | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 18/20 | 2272/2831 | 2142/2571 | 714/856 | chr3 | 38006189 | |||
| chr3:38006192 | C | T | 1 | a0001c0016 | 1 | HG01074.hp2 | synonymous_variant | LOW | c.2145C>T | p.Ser715Ser | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 18/20 | 2275/2831 | 2145/2571 | 715/856 | chr3 | 38006192 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:37991016 | C | T | 2 | a0001c0001t0001g0007 a0001c0001t0001g0080 |
8 | HG01074.hp1 HG01884.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.-87+187C>T | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 1/19 | chr3 | 37991016 | |||||||
| chr3:37991181 | G | T | 1 | a0003c0003t0001g0079 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-87+352G>T | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 1/19 | chr3 | 37991181 | |||||||
| chr3:37991323 | G | A | 5 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0034 others(2): Show |
12 | HG01981.hp2 HG02647.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.-87+494G>A | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 1/19 | chr3 | 37991323 | |||||||
| chr3:37991580 | G | T | 9 | a0001c0001t0001g0075 a0002c0002t0001g0005 a0002c0002t0001g0019 others(6): Show |
27 | HG00423.hp2 HG00544.hp1 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.-87+751G>T | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 1/19 | chr3 | 37991580 | |||||||
| chr3:37991834 | C | T | 3 | a0001c0001t0001g0007 a0001c0001t0001g0031 a0001c0001t0001g0080 |
10 | HG01074.hp1 HG01884.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.-87+1005C>T | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 1/19 | chr3 | 37991834 | |||||||
| chr3:37991855 | C | A | 1 | a0002c0006t0001g0010 | 5 | HG02602.hp2 HG02698.hp1 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.-87+1026C>A | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 1/19 | chr3 | 37991855 | |||||||
| chr3:37991879 | A | G | 1 | a0001c0001t0001g0014 | 4 | NA18945.hp1 NA18955.hp1 NA18956.hp1 others(1): Show |
intron_variant | MODIFIER | c.-87+1050A>G | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 1/19 | chr3 | 37991879 | |||||||
| chr3:37991971 | C | T | 28 | a0001c0001t0001g0007 a0001c0001t0001g0066 a0001c0001t0001g0080 others(25): Show |
76 | HG00423.hp2 HG00544.hp1 HG00741.hp2 others(73): Show |
intron_variant | MODIFIER | c.-87+1142C>T | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 1/19 | chr3 | 37991971 | |||||||
| chr3:37992025 | C | T | 2 | a0001c0001t0001g0007 a0001c0001t0001g0080 |
8 | HG01074.hp1 HG01884.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.-87+1196C>T | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 1/19 | chr3 | 37992025 | |||||||
| chr3:37992194 | T | A | 2 | a0001c0001t0001g0007 a0001c0001t0001g0080 |
8 | HG01074.hp1 HG01884.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.-87+1365T>A | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 1/19 | chr3 | 37992194 | |||||||
| chr3:37992514 | G | C | 89 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(86): Show |
321 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(318): Show |
intron_variant | MODIFIER | c.-86-1073G>C | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 1/19 | chr3 | 37992514 | |||||||
| chr3:37992780 | C | T | 1 | a0006c0012t0001g0074 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-86-807C>T | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 1/19 | chr3 | 37992780 | |||||||
| chr3:37993145 | G | A | 1 | a0001c0001t0001g0037 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-86-442G>A | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 1/19 | chr3 | 37993145 | |||||||
| chr3:37993229 | G | A | 1 | a0001c0001t0001g0038 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-86-358G>A | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 1/19 | chr3 | 37993229 | |||||||
| chr3:37993330 | A | G | 77 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(74): Show |
255 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(252): Show |
intron_variant | MODIFIER | c.-86-257A>G | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 1/19 | chr3 | 37993330 | |||||||
| chr3:37993437 | A | G | 2 | a0001c0001t0001g0007 a0001c0001t0001g0080 |
8 | HG01074.hp1 HG01884.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.-86-150A>G | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 1/19 | chr3 | 37993437 | |||||||
| chr3:37993580 | A | G | 4 | a0001c0015t0001g0036 a0002c0004t0001g0006 a0002c0004t0001g0072 others(1): Show |
10 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(7): Show |
splice_region_variant&intron_variant | LOW | c.-86-7A>G | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 1/19 | chr3 | 37993580 | |||||||
| chr3:37993829 | C | T | 1 | a0001c0001t0001g0028 | 2 | HG01106.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.61-69C>T | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 2/19 | chr3 | 37993829 | |||||||
| chr3:37994017 | G | A | 26 | a0001c0001t0001g0066 a0002c0002t0001g0005 a0002c0002t0001g0019 others(23): Show |
68 | HG00423.hp2 HG00544.hp1 HG00741.hp2 others(65): Show |
intron_variant | MODIFIER | c.135+45G>A | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 3/19 | chr3 | 37994017 | |||||||
| chr3:37994026 | G | A | 1 | a0002c0002t0001g0076 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.135+54G>A | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 3/19 | chr3 | 37994026 | |||||||
| chr3:37994051 | T | G | 1 | a0001c0001t0001g0048 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.135+79T>G | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 3/19 | chr3 | 37994051 | |||||||
| chr3:37994555 | T | C | 1 | a0001c0001t0001g0049 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.341+89T>C | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 4/19 | chr3 | 37994555 | |||||||
| chr3:37994681 | C | T | 1 | a0002c0004t0001g0073 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.341+215C>T | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 4/19 | chr3 | 37994681 | |||||||
| chr3:37994870 | T | G | 3 | a0002c0005t0001g0012 a0002c0005t0001g0065 a0007c0014t0001g0064 |
6 | HG02622.hp1 HG02965.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.341+404T>G | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 4/19 | chr3 | 37994870 | |||||||
| chr3:37994910 | T | C | 1 | a0001c0001t0001g0015 | 3 | HG02895.hp2 HG02897.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.341+444T>C | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 4/19 | chr3 | 37994910 | |||||||
| chr3:37995071 | G | C | 2 | a0001c0001t0001g0007 a0001c0001t0001g0080 |
8 | HG01074.hp1 HG01884.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.341+605G>C | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 4/19 | chr3 | 37995071 | |||||||
| chr3:37995175 | C | T | 3 | a0002c0005t0001g0012 a0002c0005t0001g0065 a0007c0014t0001g0064 |
6 | HG02622.hp1 HG02965.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.342-564C>T | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 4/19 | chr3 | 37995175 | |||||||
| chr3:37995207 | A | G | 12 | a0002c0002t0001g0005 a0002c0002t0001g0019 a0002c0002t0001g0020 others(9): Show |
39 | HG00423.hp2 HG00544.hp1 HG00741.hp2 others(36): Show |
intron_variant | MODIFIER | c.342-532A>G | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 4/19 | chr3 | 37995207 | |||||||
| chr3:37995316 | A | G | 29 | a0001c0001t0001g0007 a0001c0001t0001g0066 a0001c0001t0001g0080 others(26): Show |
77 | HG00423.hp2 HG00544.hp1 HG00741.hp2 others(74): Show |
intron_variant | MODIFIER | c.342-423A>G | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 4/19 | chr3 | 37995316 | |||||||
| chr3:37995324 | G | A | 2 | a0002c0013t0001g0071 a0004c0007t0001g0013 |
5 | HG01192.hp1 HG02055.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.342-415G>A | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 4/19 | chr3 | 37995324 | |||||||
| chr3:37995405 | A | G | 3 | a0002c0008t0001g0018 a0002c0013t0001g0071 a0004c0007t0001g0013 |
8 | HG01192.hp1 HG01884.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.342-334A>G | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 4/19 | chr3 | 37995405 | |||||||
| chr3:37995423 | C | T | 77 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(74): Show |
282 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(279): Show |
intron_variant | MODIFIER | c.342-316C>T | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 4/19 | chr3 | 37995423 | |||||||
| chr3:37995425 | T | G | 1 | a0001c0001t0001g0050 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.342-314T>G | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 4/19 | chr3 | 37995425 | |||||||
| chr3:37995463 | TAC | T | 1 | a0002c0002t0001g0020 | 3 | HG02818.hp1 HG03130.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.342-272_342-271del others(2): Show |
VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 37995463 | ||||||
| chr3:37995594 | C | A | 3 | a0002c0004t0001g0006 a0002c0004t0001g0072 a0002c0004t0001g0073 |
9 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.342-145C>A | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 4/19 | chr3 | 37995594 | |||||||
| chr3:37995668 | A | G | 3 | a0002c0005t0001g0012 a0002c0005t0001g0065 a0007c0014t0001g0064 |
6 | HG02622.hp1 HG02965.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.342-71A>G | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 4/19 | chr3 | 37995668 | |||||||
| chr3:37995718 | C | G | 1 | a0002c0006t0001g0010 | 5 | HG02602.hp2 HG02698.hp1 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.342-21C>G | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 4/19 | chr3 | 37995718 | |||||||
| chr3:37996265 | G | A | 1 | a0002c0002t0001g0032 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.450+418G>A | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 5/19 | chr3 | 37996265 | |||||||
| chr3:37996285 | G | A | 1 | a0001c0001t0001g0051 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.450+438G>A | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 5/19 | chr3 | 37996285 | |||||||
| chr3:37996401 | C | T | 1 | a0001c0001t0001g0035 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.450+554C>T | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 5/19 | chr3 | 37996401 | |||||||
| chr3:37996697 | T | C | 1 | a0002c0002t0001g0077 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.451-380T>C | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 5/19 | chr3 | 37996697 | |||||||
| chr3:37996817 | G | A | 1 | a0001c0001t0001g0021 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.451-260G>A | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 5/19 | chr3 | 37996817 | |||||||
| chr3:37996838 | A | G | 27 | a0001c0001t0001g0007 a0001c0001t0001g0080 a0002c0002t0001g0005 others(24): Show |
75 | HG00423.hp2 HG00544.hp1 HG00741.hp2 others(72): Show |
intron_variant | MODIFIER | c.451-239A>G | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 5/19 | chr3 | 37996838 | |||||||
| chr3:37996863 | G | A | 3 | a0001c0001t0001g0004 a0001c0001t0001g0052 a0005c0010t0001g0004 |
14 | HG01070.hp2 HG01071.hp1 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.451-214G>A | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 5/19 | chr3 | 37996863 | |||||||
| chr3:37997273 | G | A | 1 | a0001c0001t0001g0039 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.561+86G>A | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 6/19 | chr3 | 37997273 | |||||||
| chr3:37997441 | G | C | 2 | a0001c0001t0001g0007 a0001c0001t0001g0080 |
8 | HG01074.hp1 HG01884.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.562-42G>C | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 6/19 | chr3 | 37997441 | |||||||
| chr3:37997696 | C | T | 26 | a0001c0015t0001g0036 a0002c0002t0001g0005 a0002c0002t0001g0019 others(23): Show |
68 | HG00423.hp2 HG00544.hp1 HG00741.hp2 others(65): Show |
intron_variant | MODIFIER | c.764+11C>T | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 7/19 | chr3 | 37997696 | |||||||
| chr3:37997811 | C | T | 24 | a0002c0002t0001g0005 a0002c0002t0001g0019 a0002c0002t0001g0020 others(21): Show |
66 | HG00423.hp2 HG00544.hp1 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.764+126C>T | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 7/19 | chr3 | 37997811 | |||||||
| chr3:37997899 | G | A | 2 | a0001c0001t0001g0007 a0001c0001t0001g0080 |
8 | HG01074.hp1 HG01884.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.765-191G>A | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 7/19 | chr3 | 37997899 | |||||||
| chr3:37998435 | C | T | 1 | a0001c0001t0001g0047 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.942+71C>T | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 9/19 | chr3 | 37998435 | |||||||
| chr3:37998512 | G | A | 1 | a0001c0001t0001g0080 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.942+148G>A | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 9/19 | chr3 | 37998512 | |||||||
| chr3:37998593 | C | T | 1 | a0001c0001t0001g0063 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.942+229C>T | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 9/19 | chr3 | 37998593 | |||||||
| chr3:37998708 | C | A | 1 | a0001c0001t0001g0050 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.943-204C>A | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 9/19 | chr3 | 37998708 | |||||||
| chr3:37999135 | G | A | 1 | a0006c0012t0001g0074 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1081+85G>A | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 10/19 | chr3 | 37999135 | |||||||
| chr3:37999150 | C | T | 8 | a0002c0002t0001g0005 a0002c0002t0001g0019 a0002c0002t0001g0020 others(5): Show |
26 | HG00423.hp2 HG00544.hp1 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.1081+100C>T | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 10/19 | chr3 | 37999150 | |||||||
| chr3:37999294 | G | C | 1 | a0002c0002t0001g0078 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1082-45G>C | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 10/19 | chr3 | 37999294 | |||||||
| chr3:37999296 | G | C | 3 | a0001c0001t0001g0016 a0001c0001t0001g0038 a0002c0002t0001g0033 |
6 | HG02015.hp2 HG02027.hp1 HG02040.hp1 others(3): Show |
intron_variant | MODIFIER | c.1082-43G>C | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 10/19 | chr3 | 37999296 | |||||||
| chr3:37999296 | G | T | 2 | a0002c0004t0001g0009 a0002c0004t0001g0030 |
8 | HG01109.hp2 HG02055.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1082-43G>T | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 10/19 | chr3 | 37999296 | |||||||
| chr3:37999333 | C | A | 1 | a0003c0003t0001g0053 | 1 | NA18961.hp2 | splice_region_variant&intron_variant | LOW | c.1082-6C>A | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 10/19 | chr3 | 37999333 | |||||||
| chr3:37999447 | G | C | 1 | a0001c0001t0001g0054 | 1 | HG02683.hp1 | splice_region_variant&intron_variant | LOW | c.1182+8G>C | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 11/19 | chr3 | 37999447 | |||||||
| chr3:37999638 | G | A | 2 | a0002c0004t0001g0009 a0002c0004t0001g0030 |
8 | HG01109.hp2 HG02055.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1182+199G>A | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 11/19 | chr3 | 37999638 | |||||||
| chr3:37999644 | T | C | 1 | a0001c0001t0001g0022 | 2 | HG00408.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.1182+205T>C | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 11/19 | chr3 | 37999644 | |||||||
| chr3:37999855 | G | A | 7 | a0002c0002t0001g0005 a0002c0002t0001g0020 a0002c0002t0001g0032 others(4): Show |
23 | HG00423.hp2 HG00544.hp1 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.1182+416G>A | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 11/19 | chr3 | 37999855 | |||||||
| chr3:38000021 | G | A | 2 | a0002c0004t0001g0009 a0002c0004t0001g0030 |
8 | HG01109.hp2 HG02055.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1182+582G>A | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 11/19 | chr3 | 38000021 | |||||||
| chr3:38000248 | T | G | 1 | a0003c0003t0001g0055 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1182+809T>G | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 11/19 | chr3 | 38000248 | |||||||
| chr3:38000388 | A | G | 1 | a0002c0008t0001g0070 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1182+949A>G | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 11/19 | chr3 | 38000388 | |||||||
| chr3:38000519 | C | G | 1 | a0001c0001t0001g0062 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1183-937C>G | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 11/19 | chr3 | 38000519 | |||||||
| chr3:38000691 | T | G | 28 | a0001c0001t0001g0007 a0001c0001t0001g0080 a0001c0015t0001g0036 others(25): Show |
76 | HG00423.hp2 HG00544.hp1 HG00741.hp2 others(73): Show |
intron_variant | MODIFIER | c.1183-765T>G | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 11/19 | chr3 | 38000691 | |||||||
| chr3:38000770 | G | A | 1 | a0002c0006t0001g0010 | 5 | HG02602.hp2 HG02698.hp1 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.1183-686G>A | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 11/19 | chr3 | 38000770 | |||||||
| chr3:38000781 | G | A | 4 | a0002c0006t0001g0010 a0002c0008t0001g0018 a0002c0013t0001g0071 others(1): Show |
13 | HG01192.hp1 HG01884.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1183-675G>A | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 11/19 | chr3 | 38000781 | |||||||
| chr3:38000807 | A | C | 1 | a0001c0001t0001g0027 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1183-649A>C | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 11/19 | chr3 | 38000807 | |||||||
| chr3:38000916 | A | T | 1 | a0001c0001t0001g0061 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1183-540A>T | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 11/19 | chr3 | 38000916 | |||||||
| chr3:38000934 | A | G | 1 | a0001c0001t0001g0060 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1183-522A>G | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 11/19 | chr3 | 38000934 | |||||||
| chr3:38000953 | G | A | 7 | a0003c0003t0001g0003 a0003c0003t0001g0053 a0003c0003t0001g0056 others(4): Show |
21 | HG00597.hp1 HG01358.hp1 HG01358.hp2 others(18): Show |
intron_variant | MODIFIER | c.1183-503G>A | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 11/19 | chr3 | 38000953 | |||||||
| chr3:38000991 | A | G | 2 | a0003c0003t0001g0017 a0003c0003t0001g0026 |
5 | HG02486.hp1 HG02717.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1183-465A>G | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 11/19 | chr3 | 38000991 | |||||||
| chr3:38001232 | A | G | 1 | a0001c0001t0001g0052 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1183-224A>G | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 11/19 | chr3 | 38001232 | |||||||
| chr3:38001240 | T | C | 2 | a0002c0013t0001g0071 a0004c0007t0001g0013 |
5 | HG01192.hp1 HG02055.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1183-216T>C | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 11/19 | chr3 | 38001240 | |||||||
| chr3:38001383 | C | T | 2 | a0001c0001t0001g0011 a0001c0017t0001g0011 |
4 | NA18942.hp2 NA18967.hp2 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.1183-73C>T | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 11/19 | chr3 | 38001383 | |||||||
| chr3:38001384 | G | A | 1 | a0001c0001t0001g0062 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1183-72G>A | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 11/19 | chr3 | 38001384 | |||||||
| chr3:38002131 | C | T | 1 | a0001c0001t0001g0025 | 2 | NA18944.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.1480-265C>T | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 13/19 | chr3 | 38002131 | |||||||
| chr3:38002322 | C | A | 1 | a0002c0006t0001g0010 | 5 | HG02602.hp2 HG02698.hp1 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.1480-74C>A | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 13/19 | chr3 | 38002322 | |||||||
| chr3:38002637 | G | A | 7 | a0003c0003t0001g0003 a0003c0003t0001g0053 a0003c0003t0001g0056 others(4): Show |
21 | HG00597.hp1 HG01358.hp1 HG01358.hp2 others(18): Show |
intron_variant | MODIFIER | c.1659+62G>A | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 14/19 | chr3 | 38002637 | |||||||
| chr3:38002652 | C | G | 28 | a0001c0001t0001g0007 a0001c0001t0001g0080 a0001c0015t0001g0036 others(25): Show |
76 | HG00423.hp2 HG00544.hp1 HG00741.hp2 others(73): Show |
intron_variant | MODIFIER | c.1659+77C>G | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 14/19 | chr3 | 38002652 | |||||||
| chr3:38002836 | TTC | T | 20 | a0002c0002t0001g0005 a0002c0002t0001g0019 a0002c0002t0001g0020 others(17): Show |
53 | HG00423.hp2 HG00544.hp1 HG00741.hp2 others(50): Show |
intron_variant | MODIFIER | c.1659+262_1659+263d others(4): Show |
VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 14/19 | chr3 | 38002836 | |||||||
| chr3:38002842 | G | T | 1 | a0002c0002t0001g0076 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1659+267G>T | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 14/19 | chr3 | 38002842 | |||||||
| chr3:38002877 | G | T | 1 | a0004c0007t0001g0013 | 4 | HG01192.hp1 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1660-291G>T | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 14/19 | chr3 | 38002877 | |||||||
| chr3:38002944 | C | T | 1 | a0003c0003t0001g0056 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1660-224C>T | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 14/19 | chr3 | 38002944 | |||||||
| chr3:38002961 | G | A | 1 | a0001c0001t0001g0023 | 2 | HG02056.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.1660-207G>A | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 14/19 | chr3 | 38002961 | |||||||
| chr3:38002978 | C | T | 3 | a0002c0005t0001g0012 a0002c0005t0001g0065 a0007c0014t0001g0064 |
6 | HG02622.hp1 HG02965.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1660-190C>T | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 14/19 | chr3 | 38002978 | |||||||
| chr3:38003101 | C | T | 28 | a0001c0001t0001g0007 a0001c0001t0001g0024 a0001c0001t0001g0080 others(25): Show |
77 | HG00423.hp2 HG00544.hp1 HG00741.hp2 others(74): Show |
intron_variant | MODIFIER | c.1660-67C>T | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 14/19 | chr3 | 38003101 | |||||||
| chr3:38003411 | C | T | 1 | a0002c0008t0001g0070 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1805+98C>T | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 15/19 | chr3 | 38003411 | |||||||
| chr3:38003416 | C | T | 1 | a0001c0001t0001g0045 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1805+103C>T | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 15/19 | chr3 | 38003416 | |||||||
| chr3:38003418 | A | G | 2 | a0002c0013t0001g0071 a0004c0007t0001g0013 |
5 | HG01192.hp1 HG02055.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1805+105A>G | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 15/19 | chr3 | 38003418 | |||||||
| chr3:38003433 | C | T | 1 | a0001c0001t0001g0044 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1805+120C>T | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 15/19 | chr3 | 38003433 | |||||||
| chr3:38003460 | A | G | 27 | a0001c0001t0001g0007 a0001c0001t0001g0080 a0002c0002t0001g0005 others(24): Show |
75 | HG00423.hp2 HG00544.hp1 HG00741.hp2 others(72): Show |
intron_variant | MODIFIER | c.1805+147A>G | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 15/19 | chr3 | 38003460 | |||||||
| chr3:38003478 | G | A | 27 | a0001c0001t0001g0007 a0001c0001t0001g0080 a0002c0002t0001g0005 others(24): Show |
75 | HG00423.hp2 HG00544.hp1 HG00741.hp2 others(72): Show |
intron_variant | MODIFIER | c.1805+165G>A | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 15/19 | chr3 | 38003478 | |||||||
| chr3:38003505 | CTCA | C | 20 | a0002c0002t0001g0005 a0002c0002t0001g0019 a0002c0002t0001g0020 others(17): Show |
53 | HG00423.hp2 HG00544.hp1 HG00741.hp2 others(50): Show |
intron_variant | MODIFIER | c.1805+193_1805+195d others(5): Show |
VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 15/19 | chr3 | 38003505 | |||||||
| chr3:38003506 | T | G | 7 | a0001c0001t0001g0007 a0001c0001t0001g0080 a0002c0006t0001g0010 others(4): Show |
22 | HG01074.hp1 HG01192.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.1805+193T>G | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 15/19 | chr3 | 38003506 | |||||||
| chr3:38003507 | C | A | 7 | a0001c0001t0001g0007 a0001c0001t0001g0080 a0002c0006t0001g0010 others(4): Show |
22 | HG01074.hp1 HG01192.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.1805+194C>A | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 15/19 | chr3 | 38003507 | |||||||
| chr3:38003545 | T | A | 9 | a0002c0004t0001g0006 a0002c0004t0001g0009 a0002c0004t0001g0030 others(6): Show |
21 | HG01109.hp2 HG01167.hp1 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.1805+232T>A | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 15/19 | chr3 | 38003545 | |||||||
| chr3:38003628 | C | T | 1 | a0001c0001t0001g0059 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1805+315C>T | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 15/19 | chr3 | 38003628 | |||||||
| chr3:38003711 | G | A | 1 | a0001c0001t0001g0041 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1805+398G>A | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 15/19 | chr3 | 38003711 | |||||||
| chr3:38003739 | G | T | 1 | a0003c0003t0001g0026 | 2 | HG02717.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1805+426G>T | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 15/19 | chr3 | 38003739 | |||||||
| chr3:38003934 | G | A | 1 | a0007c0014t0001g0064 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1806-321G>A | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 15/19 | chr3 | 38003934 | |||||||
| chr3:38003969 | G | A | 1 | a0001c0001t0001g0042 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1806-286G>A | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 15/19 | chr3 | 38003969 | |||||||
| chr3:38004037 | G | A | 27 | a0001c0001t0001g0007 a0001c0001t0001g0080 a0002c0002t0001g0005 others(24): Show |
75 | HG00423.hp2 HG00544.hp1 HG00741.hp2 others(72): Show |
intron_variant | MODIFIER | c.1806-218G>A | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 15/19 | chr3 | 38004037 | |||||||
| chr3:38004047 | G | A | 2 | a0002c0005t0001g0012 a0002c0005t0001g0065 |
5 | HG02622.hp1 HG02965.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1806-208G>A | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 15/19 | chr3 | 38004047 | |||||||
| chr3:38004106 | G | A | 1 | a0002c0006t0001g0010 | 5 | HG02602.hp2 HG02698.hp1 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.1806-149G>A | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 15/19 | chr3 | 38004106 | |||||||
| chr3:38004452 | T | C | 1 | a0001c0001t0001g0057 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1950+53T>C | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 16/19 | chr3 | 38004452 | |||||||
| chr3:38004532 | A | C | 28 | a0001c0001t0001g0007 a0001c0001t0001g0080 a0001c0015t0001g0036 others(25): Show |
76 | HG00423.hp2 HG00544.hp1 HG00741.hp2 others(73): Show |
intron_variant | MODIFIER | c.1950+133A>C | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 16/19 | chr3 | 38004532 | |||||||
| chr3:38004542 | C | A | 1 | a0002c0004t0001g0030 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1950+143C>A | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 16/19 | chr3 | 38004542 | |||||||
| chr3:38004542 | C | T | 1 | a0002c0005t0001g0065 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1950+143C>T | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 16/19 | chr3 | 38004542 | |||||||
| chr3:38004559 | T | C | 2 | a0001c0001t0001g0031 a0001c0001t0001g0058 |
3 | NA18947.hp1 NA18970.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.1950+160T>C | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 16/19 | chr3 | 38004559 | |||||||
| chr3:38004655 | G | A | 1 | a0001c0001t0001g0066 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1950+256G>A | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 16/19 | chr3 | 38004655 | |||||||
| chr3:38004708 | C | T | 1 | a0002c0004t0001g0072 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1950+309C>T | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 16/19 | chr3 | 38004708 | |||||||
| chr3:38004736 | G | A | 1 | a0001c0001t0001g0025 | 2 | NA18944.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.1950+337G>A | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 16/19 | chr3 | 38004736 | |||||||
| chr3:38004761 | G | A | 1 | a0001c0001t0001g0043 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1950+362G>A | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 16/19 | chr3 | 38004761 | |||||||
| chr3:38004978 | C | T | 8 | a0002c0002t0001g0005 a0002c0002t0001g0019 a0002c0002t0001g0020 others(5): Show |
26 | HG00423.hp2 HG00544.hp1 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.1950+579C>T | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 16/19 | chr3 | 38004978 | |||||||
| chr3:38005561 | G | GA | 4 | a0002c0006t0001g0010 a0002c0008t0001g0018 a0002c0013t0001g0071 others(1): Show |
13 | HG01192.hp1 HG01884.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1951-221dupA | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr3 | 38005561 | ||||||
| chr3:38005616 | G | C | 8 | a0001c0015t0001g0036 a0002c0004t0001g0006 a0002c0004t0001g0009 others(5): Show |
20 | HG01109.hp2 HG01167.hp1 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.1951-176G>C | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 16/19 | chr3 | 38005616 | |||||||
| chr3:38005716 | C | T | 1 | a0006c0012t0001g0074 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1951-76C>T | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 16/19 | chr3 | 38005716 | |||||||
| chr3:38005717 | A | C | 1 | a0002c0002t0001g0020 | 3 | HG02818.hp1 HG03130.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1951-75A>C | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 16/19 | chr3 | 38005717 | |||||||
| chr3:38005720 | G | C | 21 | a0001c0015t0001g0036 a0002c0002t0001g0005 a0002c0002t0001g0019 others(18): Show |
54 | HG00423.hp2 HG00544.hp1 HG00741.hp2 others(51): Show |
intron_variant | MODIFIER | c.1951-72G>C | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 16/19 | chr3 | 38005720 | |||||||
| chr3:38006098 | C | T | 1 | a0001c0001t0001g0034 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2134-83C>T | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 17/19 | chr3 | 38006098 | |||||||
| chr3:38006116 | A | C | 27 | a0001c0001t0001g0007 a0001c0001t0001g0080 a0001c0015t0001g0036 others(24): Show |
73 | HG00423.hp2 HG00544.hp1 HG00741.hp2 others(70): Show |
intron_variant | MODIFIER | c.2134-65A>C | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 17/19 | chr3 | 38006116 | |||||||
| chr3:38006418 | C | T | 1 | a0001c0001t0001g0048 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.2206-31C>T | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 18/19 | chr3 | 38006418 | |||||||
| chr3:38006707 | A | AC | 3 | a0002c0005t0001g0012 a0002c0005t0001g0065 a0007c0014t0001g0064 |
6 | HG02622.hp1 HG02965.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.2457+12dupC | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr3 | 38006707 | ||||||
| chr3:38006847 | T | C | 1 | a0002c0004t0001g0067 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2458-95T>C | VILL | ENSG00000136059.16 | transcript | ENST00000383759.7 | protein_coding | 19/19 | chr3 | 38006847 |