Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 57117 |
| ensemblid | ENSG00000138785.16 |
| hgncid | 25067 |
| symbol | INTS12 |
| name | integrator complex subunit 12 |
| refseq_nuc | NM_020395.4 |
| refseq_prot | NP_065128.2 |
| ensembl_nuc | ENST00000340139.10 |
| ensembl_prot | ENSP00000340737.5 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 105682627 |
| end | 105708689 |
| strand | - |
| ver | v1.2 |
| region | chr4:105682627-105708689 |
| region5000 | chr4:105677627-105713689 |
| regionname0 | INTS12_chr4_105682627_105708689 |
| regionname5000 | INTS12_chr4_105677627_105713689 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 462 | 309 | 90 | 56 | 131 | 14 | 16 | 99 | INTS12_chr4_105677627_105713689 | INTS12 | MAATV others(457): Show |
chr4 | 105677627 | 105713689 |
| a0002 | 0/0 | 462 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | INTS12_chr4_105677627_105713689 | INTS12 | MAATV others(457): Show |
chr4 | 105677627 | 105713689 |
| a0003 | 0/0 | 462 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | INTS12_chr4_105677627_105713689 | INTS12 | MAATV others(457): Show |
chr4 | 105677627 | 105713689 |
| a0004 | 0/0 | 462 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | INTS12_chr4_105677627_105713689 | INTS12 | MAATV others(457): Show |
chr4 | 105677627 | 105713689 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1386 | 289 | 83 | 46 | 130 | 13 | 15 | INTS12_chr4_105677627_105713689 | INTS12 | ATGGC others(1381): Show |
chr4 | 105677627 | 105713689 | ||
| a0001c0002 | 0/0 | 1386 | 10 | 0 | 8 | 0 | 1 | 1 | INTS12_chr4_105677627_105713689 | INTS12 | ATGGC others(1381): Show |
chr4 | 105677627 | 105713689 | ||
| a0001c0003 | 0/0 | 1386 | 5 | 3 | 2 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | ATGGC others(1381): Show |
chr4 | 105677627 | 105713689 | ||
| a0001c0004 | 0/0 | 1386 | 3 | 3 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | ATGGC others(1381): Show |
chr4 | 105677627 | 105713689 | ||
| a0001c0005 | 0/0 | 1386 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | ATGGC others(1381): Show |
chr4 | 105677627 | 105713689 | ||
| a0001c0009 | 0/0 | 1386 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | ATGGC others(1381): Show |
chr4 | 105677627 | 105713689 | ||
| a0002c0008 | 0/0 | 1386 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | ATGGC others(1381): Show |
chr4 | 105677627 | 105713689 | ||
| a0003c0007 | 0/0 | 1386 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | ATGGC others(1381): Show |
chr4 | 105677627 | 105713689 | ||
| a0004c0006 | 0/0 | 1386 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | ATGGC others(1381): Show |
chr4 | 105677627 | 105713689 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1718 | 277 | 83 | 46 | 119 | 13 | 14 | INTS12_chr4_105677627_105713689 | INTS12 | GTTTC others(1713): Show |
chr4 | 105677627 | 105713689 |
| a0001c0001t0002 | 0/0 | 1718 | 5 | 0 | 0 | 5 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | GTTTC others(1713): Show |
chr4 | 105677627 | 105713689 |
| a0001c0001t0003 | 0/0 | 1718 | 4 | 0 | 0 | 3 | 0 | 1 | INTS12_chr4_105677627_105713689 | INTS12 | GTTTC others(1713): Show |
chr4 | 105677627 | 105713689 |
| a0001c0001t0004 | 0/0 | 1718 | 3 | 0 | 0 | 3 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | GTTTC others(1713): Show |
chr4 | 105677627 | 105713689 |
| a0001c0002t0001 | 0/0 | 1718 | 10 | 0 | 8 | 0 | 1 | 1 | INTS12_chr4_105677627_105713689 | INTS12 | GTTTC others(1713): Show |
chr4 | 105677627 | 105713689 |
| a0001c0003t0001 | 0/0 | 1718 | 5 | 3 | 2 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | GTTTC others(1713): Show |
chr4 | 105677627 | 105713689 |
| a0001c0004t0001 | 0/0 | 1718 | 3 | 3 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | GTTTC others(1713): Show |
chr4 | 105677627 | 105713689 |
| a0001c0005t0001 | 0/0 | 1718 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | GTTTC others(1713): Show |
chr4 | 105677627 | 105713689 |
| a0001c0009t0001 | 0/0 | 1718 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | GTTTC others(1713): Show |
chr4 | 105677627 | 105713689 |
| a0002c0008t0001 | 0/0 | 1718 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | GTTTC others(1713): Show |
chr4 | 105677627 | 105713689 |
| a0003c0007t0001 | 0/0 | 1718 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | GTTTC others(1713): Show |
chr4 | 105677627 | 105713689 |
| a0004c0006t0001 | 0/0 | 1718 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | GTTTC others(1713): Show |
chr4 | 105677627 | 105713689 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 1/0 | 29 | 1 | 6 | 12 | 5 | 4 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0002 | 0/0 | 18 | 4 | 4 | 9 | 0 | 1 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0003 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0004 | 0/0 | 7 | 1 | 2 | 4 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0005 | 0/0 | 6 | 4 | 2 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0006 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0008 | 0/0 | 5 | 1 | 4 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0011 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0012 | 0/0 | 3 | 1 | 0 | 0 | 1 | 1 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0015 | 0/0 | 3 | 2 | 0 | 0 | 1 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0021 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0026 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0034 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0183 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0002g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0003g0041 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0001t0004g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0002t0001g0009 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0002t0001g0019 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0002t0001g0020 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0002t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0003t0001g0018 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0003t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0003t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0003t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0004t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0004t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0004t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0005t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0001c0009t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0002c0008t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0003c0007t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| a0004c0006t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0118 | EUR | GBR | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0011 | EUR | GBR | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0015 | EUR | FIN | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | CHS | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | CHS | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | CHS | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | CHS | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG00639 | hp1 | a0001 | c0002 | t0001 | g0009 | AMR | PUR | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0041 | EAS | CHS | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG00735 | hp2 | a0001 | c0003 | t0001 | g0065 | AMR | PUR | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG00741 | hp1 | a0001 | c0002 | t0001 | g0020 | AMR | PUR | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0009 | AMR | PUR | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG01167 | hp2 | a0001 | c0002 | t0001 | g0019 | AMR | PUR | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0009 | AMR | PUR | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG01243 | hp2 | a0001 | c0003 | t0001 | g0018 | AMR | PUR | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | CLM | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | CLM | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | CLM | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | CLM | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG01346 | hp1 | a0001 | c0002 | t0001 | g0009 | AMR | CLM | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | CLM | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | CLM | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | CLM | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | CLM | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG01515 | hp1 | a0001 | c0002 | t0001 | g0019 | EUR | IBS | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0044 | EUR | IBS | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0012 | EUR | IBS | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0044 | EUR | IBS | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | ACB | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PEL | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PEL | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PEL | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG01981 | hp2 | a0001 | c0002 | t0001 | g0068 | AMR | PEL | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG02004 | hp1 | a0001 | c0002 | t0001 | g0067 | AMR | PEL | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | KHV | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | ACB | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG02056 | hp1 | a0001 | c0001 | t0003 | g0149 | EAS | KHV | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | KHV | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | KHV | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG02074 | hp1 | a0001 | c0001 | t0003 | g0175 | EAS | KHV | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | KHV | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | KHV | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | KHV | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | KHV | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG02129 | hp2 | a0001 | c0009 | t0001 | g0117 | EAS | KHV | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | KHV | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | KHV | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | ACB | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PEL | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | CDX | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | CDX | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | ACB | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG02258 | hp1 | a0001 | c0005 | t0001 | g0147 | AFR | ACB | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | ACB | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | ACB | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PEL | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PEL | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | ACB | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | KHV | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | GWD | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG02630 | hp2 | a0001 | c0004 | t0001 | g0071 | AFR | GWD | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | GWD | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | GWD | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | GWD | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | ESN | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | ESN | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | ESN | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | ESN | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | ESN | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | GWD | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | MSL | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG03098 | hp2 | a0001 | c0003 | t0001 | g0018 | AFR | MSL | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | ESN | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | ESN | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | MSL | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | MSL | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG03453 | hp1 | a0001 | c0003 | t0001 | g0066 | AFR | MSL | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | MSL | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | MSL | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0170 | SAS | PJL | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | ESN | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG03516 | hp2 | a0001 | c0004 | t0001 | g0073 | AFR | ESN | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | MSL | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | BEB | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | STU | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | STU | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG04184 | hp1 | a0001 | c0002 | t0001 | g0020 | SAS | BEB | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0041 | SAS | BEB | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0157 | SAS | STU | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | STU | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | YRI | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | YRI | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | CHB | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | CHB | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | YRI | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | YRI | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA18952 | hp2 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA18953 | hp2 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA18954 | hp1 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA18954 | hp2 | a0002 | c0008 | t0001 | g0150 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | LWK | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA19030 | hp2 | a0001 | c0003 | t0001 | g0064 | AFR | LWK | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | LWK | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | LWK | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA19060 | hp2 | a0003 | c0007 | t0001 | g0115 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA19086 | hp2 | a0004 | c0006 | t0001 | g0089 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | YRI | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA19240 | hp2 | a0001 | c0004 | t0001 | g0072 | AFR | YRI | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | ASW | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | ASW | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0056 | EUR | TSI | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0082 | EUR | TSI | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | ACB | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | ACB | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | MSL | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | MSL | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | USA | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | USA | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | USA | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | USA | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | LWK | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | LWK | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0183 | REF | REF | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0001 | REF | REF | INTS12_chr4_105677627_105713689 | INTS12 | chr4 | 105677627 | 105713689 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:105682822 | C | T | 1 | a0004 | 1 | NA19086.hp2 | missense_variant | MODERATE | c.1300G>A | p.Gly434Ser | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 8/8 | 1523/1718 | 1300/1389 | 434/462 | chr4 | 105682822 | |||
| chr4:105683151 | G | A | 1 | a0003 | 1 | NA19060.hp2 | missense_variant | MODERATE | c.971C>T | p.Ser324Leu | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 8/8 | 1194/1718 | 971/1389 | 324/462 | chr4 | 105683151 | |||
| chr4:105683278 | C | A | 1 | a0002 | 1 | NA18954.hp2 | missense_variant | MODERATE | c.844G>T | p.Val282Phe | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 8/8 | 1067/1718 | 844/1389 | 282/462 | chr4 | 105683278 | |||
| chr4:105700012 | C | T | 1 | a0001 | 5 | NA18942.hp1 NA18968.hp1 NA19005.hp1 others(2): Show |
splice_region_variant | LOW | c.-7G>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 3/8 | chr4 | 105700012 | |||||||
| chr4:105700013 | G | A | 1 | a0001 | 3 | NA18952.hp2 NA18953.hp2 NA18954.hp1 |
splice_region_variant | LOW | c.-8C>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 3/8 | chr4 | 105700013 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:105682823 | T | C | 1 | a0004c0006 | 1 | NA19086.hp2 | synonymous_variant | LOW | c.1299A>G | p.Lys433Lys | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 8/8 | 1522/1718 | 1299/1389 | 433/462 | chr4 | 105682823 | |||
| chr4:105682913 | C | T | 1 | a0001c0005 | 1 | HG02258.hp1 | synonymous_variant | LOW | c.1209G>A | p.Gly403Gly | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 8/8 | 1432/1718 | 1209/1389 | 403/462 | chr4 | 105682913 | |||
| chr4:105683033 | A | G | 1 | a0001c0002 | 10 | HG00639.hp1 HG00741.hp1 HG01109.hp1 others(7): Show |
synonymous_variant | LOW | c.1089T>C | p.Pro363Pro | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 8/8 | 1312/1718 | 1089/1389 | 363/462 | chr4 | 105683033 | |||
| chr4:105683207 | A | G | 2 | a0001c0002 a0001c0003 |
15 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(12): Show |
synonymous_variant | LOW | c.915T>C | p.Pro305Pro | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 8/8 | 1138/1718 | 915/1389 | 305/462 | chr4 | 105683207 | |||
| chr4:105692054 | G | C | 1 | a0001c0004 | 3 | HG02630.hp2 HG03516.hp2 NA19240.hp2 |
synonymous_variant | LOW | c.579C>G | p.Pro193Pro | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 6/8 | 802/1718 | 579/1389 | 193/462 | chr4 | 105692054 | |||
| chr4:105695534 | T | C | 1 | a0001c0009 | 1 | HG02129.hp2 | synonymous_variant | LOW | c.291A>G | p.Glu97Glu | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 4/8 | 514/1718 | 291/1389 | 97/462 | chr4 | 105695534 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:105682704 | A | G | 1 | a0001c0001t0003 | 4 | HG00673.hp1 HG02056.hp1 HG02074.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*29T>C | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 8/8 | 29 | chr4 | 105682704 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:105683428 | T | C | 1 | a0001c0005t0001g0147 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.805-111A>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 7/7 | chr4 | 105683428 | |||||||
| chr4:105683525 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.805-208C>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 7/7 | chr4 | 105683525 | |||||||
| chr4:105683629 | G | C | 9 | a0001c0002t0001g0009 a0001c0002t0001g0019 a0001c0002t0001g0020 others(6): Show |
15 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.805-312C>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 7/7 | chr4 | 105683629 | |||||||
| chr4:105683672 | A | C | 22 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0016 others(19): Show |
35 | HG01069.hp1 HG01192.hp1 HG01975.hp2 others(32): Show |
intron_variant | MODIFIER | c.805-355T>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 7/7 | chr4 | 105683672 | |||||||
| chr4:105683690 | C | A | 1 | a0001c0001t0001g0145 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.805-373G>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 7/7 | chr4 | 105683690 | |||||||
| chr4:105683733 | T | C | 1 | a0001c0001t0001g0118 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.805-416A>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 7/7 | chr4 | 105683733 | |||||||
| chr4:105683835 | A | G | 1 | a0001c0001t0001g0148 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.805-518T>C | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 7/7 | chr4 | 105683835 | |||||||
| chr4:105683840 | T | C | 3 | a0001c0001t0001g0033 a0001c0001t0001g0130 a0001c0001t0001g0131 |
4 | NA18971.hp1 NA19003.hp1 NA19067.hp1 others(1): Show |
intron_variant | MODIFIER | c.805-523A>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 7/7 | chr4 | 105683840 | |||||||
| chr4:105683892 | G | A | 5 | a0001c0001t0001g0070 a0001c0001t0001g0074 a0001c0004t0001g0071 others(2): Show |
5 | HG01070.hp1 HG02630.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.805-575C>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 7/7 | chr4 | 105683892 | |||||||
| chr4:105684085 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.805-768C>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 7/7 | chr4 | 105684085 | |||||||
| chr4:105684136 | C | T | 1 | a0001c0002t0001g0067 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.805-819G>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 7/7 | chr4 | 105684136 | |||||||
| chr4:105684302 | T | C | 4 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0075 others(1): Show |
6 | HG01243.hp1 HG01884.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.805-985A>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 7/7 | chr4 | 105684302 | |||||||
| chr4:105684563 | A | C | 9 | a0001c0002t0001g0009 a0001c0002t0001g0019 a0001c0002t0001g0020 others(6): Show |
15 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.805-1246T>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 7/7 | chr4 | 105684563 | |||||||
| chr4:105684795 | T | A | 2 | a0001c0001t0001g0096 a0001c0001t0001g0097 |
2 | HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.805-1478A>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 7/7 | chr4 | 105684795 | |||||||
| chr4:105684859 | C | T | 3 | a0001c0001t0001g0043 a0001c0001t0001g0187 a0001c0001t0001g0193 |
4 | NA18990.hp1 NA18994.hp2 NA19004.hp2 others(1): Show |
intron_variant | MODIFIER | c.805-1542G>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 7/7 | chr4 | 105684859 | |||||||
| chr4:105685013 | A | T | 1 | a0001c0001t0001g0129 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.804+1679T>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 7/7 | chr4 | 105685013 | |||||||
| chr4:105685154 | T | C | 4 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0075 others(1): Show |
6 | HG01243.hp1 HG01884.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.804+1538A>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 7/7 | chr4 | 105685154 | |||||||
| chr4:105685392 | C | T | 1 | a0001c0005t0001g0147 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.804+1300G>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 7/7 | chr4 | 105685392 | |||||||
| chr4:105685412 | C | A | 18 | a0001c0001t0001g0015 a0001c0001t0001g0043 a0001c0001t0001g0044 others(15): Show |
22 | HG00280.hp2 HG01081.hp1 HG01516.hp1 others(19): Show |
intron_variant | MODIFIER | c.804+1280G>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 7/7 | chr4 | 105685412 | |||||||
| chr4:105685451 | A | G | 9 | a0001c0002t0001g0009 a0001c0002t0001g0019 a0001c0002t0001g0020 others(6): Show |
15 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.804+1241T>C | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 7/7 | chr4 | 105685451 | |||||||
| chr4:105685660 | AT | A | 5 | a0001c0002t0001g0009 a0001c0002t0001g0019 a0001c0002t0001g0020 others(2): Show |
10 | HG00639.hp1 HG00741.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.804+1031delA | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 7/7 | chr4 | 105685660 | |||||||
| chr4:105685694 | T | G | 3 | a0001c0001t0001g0151 a0001c0001t0001g0154 a0001c0001t0001g0165 |
3 | HG02074.hp2 NA18974.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.804+998A>C | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 7/7 | chr4 | 105685694 | |||||||
| chr4:105685816 | T | C | 1 | a0001c0001t0001g0060 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.804+876A>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 7/7 | chr4 | 105685816 | |||||||
| chr4:105686084 | T | C | 94 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(91): Show |
141 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.804+608A>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 7/7 | chr4 | 105686084 | |||||||
| chr4:105686157 | G | A | 3 | a0001c0001t0001g0114 a0001c0001t0001g0132 a0001c0001t0001g0152 |
3 | HG00642.hp2 HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.804+535C>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 7/7 | chr4 | 105686157 | |||||||
| chr4:105686336 | G | A | 1 | a0001c0001t0001g0191 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.804+356C>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 7/7 | chr4 | 105686336 | |||||||
| chr4:105686389 | T | C | 1 | a0001c0001t0001g0153 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.804+303A>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 7/7 | chr4 | 105686389 | |||||||
| chr4:105686650 | A | T | 1 | a0001c0001t0001g0113 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.804+42T>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 7/7 | chr4 | 105686650 | |||||||
| chr4:105687054 | G | A | 1 | a0001c0001t0001g0122 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.658-216C>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 6/7 | chr4 | 105687054 | |||||||
| chr4:105687821 | C | T | 3 | a0001c0001t0001g0022 a0001c0001t0001g0075 a0001c0001t0001g0076 |
4 | HG01884.hp1 HG02559.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.658-983G>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 6/7 | chr4 | 105687821 | |||||||
| chr4:105687908 | G | A | 2 | a0001c0001t0001g0137 a0001c0001t0001g0157 |
2 | HG04199.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.658-1070C>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 6/7 | chr4 | 105687908 | |||||||
| chr4:105688247 | G | A | 4 | a0001c0001t0001g0007 a0001c0001t0001g0111 a0001c0001t0001g0119 others(1): Show |
8 | HG00438.hp2 NA18944.hp1 NA18946.hp1 others(5): Show |
intron_variant | MODIFIER | c.658-1409C>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 6/7 | chr4 | 105688247 | |||||||
| chr4:105689193 | T | C | 1 | a0001c0001t0001g0154 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.658-2355A>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 6/7 | chr4 | 105689193 | |||||||
| chr4:105689211 | G | A | 3 | a0001c0001t0001g0032 a0001c0001t0001g0129 a0001c0001t0001g0162 |
4 | HG00408.hp2 NA18747.hp1 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.658-2373C>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 6/7 | chr4 | 105689211 | |||||||
| chr4:105689241 | C | T | 1 | a0001c0001t0001g0039 | 2 | NA19002.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.658-2403G>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 6/7 | chr4 | 105689241 | |||||||
| chr4:105689274 | G | A | 1 | a0001c0001t0001g0027 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.658-2436C>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 6/7 | chr4 | 105689274 | |||||||
| chr4:105689280 | T | A | 2 | a0001c0001t0001g0030 a0003c0007t0001g0115 |
3 | HG00544.hp2 NA18979.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.658-2442A>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 6/7 | chr4 | 105689280 | |||||||
| chr4:105689499 | C | T | 4 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0075 others(1): Show |
6 | HG01243.hp1 HG01884.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.657+2477G>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 6/7 | chr4 | 105689499 | |||||||
| chr4:105689502 | A | G | 1 | a0001c0001t0001g0155 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.657+2474T>C | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 6/7 | chr4 | 105689502 | |||||||
| chr4:105689642 | C | A | 3 | a0001c0001t0001g0026 a0001c0001t0001g0079 a0001c0001t0001g0098 |
4 | HG01175.hp2 HG02145.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.657+2334G>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 6/7 | chr4 | 105689642 | |||||||
| chr4:105689764 | G | C | 2 | a0001c0001t0001g0061 a0001c0001t0001g0063 |
2 | HG02055.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.657+2212C>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 6/7 | chr4 | 105689764 | |||||||
| chr4:105689774 | C | T | 5 | a0001c0002t0001g0009 a0001c0002t0001g0019 a0001c0002t0001g0020 others(2): Show |
10 | HG00639.hp1 HG00741.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.657+2202G>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 6/7 | chr4 | 105689774 | |||||||
| chr4:105689782 | T | C | 1 | a0001c0001t0001g0127 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.657+2194A>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 6/7 | chr4 | 105689782 | |||||||
| chr4:105689857 | G | A | 3 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0093 |
3 | HG02896.hp1 HG02897.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.657+2119C>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 6/7 | chr4 | 105689857 | |||||||
| chr4:105690052 | A | T | 2 | a0001c0001t0001g0096 a0001c0001t0001g0097 |
2 | HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.657+1924T>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 6/7 | chr4 | 105690052 | |||||||
| chr4:105690103 | A | C | 95 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(92): Show |
142 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.657+1873T>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 6/7 | chr4 | 105690103 | |||||||
| chr4:105690380 | A | C | 9 | a0001c0002t0001g0009 a0001c0002t0001g0019 a0001c0002t0001g0020 others(6): Show |
15 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.657+1596T>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 6/7 | chr4 | 105690380 | |||||||
| chr4:105690458 | CAT | C | 26 | a0001c0001t0001g0002 a0001c0001t0001g0023 a0001c0001t0001g0024 others(23): Show |
48 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.657+1516_657+1517d others(4): Show |
INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 6/7 | chr4 | 105690458 | |||||||
| chr4:105690486 | G | A | 2 | a0001c0003t0001g0018 a0001c0003t0001g0065 |
3 | HG00735.hp2 HG01243.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.657+1490C>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 6/7 | chr4 | 105690486 | |||||||
| chr4:105690648 | A | G | 1 | a0001c0001t0001g0180 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.657+1328T>C | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 6/7 | chr4 | 105690648 | |||||||
| chr4:105690950 | G | T | 4 | a0001c0003t0001g0018 a0001c0003t0001g0064 a0001c0003t0001g0065 others(1): Show |
5 | HG00735.hp2 HG01243.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.657+1026C>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 6/7 | chr4 | 105690950 | |||||||
| chr4:105691119 | C | G | 1 | a0001c0001t0001g0144 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.657+857G>C | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 6/7 | chr4 | 105691119 | |||||||
| chr4:105691461 | T | C | 1 | a0001c0001t0001g0191 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.657+515A>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 6/7 | chr4 | 105691461 | |||||||
| chr4:105691576 | G | A | 7 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0127 others(4): Show |
9 | HG00544.hp1 NA18939.hp1 NA18949.hp1 others(6): Show |
intron_variant | MODIFIER | c.657+400C>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 6/7 | chr4 | 105691576 | |||||||
| chr4:105691692 | T | C | 3 | a0001c0001t0001g0022 a0001c0001t0001g0075 a0001c0001t0001g0076 |
4 | HG01884.hp1 HG02559.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.657+284A>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 6/7 | chr4 | 105691692 | |||||||
| chr4:105691696 | T | C | 4 | a0001c0001t0001g0038 a0001c0001t0001g0155 a0001c0001t0001g0161 others(1): Show |
5 | HG01433.hp2 NA18990.hp2 NA18995.hp2 others(2): Show |
intron_variant | MODIFIER | c.657+280A>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 6/7 | chr4 | 105691696 | |||||||
| chr4:105691837 | A | T | 4 | a0001c0003t0001g0018 a0001c0003t0001g0064 a0001c0003t0001g0065 others(1): Show |
5 | HG00735.hp2 HG01243.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.657+139T>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 6/7 | chr4 | 105691837 | |||||||
| chr4:105691839 | A | G | 14 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0069 others(11): Show |
16 | HG01070.hp1 HG01243.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.657+137T>C | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 6/7 | chr4 | 105691839 | |||||||
| chr4:105691929 | A | C | 2 | a0001c0001t0001g0137 a0001c0001t0001g0157 |
2 | HG04199.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.657+47T>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 6/7 | chr4 | 105691929 | |||||||
| chr4:105692342 | G | C | 1 | a0001c0001t0001g0095 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.498-207C>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 5/7 | chr4 | 105692342 | |||||||
| chr4:105692479 | G | A | 4 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0075 others(1): Show |
6 | HG01243.hp1 HG01884.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.498-344C>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 5/7 | chr4 | 105692479 | |||||||
| chr4:105692483 | C | CA | 20 | a0001c0001t0001g0022 a0001c0001t0001g0046 a0001c0001t0001g0075 others(17): Show |
21 | HG00642.hp1 HG00735.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.498-349dupT | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 5/7 | chr4 | 105692483 | |||||||
| chr4:105692483 | CA | C | 6 | a0001c0001t0001g0050 a0001c0001t0001g0107 a0001c0001t0001g0134 others(3): Show |
6 | HG01167.hp1 HG02630.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.498-349delT | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 5/7 | chr4 | 105692483 | |||||||
| chr4:105692596 | T | C | 5 | a0001c0002t0001g0009 a0001c0002t0001g0019 a0001c0002t0001g0020 others(2): Show |
10 | HG00639.hp1 HG00741.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.498-461A>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 5/7 | chr4 | 105692596 | |||||||
| chr4:105692664 | A | G | 54 | a0001c0001t0001g0002 a0001c0001t0001g0021 a0001c0001t0001g0022 others(51): Show |
84 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.498-529T>C | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 5/7 | chr4 | 105692664 | |||||||
| chr4:105693127 | T | G | 1 | a0001c0001t0001g0138 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.497+172A>C | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 5/7 | chr4 | 105693127 | |||||||
| chr4:105693180 | A | C | 1 | a0001c0001t0001g0160 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.497+119T>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 5/7 | chr4 | 105693180 | |||||||
| chr4:105693539 | T | C | 1 | a0001c0001t0001g0177 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.310-53A>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 4/7 | chr4 | 105693539 | |||||||
| chr4:105693570 | T | C | 4 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0075 others(1): Show |
6 | HG01243.hp1 HG01884.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.310-84A>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 4/7 | chr4 | 105693570 | |||||||
| chr4:105693598 | T | G | 11 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0046 others(8): Show |
22 | HG01069.hp1 HG01192.hp1 HG01975.hp2 others(19): Show |
intron_variant | MODIFIER | c.310-112A>C | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 4/7 | chr4 | 105693598 | |||||||
| chr4:105693620 | G | A | 1 | a0001c0001t0001g0021 | 2 | HG01243.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.310-134C>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 4/7 | chr4 | 105693620 | |||||||
| chr4:105693649 | T | C | 19 | a0001c0001t0001g0015 a0001c0001t0001g0043 a0001c0001t0001g0044 others(16): Show |
23 | HG00280.hp2 HG01081.hp1 HG01516.hp1 others(20): Show |
intron_variant | MODIFIER | c.310-163A>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 4/7 | chr4 | 105693649 | |||||||
| chr4:105693869 | CA | C | 9 | a0001c0002t0001g0009 a0001c0002t0001g0019 a0001c0002t0001g0020 others(6): Show |
15 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.310-384delT | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 4/7 | chr4 | 105693869 | |||||||
| chr4:105693874 | T | C | 1 | a0001c0001t0003g0175 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.310-388A>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 4/7 | chr4 | 105693874 | |||||||
| chr4:105694446 | C | T | 9 | a0001c0002t0001g0009 a0001c0002t0001g0019 a0001c0002t0001g0020 others(6): Show |
15 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.310-960G>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 4/7 | chr4 | 105694446 | |||||||
| chr4:105694480 | C | T | 1 | a0001c0001t0001g0101 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.310-994G>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 4/7 | chr4 | 105694480 | |||||||
| chr4:105694581 | T | C | 4 | a0001c0003t0001g0018 a0001c0003t0001g0064 a0001c0003t0001g0065 others(1): Show |
5 | HG00735.hp2 HG01243.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.309+935A>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 4/7 | chr4 | 105694581 | |||||||
| chr4:105694865 | C | T | 1 | a0001c0001t0001g0191 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.309+651G>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 4/7 | chr4 | 105694865 | |||||||
| chr4:105694885 | T | G | 1 | a0001c0001t0001g0192 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.309+631A>C | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 4/7 | chr4 | 105694885 | |||||||
| chr4:105694987 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.309+529G>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 4/7 | chr4 | 105694987 | |||||||
| chr4:105695034 | C | T | 9 | a0001c0002t0001g0009 a0001c0002t0001g0019 a0001c0002t0001g0020 others(6): Show |
15 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.309+482G>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 4/7 | chr4 | 105695034 | |||||||
| chr4:105695041 | C | A | 5 | a0001c0002t0001g0009 a0001c0002t0001g0019 a0001c0002t0001g0020 others(2): Show |
10 | HG00639.hp1 HG00741.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.309+475G>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 4/7 | chr4 | 105695041 | |||||||
| chr4:105695043 | C | G | 1 | a0001c0001t0001g0087 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.309+473G>C | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 4/7 | chr4 | 105695043 | |||||||
| chr4:105695057 | C | T | 9 | a0001c0002t0001g0009 a0001c0002t0001g0019 a0001c0002t0001g0020 others(6): Show |
15 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.309+459G>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 4/7 | chr4 | 105695057 | |||||||
| chr4:105695210 | C | T | 18 | a0001c0001t0001g0015 a0001c0001t0001g0043 a0001c0001t0001g0044 others(15): Show |
22 | HG00280.hp2 HG01081.hp1 HG01516.hp1 others(19): Show |
intron_variant | MODIFIER | c.309+306G>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 4/7 | chr4 | 105695210 | |||||||
| chr4:105695935 | C | A | 9 | a0001c0002t0001g0009 a0001c0002t0001g0019 a0001c0002t0001g0020 others(6): Show |
15 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.157-267G>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 3/7 | chr4 | 105695935 | |||||||
| chr4:105695979 | G | A | 18 | a0001c0001t0001g0015 a0001c0001t0001g0043 a0001c0001t0001g0044 others(15): Show |
22 | HG00280.hp2 HG01081.hp1 HG01516.hp1 others(19): Show |
intron_variant | MODIFIER | c.157-311C>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 3/7 | chr4 | 105695979 | |||||||
| chr4:105695996 | G | C | 1 | a0001c0001t0001g0086 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.157-328C>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 3/7 | chr4 | 105695996 | |||||||
| chr4:105696014 | G | A | 29 | a0001c0001t0001g0002 a0001c0001t0001g0023 a0001c0001t0001g0024 others(26): Show |
51 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.157-346C>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 3/7 | chr4 | 105696014 | |||||||
| chr4:105696044 | G | A | 1 | a0001c0001t0001g0139 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.157-376C>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 3/7 | chr4 | 105696044 | |||||||
| chr4:105696093 | C | T | 3 | a0001c0001t0001g0011 a0001c0001t0001g0112 a0001c0001t0001g0118 |
5 | HG00099.hp2 HG00140.hp1 HG00735.hp1 others(2): Show |
intron_variant | MODIFIER | c.157-425G>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 3/7 | chr4 | 105696093 | |||||||
| chr4:105696133 | G | A | 2 | a0001c0002t0001g0009 a0001c0002t0001g0020 |
6 | HG00639.hp1 HG00741.hp1 HG01109.hp1 others(3): Show |
intron_variant | MODIFIER | c.157-465C>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 3/7 | chr4 | 105696133 | |||||||
| chr4:105696204 | G | A | 9 | a0001c0002t0001g0009 a0001c0002t0001g0019 a0001c0002t0001g0020 others(6): Show |
15 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.157-536C>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 3/7 | chr4 | 105696204 | |||||||
| chr4:105696394 | T | A | 4 | a0001c0001t0001g0014 a0001c0001t0001g0039 a0001c0001t0001g0124 others(1): Show |
7 | NA18747.hp2 NA18952.hp1 NA18953.hp1 others(4): Show |
intron_variant | MODIFIER | c.157-726A>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 3/7 | chr4 | 105696394 | |||||||
| chr4:105697062 | A | G | 9 | a0001c0002t0001g0009 a0001c0002t0001g0019 a0001c0002t0001g0020 others(6): Show |
15 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.157-1394T>C | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 3/7 | chr4 | 105697062 | |||||||
| chr4:105697205 | T | C | 18 | a0001c0001t0001g0015 a0001c0001t0001g0043 a0001c0001t0001g0044 others(15): Show |
22 | HG00280.hp2 HG01081.hp1 HG01516.hp1 others(19): Show |
intron_variant | MODIFIER | c.157-1537A>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 3/7 | chr4 | 105697205 | |||||||
| chr4:105697344 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.157-1676C>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 3/7 | chr4 | 105697344 | |||||||
| chr4:105697382 | T | C | 1 | a0001c0001t0001g0101 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.157-1714A>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 3/7 | chr4 | 105697382 | |||||||
| chr4:105697429 | G | GA | 5 | a0001c0002t0001g0009 a0001c0002t0001g0019 a0001c0002t0001g0020 others(2): Show |
10 | HG00639.hp1 HG00741.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.157-1762dupT | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 3/7 | chr4 | 105697429 | |||||||
| chr4:105697459 | C | A | 1 | a0001c0001t0001g0156 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.157-1791G>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 3/7 | chr4 | 105697459 | |||||||
| chr4:105697597 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.157-1929G>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 3/7 | chr4 | 105697597 | |||||||
| chr4:105697705 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.157-2037C>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 3/7 | chr4 | 105697705 | |||||||
| chr4:105697791 | T | C | 14 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0069 others(11): Show |
16 | HG01070.hp1 HG01243.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.156+2059A>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 3/7 | chr4 | 105697791 | |||||||
| chr4:105697793 | T | C | 5 | a0001c0001t0001g0070 a0001c0001t0001g0074 a0001c0004t0001g0071 others(2): Show |
5 | HG01070.hp1 HG02630.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.156+2057A>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 3/7 | chr4 | 105697793 | |||||||
| chr4:105697912 | T | C | 29 | a0001c0001t0001g0002 a0001c0001t0001g0023 a0001c0001t0001g0024 others(26): Show |
51 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.156+1938A>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 3/7 | chr4 | 105697912 | |||||||
| chr4:105697914 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.156+1936C>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 3/7 | chr4 | 105697914 | |||||||
| chr4:105697983 | G | T | 9 | a0001c0002t0001g0009 a0001c0002t0001g0019 a0001c0002t0001g0020 others(6): Show |
15 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.156+1867C>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 3/7 | chr4 | 105697983 | |||||||
| chr4:105698072 | A | G | 3 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0093 |
3 | HG02896.hp1 HG02897.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.156+1778T>C | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 3/7 | chr4 | 105698072 | |||||||
| chr4:105698156 | C | T | 18 | a0001c0001t0001g0015 a0001c0001t0001g0043 a0001c0001t0001g0044 others(15): Show |
22 | HG00280.hp2 HG01081.hp1 HG01516.hp1 others(19): Show |
intron_variant | MODIFIER | c.156+1694G>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 3/7 | chr4 | 105698156 | |||||||
| chr4:105698187 | T | A | 1 | a0001c0001t0001g0101 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.156+1663A>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 3/7 | chr4 | 105698187 | |||||||
| chr4:105698220 | T | A | 12 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0046 others(9): Show |
23 | HG01069.hp1 HG01192.hp1 HG01975.hp2 others(20): Show |
intron_variant | MODIFIER | c.156+1630A>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 3/7 | chr4 | 105698220 | |||||||
| chr4:105698554 | A | AT | 45 | a0001c0001t0001g0002 a0001c0001t0001g0021 a0001c0001t0001g0022 others(42): Show |
69 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.156+1295dupA | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 3/7 | chr4 | 105698554 | |||||||
| chr4:105698571 | A | G | 1 | a0001c0001t0001g0158 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.156+1279T>C | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 3/7 | chr4 | 105698571 | |||||||
| chr4:105698852 | G | A | 2 | a0001c0003t0001g0018 a0001c0003t0001g0065 |
3 | HG00735.hp2 HG01243.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.156+998C>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 3/7 | chr4 | 105698852 | |||||||
| chr4:105699040 | A | C | 5 | a0001c0001t0001g0036 a0001c0001t0001g0128 a0001c0001t0001g0135 others(2): Show |
6 | NA18939.hp1 NA18949.hp1 NA19000.hp1 others(3): Show |
intron_variant | MODIFIER | c.156+810T>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 3/7 | chr4 | 105699040 | |||||||
| chr4:105699348 | T | C | 3 | a0001c0001t0001g0028 a0001c0001t0001g0105 a0001c0001t0001g0106 |
4 | HG01928.hp1 HG01952.hp1 HG02148.hp1 others(1): Show |
intron_variant | MODIFIER | c.156+502A>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 3/7 | chr4 | 105699348 | |||||||
| chr4:105699370 | C | T | 1 | a0001c0001t0001g0182 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.156+480G>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 3/7 | chr4 | 105699370 | |||||||
| chr4:105699468 | T | C | 2 | a0001c0001t0001g0006 a0001c0001t0001g0173 |
7 | NA18993.hp2 NA19007.hp1 NA19060.hp1 others(4): Show |
intron_variant | MODIFIER | c.156+382A>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 3/7 | chr4 | 105699468 | |||||||
| chr4:105699601 | G | A | 1 | a0001c0001t0001g0119 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.156+249C>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 3/7 | chr4 | 105699601 | |||||||
| chr4:105699669 | C | G | 1 | a0001c0001t0001g0070 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.156+181G>C | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 3/7 | chr4 | 105699669 | |||||||
| chr4:105699757 | C | T | 1 | a0001c0001t0001g0134 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.156+93G>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 3/7 | chr4 | 105699757 | |||||||
| chr4:105699808 | G | A | 3 | a0001c0001t0001g0043 a0001c0001t0001g0187 a0001c0001t0001g0193 |
4 | NA18990.hp1 NA18994.hp2 NA19004.hp2 others(1): Show |
intron_variant | MODIFIER | c.156+42C>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 3/7 | chr4 | 105699808 | |||||||
| chr4:105699826 | C | T | 5 | a0001c0002t0001g0009 a0001c0002t0001g0019 a0001c0002t0001g0020 others(2): Show |
10 | HG00639.hp1 HG00741.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.156+24G>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 3/7 | chr4 | 105699826 | |||||||
| chr4:105700100 | A | G | 4 | a0001c0003t0001g0018 a0001c0003t0001g0064 a0001c0003t0001g0065 others(1): Show |
5 | HG00735.hp2 HG01243.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9-86T>C | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105700100 | |||||||
| chr4:105700101 | T | C | 1 | a0001c0001t0001g0162 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-9-87A>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105700101 | |||||||
| chr4:105700351 | G | C | 9 | a0001c0002t0001g0009 a0001c0002t0001g0019 a0001c0002t0001g0020 others(6): Show |
15 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-9-337C>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105700351 | |||||||
| chr4:105700361 | C | T | 6 | a0001c0001t0001g0070 a0001c0001t0001g0074 a0001c0001t0001g0189 others(3): Show |
6 | HG01070.hp1 HG02630.hp2 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9-347G>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105700361 | |||||||
| chr4:105700486 | T | C | 54 | a0001c0001t0001g0002 a0001c0001t0001g0021 a0001c0001t0001g0022 others(51): Show |
84 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.-9-472A>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105700486 | |||||||
| chr4:105700553 | A | C | 1 | a0001c0001t0001g0094 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-9-539T>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105700553 | |||||||
| chr4:105700589 | T | C | 2 | a0001c0001t0001g0137 a0001c0001t0001g0157 |
2 | HG04199.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.-9-575A>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105700589 | |||||||
| chr4:105700706 | A | AAC | 20 | a0001c0001t0001g0013 a0001c0001t0001g0034 a0001c0001t0001g0078 others(17): Show |
23 | HG01256.hp2 HG01928.hp1 HG02129.hp1 others(20): Show |
intron_variant | MODIFIER | c.-9-694_-9-693dupGT | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105700706 | |||||||
| chr4:105700706 | A | AACAC | 8 | a0001c0001t0001g0008 a0001c0001t0001g0029 a0001c0001t0001g0057 others(5): Show |
13 | HG01069.hp2 HG01167.hp1 HG01346.hp2 others(10): Show |
intron_variant | MODIFIER | c.-9-696_-9-693dupGT others(2): Show |
INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105700706 | |||||||
| chr4:105700706 | A | AACACAC | 5 | a0001c0001t0001g0021 a0001c0001t0001g0052 a0001c0001t0001g0053 others(2): Show |
6 | HG01243.hp1 HG02559.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9-698_-9-693dupGT others(4): Show |
INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105700706 | |||||||
| chr4:105700706 | A | AACACACA others(1): Show |
18 | a0001c0001t0001g0002 a0001c0001t0001g0022 a0001c0001t0001g0027 others(15): Show |
37 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.-9-700_-9-693dupGT others(6): Show |
INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105700706 | |||||||
| chr4:105700706 | A | AACACACA others(3): Show |
16 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0025 others(13): Show |
30 | HG00741.hp1 HG01069.hp1 HG01175.hp2 others(27): Show |
intron_variant | MODIFIER | c.-9-702_-9-693dupGT others(8): Show |
INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105700706 | |||||||
| chr4:105700706 | A | AACACACA others(5): Show |
13 | a0001c0001t0001g0024 a0001c0001t0001g0049 a0001c0001t0001g0054 others(10): Show |
18 | HG00639.hp1 HG01109.hp1 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.-9-704_-9-693dupGT others(10): Show |
INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105700706 | |||||||
| chr4:105700706 | A | AACACACA others(7): Show |
11 | a0001c0001t0001g0016 a0001c0001t0001g0023 a0001c0001t0001g0062 others(8): Show |
14 | HG00735.hp2 HG01243.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.-9-706_-9-693dupGT others(12): Show |
INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105700706 | |||||||
| chr4:105700706 | A | AACACACA others(9): Show |
8 | a0001c0001t0001g0081 a0001c0001t0001g0090 a0001c0001t0001g0180 others(5): Show |
8 | HG02630.hp2 HG02809.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.-9-708_-9-693dupGT others(14): Show |
INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105700706 | |||||||
| chr4:105700706 | A | AACACACA others(11): Show |
7 | a0001c0001t0001g0015 a0001c0001t0001g0061 a0001c0001t0001g0178 others(4): Show |
9 | HG00280.hp2 HG02015.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.-9-710_-9-693dupGT others(16): Show |
INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105700706 | |||||||
| chr4:105700706 | A | AACACACA others(13): Show |
4 | a0001c0001t0001g0044 a0001c0001t0001g0182 a0001c0001t0001g0184 others(1): Show |
5 | HG01516.hp1 HG01517.hp2 HG02071.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9-712_-9-693dupGT others(18): Show |
INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105700706 | |||||||
| chr4:105700706 | A | AACACACA others(15): Show |
2 | a0001c0001t0001g0097 a0001c0001t0001g0177 |
2 | HG02523.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-9-714_-9-693dupGT others(20): Show |
INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105700706 | |||||||
| chr4:105700706 | A | AACACACA others(17): Show |
1 | a0001c0001t0001g0190 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-9-716_-9-693dupGT others(22): Show |
INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105700706 | |||||||
| chr4:105700706 | A | ACACACAC others(4): Show |
1 | a0001c0001t0001g0048 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.-9-693_-9-692insGT others(9): Show |
INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105700706 | |||||||
| chr4:105700706 | A | ACACACAC others(10): Show |
1 | a0001c0001t0001g0043 | 2 | NA18994.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.-9-693_-9-692insGT others(15): Show |
INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105700706 | |||||||
| chr4:105700706 | A | ACACACAC others(12): Show |
1 | a0001c0001t0001g0179 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-9-693_-9-692insGT others(17): Show |
INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105700706 | |||||||
| chr4:105700706 | A | ACACACAC others(18): Show |
1 | a0001c0001t0001g0096 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-9-693_-9-692insGT others(23): Show |
INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105700706 | |||||||
| chr4:105700706 | AACACAC | A | 2 | a0001c0001t0001g0017 a0001c0001t0001g0158 |
3 | HG02615.hp1 HG02818.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.-9-698_-9-693delGT others(4): Show |
INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105700706 | |||||||
| chr4:105700861 | C | A | 1 | a0001c0001t0001g0159 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-9-847G>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105700861 | |||||||
| chr4:105701033 | T | C | 9 | a0001c0002t0001g0009 a0001c0002t0001g0019 a0001c0002t0001g0020 others(6): Show |
15 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-9-1019A>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105701033 | |||||||
| chr4:105701233 | CT | C | 65 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0015 others(62): Show |
85 | HG00280.hp2 HG00408.hp2 HG01069.hp1 others(82): Show |
intron_variant | MODIFIER | c.-9-1220delA | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105701233 | |||||||
| chr4:105701233 | CTT | C | 39 | a0001c0001t0001g0002 a0001c0001t0001g0023 a0001c0001t0001g0024 others(36): Show |
67 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.-9-1221_-9-1220del others(2): Show |
INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105701233 | |||||||
| chr4:105701353 | T | A | 2 | a0001c0001t0001g0096 a0001c0001t0001g0097 |
2 | HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-9-1339A>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105701353 | |||||||
| chr4:105701416 | T | C | 1 | a0001c0001t0001g0163 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-9-1402A>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105701416 | |||||||
| chr4:105701473 | A | C | 6 | a0001c0001t0001g0015 a0001c0001t0001g0178 a0001c0001t0001g0179 others(3): Show |
8 | HG00280.hp2 HG01081.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.-9-1459T>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105701473 | |||||||
| chr4:105701603 | C | T | 1 | a0001c0001t0001g0080 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.-9-1589G>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105701603 | |||||||
| chr4:105701880 | C | G | 1 | a0001c0001t0001g0138 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-10+1768G>C | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105701880 | |||||||
| chr4:105702066 | A | G | 9 | a0001c0002t0001g0009 a0001c0002t0001g0019 a0001c0002t0001g0020 others(6): Show |
15 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-10+1582T>C | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105702066 | |||||||
| chr4:105702130 | C | CT | 27 | a0001c0001t0001g0012 a0001c0001t0001g0022 a0001c0001t0001g0034 others(24): Show |
31 | HG00597.hp1 HG01346.hp2 HG01517.hp1 others(28): Show |
intron_variant | MODIFIER | c.-10+1517dupA | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105702130 | |||||||
| chr4:105702130 | C | CTT | 8 | a0001c0001t0001g0070 a0001c0002t0001g0009 a0001c0002t0001g0019 others(5): Show |
14 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.-10+1516_-10+1517d others(4): Show |
INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105702130 | |||||||
| chr4:105702130 | CT | C | 7 | a0001c0001t0001g0048 a0001c0001t0001g0058 a0001c0001t0001g0084 others(4): Show |
7 | HG01167.hp1 HG02155.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.-10+1517delA | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105702130 | |||||||
| chr4:105702180 | G | A | 1 | a0001c0001t0001g0191 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-10+1468C>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105702180 | |||||||
| chr4:105702285 | G | A | 9 | a0001c0002t0001g0009 a0001c0002t0001g0019 a0001c0002t0001g0020 others(6): Show |
15 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-10+1363C>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105702285 | |||||||
| chr4:105702425 | C | T | 3 | a0001c0001t0001g0028 a0001c0001t0001g0105 a0001c0001t0001g0106 |
4 | HG01928.hp1 HG01952.hp1 HG02148.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10+1223G>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105702425 | |||||||
| chr4:105702464 | A | T | 4 | a0001c0003t0001g0018 a0001c0003t0001g0064 a0001c0003t0001g0065 others(1): Show |
5 | HG00735.hp2 HG01243.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-10+1184T>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105702464 | |||||||
| chr4:105702517 | A | T | 9 | a0001c0002t0001g0009 a0001c0002t0001g0019 a0001c0002t0001g0020 others(6): Show |
15 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-10+1131T>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105702517 | |||||||
| chr4:105702879 | A | G | 1 | a0001c0001t0001g0190 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-10+769T>C | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105702879 | |||||||
| chr4:105703128 | C | T | 5 | a0001c0002t0001g0009 a0001c0002t0001g0019 a0001c0002t0001g0020 others(2): Show |
10 | HG00639.hp1 HG00741.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.-10+520G>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105703128 | |||||||
| chr4:105703309 | A | C | 1 | a0001c0001t0001g0132 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-10+339T>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105703309 | |||||||
| chr4:105703345 | T | C | 5 | a0001c0002t0001g0009 a0001c0002t0001g0019 a0001c0002t0001g0020 others(2): Show |
10 | HG00639.hp1 HG00741.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.-10+303A>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105703345 | |||||||
| chr4:105703372 | C | T | 5 | a0001c0002t0001g0009 a0001c0002t0001g0019 a0001c0002t0001g0020 others(2): Show |
10 | HG00639.hp1 HG00741.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.-10+276G>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105703372 | |||||||
| chr4:105703415 | A | T | 1 | a0001c0001t0001g0021 | 2 | HG01243.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.-10+233T>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105703415 | |||||||
| chr4:105703576 | C | A | 3 | a0001c0001t0001g0069 a0001c0001t0001g0077 a0001c0001t0001g0078 |
3 | HG02257.hp1 HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-10+72G>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105703576 | |||||||
| chr4:105703614 | A | G | 1 | a0001c0001t0001g0191 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-10+34T>C | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105703614 | |||||||
| chr4:105703643 | C | T | 9 | a0001c0002t0001g0009 a0001c0002t0001g0019 a0001c0002t0001g0020 others(6): Show |
15 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(12): Show |
splice_region_variant&intron_variant | LOW | c.-10+5G>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 2/7 | chr4 | 105703643 | |||||||
| chr4:105703969 | T | C | 1 | a0001c0001t0001g0191 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-171-160A>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 1/7 | chr4 | 105703969 | |||||||
| chr4:105704014 | C | CT | 19 | a0001c0001t0001g0015 a0001c0001t0001g0043 a0001c0001t0001g0083 others(16): Show |
22 | HG00280.hp2 HG01081.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.-171-206dupA | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 1/7 | chr4 | 105704014 | |||||||
| chr4:105704015 | T | C | 1 | a0001c0001t0001g0165 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-171-206A>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 1/7 | chr4 | 105704015 | |||||||
| chr4:105704106 | G | T | 94 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(91): Show |
141 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.-171-297C>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 1/7 | chr4 | 105704106 | |||||||
| chr4:105704223 | G | A | 4 | a0001c0003t0001g0018 a0001c0003t0001g0064 a0001c0003t0001g0065 others(1): Show |
5 | HG00735.hp2 HG01243.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-171-414C>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 1/7 | chr4 | 105704223 | |||||||
| chr4:105704250 | A | G | 1 | a0001c0001t0001g0060 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-171-441T>C | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 1/7 | chr4 | 105704250 | |||||||
| chr4:105704253 | C | T | 2 | a0001c0001t0001g0102 a0001c0001t0001g0103 |
2 | HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-171-444G>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 1/7 | chr4 | 105704253 | |||||||
| chr4:105704305 | A | C | 1 | a0001c0001t0001g0082 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-171-496T>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 1/7 | chr4 | 105704305 | |||||||
| chr4:105704479 | G | A | 18 | a0001c0001t0001g0015 a0001c0001t0001g0043 a0001c0001t0001g0044 others(15): Show |
22 | HG00280.hp2 HG01081.hp1 HG01516.hp1 others(19): Show |
intron_variant | MODIFIER | c.-171-670C>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 1/7 | chr4 | 105704479 | |||||||
| chr4:105704917 | A | T | 12 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0069 others(9): Show |
14 | HG01070.hp1 HG01243.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.-171-1108T>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 1/7 | chr4 | 105704917 | |||||||
| chr4:105705026 | T | G | 1 | a0001c0001t0001g0166 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-171-1217A>C | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 1/7 | chr4 | 105705026 | |||||||
| chr4:105705027 | C | A | 22 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0016 others(19): Show |
35 | HG01069.hp1 HG01192.hp1 HG01975.hp2 others(32): Show |
intron_variant | MODIFIER | c.-171-1218G>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 1/7 | chr4 | 105705027 | |||||||
| chr4:105705115 | G | A | 1 | a0001c0001t0001g0059 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-171-1306C>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 1/7 | chr4 | 105705115 | |||||||
| chr4:105705218 | T | C | 1 | a0001c0001t0001g0167 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-171-1409A>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 1/7 | chr4 | 105705218 | |||||||
| chr4:105705232 | C | T | 3 | a0001c0001t0001g0033 a0001c0001t0001g0130 a0001c0001t0001g0131 |
4 | NA18971.hp1 NA19003.hp1 NA19067.hp1 others(1): Show |
intron_variant | MODIFIER | c.-171-1423G>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 1/7 | chr4 | 105705232 | |||||||
| chr4:105705359 | A | G | 1 | a0001c0001t0001g0069 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-171-1550T>C | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 1/7 | chr4 | 105705359 | |||||||
| chr4:105705406 | A | T | 2 | a0001c0001t0001g0032 a0001c0001t0001g0129 |
3 | NA18747.hp1 NA19007.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.-171-1597T>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 1/7 | chr4 | 105705406 | |||||||
| chr4:105705513 | GCCAAAAA others(9): Show |
G | 4 | a0001c0003t0001g0018 a0001c0003t0001g0064 a0001c0003t0001g0065 others(1): Show |
5 | HG00735.hp2 HG01243.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-171-1720_-171-170 others(20): Show |
INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 1/7 | chr4 | 105705513 | |||||||
| chr4:105705712 | T | C | 1 | a0001c0001t0001g0060 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-171-1903A>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 1/7 | chr4 | 105705712 | |||||||
| chr4:105705728 | A | G | 1 | a0001c0001t0001g0053 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-171-1919T>C | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 1/7 | chr4 | 105705728 | |||||||
| chr4:105706244 | A | G | 1 | a0001c0001t0001g0081 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-172+2394T>C | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 1/7 | chr4 | 105706244 | |||||||
| chr4:105706254 | C | CT | 8 | a0001c0001t0001g0080 a0001c0001t0001g0124 a0001c0001t0001g0126 others(5): Show |
8 | HG02523.hp1 HG02965.hp2 NA18952.hp1 others(5): Show |
intron_variant | MODIFIER | c.-172+2383dupA | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 1/7 | chr4 | 105706254 | |||||||
| chr4:105706254 | CT | C | 10 | a0001c0001t0001g0040 a0001c0001t0001g0061 a0001c0001t0001g0062 others(7): Show |
11 | HG01257.hp1 HG02055.hp1 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.-172+2383delA | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 1/7 | chr4 | 105706254 | |||||||
| chr4:105706254 | CTT | C | 9 | a0001c0002t0001g0009 a0001c0002t0001g0019 a0001c0002t0001g0020 others(6): Show |
15 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-172+2382_-172+238 others(6): Show |
INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 1/7 | chr4 | 105706254 | |||||||
| chr4:105706410 | G | A | 1 | a0001c0001t0001g0171 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-172+2228C>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 1/7 | chr4 | 105706410 | |||||||
| chr4:105706469 | C | T | 1 | a0001c0001t0001g0191 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-172+2169G>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 1/7 | chr4 | 105706469 | |||||||
| chr4:105706532 | G | A | 1 | a0001c0001t0001g0101 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-172+2106C>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 1/7 | chr4 | 105706532 | |||||||
| chr4:105706553 | A | C | 1 | a0001c0001t0001g0105 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-172+2085T>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 1/7 | chr4 | 105706553 | |||||||
| chr4:105706618 | G | A | 1 | a0001c0001t0001g0190 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-172+2020C>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 1/7 | chr4 | 105706618 | |||||||
| chr4:105706652 | C | T | 1 | a0001c0001t0002g0123 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-172+1986G>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 1/7 | chr4 | 105706652 | |||||||
| chr4:105706681 | C | T | 18 | a0001c0001t0001g0015 a0001c0001t0001g0043 a0001c0001t0001g0044 others(15): Show |
22 | HG00280.hp2 HG01081.hp1 HG01516.hp1 others(19): Show |
intron_variant | MODIFIER | c.-172+1957G>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 1/7 | chr4 | 105706681 | |||||||
| chr4:105706696 | C | T | 1 | a0001c0001t0001g0079 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-172+1942G>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 1/7 | chr4 | 105706696 | |||||||
| chr4:105706791 | C | T | 19 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0011 others(16): Show |
36 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(33): Show |
intron_variant | MODIFIER | c.-172+1847G>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 1/7 | chr4 | 105706791 | |||||||
| chr4:105706792 | G | A | 1 | a0001c0001t0001g0172 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-172+1846C>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 1/7 | chr4 | 105706792 | |||||||
| chr4:105706807 | A | C | 5 | a0001c0001t0001g0005 a0001c0001t0001g0049 a0001c0001t0001g0050 others(2): Show |
10 | HG01069.hp1 HG01192.hp1 HG01975.hp2 others(7): Show |
intron_variant | MODIFIER | c.-172+1831T>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 1/7 | chr4 | 105706807 | |||||||
| chr4:105707065 | A | T | 4 | a0001c0001t0001g0003 a0001c0001t0001g0046 a0001c0001t0001g0047 others(1): Show |
10 | HG02109.hp2 HG02615.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.-172+1573T>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 1/7 | chr4 | 105707065 | |||||||
| chr4:105707223 | G | T | 12 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0069 others(9): Show |
14 | HG01070.hp1 HG01243.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.-172+1415C>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 1/7 | chr4 | 105707223 | |||||||
| chr4:105707316 | A | AT | 16 | a0001c0001t0001g0028 a0001c0001t0001g0105 a0001c0001t0001g0106 others(13): Show |
23 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.-172+1321dupA | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 1/7 | chr4 | 105707316 | |||||||
| chr4:105707316 | AT | A | 11 | a0001c0001t0001g0006 a0001c0001t0001g0042 a0001c0001t0001g0102 others(8): Show |
18 | HG00673.hp1 HG01069.hp2 HG02056.hp2 others(15): Show |
intron_variant | MODIFIER | c.-172+1321delA | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 1/7 | chr4 | 105707316 | |||||||
| chr4:105707500 | A | T | 1 | a0001c0001t0004g0010 | 3 | NA18952.hp2 NA18953.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.-172+1138T>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 1/7 | chr4 | 105707500 | |||||||
| chr4:105707798 | C | T | 9 | a0001c0002t0001g0009 a0001c0002t0001g0019 a0001c0002t0001g0020 others(6): Show |
15 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-172+840G>A | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 1/7 | chr4 | 105707798 | |||||||
| chr4:105707852 | G | A | 94 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(91): Show |
141 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.-172+786C>T | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 1/7 | chr4 | 105707852 | |||||||
| chr4:105708089 | A | C | 53 | a0001c0001t0001g0002 a0001c0001t0001g0021 a0001c0001t0001g0022 others(50): Show |
83 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(80): Show |
intron_variant | MODIFIER | c.-172+549T>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 1/7 | chr4 | 105708089 | |||||||
| chr4:105708140 | T | C | 1 | a0001c0001t0001g0193 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-172+498A>G | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 1/7 | chr4 | 105708140 | |||||||
| chr4:105708410 | A | G | 22 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0016 others(19): Show |
35 | HG01069.hp1 HG01192.hp1 HG01975.hp2 others(32): Show |
intron_variant | MODIFIER | c.-172+228T>C | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 1/7 | chr4 | 105708410 | |||||||
| chr4:105708481 | A | G | 1 | a0001c0001t0001g0045 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.-172+157T>C | INTS12 | ENSG00000138785.16 | transcript | ENST00000340139.10 | protein_coding | 1/7 | chr4 | 105708481 |