Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 2638 |
| ensemblid | ENSG00000145321.13 |
| hgncid | 4187 |
| symbol | GC |
| name | GC vitamin D binding protein |
| refseq_nuc | NM_000583.4 |
| refseq_prot | NP_000574.2 |
| ensembl_nuc | ENST00000273951.13 |
| ensembl_prot | ENSP00000273951.8 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 71741697 |
| end | 71784079 |
| strand | - |
| ver | v1.2 |
| region | chr4:71741697-71784079 |
| region5000 | chr4:71736697-71789079 |
| regionname0 | GC_chr4_71741697_71784079 |
| regionname5000 | GC_chr4_71736697_71789079 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 474 | 194 | 75 | 17 | 94 | 0 | 8 | 76 | GC_chr4_71736697_71789079 | GC | MKRVL others(469): Show |
chr4 | 71736697 | 71789079 |
| a0002 | 0/1 | 474 | 101 | 10 | 21 | 48 | 7 | 14 | 34 | GC_chr4_71736697_71789079 | GC | MKRVL others(469): Show |
chr4 | 71736697 | 71789079 |
| a0003 | 0/0 | 474 | 81 | 9 | 14 | 47 | 1 | 10 | 39 | GC_chr4_71736697_71789079 | GC | MKRVL others(469): Show |
chr4 | 71736697 | 71789079 |
| a0004 | 0/0 | 474 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | GC_chr4_71736697_71789079 | GC | MKRVL others(469): Show |
chr4 | 71736697 | 71789079 |
| a0005 | 1/0 | 474 | 2 | 1 | 0 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | MKRVL others(469): Show |
chr4 | 71736697 | 71789079 |
| a0006 | 0/0 | 474 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | GC_chr4_71736697_71789079 | GC | MKRVL others(469): Show |
chr4 | 71736697 | 71789079 |
| a0007 | 0/0 | 474 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | MKRVL others(469): Show |
chr4 | 71736697 | 71789079 |
| a0008 | 0/0 | 474 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | MKRVL others(469): Show |
chr4 | 71736697 | 71789079 |
| a0009 | 0/0 | 474 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | MKRVL others(469): Show |
chr4 | 71736697 | 71789079 |
| a0010 | 0/0 | 474 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GC_chr4_71736697_71789079 | GC | MKRVL others(469): Show |
chr4 | 71736697 | 71789079 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1422 | 121 | 35 | 12 | 66 | 0 | 8 | GC_chr4_71736697_71789079 | GC | ATGAA others(1417): Show |
chr4 | 71736697 | 71789079 | ||
| a0001c0004 | 0/0 | 1422 | 47 | 19 | 4 | 24 | 0 | 0 | GC_chr4_71736697_71789079 | GC | ATGAA others(1417): Show |
chr4 | 71736697 | 71789079 | ||
| a0001c0005 | 0/0 | 1422 | 14 | 13 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | ATGAA others(1417): Show |
chr4 | 71736697 | 71789079 | ||
| a0001c0007 | 0/0 | 1422 | 3 | 0 | 0 | 3 | 0 | 0 | GC_chr4_71736697_71789079 | GC | ATGAA others(1417): Show |
chr4 | 71736697 | 71789079 | ||
| a0001c0008 | 0/0 | 1422 | 3 | 3 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | ATGAA others(1417): Show |
chr4 | 71736697 | 71789079 | ||
| a0001c0009 | 0/0 | 1422 | 2 | 2 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | ATGAA others(1417): Show |
chr4 | 71736697 | 71789079 | ||
| a0001c0011 | 0/0 | 1422 | 2 | 2 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | ATGAA others(1417): Show |
chr4 | 71736697 | 71789079 | ||
| a0001c0015 | 0/0 | 1422 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | ATGAA others(1417): Show |
chr4 | 71736697 | 71789079 | ||
| a0001c0020 | 0/0 | 1422 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | ATGAA others(1417): Show |
chr4 | 71736697 | 71789079 | ||
| a0002c0002 | 0/1 | 1422 | 99 | 10 | 20 | 48 | 6 | 14 | GC_chr4_71736697_71789079 | GC | ATGAA others(1417): Show |
chr4 | 71736697 | 71789079 | ||
| a0002c0010 | 0/0 | 1422 | 2 | 0 | 1 | 0 | 1 | 0 | GC_chr4_71736697_71789079 | GC | ATGAA others(1417): Show |
chr4 | 71736697 | 71789079 | ||
| a0003c0003 | 0/0 | 1422 | 81 | 9 | 14 | 47 | 1 | 10 | GC_chr4_71736697_71789079 | GC | ATGAA others(1417): Show |
chr4 | 71736697 | 71789079 | ||
| a0004c0006 | 0/0 | 1422 | 4 | 0 | 0 | 4 | 0 | 0 | GC_chr4_71736697_71789079 | GC | ATGAA others(1417): Show |
chr4 | 71736697 | 71789079 | ||
| a0005c0012 | 1/0 | 1422 | 2 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | ATGAA others(1417): Show |
chr4 | 71736697 | 71789079 | ||
| a0006c0013 | 0/0 | 1422 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | ATGAA others(1417): Show |
chr4 | 71736697 | 71789079 | ||
| a0006c0014 | 0/0 | 1422 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | ATGAA others(1417): Show |
chr4 | 71736697 | 71789079 | ||
| a0007c0017 | 0/0 | 1422 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | ATGAA others(1417): Show |
chr4 | 71736697 | 71789079 | ||
| a0008c0016 | 0/0 | 1422 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | ATGAA others(1417): Show |
chr4 | 71736697 | 71789079 | ||
| a0009c0019 | 0/0 | 1422 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | ATGAA others(1417): Show |
chr4 | 71736697 | 71789079 | ||
| a0010c0018 | 0/0 | 1422 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | ATGAA others(1417): Show |
chr4 | 71736697 | 71789079 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1685 | 38 | 21 | 2 | 13 | 0 | 2 | GC_chr4_71736697_71789079 | GC | ACCAC others(1680): Show |
chr4 | 71736697 | 71789079 |
| a0001c0001t0002 | 0/0 | 1685 | 83 | 14 | 10 | 53 | 0 | 6 | GC_chr4_71736697_71789079 | GC | ACCAC others(1680): Show |
chr4 | 71736697 | 71789079 |
| a0001c0004t0001 | 0/0 | 1685 | 46 | 18 | 4 | 24 | 0 | 0 | GC_chr4_71736697_71789079 | GC | ACCAC others(1680): Show |
chr4 | 71736697 | 71789079 |
| a0001c0004t0002 | 0/0 | 1685 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | ACCAC others(1680): Show |
chr4 | 71736697 | 71789079 |
| a0001c0005t0001 | 0/0 | 1685 | 12 | 11 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | ACCAC others(1680): Show |
chr4 | 71736697 | 71789079 |
| a0001c0005t0002 | 0/0 | 1685 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | ACCAC others(1680): Show |
chr4 | 71736697 | 71789079 |
| a0001c0005t0003 | 0/0 | 1685 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | ACCAC others(1680): Show |
chr4 | 71736697 | 71789079 |
| a0001c0007t0001 | 0/0 | 1685 | 3 | 0 | 0 | 3 | 0 | 0 | GC_chr4_71736697_71789079 | GC | ACCAC others(1680): Show |
chr4 | 71736697 | 71789079 |
| a0001c0008t0001 | 0/0 | 1685 | 3 | 3 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | ACCAC others(1680): Show |
chr4 | 71736697 | 71789079 |
| a0001c0009t0001 | 0/0 | 1685 | 2 | 2 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | ACCAC others(1680): Show |
chr4 | 71736697 | 71789079 |
| a0001c0011t0002 | 0/0 | 1685 | 2 | 2 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | ACCAC others(1680): Show |
chr4 | 71736697 | 71789079 |
| a0001c0015t0001 | 0/0 | 1685 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | ACCAC others(1680): Show |
chr4 | 71736697 | 71789079 |
| a0001c0020t0001 | 0/0 | 1685 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | ACCAC others(1680): Show |
chr4 | 71736697 | 71789079 |
| a0002c0002t0001 | 0/1 | 1685 | 87 | 8 | 19 | 39 | 6 | 14 | GC_chr4_71736697_71789079 | GC | ACCAC others(1680): Show |
chr4 | 71736697 | 71789079 |
| a0002c0002t0002 | 0/0 | 1685 | 12 | 2 | 1 | 9 | 0 | 0 | GC_chr4_71736697_71789079 | GC | ACCAC others(1680): Show |
chr4 | 71736697 | 71789079 |
| a0002c0010t0001 | 0/0 | 1685 | 2 | 0 | 1 | 0 | 1 | 0 | GC_chr4_71736697_71789079 | GC | ACCAC others(1680): Show |
chr4 | 71736697 | 71789079 |
| a0003c0003t0001 | 0/0 | 1685 | 73 | 4 | 14 | 45 | 1 | 9 | GC_chr4_71736697_71789079 | GC | ACCAC others(1680): Show |
chr4 | 71736697 | 71789079 |
| a0003c0003t0002 | 0/0 | 1685 | 4 | 1 | 0 | 2 | 0 | 1 | GC_chr4_71736697_71789079 | GC | ACCAC others(1680): Show |
chr4 | 71736697 | 71789079 |
| a0003c0003t0003 | 0/0 | 1685 | 4 | 4 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | ACCAC others(1680): Show |
chr4 | 71736697 | 71789079 |
| a0004c0006t0001 | 0/0 | 1685 | 4 | 0 | 0 | 4 | 0 | 0 | GC_chr4_71736697_71789079 | GC | ACCAC others(1680): Show |
chr4 | 71736697 | 71789079 |
| a0005c0012t0001 | 1/0 | 1685 | 2 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | ACCAC others(1680): Show |
chr4 | 71736697 | 71789079 |
| a0006c0013t0002 | 0/0 | 1685 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | ACCAC others(1680): Show |
chr4 | 71736697 | 71789079 |
| a0006c0014t0002 | 0/0 | 1685 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | ACCAC others(1680): Show |
chr4 | 71736697 | 71789079 |
| a0007c0017t0001 | 0/0 | 1685 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | ACCAC others(1680): Show |
chr4 | 71736697 | 71789079 |
| a0008c0016t0001 | 0/0 | 1685 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | ACCAC others(1680): Show |
chr4 | 71736697 | 71789079 |
| a0009c0019t0001 | 0/0 | 1685 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | ACCAC others(1680): Show |
chr4 | 71736697 | 71789079 |
| a0010c0018t0002 | 0/0 | 1685 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | ACCAC others(1680): Show |
chr4 | 71736697 | 71789079 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0002g0001 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0002g0008 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0002g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0002g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0002g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0002g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0002g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0002g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0002g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0002g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0002g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0002g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0002g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0002g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0001t0002g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0004t0001g0003 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0004t0001g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0004t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0004t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0004t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0004t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0004t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0004t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0004t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0004t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0004t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0004t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0004t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0004t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0004t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0004t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0004t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0004t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0004t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0004t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0004t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0004t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0004t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0004t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0004t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0004t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0004t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0004t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0004t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0004t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0004t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0004t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0004t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0004t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0004t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0004t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0004t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0005t0001g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0005t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0005t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0005t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0005t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0005t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0005t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0005t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0005t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0005t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0005t0003g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0007t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0007t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0008t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0008t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0009t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0009t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0011t0002g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0015t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0001c0020t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0002c0002t0001g0005 | 0/0 | 4 | 1 | 1 | 0 | 1 | 1 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0002c0002t0001g0006 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0002c0002t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0002c0002t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0002c0002t0001g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0002c0002t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0002c0002t0001g0022 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0002c0002t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0002c0002t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0002c0002t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0002c0002t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0002c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0002c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0002c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0002c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0002c0002t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0002c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0002c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0002c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0002c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0002c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0002c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0002c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0002c0002t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0002c0002t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0002c0002t0001g0122 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0002c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0002c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0002c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0002c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0002c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0002c0002t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0002c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0002c0002t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0002c0002t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0002c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0002c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0002c0002t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0002c0002t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0002c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0002c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0002c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0002c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0002c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0002c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0002c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0002c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0002c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0002c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0002c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0002c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0002c0002t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0002c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0002c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0002c0002t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0002c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0002c0002t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0002c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0002c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0002c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0002c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0002c0002t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0002c0002t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0002c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0002c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0002c0002t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0002c0002t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0002c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0002c0002t0002g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0002c0002t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0002c0002t0002g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0002c0002t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0002c0002t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0002c0002t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0002c0002t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0002c0002t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0002c0002t0002g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0002c0002t0002g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0002c0002t0002g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0002c0010t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0002c0010t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0003c0003t0001g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0003c0003t0001g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0003c0003t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0003c0003t0001g0011 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0003c0003t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0003c0003t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0003c0003t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0003c0003t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0003c0003t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0003c0003t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0003c0003t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0003c0003t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0003c0003t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0003c0003t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0003c0003t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0003c0003t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0003c0003t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0003c0003t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0003c0003t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0003c0003t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0003c0003t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0003c0003t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0003c0003t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0003c0003t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0003c0003t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0003c0003t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0003c0003t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0003c0003t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0003c0003t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0003c0003t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0003c0003t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0003c0003t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0003c0003t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0003c0003t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0003c0003t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0003c0003t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0003c0003t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0003c0003t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0003c0003t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0003c0003t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0003c0003t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0003c0003t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0003c0003t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0003c0003t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0003c0003t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0003c0003t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0003c0003t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0003c0003t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0003c0003t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0003c0003t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0003c0003t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0003c0003t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0003c0003t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0003c0003t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0003c0003t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0003c0003t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0003c0003t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0003c0003t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0003c0003t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0003c0003t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0003c0003t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0003c0003t0002g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0003c0003t0002g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0003c0003t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0003c0003t0003g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0003c0003t0003g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0003c0003t0003g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0003c0003t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0004c0006t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0004c0006t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0004c0006t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0004c0006t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0005c0012t0001g0137 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0005c0012t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0006c0013t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0006c0014t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0007c0017t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0008c0016t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0009c0019t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| a0010c0018t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0003 | c0003 | t0001 | g0098 | EUR | GBR | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG00140 | hp2 | a0002 | c0010 | t0001 | g0150 | EUR | GBR | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG00280 | hp1 | a0002 | c0002 | t0001 | g0236 | EUR | FIN | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG00280 | hp2 | a0002 | c0002 | t0001 | g0174 | EUR | FIN | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG00408 | hp1 | a0002 | c0002 | t0001 | g0162 | EAS | CHS | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG00408 | hp2 | a0001 | c0007 | t0001 | g0028 | EAS | CHS | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0267 | EAS | CHS | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG00423 | hp2 | a0002 | c0002 | t0001 | g0199 | EAS | CHS | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG00438 | hp1 | a0003 | c0003 | t0002 | g0291 | EAS | CHS | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG00438 | hp2 | a0001 | c0004 | t0001 | g0007 | EAS | CHS | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG00544 | hp1 | a0003 | c0003 | t0001 | g0047 | EAS | CHS | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0278 | EAS | CHS | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG00558 | hp1 | a0003 | c0003 | t0001 | g0011 | EAS | CHS | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG00558 | hp2 | a0001 | c0004 | t0001 | g0222 | EAS | CHS | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG00597 | hp1 | a0002 | c0002 | t0002 | g0325 | EAS | CHS | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0263 | EAS | CHS | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG00609 | hp1 | a0003 | c0003 | t0001 | g0078 | EAS | CHS | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0254 | EAS | CHS | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG00621 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | CHS | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG00621 | hp2 | a0002 | c0002 | t0002 | g0296 | EAS | CHS | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG00639 | hp1 | a0003 | c0003 | t0001 | g0075 | AMR | PUR | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0315 | AMR | PUR | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG00642 | hp1 | a0003 | c0003 | t0001 | g0037 | AMR | PUR | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG00642 | hp2 | a0002 | c0002 | t0001 | g0175 | AMR | PUR | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG00735 | hp1 | a0002 | c0002 | t0001 | g0027 | AMR | PUR | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG00735 | hp2 | a0002 | c0002 | t0001 | g0005 | AMR | PUR | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG00741 | hp1 | a0002 | c0002 | t0001 | g0059 | AMR | PUR | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG00741 | hp2 | a0003 | c0003 | t0001 | g0038 | AMR | PUR | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG01071 | hp1 | a0002 | c0002 | t0001 | g0024 | AMR | PUR | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG01071 | hp2 | a0003 | c0003 | t0001 | g0072 | AMR | PUR | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG01106 | hp1 | a0002 | c0002 | t0001 | g0169 | AMR | PUR | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0247 | AMR | PUR | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG01109 | hp1 | a0003 | c0003 | t0001 | g0049 | AMR | PUR | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0253 | AMR | PUR | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0241 | AMR | PUR | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG01167 | hp2 | a0002 | c0002 | t0001 | g0143 | AMR | PUR | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG01169 | hp1 | a0002 | c0002 | t0001 | g0142 | AMR | PUR | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG01169 | hp2 | a0002 | c0002 | t0001 | g0027 | AMR | PUR | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0301 | AMR | PUR | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG01192 | hp2 | a0002 | c0002 | t0001 | g0153 | AMR | PUR | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG01243 | hp1 | a0001 | c0005 | t0001 | g0124 | AMR | PUR | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG01243 | hp2 | a0001 | c0004 | t0001 | g0109 | AMR | PUR | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG01255 | hp1 | a0002 | c0002 | t0002 | g0322 | AMR | CLM | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG01255 | hp2 | a0003 | c0003 | t0001 | g0011 | AMR | CLM | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | CLM | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | CLM | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG01258 | hp1 | a0002 | c0010 | t0001 | g0151 | AMR | CLM | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | CLM | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG01358 | hp1 | a0002 | c0002 | t0001 | g0119 | AMR | CLM | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG01358 | hp2 | a0003 | c0003 | t0001 | g0099 | AMR | CLM | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG01361 | hp1 | a0002 | c0002 | t0001 | g0154 | AMR | CLM | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG01361 | hp2 | a0001 | c0004 | t0001 | g0003 | AMR | CLM | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG01496 | hp1 | a0003 | c0003 | t0001 | g0092 | AMR | CLM | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG01496 | hp2 | a0002 | c0002 | t0001 | g0022 | AMR | CLM | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG01515 | hp1 | a0002 | c0002 | t0001 | g0123 | EUR | IBS | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG01515 | hp2 | a0002 | c0002 | t0001 | g0167 | EUR | IBS | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG01884 | hp1 | a0003 | c0003 | t0001 | g0139 | AFR | ACB | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG01884 | hp2 | a0001 | c0008 | t0001 | g0105 | AFR | ACB | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG01928 | hp1 | a0003 | c0003 | t0001 | g0103 | AMR | PEL | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG01928 | hp2 | a0002 | c0002 | t0001 | g0024 | AMR | PEL | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG01934 | hp1 | a0002 | c0002 | t0001 | g0025 | AMR | PEL | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG01934 | hp2 | a0003 | c0003 | t0001 | g0152 | AMR | PEL | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0248 | AMR | PEL | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG01943 | hp2 | a0003 | c0003 | t0001 | g0173 | AMR | PEL | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG01978 | hp1 | a0001 | c0004 | t0001 | g0215 | AMR | PEL | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG01978 | hp2 | a0002 | c0002 | t0001 | g0184 | AMR | PEL | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0314 | AMR | PEL | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG01981 | hp2 | a0003 | c0003 | t0001 | g0079 | AMR | PEL | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0256 | EAS | KHV | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG02015 | hp2 | a0002 | c0002 | t0001 | g0074 | EAS | KHV | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG02040 | hp1 | a0002 | c0002 | t0001 | g0177 | EAS | KHV | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0274 | EAS | KHV | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG02055 | hp1 | a0003 | c0003 | t0002 | g0284 | AFR | ACB | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | ACB | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG02056 | hp1 | a0002 | c0002 | t0001 | g0140 | EAS | KHV | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0260 | EAS | KHV | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG02071 | hp1 | a0003 | c0003 | t0001 | g0011 | EAS | KHV | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0282 | EAS | KHV | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG02074 | hp1 | a0002 | c0002 | t0001 | g0161 | EAS | KHV | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG02074 | hp2 | a0003 | c0003 | t0001 | g0081 | EAS | KHV | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG02080 | hp1 | a0002 | c0002 | t0002 | g0245 | EAS | KHV | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0304 | EAS | KHV | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG02083 | hp1 | a0003 | c0003 | t0001 | g0004 | EAS | KHV | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG02083 | hp2 | a0002 | c0002 | t0002 | g0034 | EAS | KHV | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG02135 | hp1 | a0001 | c0004 | t0001 | g0213 | EAS | KHV | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG02135 | hp2 | a0002 | c0002 | t0002 | g0295 | EAS | KHV | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG02145 | hp2 | a0001 | c0004 | t0001 | g0226 | AFR | ACB | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG02148 | hp1 | a0002 | c0002 | t0001 | g0185 | AMR | PEL | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG02148 | hp2 | a0003 | c0003 | t0001 | g0080 | AMR | PEL | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG02155 | hp1 | a0002 | c0002 | t0002 | g0034 | EAS | CDX | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG02155 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | CDX | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0261 | EAS | CDX | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG02165 | hp2 | a0003 | c0003 | t0001 | g0085 | EAS | CDX | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG02257 | hp1 | a0003 | c0003 | t0001 | g0039 | AFR | ACB | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0300 | AFR | ACB | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | ACB | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG02258 | hp2 | a0003 | c0003 | t0003 | g0048 | AFR | ACB | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG02273 | hp1 | a0001 | c0004 | t0001 | g0003 | AMR | PEL | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | PEL | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG02280 | hp1 | a0001 | c0004 | t0001 | g0234 | AFR | ACB | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG02280 | hp2 | a0001 | c0009 | t0001 | g0192 | AFR | ACB | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | PEL | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG02300 | hp2 | a0002 | c0002 | t0001 | g0025 | AMR | PEL | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG02451 | hp1 | a0002 | c0002 | t0001 | g0005 | AFR | ACB | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG02451 | hp2 | a0001 | c0005 | t0001 | g0014 | AFR | ACB | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0318 | EAS | KHV | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0317 | EAS | KHV | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG02572 | hp1 | a0001 | c0004 | t0001 | g0228 | AFR | GWD | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG02572 | hp2 | a0001 | c0005 | t0001 | g0126 | AFR | GWD | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0268 | SAS | PJL | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG02615 | hp1 | a0002 | c0002 | t0001 | g0016 | AFR | GWD | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG02615 | hp2 | a0003 | c0003 | t0003 | g0054 | AFR | GWD | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | GWD | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0289 | AFR | GWD | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG02630 | hp2 | a0002 | c0002 | t0001 | g0172 | AFR | GWD | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG02647 | hp1 | a0003 | c0003 | t0003 | g0114 | AFR | GWD | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG02647 | hp2 | a0008 | c0016 | t0001 | g0195 | AFR | GWD | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG02717 | hp1 | a0001 | c0008 | t0001 | g0018 | AFR | GWD | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG02717 | hp2 | a0001 | c0004 | t0001 | g0227 | AFR | GWD | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG02723 | hp1 | a0003 | c0003 | t0001 | g0239 | AFR | GWD | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG02723 | hp2 | a0001 | c0004 | t0001 | g0111 | AFR | GWD | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG02735 | hp1 | a0002 | c0002 | t0001 | g0183 | SAS | PJL | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG02735 | hp2 | a0002 | c0002 | t0001 | g0155 | SAS | PJL | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0283 | SAS | PJL | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG02738 | hp2 | a0002 | c0002 | t0001 | g0168 | SAS | PJL | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0243 | AFR | GWD | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG02809 | hp2 | a0001 | c0005 | t0001 | g0141 | AFR | GWD | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | GWD | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG02818 | hp2 | a0001 | c0011 | t0002 | g0032 | AFR | GWD | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG02886 | hp2 | a0001 | c0004 | t0001 | g0019 | AFR | GWD | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG02895 | hp1 | a0001 | c0004 | t0001 | g0020 | AFR | GWD | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG02895 | hp2 | a0002 | c0002 | t0001 | g0016 | AFR | GWD | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG02896 | hp1 | a0001 | c0004 | t0001 | g0211 | AFR | GWD | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG02896 | hp2 | a0002 | c0002 | t0001 | g0016 | AFR | GWD | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG02897 | hp1 | a0001 | c0004 | t0001 | g0020 | AFR | GWD | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG02897 | hp2 | a0001 | c0004 | t0001 | g0210 | AFR | GWD | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | ESN | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0308 | AFR | ESN | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0293 | AFR | ESN | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG02970 | hp1 | a0001 | c0008 | t0001 | g0018 | AFR | ESN | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG02970 | hp2 | a0001 | c0005 | t0001 | g0014 | AFR | ESN | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG02976 | hp1 | a0002 | c0002 | t0002 | g0251 | AFR | ESN | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG02976 | hp2 | a0001 | c0009 | t0001 | g0191 | AFR | ESN | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG03017 | hp1 | a0002 | c0002 | t0001 | g0170 | SAS | PJL | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG03017 | hp2 | a0002 | c0002 | t0001 | g0108 | SAS | PJL | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0288 | AFR | GWD | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG03098 | hp1 | a0009 | c0019 | t0001 | g0116 | AFR | MSL | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG03098 | hp2 | a0001 | c0005 | t0003 | g0128 | AFR | MSL | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG03130 | hp1 | a0003 | c0003 | t0001 | g0058 | AFR | ESN | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | ESN | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | ESN | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0290 | AFR | ESN | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG03195 | hp2 | a0001 | c0005 | t0001 | g0014 | AFR | ESN | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0242 | AFR | MSL | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG03209 | hp2 | a0001 | c0011 | t0002 | g0032 | AFR | MSL | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0030 | AFR | MSL | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | MSL | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG03453 | hp1 | a0001 | c0005 | t0001 | g0129 | AFR | MSL | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | MSL | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG03486 | hp1 | a0001 | c0005 | t0001 | g0021 | AFR | MSL | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG03486 | hp2 | a0001 | c0004 | t0001 | g0225 | AFR | MSL | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG03490 | hp1 | a0002 | c0002 | t0001 | g0107 | SAS | PJL | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG03490 | hp2 | a0003 | c0003 | t0001 | g0071 | SAS | PJL | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0240 | AFR | ESN | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG03516 | hp2 | a0001 | c0004 | t0001 | g0110 | AFR | ESN | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG03540 | hp1 | a0001 | c0004 | t0001 | g0220 | AFR | GWD | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG03579 | hp1 | a0001 | c0004 | t0001 | g0233 | AFR | MSL | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG03579 | hp2 | a0001 | c0005 | t0001 | g0127 | AFR | MSL | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG03654 | hp1 | a0002 | c0002 | t0001 | g0022 | SAS | PJL | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG03654 | hp2 | a0003 | c0003 | t0001 | g0100 | SAS | PJL | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG03669 | hp1 | a0002 | c0002 | t0001 | g0005 | SAS | PJL | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG03669 | hp2 | a0003 | c0003 | t0002 | g0287 | SAS | PJL | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0299 | SAS | STU | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG03688 | hp2 | a0003 | c0003 | t0001 | g0190 | SAS | STU | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG03704 | hp1 | a0003 | c0003 | t0001 | g0091 | SAS | PJL | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG03704 | hp2 | a0002 | c0002 | t0001 | g0156 | SAS | PJL | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG03710 | hp1 | a0002 | c0002 | t0001 | g0182 | SAS | PJL | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG03710 | hp2 | a0003 | c0003 | t0001 | g0065 | SAS | PJL | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG03831 | hp1 | a0002 | c0002 | t0001 | g0187 | SAS | BEB | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0306 | SAS | BEB | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | BEB | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG03834 | hp2 | a0003 | c0003 | t0001 | g0093 | SAS | BEB | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0249 | SAS | BEB | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG03927 | hp2 | a0003 | c0003 | t0001 | g0120 | SAS | BEB | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG03942 | hp1 | a0002 | c0002 | t0001 | g0163 | SAS | BEB | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0307 | SAS | BEB | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG04115 | hp1 | a0003 | c0003 | t0001 | g0060 | SAS | STU | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG04115 | hp2 | a0002 | c0002 | t0001 | g0171 | SAS | STU | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG04199 | hp1 | a0002 | c0002 | t0001 | g0006 | SAS | STU | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG04199 | hp2 | a0003 | c0003 | t0001 | g0086 | SAS | STU | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA18522 | hp1 | a0001 | c0004 | t0002 | g0250 | AFR | YRI | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA18522 | hp2 | a0002 | c0002 | t0001 | g0219 | AFR | YRI | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0303 | EAS | CHB | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0262 | EAS | CHB | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0031 | AFR | YRI | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA18906 | hp2 | a0005 | c0012 | t0001 | g0198 | AFR | YRI | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA18940 | hp1 | a0006 | c0014 | t0002 | g0320 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA18940 | hp2 | a0002 | c0002 | t0001 | g0023 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA18941 | hp1 | a0003 | c0003 | t0001 | g0002 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA18941 | hp2 | a0003 | c0003 | t0002 | g0258 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA18943 | hp1 | a0001 | c0007 | t0001 | g0208 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA18943 | hp2 | a0002 | c0002 | t0001 | g0040 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA18944 | hp1 | a0001 | c0004 | t0001 | g0214 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA18944 | hp2 | a0003 | c0003 | t0001 | g0089 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA18945 | hp1 | a0003 | c0003 | t0001 | g0012 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA18945 | hp2 | a0004 | c0006 | t0001 | g0229 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA18946 | hp2 | a0002 | c0002 | t0001 | g0176 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA18947 | hp1 | a0003 | c0003 | t0001 | g0064 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0298 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA18949 | hp2 | a0003 | c0003 | t0001 | g0004 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA18950 | hp1 | a0002 | c0002 | t0001 | g0015 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA18950 | hp2 | a0003 | c0003 | t0001 | g0002 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA18951 | hp1 | a0001 | c0004 | t0001 | g0003 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA18953 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA18953 | hp2 | a0002 | c0002 | t0002 | g0312 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA18954 | hp2 | a0003 | c0003 | t0001 | g0102 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0316 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA18957 | hp1 | a0002 | c0002 | t0001 | g0066 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0279 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0280 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0255 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA18961 | hp1 | a0003 | c0003 | t0001 | g0077 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA18961 | hp2 | a0002 | c0002 | t0002 | g0311 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA18962 | hp1 | a0002 | c0002 | t0001 | g0015 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA18962 | hp2 | a0003 | c0003 | t0001 | g0010 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA18963 | hp1 | a0002 | c0002 | t0001 | g0062 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA18965 | hp1 | a0004 | c0006 | t0001 | g0209 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA18965 | hp2 | a0003 | c0003 | t0001 | g0045 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0302 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA18967 | hp1 | a0001 | c0007 | t0001 | g0028 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA18967 | hp2 | a0003 | c0003 | t0001 | g0068 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0292 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA18970 | hp1 | a0006 | c0013 | t0002 | g0319 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA18970 | hp2 | a0003 | c0003 | t0001 | g0164 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA18971 | hp2 | a0003 | c0003 | t0001 | g0010 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA18972 | hp1 | a0004 | c0006 | t0001 | g0132 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA18972 | hp2 | a0002 | c0002 | t0001 | g0157 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA18973 | hp1 | a0003 | c0003 | t0001 | g0076 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA18973 | hp2 | a0002 | c0002 | t0001 | g0160 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA18975 | hp1 | a0001 | c0004 | t0001 | g0003 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA18975 | hp2 | a0002 | c0002 | t0001 | g0042 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0310 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA18978 | hp1 | a0003 | c0003 | t0001 | g0002 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA18979 | hp2 | a0001 | c0004 | t0001 | g0231 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA18982 | hp1 | a0010 | c0018 | t0002 | g0313 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA18982 | hp2 | a0002 | c0002 | t0001 | g0133 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA18983 | hp2 | a0002 | c0002 | t0001 | g0131 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA18988 | hp1 | a0001 | c0004 | t0001 | g0204 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA18988 | hp2 | a0003 | c0003 | t0001 | g0097 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA18989 | hp1 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA18989 | hp2 | a0001 | c0004 | t0001 | g0203 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA18990 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA18991 | hp1 | a0001 | c0004 | t0001 | g0029 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA18992 | hp2 | a0003 | c0003 | t0001 | g0070 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA18994 | hp1 | a0003 | c0003 | t0001 | g0165 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA18994 | hp2 | a0002 | c0002 | t0001 | g0061 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA18997 | hp1 | a0003 | c0003 | t0001 | g0095 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA18997 | hp2 | a0001 | c0004 | t0001 | g0218 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA18998 | hp1 | a0003 | c0003 | t0001 | g0087 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA18998 | hp2 | a0001 | c0004 | t0001 | g0217 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA19000 | hp2 | a0001 | c0004 | t0001 | g0221 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA19001 | hp1 | a0003 | c0003 | t0001 | g0010 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA19002 | hp1 | a0003 | c0003 | t0001 | g0207 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA19002 | hp2 | a0003 | c0003 | t0001 | g0090 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA19009 | hp1 | a0002 | c0002 | t0001 | g0147 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0286 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA19010 | hp1 | a0003 | c0003 | t0001 | g0057 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0297 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA19011 | hp1 | a0004 | c0006 | t0001 | g0180 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA19012 | hp1 | a0001 | c0004 | t0001 | g0197 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA19012 | hp2 | a0003 | c0003 | t0001 | g0082 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA19030 | hp1 | a0001 | c0020 | t0001 | g0104 | AFR | LWK | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | LWK | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0324 | AFR | LWK | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | LWK | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA19054 | hp1 | a0001 | c0004 | t0001 | g0007 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA19056 | hp1 | a0002 | c0002 | t0001 | g0135 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA19056 | hp2 | a0002 | c0002 | t0001 | g0063 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA19057 | hp1 | a0003 | c0003 | t0001 | g0041 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA19058 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA19059 | hp1 | a0003 | c0003 | t0001 | g0044 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA19059 | hp2 | a0001 | c0004 | t0001 | g0232 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA19062 | hp1 | a0002 | c0002 | t0001 | g0067 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA19062 | hp2 | a0003 | c0003 | t0001 | g0179 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA19063 | hp1 | a0002 | c0002 | t0002 | g0294 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0281 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA19064 | hp2 | a0002 | c0002 | t0001 | g0015 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA19065 | hp2 | a0003 | c0003 | t0001 | g0073 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA19066 | hp1 | a0003 | c0003 | t0001 | g0002 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA19066 | hp2 | a0002 | c0002 | t0001 | g0023 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA19068 | hp1 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA19068 | hp2 | a0002 | c0002 | t0001 | g0146 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA19070 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA19074 | hp1 | a0003 | c0003 | t0001 | g0004 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA19074 | hp2 | a0001 | c0004 | t0001 | g0003 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA19075 | hp1 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA19075 | hp2 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA19076 | hp1 | a0001 | c0004 | t0001 | g0205 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA19076 | hp2 | a0001 | c0001 | t0002 | g0305 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA19077 | hp1 | a0001 | c0004 | t0001 | g0029 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0309 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA19078 | hp1 | a0001 | c0004 | t0001 | g0216 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA19078 | hp2 | a0003 | c0003 | t0001 | g0056 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA19080 | hp1 | a0003 | c0003 | t0001 | g0012 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA19080 | hp2 | a0001 | c0004 | t0001 | g0007 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA19081 | hp1 | a0003 | c0003 | t0001 | g0004 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA19081 | hp2 | a0001 | c0004 | t0001 | g0007 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0276 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA19083 | hp2 | a0003 | c0003 | t0001 | g0002 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA19085 | hp1 | a0002 | c0002 | t0001 | g0134 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA19085 | hp2 | a0003 | c0003 | t0001 | g0084 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0269 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA19086 | hp2 | a0003 | c0003 | t0001 | g0012 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA19087 | hp1 | a0002 | c0002 | t0001 | g0159 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA19087 | hp2 | a0001 | c0015 | t0001 | g0088 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA19088 | hp1 | a0002 | c0002 | t0001 | g0053 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA19088 | hp2 | a0001 | c0004 | t0001 | g0212 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA19090 | hp2 | a0002 | c0002 | t0001 | g0046 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA19091 | hp1 | a0001 | c0004 | t0001 | g0230 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA19091 | hp2 | a0003 | c0003 | t0001 | g0101 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0030 | AFR | YRI | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | YRI | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA20129 | hp1 | a0002 | c0002 | t0001 | g0235 | AFR | ASW | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | ASW | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA20752 | hp1 | a0002 | c0002 | t0001 | g0005 | EUR | TSI | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA20752 | hp2 | a0002 | c0002 | t0001 | g0166 | EUR | TSI | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG01123 | hp1 | a0002 | c0002 | t0001 | g0136 | AMR | CLM | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG01123 | hp2 | a0003 | c0003 | t0001 | g0178 | AMR | CLM | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG02109 | hp1 | a0007 | c0017 | t0001 | g0106 | AFR | ACB | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG02109 | hp2 | a0001 | c0005 | t0002 | g0244 | AFR | ACB | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG02486 | hp1 | a0001 | c0004 | t0001 | g0223 | AFR | ACB | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG02486 | hp2 | a0001 | c0005 | t0001 | g0130 | AFR | ACB | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG02559 | hp1 | a0001 | c0004 | t0001 | g0019 | AFR | ACB | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG02559 | hp2 | a0001 | c0004 | t0001 | g0206 | AFR | ACB | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG03471 | hp1 | a0001 | c0005 | t0001 | g0021 | AFR | MSL | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG03471 | hp2 | a0003 | c0003 | t0003 | g0094 | AFR | MSL | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0252 | AFR | USA | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| HG06807 | hp2 | a0001 | c0005 | t0001 | g0125 | AFR | USA | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0321 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA18955 | hp2 | a0002 | c0002 | t0001 | g0158 | EAS | JPT | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0031 | AFR | USA | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA20300 | hp2 | a0002 | c0002 | t0001 | g0117 | AFR | USA | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA21309 | hp1 | a0001 | c0004 | t0001 | g0224 | AFR | LWK | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| NA21309 | hp2 | a0002 | c0002 | t0002 | g0323 | AFR | LWK | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0001 | g0122 | REF | REF | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| homoSapiens | grch38p0 | a0005 | c0012 | t0001 | g0137 | REF | REF | GC_chr4_71736697_71789079 | GC | chr4 | 71736697 | 71789079 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:71752579 | T | C | 9 | a0001 a0002 a0003 others(6): Show |
385 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(382): Show |
missense_variant | MODERATE | c.1334A>G | p.His445Arg | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/13 | 1395/1685 | 1334/1425 | 445/474 | chr4 | 71752579 | |||
| chr4:71752580 | G | A | 2 | a0001 a0004 |
7 | HG00408.hp2 NA18943.hp1 NA18945.hp2 others(4): Show |
missense_variant | MODERATE | c.1333C>T | p.His445Tyr | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/13 | 1394/1685 | 1333/1425 | 445/474 | chr4 | 71752580 | |||
| chr4:71752606 | G | T | 1 | a0003 | 81 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(78): Show |
missense_variant | MODERATE | c.1307C>A | p.Thr436Lys | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/13 | 1368/1685 | 1307/1425 | 436/474 | chr4 | 71752606 | |||
| chr4:71752617 | A | C | 3 | a0002 a0007 a0010 |
102 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(99): Show |
missense_variant | MODERATE | c.1296T>G | p.Asp432Glu | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/13 | 1357/1685 | 1296/1425 | 432/474 | chr4 | 71752617 | |||
| chr4:71754445 | A | G | 1 | a0008 | 1 | HG02647.hp2 | missense_variant | MODERATE | c.1228T>C | p.Tyr410His | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 10/13 | 1289/1685 | 1228/1425 | 410/474 | chr4 | 71754445 | |||
| chr4:71754495 | T | C | 1 | a0010 | 1 | NA18982.hp1 | missense_variant | MODERATE | c.1178A>G | p.Lys393Arg | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 10/13 | 1239/1685 | 1178/1425 | 393/474 | chr4 | 71754495 | |||
| chr4:71755091 | T | C | 1 | a0004 | 4 | NA18945.hp2 NA18965.hp1 NA18972.hp1 others(1): Show |
missense_variant | MODERATE | c.1051A>G | p.Ser351Gly | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 9/13 | 1112/1685 | 1051/1425 | 351/474 | chr4 | 71755091 | |||
| chr4:71756746 | C | G | 1 | a0007 | 1 | HG02109.hp1 | missense_variant | MODERATE | c.1000G>C | p.Val334Leu | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 8/13 | 1061/1685 | 1000/1425 | 334/474 | chr4 | 71756746 | |||
| chr4:71763435 | G | C | 1 | a0009 | 1 | HG03098.hp1 | missense_variant | MODERATE | c.674C>G | p.Ala225Gly | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/13 | 735/1685 | 674/1425 | 225/474 | chr4 | 71763435 | |||
| chr4:71769397 | C | T | 1 | a0006 | 2 | NA18940.hp1 NA18970.hp1 |
missense_variant | MODERATE | c.62G>A | p.Arg21Gln | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 2/13 | 123/1685 | 62/1425 | 21/474 | chr4 | 71769397 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:71752640 | G | T | 1 | a0001c0011 | 2 | HG02818.hp2 HG03209.hp2 |
synonymous_variant | LOW | c.1273C>A | p.Arg425Arg | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/13 | 1334/1685 | 1273/1425 | 425/474 | chr4 | 71752640 | |||
| chr4:71755071 | C | T | 1 | a0002c0010 | 2 | HG00140.hp2 HG01258.hp1 |
synonymous_variant | LOW | c.1071G>A | p.Pro357Pro | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 9/13 | 1132/1685 | 1071/1425 | 357/474 | chr4 | 71755071 | |||
| chr4:71756849 | A | G | 7 | a0001c0004 a0001c0007 a0001c0008 others(4): Show |
60 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(57): Show |
synonymous_variant | LOW | c.897T>C | p.Cys299Cys | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 8/13 | 958/1685 | 897/1425 | 299/474 | chr4 | 71756849 | |||
| chr4:71756909 | A | C | 1 | a0001c0015 | 1 | NA19087.hp2 | synonymous_variant | LOW | c.837T>G | p.Pro279Pro | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 8/13 | 898/1685 | 837/1425 | 279/474 | chr4 | 71756909 | |||
| chr4:71763912 | A | G | 1 | a0001c0009 | 2 | HG02280.hp2 HG02976.hp2 |
synonymous_variant | LOW | c.498T>C | p.Asn166Asn | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 5/13 | 559/1685 | 498/1425 | 166/474 | chr4 | 71763912 | |||
| chr4:71765497 | G | A | 2 | a0001c0008 a0001c0020 |
4 | HG01884.hp2 HG02717.hp1 HG02970.hp1 others(1): Show |
synonymous_variant | LOW | c.408C>T | p.Tyr136Tyr | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 4/13 | 469/1685 | 408/1425 | 136/474 | chr4 | 71765497 | |||
| chr4:71765623 | C | T | 1 | a0001c0005 | 14 | HG01243.hp1 HG02109.hp2 HG02451.hp2 others(11): Show |
synonymous_variant | LOW | c.282G>A | p.Lys94Lys | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 4/13 | 343/1685 | 282/1425 | 94/474 | chr4 | 71765623 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:71741766 | A | G | 2 | a0001c0005t0003 a0003c0003t0003 |
5 | HG02258.hp2 HG02615.hp2 HG02647.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*130T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 13/13 | 4410 | chr4 | 71741766 | ||||||
| chr4:71784057 | G | A | 9 | a0001c0001t0002 a0001c0004t0002 a0001c0005t0002 others(6): Show |
106 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(103): Show |
5_prime_UTR_variant | MODIFIER | c.-39C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/13 | 39 | chr4 | 71784057 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:71741918 | G | A | 1 | a0001c0008t0001g0105 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.*26-48C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71741918 | |||||||
| chr4:71741961 | T | G | 46 | a0001c0001t0001g0035 a0001c0001t0001g0043 a0001c0001t0001g0051 others(43): Show |
52 | HG00423.hp1 HG01106.hp2 HG01884.hp1 others(49): Show |
intron_variant | MODIFIER | c.*26-91A>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71741961 | |||||||
| chr4:71742240 | A | G | 1 | a0001c0001t0002g0318 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.*26-370T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71742240 | |||||||
| chr4:71742317 | G | A | 7 | a0001c0001t0001g0026 a0001c0001t0001g0113 a0001c0001t0001g0121 others(4): Show |
8 | HG02622.hp1 HG02630.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.*26-447C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71742317 | |||||||
| chr4:71742398 | C | T | 142 | a0001c0001t0002g0253 a0001c0001t0002g0301 a0001c0004t0001g0217 others(139): Show |
172 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.*26-528G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71742398 | |||||||
| chr4:71742604 | T | C | 1 | a0003c0003t0001g0072 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.*26-734A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71742604 | |||||||
| chr4:71742647 | C | T | 64 | a0001c0004t0001g0217 a0001c0004t0001g0218 a0001c0005t0001g0129 others(61): Show |
77 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.*26-777G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71742647 | |||||||
| chr4:71742666 | T | G | 63 | a0001c0004t0001g0217 a0001c0004t0001g0218 a0001c0005t0001g0129 others(60): Show |
76 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.*26-796A>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71742666 | |||||||
| chr4:71742699 | G | A | 1 | a0001c0007t0001g0208 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.*26-829C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71742699 | |||||||
| chr4:71742712 | C | CGCCTGTA others(1461): Show |
3 | a0001c0001t0001g0145 a0001c0001t0001g0148 a0001c0001t0001g0149 |
3 | NA18951.hp2 NA18993.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.*26-843_*26-842ins others(1468): Show |
GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71742712 | |||||||
| chr4:71742789 | A | G | 1 | a0001c0001t0002g0304 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.*26-919T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71742789 | |||||||
| chr4:71742915 | G | A | 67 | a0001c0001t0001g0052 a0001c0001t0001g0055 a0001c0001t0001g0069 others(64): Show |
76 | HG00544.hp2 HG00597.hp2 HG00609.hp2 others(73): Show |
intron_variant | MODIFIER | c.*26-1045C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71742915 | |||||||
| chr4:71742952 | C | T | 4 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0009t0001g0191 others(1): Show |
4 | HG02280.hp2 HG02922.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.*26-1082G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71742952 | |||||||
| chr4:71743075 | A | G | 45 | a0001c0004t0001g0003 a0001c0004t0001g0007 a0001c0004t0001g0019 others(42): Show |
57 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.*26-1205T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71743075 | |||||||
| chr4:71743099 | T | C | 1 | a0003c0003t0001g0103 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.*26-1229A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71743099 | |||||||
| chr4:71743211 | G | T | 12 | a0003c0003t0001g0002 a0003c0003t0001g0004 a0003c0003t0001g0010 others(9): Show |
21 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(18): Show |
intron_variant | MODIFIER | c.*26-1341C>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71743211 | |||||||
| chr4:71743295 | C | A | 11 | a0001c0001t0001g0144 a0001c0001t0001g0196 a0001c0001t0002g0255 others(8): Show |
11 | HG03834.hp1 NA18957.hp2 NA18960.hp2 others(8): Show |
intron_variant | MODIFIER | c.*26-1425G>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71743295 | |||||||
| chr4:71743377 | A | C | 111 | a0001c0001t0001g0052 a0001c0001t0001g0055 a0001c0001t0001g0069 others(108): Show |
132 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(129): Show |
intron_variant | MODIFIER | c.*26-1507T>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71743377 | |||||||
| chr4:71743568 | T | C | 7 | a0001c0001t0001g0026 a0001c0001t0001g0113 a0001c0001t0001g0121 others(4): Show |
8 | HG02622.hp1 HG02630.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.*26-1698A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71743568 | |||||||
| chr4:71743681 | C | T | 64 | a0001c0004t0001g0217 a0001c0004t0001g0218 a0001c0005t0001g0129 others(61): Show |
77 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.*26-1811G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71743681 | |||||||
| chr4:71743808 | G | A | 1 | a0001c0001t0002g0253 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.*26-1938C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71743808 | |||||||
| chr4:71743840 | T | C | 1 | a0003c0003t0001g0152 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.*26-1970A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71743840 | |||||||
| chr4:71743972 | G | A | 1 | a0003c0003t0003g0054 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.*26-2102C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71743972 | |||||||
| chr4:71744122 | G | T | 50 | a0001c0004t0001g0003 a0001c0004t0001g0007 a0001c0004t0001g0019 others(47): Show |
62 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.*25+2029C>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71744122 | |||||||
| chr4:71744217 | C | T | 45 | a0001c0004t0001g0003 a0001c0004t0001g0007 a0001c0004t0001g0019 others(42): Show |
57 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.*25+1934G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71744217 | |||||||
| chr4:71744238 | A | G | 1 | a0003c0003t0001g0060 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.*25+1913T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71744238 | |||||||
| chr4:71744286 | C | CA | 71 | a0001c0001t0001g0013 a0001c0001t0001g0036 a0001c0001t0001g0138 others(68): Show |
87 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.*25+1864dupT | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71744286 | |||||||
| chr4:71744286 | C | CAA | 9 | a0001c0004t0001g0203 a0001c0004t0001g0214 a0001c0004t0001g0215 others(6): Show |
9 | HG01978.hp1 HG01978.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.*25+1863_*25+1864d others(4): Show |
GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71744286 | |||||||
| chr4:71744286 | CA | C | 10 | a0001c0001t0001g0096 a0001c0001t0001g0193 a0001c0001t0001g0194 others(7): Show |
12 | HG01109.hp2 HG01167.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.*25+1864delT | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71744286 | |||||||
| chr4:71744297 | A | C | 1 | a0001c0001t0002g0247 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.*25+1854T>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71744297 | |||||||
| chr4:71744303 | A | C | 1 | a0001c0001t0002g0316 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.*25+1848T>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71744303 | |||||||
| chr4:71744304 | C | A | 77 | a0001c0001t0002g0301 a0002c0002t0001g0005 a0002c0002t0001g0006 others(74): Show |
94 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.*25+1847G>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71744304 | |||||||
| chr4:71744331 | C | T | 1 | a0001c0005t0002g0244 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.*25+1820G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71744331 | |||||||
| chr4:71744389 | G | GCGGT | 4 | a0001c0001t0002g0252 a0001c0001t0002g0290 a0001c0001t0002g0293 others(1): Show |
4 | HG02965.hp1 HG02965.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.*25+1758_*25+1761d others(6): Show |
GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71744389 | |||||||
| chr4:71744435 | GGAGACAG others(3): Show |
G | 63 | a0001c0004t0001g0217 a0001c0004t0001g0218 a0001c0005t0001g0129 others(60): Show |
76 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.*25+1706_*25+1715d others(12): Show |
GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71744435 | |||||||
| chr4:71744458 | C | CA | 175 | a0001c0001t0001g0013 a0001c0001t0001g0036 a0001c0001t0001g0050 others(172): Show |
214 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.*25+1692dupT | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71744458 | |||||||
| chr4:71744458 | C | CAA | 25 | a0001c0001t0001g0026 a0001c0001t0001g0113 a0001c0001t0001g0188 others(22): Show |
30 | HG00408.hp1 HG01243.hp1 HG01978.hp1 others(27): Show |
intron_variant | MODIFIER | c.*25+1691_*25+1692d others(4): Show |
GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71744458 | |||||||
| chr4:71744458 | CA | C | 61 | a0001c0001t0002g0246 a0001c0001t0002g0302 a0001c0004t0001g0217 others(58): Show |
74 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.*25+1692delT | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71744458 | |||||||
| chr4:71744491 | C | A | 242 | a0001c0001t0001g0013 a0001c0001t0001g0026 a0001c0001t0001g0035 others(239): Show |
288 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(285): Show |
intron_variant | MODIFIER | c.*25+1660G>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71744491 | |||||||
| chr4:71744828 | G | A | 45 | a0001c0004t0001g0003 a0001c0004t0001g0007 a0001c0004t0001g0019 others(42): Show |
57 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.*25+1323C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71744828 | |||||||
| chr4:71744834 | G | GA | 44 | a0001c0001t0001g0035 a0001c0001t0001g0043 a0001c0001t0001g0051 others(41): Show |
50 | HG00423.hp1 HG01106.hp2 HG01943.hp1 others(47): Show |
intron_variant | MODIFIER | c.*25+1316dupT | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71744834 | |||||||
| chr4:71744877 | C | T | 1 | a0001c0001t0002g0253 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.*25+1274G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71744877 | |||||||
| chr4:71745037 | T | C | 3 | a0002c0002t0001g0016 a0002c0002t0001g0172 a0002c0002t0001g0219 |
5 | HG02615.hp1 HG02630.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.*25+1114A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71745037 | |||||||
| chr4:71745113 | C | T | 3 | a0001c0004t0001g0206 a0001c0004t0001g0210 a0001c0004t0001g0211 |
3 | HG02559.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.*25+1038G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71745113 | |||||||
| chr4:71745133 | C | T | 13 | a0001c0001t0001g0013 a0001c0001t0001g0036 a0001c0001t0001g0050 others(10): Show |
18 | HG01167.hp1 HG01257.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.*25+1018G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71745133 | |||||||
| chr4:71745245 | T | C | 3 | a0001c0001t0001g0145 a0001c0001t0001g0148 a0001c0001t0001g0149 |
3 | NA18951.hp2 NA18993.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.*25+906A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71745245 | |||||||
| chr4:71745361 | G | T | 1 | a0003c0003t0001g0239 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.*25+790C>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71745361 | |||||||
| chr4:71745465 | T | C | 1 | a0009c0019t0001g0116 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.*25+686A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71745465 | |||||||
| chr4:71745498 | A | G | 45 | a0001c0004t0001g0003 a0001c0004t0001g0007 a0001c0004t0001g0019 others(42): Show |
57 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.*25+653T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71745498 | |||||||
| chr4:71745652 | CTA | C | 18 | a0001c0001t0001g0013 a0001c0001t0001g0036 a0001c0001t0001g0050 others(15): Show |
23 | HG01167.hp1 HG01257.hp1 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.*25+497_*25+498del others(2): Show |
GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71745652 | |||||||
| chr4:71745805 | A | T | 2 | a0003c0003t0001g0076 a0003c0003t0001g0077 |
2 | NA18961.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.*25+346T>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71745805 | |||||||
| chr4:71745843 | A | G | 1 | a0003c0003t0001g0091 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.*25+308T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71745843 | |||||||
| chr4:71745941 | C | T | 7 | a0001c0001t0001g0026 a0001c0001t0001g0113 a0001c0001t0001g0121 others(4): Show |
8 | HG02622.hp1 HG02630.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.*25+210G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71745941 | |||||||
| chr4:71745973 | G | C | 76 | a0001c0001t0002g0301 a0002c0002t0001g0005 a0002c0002t0001g0006 others(73): Show |
93 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.*25+178C>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71745973 | |||||||
| chr4:71745973 | G | T | 1 | a0002c0002t0001g0167 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.*25+178C>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71745973 | |||||||
| chr4:71745982 | G | A | 13 | a0001c0001t0001g0050 a0001c0001t0001g0112 a0001c0001t0001g0181 others(10): Show |
16 | HG01257.hp1 HG02258.hp2 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.*25+169C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 12/12 | chr4 | 71745982 | |||||||
| chr4:71746284 | AAATCTTG others(19): Show |
A | 1 | a0001c0004t0001g0218 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1396-105_1396-80de others(27): Show |
GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71746284 | |||||||
| chr4:71746501 | A | T | 7 | a0001c0001t0001g0026 a0001c0001t0001g0113 a0001c0001t0001g0121 others(4): Show |
8 | HG02622.hp1 HG02630.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1396-296T>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71746501 | |||||||
| chr4:71746517 | G | A | 105 | a0001c0001t0001g0052 a0001c0001t0001g0055 a0001c0001t0001g0069 others(102): Show |
126 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.1396-312C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71746517 | |||||||
| chr4:71746531 | G | A | 1 | a0002c0002t0001g0182 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1396-326C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71746531 | |||||||
| chr4:71746576 | T | G | 1 | a0002c0002t0002g0251 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1396-371A>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71746576 | |||||||
| chr4:71746772 | T | TA | 18 | a0001c0001t0001g0035 a0001c0001t0001g0050 a0001c0001t0001g0096 others(15): Show |
19 | HG01167.hp1 HG02074.hp1 HG02622.hp2 others(16): Show |
intron_variant | MODIFIER | c.1396-568dupT | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71746772 | |||||||
| chr4:71746772 | T | TAA | 101 | a0001c0001t0001g0026 a0001c0001t0001g0043 a0001c0001t0001g0051 others(98): Show |
123 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.1396-569_1396-568d others(4): Show |
GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71746772 | |||||||
| chr4:71746772 | T | TAAA | 79 | a0001c0001t0001g0052 a0001c0001t0001g0055 a0001c0001t0001g0069 others(76): Show |
92 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.1396-570_1396-568d others(5): Show |
GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71746772 | |||||||
| chr4:71746772 | T | TAAAA | 43 | a0001c0001t0001g0196 a0001c0001t0002g0253 a0001c0001t0002g0257 others(40): Show |
53 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(50): Show |
intron_variant | MODIFIER | c.1396-571_1396-568d others(6): Show |
GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71746772 | |||||||
| chr4:71746772 | T | TAAAAA | 9 | a0001c0004t0001g0203 a0001c0004t0001g0204 a0001c0004t0001g0213 others(6): Show |
9 | HG01978.hp1 HG02135.hp1 NA18943.hp1 others(6): Show |
intron_variant | MODIFIER | c.1396-572_1396-568d others(7): Show |
GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71746772 | |||||||
| chr4:71746772 | T | TAAAAAAA others(9): Show |
1 | a0001c0009t0001g0191 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1396-583_1396-568d others(18): Show |
GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71746772 | |||||||
| chr4:71746772 | T | TAAAAAAA others(10): Show |
2 | a0001c0001t0001g0193 a0001c0009t0001g0192 |
2 | HG02280.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1396-584_1396-568d others(19): Show |
GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71746772 | |||||||
| chr4:71746772 | T | TAAAAAAA others(11): Show |
1 | a0001c0001t0001g0194 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1396-585_1396-568d others(20): Show |
GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71746772 | |||||||
| chr4:71746772 | TA | T | 54 | a0003c0003t0001g0002 a0003c0003t0001g0004 a0003c0003t0001g0010 others(51): Show |
67 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.1396-568delT | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71746772 | |||||||
| chr4:71746899 | G | A | 9 | a0001c0001t0001g0050 a0001c0001t0001g0112 a0001c0001t0001g0181 others(6): Show |
12 | HG01257.hp1 HG02809.hp1 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.1396-694C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71746899 | |||||||
| chr4:71746926 | GGGA | G | 104 | a0001c0001t0001g0052 a0001c0001t0001g0055 a0001c0001t0001g0069 others(101): Show |
123 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(120): Show |
intron_variant | MODIFIER | c.1396-724_1396-722d others(5): Show |
GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71746926 | |||||||
| chr4:71746970 | C | A | 1 | a0001c0001t0002g0318 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1396-765G>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71746970 | |||||||
| chr4:71746970 | C | G | 42 | a0001c0001t0001g0035 a0001c0001t0001g0043 a0001c0001t0001g0051 others(39): Show |
48 | HG00423.hp1 HG01106.hp2 HG01943.hp1 others(45): Show |
intron_variant | MODIFIER | c.1396-765G>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71746970 | |||||||
| chr4:71746980 | A | C | 2 | a0001c0004t0001g0210 a0001c0004t0001g0211 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1396-775T>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71746980 | |||||||
| chr4:71747114 | G | A | 1 | a0001c0001t0002g0261 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1396-909C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71747114 | |||||||
| chr4:71747185 | T | G | 100 | a0001c0001t0001g0052 a0001c0001t0001g0055 a0001c0001t0001g0069 others(97): Show |
119 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(116): Show |
intron_variant | MODIFIER | c.1396-980A>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71747185 | |||||||
| chr4:71747194 | T | C | 43 | a0001c0001t0001g0035 a0001c0001t0001g0043 a0001c0001t0001g0051 others(40): Show |
49 | HG00423.hp1 HG01106.hp2 HG01943.hp1 others(46): Show |
intron_variant | MODIFIER | c.1396-989A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71747194 | |||||||
| chr4:71747206 | A | G | 1 | a0001c0001t0001g0240 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1396-1001T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71747206 | |||||||
| chr4:71747258 | T | A | 103 | a0001c0001t0001g0052 a0001c0001t0001g0055 a0001c0001t0001g0069 others(100): Show |
122 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.1396-1053A>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71747258 | |||||||
| chr4:71747319 | A | C | 85 | a0001c0001t0002g0301 a0002c0002t0001g0005 a0002c0002t0001g0006 others(82): Show |
104 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.1396-1114T>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71747319 | |||||||
| chr4:71747326 | T | C | 1 | a0001c0004t0001g0216 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1396-1121A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71747326 | |||||||
| chr4:71747526 | G | GGTATCAA others(19): Show |
1 | a0001c0004t0001g0218 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1396-1347_1396-132 others(30): Show |
GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71747526 | |||||||
| chr4:71747770 | A | G | 4 | a0003c0003t0003g0048 a0003c0003t0003g0054 a0003c0003t0003g0094 others(1): Show |
4 | HG02258.hp2 HG02615.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1396-1565T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71747770 | |||||||
| chr4:71747774 | T | A | 11 | a0001c0001t0002g0242 a0001c0001t0002g0324 a0001c0005t0001g0014 others(8): Show |
14 | HG01243.hp1 HG02109.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.1396-1569A>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71747774 | |||||||
| chr4:71747849 | G | A | 43 | a0001c0001t0001g0035 a0001c0001t0001g0043 a0001c0001t0001g0051 others(40): Show |
49 | HG00423.hp1 HG01106.hp2 HG01943.hp1 others(46): Show |
intron_variant | MODIFIER | c.1396-1644C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71747849 | |||||||
| chr4:71747914 | A | G | 2 | a0003c0003t0001g0072 a0003c0003t0001g0075 |
2 | HG00639.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1396-1709T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71747914 | |||||||
| chr4:71747976 | A | C | 4 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0009t0001g0191 others(1): Show |
4 | HG02280.hp2 HG02922.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1396-1771T>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71747976 | |||||||
| chr4:71748075 | T | C | 188 | a0001c0001t0001g0052 a0001c0001t0001g0055 a0001c0001t0001g0069 others(185): Show |
226 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(223): Show |
intron_variant | MODIFIER | c.1396-1870A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71748075 | |||||||
| chr4:71748123 | G | A | 51 | a0001c0001t0001g0052 a0001c0001t0001g0055 a0001c0001t0001g0069 others(48): Show |
58 | HG00544.hp2 HG00597.hp2 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.1396-1918C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71748123 | |||||||
| chr4:71748266 | A | G | 1 | a0002c0002t0001g0168 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1396-2061T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71748266 | |||||||
| chr4:71748326 | A | G | 1 | a0002c0002t0002g0251 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1396-2121T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71748326 | |||||||
| chr4:71748423 | A | C | 184 | a0001c0001t0001g0052 a0001c0001t0001g0055 a0001c0001t0001g0069 others(181): Show |
222 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.1396-2218T>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71748423 | |||||||
| chr4:71748439 | A | G | 4 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0009t0001g0191 others(1): Show |
4 | HG02280.hp2 HG02922.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1396-2234T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71748439 | |||||||
| chr4:71748550 | G | C | 62 | a0003c0003t0001g0002 a0003c0003t0001g0004 a0003c0003t0001g0010 others(59): Show |
75 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.1396-2345C>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71748550 | |||||||
| chr4:71748669 | C | T | 1 | a0002c0002t0001g0154 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1396-2464G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71748669 | |||||||
| chr4:71748785 | G | A | 1 | a0003c0003t0001g0058 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1396-2580C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71748785 | |||||||
| chr4:71748870 | A | G | 1 | a0001c0001t0002g0278 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1396-2665T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71748870 | |||||||
| chr4:71749051 | A | C | 1 | a0002c0002t0001g0167 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1396-2846T>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71749051 | |||||||
| chr4:71749054 | G | A | 1 | a0003c0003t0001g0139 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1396-2849C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71749054 | |||||||
| chr4:71749307 | G | A | 1 | a0003c0003t0001g0101 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1396-3102C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71749307 | |||||||
| chr4:71749488 | T | C | 1 | a0001c0001t0002g0282 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1395+3030A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71749488 | |||||||
| chr4:71749645 | A | G | 64 | a0003c0003t0001g0002 a0003c0003t0001g0004 a0003c0003t0001g0010 others(61): Show |
77 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.1395+2873T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71749645 | |||||||
| chr4:71749901 | G | A | 1 | a0001c0001t0002g0253 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1395+2617C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71749901 | |||||||
| chr4:71749904 | T | C | 4 | a0001c0001t0001g0026 a0001c0001t0001g0113 a0001c0001t0001g0188 others(1): Show |
5 | HG02622.hp1 HG02818.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.1395+2614A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71749904 | |||||||
| chr4:71749947 | A | C | 1 | a0003c0003t0001g0079 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1395+2571T>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71749947 | |||||||
| chr4:71750116 | A | G | 184 | a0001c0001t0001g0052 a0001c0001t0001g0055 a0001c0001t0001g0069 others(181): Show |
222 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.1395+2402T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71750116 | |||||||
| chr4:71750185 | C | T | 1 | a0001c0005t0003g0128 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1395+2333G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71750185 | |||||||
| chr4:71750292 | T | C | 1 | a0001c0001t0002g0241 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1395+2226A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71750292 | |||||||
| chr4:71750425 | A | G | 7 | a0001c0004t0001g0019 a0001c0004t0001g0020 a0001c0004t0001g0109 others(4): Show |
9 | HG01243.hp2 HG01884.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1395+2093T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71750425 | |||||||
| chr4:71750606 | C | T | 3 | a0002c0002t0001g0142 a0002c0002t0001g0143 a0002c0002t0001g0174 |
3 | HG00280.hp2 HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1395+1912G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71750606 | |||||||
| chr4:71750610 | C | T | 133 | a0001c0001t0002g0301 a0001c0004t0001g0003 a0001c0004t0001g0007 others(130): Show |
164 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.1395+1908G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71750610 | |||||||
| chr4:71750695 | G | A | 4 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0009t0001g0191 others(1): Show |
4 | HG02280.hp2 HG02922.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1395+1823C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71750695 | |||||||
| chr4:71750809 | C | A | 1 | a0001c0001t0002g0275 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1395+1709G>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71750809 | |||||||
| chr4:71750872 | G | C | 41 | a0001c0004t0001g0003 a0001c0004t0001g0007 a0001c0004t0001g0029 others(38): Show |
51 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.1395+1646C>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71750872 | |||||||
| chr4:71750900 | CA | C | 131 | a0001c0001t0001g0013 a0001c0001t0001g0026 a0001c0001t0001g0035 others(128): Show |
156 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(153): Show |
intron_variant | MODIFIER | c.1395+1617delT | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71750900 | |||||||
| chr4:71750900 | CAA | C | 188 | a0001c0001t0001g0052 a0001c0001t0001g0055 a0001c0001t0001g0069 others(185): Show |
226 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(223): Show |
intron_variant | MODIFIER | c.1395+1616_1395+161 others(6): Show |
GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71750900 | |||||||
| chr4:71750901 | A | C | 3 | a0003c0003t0001g0079 a0003c0003t0001g0080 a0003c0003t0001g0152 |
3 | HG01934.hp2 HG01981.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.1395+1617T>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71750901 | |||||||
| chr4:71750912 | G | A | 2 | a0003c0003t0001g0041 a0003c0003t0001g0064 |
2 | NA18947.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.1395+1606C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71750912 | |||||||
| chr4:71750912 | G | C | 19 | a0001c0001t0001g0013 a0001c0001t0001g0036 a0001c0001t0001g0050 others(16): Show |
24 | HG01167.hp1 HG01257.hp1 HG02145.hp1 others(21): Show |
intron_variant | MODIFIER | c.1395+1606C>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71750912 | |||||||
| chr4:71750938 | G | A | 1 | a0001c0001t0002g0324 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1395+1580C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71750938 | |||||||
| chr4:71751007 | T | C | 1 | a0003c0003t0001g0081 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1395+1511A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71751007 | |||||||
| chr4:71751098 | A | G | 1 | a0002c0002t0001g0235 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1395+1420T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71751098 | |||||||
| chr4:71751165 | C | T | 5 | a0001c0001t0002g0008 a0001c0001t0002g0314 a0001c0001t0002g0315 others(2): Show |
8 | HG00639.hp2 HG01257.hp2 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1395+1353G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71751165 | |||||||
| chr4:71751215 | G | A | 133 | a0001c0001t0002g0301 a0001c0004t0001g0003 a0001c0004t0001g0007 others(130): Show |
164 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.1395+1303C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71751215 | |||||||
| chr4:71751247 | G | T | 1 | a0003c0003t0001g0239 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1395+1271C>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71751247 | |||||||
| chr4:71751296 | A | G | 1 | a0002c0002t0002g0251 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1395+1222T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71751296 | |||||||
| chr4:71751421 | C | G | 50 | a0001c0001t0001g0052 a0001c0001t0001g0055 a0001c0001t0001g0069 others(47): Show |
56 | HG00544.hp2 HG00597.hp2 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.1395+1097G>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71751421 | |||||||
| chr4:71751627 | A | G | 2 | a0003c0003t0001g0056 a0003c0003t0001g0070 |
2 | NA18992.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.1395+891T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71751627 | |||||||
| chr4:71751675 | G | C | 4 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0009t0001g0191 others(1): Show |
4 | HG02280.hp2 HG02922.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1395+843C>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71751675 | |||||||
| chr4:71751840 | T | TA | 62 | a0001c0020t0001g0104 a0003c0003t0001g0002 a0003c0003t0001g0004 others(59): Show |
73 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.1395+677dupT | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71751840 | |||||||
| chr4:71752058 | A | G | 63 | a0001c0001t0002g0241 a0003c0003t0001g0002 a0003c0003t0001g0004 others(60): Show |
74 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.1395+460T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71752058 | |||||||
| chr4:71752077 | C | T | 1 | a0001c0001t0002g0303 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1395+441G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71752077 | |||||||
| chr4:71752107 | C | T | 1 | a0001c0001t0002g0303 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1395+411G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71752107 | |||||||
| chr4:71752341 | A | G | 4 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0009t0001g0191 others(1): Show |
4 | HG02280.hp2 HG02922.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1395+177T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71752341 | |||||||
| chr4:71752469 | C | T | 1 | a0001c0001t0002g0253 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1395+49G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71752469 | |||||||
| chr4:71752484 | C | G | 7 | a0001c0001t0001g0026 a0001c0001t0001g0113 a0001c0001t0001g0121 others(4): Show |
8 | HG02622.hp1 HG02630.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1395+34G>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 11/12 | chr4 | 71752484 | |||||||
| chr4:71752890 | T | G | 3 | a0002c0002t0001g0142 a0002c0002t0001g0143 a0002c0002t0001g0174 |
3 | HG00280.hp2 HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1263-240A>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 10/12 | chr4 | 71752890 | |||||||
| chr4:71753029 | CT | C | 7 | a0001c0001t0001g0145 a0001c0001t0001g0148 a0001c0001t0001g0149 others(4): Show |
8 | HG00609.hp2 HG02015.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.1263-380delA | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 10/12 | chr4 | 71753029 | |||||||
| chr4:71753194 | A | T | 1 | a0002c0002t0001g0066 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1263-544T>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 10/12 | chr4 | 71753194 | |||||||
| chr4:71753268 | G | C | 8 | a0001c0001t0001g0050 a0001c0001t0001g0112 a0001c0001t0001g0181 others(5): Show |
11 | HG01257.hp1 HG02809.hp1 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.1263-618C>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 10/12 | chr4 | 71753268 | |||||||
| chr4:71753431 | T | C | 49 | a0001c0001t0002g0253 a0001c0004t0001g0003 a0001c0004t0001g0007 others(46): Show |
61 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.1263-781A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 10/12 | chr4 | 71753431 | |||||||
| chr4:71753448 | G | T | 1 | a0001c0001t0001g0238 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1263-798C>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 10/12 | chr4 | 71753448 | |||||||
| chr4:71753484 | C | CA | 90 | a0001c0001t0001g0035 a0001c0001t0001g0043 a0001c0001t0001g0051 others(87): Show |
108 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.1263-835dupT | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 10/12 | chr4 | 71753484 | |||||||
| chr4:71753484 | CA | C | 9 | a0001c0001t0001g0026 a0001c0001t0001g0113 a0001c0001t0001g0121 others(6): Show |
10 | HG02622.hp1 HG02630.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.1263-835delT | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 10/12 | chr4 | 71753484 | |||||||
| chr4:71753499 | A | G | 11 | a0001c0001t0001g0026 a0001c0001t0001g0113 a0001c0001t0001g0121 others(8): Show |
12 | HG02280.hp2 HG02622.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.1263-849T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 10/12 | chr4 | 71753499 | |||||||
| chr4:71753674 | T | C | 1 | a0001c0001t0001g0121 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1262+737A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 10/12 | chr4 | 71753674 | |||||||
| chr4:71753955 | A | ATAT | 7 | a0001c0001t0001g0026 a0001c0001t0001g0113 a0001c0001t0001g0121 others(4): Show |
8 | HG02622.hp1 HG02630.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1262+453_1262+455d others(5): Show |
GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 10/12 | chr4 | 71753955 | |||||||
| chr4:71753957 | ATTTTTAT others(6): Show |
A | 4 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0009t0001g0191 others(1): Show |
4 | HG02280.hp2 HG02922.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1262+441_1262+453d others(15): Show |
GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 10/12 | chr4 | 71753957 | |||||||
| chr4:71754081 | G | A | 47 | a0001c0004t0001g0003 a0001c0004t0001g0007 a0001c0004t0001g0019 others(44): Show |
59 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.1262+330C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 10/12 | chr4 | 71754081 | |||||||
| chr4:71754279 | A | C | 59 | a0001c0001t0001g0013 a0001c0001t0001g0036 a0001c0001t0001g0050 others(56): Show |
76 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.1262+132T>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 10/12 | chr4 | 71754279 | |||||||
| chr4:71754537 | A | C | 1 | a0001c0001t0001g0240 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1165-29T>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 9/12 | chr4 | 71754537 | |||||||
| chr4:71754597 | T | TCAGTATG others(11): Show |
1 | a0001c0001t0002g0253 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1165-90_1165-89ins others(18): Show |
GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 9/12 | chr4 | 71754597 | |||||||
| chr4:71754831 | TCCCAACA others(8): Show |
T | 1 | a0002c0002t0001g0199 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1164+132_1164+146d others(17): Show |
GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 9/12 | chr4 | 71754831 | |||||||
| chr4:71754840 | T | C | 3 | a0002c0002t0001g0153 a0002c0002t0001g0166 a0002c0002t0001g0175 |
3 | HG00642.hp2 HG01192.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1164+138A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 9/12 | chr4 | 71754840 | |||||||
| chr4:71754860 | C | T | 1 | a0005c0012t0001g0198 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1164+118G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 9/12 | chr4 | 71754860 | |||||||
| chr4:71755148 | C | CTATT | 6 | a0001c0001t0001g0013 a0001c0001t0001g0036 a0001c0001t0001g0138 others(3): Show |
8 | HG02145.hp1 HG02258.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.1035-45_1035-42dup others(4): Show |
GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 8/12 | chr4 | 71755148 | |||||||
| chr4:71755148 | C | CTATTTAT others(1): Show |
148 | a0001c0001t0001g0026 a0001c0001t0001g0083 a0001c0001t0001g0096 others(145): Show |
179 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.1035-49_1035-42dup others(8): Show |
GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 8/12 | chr4 | 71755148 | |||||||
| chr4:71755148 | C | CTATTTAT others(5): Show |
83 | a0001c0001t0001g0043 a0001c0001t0001g0051 a0001c0001t0001g0052 others(80): Show |
98 | HG00544.hp2 HG00597.hp2 HG00609.hp2 others(95): Show |
intron_variant | MODIFIER | c.1035-53_1035-42dup others(12): Show |
GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 8/12 | chr4 | 71755148 | |||||||
| chr4:71755148 | C | CTATTTAT others(9): Show |
30 | a0001c0001t0001g0035 a0001c0001t0001g0050 a0001c0001t0001g0181 others(27): Show |
33 | HG00423.hp1 HG01106.hp2 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.1035-57_1035-42dup others(16): Show |
GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 8/12 | chr4 | 71755148 | |||||||
| chr4:71755148 | C | CTATTTAT others(13): Show |
3 | a0001c0001t0001g0112 a0001c0001t0002g0273 a0001c0001t0002g0306 |
3 | HG03831.hp2 NA18946.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1035-61_1035-42dup others(20): Show |
GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 8/12 | chr4 | 71755148 | |||||||
| chr4:71755222 | G | T | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | NA18951.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.1035-115C>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 8/12 | chr4 | 71755222 | |||||||
| chr4:71755245 | C | G | 1 | a0002c0002t0002g0251 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1035-138G>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 8/12 | chr4 | 71755245 | |||||||
| chr4:71755287 | C | T | 3 | a0003c0003t0001g0098 a0003c0003t0001g0099 a0003c0003t0001g0103 |
3 | HG00140.hp1 HG01358.hp2 HG01928.hp1 |
intron_variant | MODIFIER | c.1035-180G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 8/12 | chr4 | 71755287 | |||||||
| chr4:71755324 | G | A | 7 | a0001c0004t0001g0223 a0001c0004t0001g0224 a0001c0004t0001g0225 others(4): Show |
7 | HG02145.hp2 HG02486.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1035-217C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 8/12 | chr4 | 71755324 | |||||||
| chr4:71755335 | G | A | 2 | a0002c0002t0001g0153 a0002c0002t0001g0175 |
2 | HG00642.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.1035-228C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 8/12 | chr4 | 71755335 | |||||||
| chr4:71755406 | G | A | 1 | a0008c0016t0001g0195 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1035-299C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 8/12 | chr4 | 71755406 | |||||||
| chr4:71755678 | T | C | 1 | a0002c0002t0001g0022 | 2 | HG01496.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.1035-571A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 8/12 | chr4 | 71755678 | |||||||
| chr4:71755753 | T | C | 3 | a0001c0001t0001g0051 a0001c0001t0002g0306 a0001c0001t0002g0307 |
3 | HG02602.hp1 HG03831.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1035-646A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 8/12 | chr4 | 71755753 | |||||||
| chr4:71755790 | G | C | 1 | a0002c0002t0002g0251 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1035-683C>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 8/12 | chr4 | 71755790 | |||||||
| chr4:71755896 | A | G | 318 | a0001c0001t0001g0013 a0001c0001t0001g0026 a0001c0001t0001g0035 others(315): Show |
381 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(378): Show |
intron_variant | MODIFIER | c.1035-789T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 8/12 | chr4 | 71755896 | |||||||
| chr4:71755957 | T | G | 82 | a0002c0002t0001g0005 a0002c0002t0001g0006 a0002c0002t0001g0009 others(79): Show |
101 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.1034+755A>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 8/12 | chr4 | 71755957 | |||||||
| chr4:71755962 | C | T | 61 | a0001c0001t0001g0013 a0001c0001t0001g0036 a0001c0001t0001g0050 others(58): Show |
78 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.1034+750G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 8/12 | chr4 | 71755962 | |||||||
| chr4:71755972 | G | T | 1 | a0004c0006t0001g0180 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1034+740C>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 8/12 | chr4 | 71755972 | |||||||
| chr4:71756014 | T | C | 4 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0009t0001g0191 others(1): Show |
4 | HG02280.hp2 HG02922.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1034+698A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 8/12 | chr4 | 71756014 | |||||||
| chr4:71756039 | A | G | 48 | a0001c0004t0001g0003 a0001c0004t0001g0007 a0001c0004t0001g0019 others(45): Show |
60 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.1034+673T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 8/12 | chr4 | 71756039 | |||||||
| chr4:71756108 | GA | G | 248 | a0001c0001t0001g0035 a0001c0001t0001g0043 a0001c0001t0001g0051 others(245): Show |
293 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.1034+603delT | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 8/12 | chr4 | 71756108 | |||||||
| chr4:71756116 | T | A | 61 | a0001c0001t0001g0013 a0001c0001t0001g0036 a0001c0001t0001g0050 others(58): Show |
78 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.1034+596A>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 8/12 | chr4 | 71756116 | |||||||
| chr4:71756513 | C | A | 1 | a0003c0003t0001g0239 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1034+199G>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 8/12 | chr4 | 71756513 | |||||||
| chr4:71756686 | A | C | 322 | a0001c0001t0001g0013 a0001c0001t0001g0026 a0001c0001t0001g0035 others(319): Show |
385 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(382): Show |
intron_variant | MODIFIER | c.1034+26T>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 8/12 | chr4 | 71756686 | |||||||
| chr4:71756929 | G | T | 1 | a0005c0012t0001g0198 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.832-15C>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 7/12 | chr4 | 71756929 | |||||||
| chr4:71756942 | T | C | 12 | a0001c0001t0002g0242 a0001c0005t0001g0014 a0001c0005t0001g0021 others(9): Show |
15 | HG01243.hp1 HG02109.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.832-28A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 7/12 | chr4 | 71756942 | |||||||
| chr4:71756973 | A | T | 1 | a0002c0002t0001g0159 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.832-59T>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 7/12 | chr4 | 71756973 | |||||||
| chr4:71757047 | G | A | 4 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0009t0001g0191 others(1): Show |
4 | HG02280.hp2 HG02922.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.832-133C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 7/12 | chr4 | 71757047 | |||||||
| chr4:71757074 | C | T | 1 | a0001c0001t0002g0268 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.832-160G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 7/12 | chr4 | 71757074 | |||||||
| chr4:71757200 | A | T | 1 | a0003c0003t0001g0071 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.832-286T>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 7/12 | chr4 | 71757200 | |||||||
| chr4:71757314 | C | A | 2 | a0002c0002t0002g0295 a0002c0002t0002g0296 |
2 | HG00621.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.832-400G>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 7/12 | chr4 | 71757314 | |||||||
| chr4:71757358 | C | T | 10 | a0002c0002t0001g0024 a0002c0002t0001g0025 a0002c0002t0001g0131 others(7): Show |
12 | HG01071.hp1 HG01123.hp1 HG01928.hp2 others(9): Show |
intron_variant | MODIFIER | c.832-444G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 7/12 | chr4 | 71757358 | |||||||
| chr4:71757495 | T | TA | 67 | a0001c0001t0001g0013 a0001c0001t0001g0036 a0001c0001t0001g0050 others(64): Show |
87 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.831+546dupT | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 7/12 | chr4 | 71757495 | |||||||
| chr4:71757552 | G | A | 1 | a0001c0004t0001g0217 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.831+490C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 7/12 | chr4 | 71757552 | |||||||
| chr4:71757607 | A | AATG | 187 | a0001c0001t0001g0026 a0001c0001t0001g0035 a0001c0001t0001g0043 others(184): Show |
220 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.831+432_831+434dup others(3): Show |
GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 7/12 | chr4 | 71757607 | |||||||
| chr4:71757609 | T | TGAC | 68 | a0002c0002t0001g0040 a0002c0002t0001g0074 a0002c0002t0001g0176 others(65): Show |
81 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.831+432_831+433ins others(3): Show |
GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 7/12 | chr4 | 71757609 | |||||||
| chr4:71757630 | A | G | 60 | a0001c0001t0001g0013 a0001c0001t0001g0036 a0001c0001t0001g0050 others(57): Show |
77 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.831+412T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 7/12 | chr4 | 71757630 | |||||||
| chr4:71757667 | G | A | 4 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0009t0001g0191 others(1): Show |
4 | HG02280.hp2 HG02922.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.831+375C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 7/12 | chr4 | 71757667 | |||||||
| chr4:71757915 | C | T | 1 | a0001c0004t0001g0020 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.831+127G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 7/12 | chr4 | 71757915 | |||||||
| chr4:71757936 | C | A | 4 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0009t0001g0191 others(1): Show |
4 | HG02280.hp2 HG02922.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.831+106G>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 7/12 | chr4 | 71757936 | |||||||
| chr4:71758212 | T | C | 4 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0009t0001g0191 others(1): Show |
4 | HG02280.hp2 HG02922.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.702-41A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71758212 | |||||||
| chr4:71758296 | G | A | 1 | a0003c0003t0001g0065 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.702-125C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71758296 | |||||||
| chr4:71758418 | C | T | 54 | a0001c0001t0001g0052 a0001c0001t0001g0055 a0001c0001t0001g0069 others(51): Show |
61 | HG00544.hp2 HG00597.hp2 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.702-247G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71758418 | |||||||
| chr4:71758448 | A | C | 1 | a0001c0004t0001g0020 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.702-277T>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71758448 | |||||||
| chr4:71758553 | T | C | 1 | a0003c0003t0001g0089 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.702-382A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71758553 | |||||||
| chr4:71758624 | A | G | 1 | a0003c0003t0001g0070 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.702-453T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71758624 | |||||||
| chr4:71758784 | T | C | 56 | a0001c0001t0001g0013 a0001c0001t0001g0036 a0001c0001t0001g0050 others(53): Show |
73 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.702-613A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71758784 | |||||||
| chr4:71759013 | C | T | 7 | a0001c0001t0001g0026 a0001c0001t0001g0113 a0001c0001t0001g0121 others(4): Show |
8 | HG02622.hp1 HG02630.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.702-842G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71759013 | |||||||
| chr4:71759035 | T | C | 1 | a0001c0001t0001g0112 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.702-864A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71759035 | |||||||
| chr4:71759071 | A | G | 2 | a0001c0001t0001g0240 a0003c0003t0001g0239 |
2 | HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.702-900T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71759071 | |||||||
| chr4:71759135 | A | G | 2 | a0001c0001t0001g0112 a0001c0011t0002g0032 |
3 | HG02818.hp2 HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.702-964T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71759135 | |||||||
| chr4:71759376 | A | G | 1 | a0001c0020t0001g0104 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.702-1205T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71759376 | |||||||
| chr4:71759380 | A | C | 122 | a0001c0001t0001g0013 a0001c0001t0001g0036 a0001c0001t0001g0050 others(119): Show |
152 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.702-1209T>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71759380 | |||||||
| chr4:71759545 | A | G | 4 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0009t0001g0191 others(1): Show |
4 | HG02280.hp2 HG02922.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.702-1374T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71759545 | |||||||
| chr4:71759626 | A | G | 1 | a0002c0002t0001g0163 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.702-1455T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71759626 | |||||||
| chr4:71759718 | TACC | T | 55 | a0001c0001t0001g0013 a0001c0001t0001g0036 a0001c0001t0001g0050 others(52): Show |
72 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.702-1550_702-1548d others(5): Show |
GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71759718 | |||||||
| chr4:71759759 | C | G | 318 | a0001c0001t0001g0013 a0001c0001t0001g0026 a0001c0001t0001g0035 others(315): Show |
381 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(378): Show |
intron_variant | MODIFIER | c.702-1588G>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71759759 | |||||||
| chr4:71759782 | C | A | 1 | a0003c0003t0001g0084 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.702-1611G>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71759782 | |||||||
| chr4:71760041 | G | GT | 9 | a0001c0001t0001g0237 a0001c0001t0002g0297 a0001c0004t0001g0203 others(6): Show |
10 | HG00408.hp2 HG02258.hp1 NA18943.hp1 others(7): Show |
intron_variant | MODIFIER | c.702-1871dupA | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71760041 | |||||||
| chr4:71760041 | GT | G | 244 | a0001c0001t0001g0026 a0001c0001t0001g0035 a0001c0001t0001g0043 others(241): Show |
290 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.702-1871delA | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71760041 | |||||||
| chr4:71760055 | T | G | 7 | a0002c0002t0001g0040 a0003c0003t0001g0002 a0003c0003t0001g0004 others(4): Show |
16 | HG02083.hp1 HG02165.hp2 NA18941.hp1 others(13): Show |
intron_variant | MODIFIER | c.702-1884A>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71760055 | |||||||
| chr4:71760065 | C | T | 1 | a0001c0001t0002g0242 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.702-1894G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71760065 | |||||||
| chr4:71760183 | A | C | 57 | a0001c0001t0001g0013 a0001c0001t0001g0036 a0001c0001t0001g0050 others(54): Show |
74 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.702-2012T>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71760183 | |||||||
| chr4:71760191 | C | G | 8 | a0002c0002t0001g0015 a0002c0002t0001g0023 a0002c0002t0001g0146 others(5): Show |
11 | HG00408.hp1 HG02074.hp1 NA18940.hp2 others(8): Show |
intron_variant | MODIFIER | c.702-2020G>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71760191 | |||||||
| chr4:71760210 | A | AT | 58 | a0001c0001t0001g0035 a0001c0001t0001g0193 a0001c0001t0001g0194 others(55): Show |
71 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.702-2040dupA | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71760210 | |||||||
| chr4:71760210 | AT | A | 8 | a0001c0001t0001g0026 a0001c0001t0001g0113 a0001c0001t0001g0121 others(5): Show |
9 | HG02622.hp1 HG02630.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.702-2040delA | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71760210 | |||||||
| chr4:71760246 | G | T | 259 | a0001c0001t0001g0026 a0001c0001t0001g0035 a0001c0001t0001g0043 others(256): Show |
305 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.702-2075C>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71760246 | |||||||
| chr4:71760327 | C | A | 252 | a0001c0001t0001g0035 a0001c0001t0001g0043 a0001c0001t0001g0051 others(249): Show |
297 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.702-2156G>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71760327 | |||||||
| chr4:71760371 | C | G | 258 | a0001c0001t0001g0026 a0001c0001t0001g0035 a0001c0001t0001g0043 others(255): Show |
304 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(301): Show |
intron_variant | MODIFIER | c.702-2200G>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71760371 | |||||||
| chr4:71760377 | C | T | 1 | a0002c0002t0001g0154 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.702-2206G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71760377 | |||||||
| chr4:71760386 | A | T | 90 | a0001c0004t0001g0223 a0001c0004t0001g0224 a0001c0004t0001g0225 others(87): Show |
109 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.702-2215T>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71760386 | |||||||
| chr4:71760397 | C | T | 1 | a0001c0001t0001g0035 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.702-2226G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71760397 | |||||||
| chr4:71760423 | T | C | 1 | a0001c0020t0001g0104 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.702-2252A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71760423 | |||||||
| chr4:71760490 | G | A | 1 | a0002c0002t0001g0146 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.702-2319C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71760490 | |||||||
| chr4:71760522 | G | A | 1 | a0001c0020t0001g0104 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.702-2351C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71760522 | |||||||
| chr4:71760713 | G | C | 1 | a0001c0015t0001g0088 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.702-2542C>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71760713 | |||||||
| chr4:71760771 | T | C | 58 | a0001c0001t0001g0026 a0001c0001t0001g0035 a0001c0001t0001g0051 others(55): Show |
70 | HG00597.hp1 HG00621.hp2 HG00639.hp2 others(67): Show |
intron_variant | MODIFIER | c.702-2600A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71760771 | |||||||
| chr4:71760840 | T | C | 2 | a0002c0002t0002g0322 a0002c0002t0002g0323 |
2 | HG01255.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.701+2568A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71760840 | |||||||
| chr4:71760999 | C | T | 7 | a0001c0001t0001g0013 a0001c0001t0001g0138 a0001c0001t0001g0193 others(4): Show |
9 | HG02145.hp1 HG02258.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.701+2409G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71760999 | |||||||
| chr4:71761000 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.701+2408C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71761000 | |||||||
| chr4:71761061 | G | C | 11 | a0001c0001t0001g0036 a0001c0001t0001g0115 a0001c0001t0001g0118 others(8): Show |
13 | HG01109.hp2 HG01243.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.701+2347C>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71761061 | |||||||
| chr4:71761144 | T | A | 16 | a0001c0001t0001g0036 a0001c0001t0001g0115 a0001c0001t0001g0118 others(13): Show |
21 | HG00735.hp2 HG01109.hp2 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.701+2264A>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71761144 | |||||||
| chr4:71761282 | C | T | 22 | a0001c0001t0001g0115 a0001c0001t0001g0118 a0001c0001t0001g0193 others(19): Show |
27 | HG00735.hp2 HG01109.hp2 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.701+2126G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71761282 | |||||||
| chr4:71761411 | G | A | 3 | a0001c0008t0001g0018 a0001c0008t0001g0105 a0001c0020t0001g0104 |
4 | HG01884.hp2 HG02717.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.701+1997C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71761411 | |||||||
| chr4:71761610 | G | A | 11 | a0001c0001t0001g0052 a0001c0001t0002g0262 a0001c0001t0002g0265 others(8): Show |
11 | HG00423.hp1 HG02040.hp2 NA18612.hp2 others(8): Show |
intron_variant | MODIFIER | c.701+1798C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71761610 | |||||||
| chr4:71761967 | A | T | 28 | a0001c0001t0001g0036 a0001c0001t0001g0115 a0001c0001t0001g0118 others(25): Show |
36 | HG00735.hp2 HG01109.hp2 HG01243.hp1 others(33): Show |
intron_variant | MODIFIER | c.701+1441T>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71761967 | |||||||
| chr4:71762026 | C | T | 1 | a0001c0001t0001g0035 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.701+1382G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71762026 | |||||||
| chr4:71762080 | G | C | 148 | a0001c0001t0001g0043 a0001c0001t0001g0055 a0001c0001t0001g0069 others(145): Show |
176 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.701+1328C>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71762080 | |||||||
| chr4:71762092 | A | T | 1 | a0002c0002t0001g0119 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.701+1316T>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71762092 | |||||||
| chr4:71762281 | T | C | 1 | a0001c0004t0001g0228 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.701+1127A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71762281 | |||||||
| chr4:71762286 | C | T | 59 | a0001c0001t0001g0026 a0001c0001t0001g0035 a0001c0001t0001g0051 others(56): Show |
71 | HG00423.hp2 HG00597.hp1 HG00621.hp2 others(68): Show |
intron_variant | MODIFIER | c.701+1122G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71762286 | |||||||
| chr4:71762474 | G | T | 1 | a0001c0005t0001g0130 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.701+934C>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71762474 | |||||||
| chr4:71762506 | A | G | 17 | a0001c0001t0001g0036 a0001c0001t0001g0115 a0001c0001t0001g0118 others(14): Show |
22 | HG00735.hp2 HG01109.hp2 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.701+902T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71762506 | |||||||
| chr4:71762549 | G | A | 1 | a0003c0003t0001g0044 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.701+859C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71762549 | |||||||
| chr4:71762588 | T | C | 1 | a0002c0002t0001g0147 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.701+820A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71762588 | |||||||
| chr4:71762667 | G | A | 1 | a0003c0003t0001g0086 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.701+741C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71762667 | |||||||
| chr4:71762686 | C | A | 2 | a0001c0015t0001g0088 a0003c0003t0001g0087 |
2 | NA18998.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.701+722G>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71762686 | |||||||
| chr4:71762731 | C | T | 1 | a0001c0001t0002g0292 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.701+677G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71762731 | |||||||
| chr4:71762774 | C | T | 11 | a0001c0005t0001g0014 a0001c0005t0001g0021 a0001c0005t0001g0124 others(8): Show |
14 | HG01243.hp1 HG02109.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.701+634G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71762774 | |||||||
| chr4:71762940 | T | G | 1 | a0001c0004t0001g0020 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.701+468A>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71762940 | |||||||
| chr4:71763157 | A | G | 1 | a0001c0001t0001g0036 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.701+251T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71763157 | |||||||
| chr4:71763167 | T | C | 16 | a0001c0001t0001g0115 a0001c0001t0001g0118 a0001c0001t0002g0253 others(13): Show |
21 | HG00735.hp2 HG01109.hp2 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.701+241A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71763167 | |||||||
| chr4:71763169 | T | A | 16 | a0001c0001t0001g0115 a0001c0001t0001g0118 a0001c0001t0002g0253 others(13): Show |
21 | HG00735.hp2 HG01109.hp2 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.701+239A>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71763169 | |||||||
| chr4:71763240 | G | A | 3 | a0001c0008t0001g0018 a0001c0008t0001g0105 a0001c0020t0001g0104 |
4 | HG01884.hp2 HG02717.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.701+168C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71763240 | |||||||
| chr4:71763252 | G | A | 103 | a0001c0001t0001g0013 a0001c0001t0001g0026 a0001c0001t0001g0035 others(100): Show |
120 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(117): Show |
intron_variant | MODIFIER | c.701+156C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71763252 | |||||||
| chr4:71763257 | C | T | 4 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0009t0001g0191 others(1): Show |
4 | HG02280.hp2 HG02922.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.701+151G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 6/12 | chr4 | 71763257 | |||||||
| chr4:71763690 | G | T | 6 | a0001c0001t0002g0246 a0001c0001t0002g0247 a0001c0001t0002g0248 others(3): Show |
6 | HG01106.hp2 HG01943.hp1 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.606+114C>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 5/12 | chr4 | 71763690 | |||||||
| chr4:71763711 | A | G | 3 | a0001c0008t0001g0018 a0001c0008t0001g0105 a0001c0020t0001g0104 |
4 | HG01884.hp2 HG02717.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.606+93T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 5/12 | chr4 | 71763711 | |||||||
| chr4:71763772 | C | T | 1 | a0001c0001t0002g0265 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.606+32G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 5/12 | chr4 | 71763772 | |||||||
| chr4:71763785 | T | A | 2 | a0003c0003t0001g0089 a0003c0003t0001g0102 |
2 | NA18944.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.606+19A>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 5/12 | chr4 | 71763785 | |||||||
| chr4:71763952 | T | C | 2 | a0002c0002t0001g0235 a0002c0002t0001g0236 |
2 | HG00280.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.474-16A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 4/12 | chr4 | 71763952 | |||||||
| chr4:71763960 | G | T | 11 | a0001c0005t0001g0014 a0001c0005t0001g0021 a0001c0005t0001g0124 others(8): Show |
14 | HG01243.hp1 HG02109.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.474-24C>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 4/12 | chr4 | 71763960 | |||||||
| chr4:71764010 | T | A | 1 | a0002c0002t0001g0182 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.474-74A>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 4/12 | chr4 | 71764010 | |||||||
| chr4:71764085 | G | A | 2 | a0001c0004t0001g0220 a0002c0002t0001g0183 |
2 | HG02735.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.474-149C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 4/12 | chr4 | 71764085 | |||||||
| chr4:71764192 | G | A | 1 | a0003c0003t0001g0089 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.474-256C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 4/12 | chr4 | 71764192 | |||||||
| chr4:71764222 | T | C | 11 | a0001c0005t0001g0014 a0001c0005t0001g0021 a0001c0005t0001g0124 others(8): Show |
14 | HG01243.hp1 HG02109.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.474-286A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 4/12 | chr4 | 71764222 | |||||||
| chr4:71764345 | G | A | 1 | a0002c0002t0001g0183 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.474-409C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 4/12 | chr4 | 71764345 | |||||||
| chr4:71764438 | C | T | 1 | a0002c0002t0001g0156 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.474-502G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 4/12 | chr4 | 71764438 | |||||||
| chr4:71764493 | A | C | 6 | a0001c0001t0002g0262 a0001c0001t0002g0265 a0001c0001t0002g0266 others(3): Show |
6 | HG00423.hp1 NA18612.hp2 NA18960.hp1 others(3): Show |
intron_variant | MODIFIER | c.474-557T>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 4/12 | chr4 | 71764493 | |||||||
| chr4:71764508 | G | A | 3 | a0001c0001t0001g0051 a0001c0001t0002g0306 a0001c0001t0002g0307 |
3 | HG02602.hp1 HG03831.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.474-572C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 4/12 | chr4 | 71764508 | |||||||
| chr4:71764680 | T | C | 4 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(1): Show |
4 | HG00423.hp2 NA18954.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.474-744A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 4/12 | chr4 | 71764680 | |||||||
| chr4:71764699 | G | A | 9 | a0001c0001t0001g0013 a0001c0001t0001g0050 a0001c0001t0001g0112 others(6): Show |
13 | HG02145.hp1 HG02258.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.473+733C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 4/12 | chr4 | 71764699 | |||||||
| chr4:71764810 | G | C | 44 | a0001c0001t0001g0013 a0001c0001t0001g0050 a0001c0001t0001g0052 others(41): Show |
49 | HG00423.hp1 HG00544.hp2 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.473+622C>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 4/12 | chr4 | 71764810 | |||||||
| chr4:71764867 | C | T | 11 | a0001c0005t0001g0014 a0001c0005t0001g0021 a0001c0005t0001g0124 others(8): Show |
14 | HG01243.hp1 HG02109.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.473+565G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 4/12 | chr4 | 71764867 | |||||||
| chr4:71764925 | C | A | 59 | a0001c0001t0001g0013 a0001c0001t0001g0036 a0001c0001t0001g0050 others(56): Show |
68 | HG00423.hp1 HG00544.hp2 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.473+507G>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 4/12 | chr4 | 71764925 | |||||||
| chr4:71764936 | T | C | 1 | a0001c0001t0001g0036 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.473+496A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 4/12 | chr4 | 71764936 | |||||||
| chr4:71765258 | G | A | 1 | a0003c0003t0001g0090 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.473+174C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 4/12 | chr4 | 71765258 | |||||||
| chr4:71765831 | T | A | 1 | a0003c0003t0001g0044 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.262-188A>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 3/12 | chr4 | 71765831 | |||||||
| chr4:71765851 | C | A | 1 | a0003c0003t0001g0091 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.262-208G>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 3/12 | chr4 | 71765851 | |||||||
| chr4:71765922 | A | G | 6 | a0001c0001t0001g0050 a0001c0001t0001g0112 a0001c0001t0002g0030 others(3): Show |
8 | HG02809.hp1 HG03209.hp1 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.262-279T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 3/12 | chr4 | 71765922 | |||||||
| chr4:71765951 | G | A | 44 | a0001c0001t0001g0013 a0001c0001t0001g0050 a0001c0001t0001g0052 others(41): Show |
49 | HG00423.hp1 HG00544.hp2 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.262-308C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 3/12 | chr4 | 71765951 | |||||||
| chr4:71766018 | T | C | 282 | a0001c0001t0001g0013 a0001c0001t0001g0026 a0001c0001t0001g0035 others(279): Show |
336 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.262-375A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 3/12 | chr4 | 71766018 | |||||||
| chr4:71766027 | T | C | 223 | a0001c0001t0001g0013 a0001c0001t0001g0036 a0001c0001t0001g0043 others(220): Show |
265 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.262-384A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 3/12 | chr4 | 71766027 | |||||||
| chr4:71766182 | C | A | 17 | a0001c0001t0001g0036 a0001c0001t0001g0115 a0001c0001t0001g0118 others(14): Show |
22 | HG00735.hp2 HG01109.hp2 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.262-539G>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 3/12 | chr4 | 71766182 | |||||||
| chr4:71766190 | G | T | 17 | a0001c0001t0001g0036 a0001c0001t0001g0115 a0001c0001t0001g0118 others(14): Show |
22 | HG00735.hp2 HG01109.hp2 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.262-547C>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 3/12 | chr4 | 71766190 | |||||||
| chr4:71766309 | T | C | 1 | a0003c0003t0001g0092 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.262-666A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 3/12 | chr4 | 71766309 | |||||||
| chr4:71766491 | A | G | 3 | a0001c0001t0001g0013 a0001c0001t0001g0138 a0001c0001t0001g0237 |
5 | HG02145.hp1 HG02258.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.262-848T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 3/12 | chr4 | 71766491 | |||||||
| chr4:71766568 | T | C | 1 | a0002c0002t0001g0117 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.262-925A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 3/12 | chr4 | 71766568 | |||||||
| chr4:71766614 | T | C | 11 | a0001c0005t0001g0014 a0001c0005t0001g0021 a0001c0005t0001g0124 others(8): Show |
14 | HG01243.hp1 HG02109.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.262-971A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 3/12 | chr4 | 71766614 | |||||||
| chr4:71766689 | C | T | 59 | a0001c0001t0001g0026 a0001c0001t0001g0035 a0001c0001t0001g0051 others(56): Show |
71 | HG00423.hp2 HG00597.hp1 HG00621.hp2 others(68): Show |
intron_variant | MODIFIER | c.262-1046G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 3/12 | chr4 | 71766689 | |||||||
| chr4:71766690 | G | A | 44 | a0001c0001t0001g0013 a0001c0001t0001g0050 a0001c0001t0001g0052 others(41): Show |
49 | HG00423.hp1 HG00544.hp2 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.262-1047C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 3/12 | chr4 | 71766690 | |||||||
| chr4:71766794 | C | A | 2 | a0001c0001t0002g0252 a0001c0001t0002g0308 |
2 | HG02965.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.262-1151G>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 3/12 | chr4 | 71766794 | |||||||
| chr4:71766924 | C | T | 3 | a0001c0008t0001g0018 a0001c0008t0001g0105 a0001c0020t0001g0104 |
4 | HG01884.hp2 HG02717.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.262-1281G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 3/12 | chr4 | 71766924 | |||||||
| chr4:71766925 | C | T | 3 | a0003c0003t0001g0098 a0003c0003t0001g0099 a0003c0003t0001g0103 |
3 | HG00140.hp1 HG01358.hp2 HG01928.hp1 |
intron_variant | MODIFIER | c.262-1282G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 3/12 | chr4 | 71766925 | |||||||
| chr4:71766926 | A | G | 265 | a0001c0001t0001g0013 a0001c0001t0001g0026 a0001c0001t0001g0035 others(262): Show |
314 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(311): Show |
intron_variant | MODIFIER | c.262-1283T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 3/12 | chr4 | 71766926 | |||||||
| chr4:71767065 | C | G | 1 | a0003c0003t0001g0060 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.261+1236G>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 3/12 | chr4 | 71767065 | |||||||
| chr4:71767149 | A | T | 11 | a0001c0005t0001g0014 a0001c0005t0001g0021 a0001c0005t0001g0124 others(8): Show |
14 | HG01243.hp1 HG02109.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.261+1152T>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 3/12 | chr4 | 71767149 | |||||||
| chr4:71767214 | C | T | 16 | a0001c0001t0001g0115 a0001c0001t0001g0118 a0001c0001t0002g0253 others(13): Show |
21 | HG00735.hp2 HG01109.hp2 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.261+1087G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 3/12 | chr4 | 71767214 | |||||||
| chr4:71767215 | A | G | 1 | a0002c0002t0001g0155 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.261+1086T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 3/12 | chr4 | 71767215 | |||||||
| chr4:71767255 | G | A | 1 | a0001c0004t0001g0111 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.261+1046C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 3/12 | chr4 | 71767255 | |||||||
| chr4:71767608 | G | GAT | 77 | a0001c0001t0001g0026 a0001c0001t0001g0035 a0001c0001t0001g0036 others(74): Show |
93 | HG00423.hp2 HG00597.hp1 HG00621.hp2 others(90): Show |
intron_variant | MODIFIER | c.261+691_261+692dup others(2): Show |
GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 3/12 | chr4 | 71767608 | |||||||
| chr4:71767647 | G | A | 2 | a0001c0004t0001g0205 a0001c0004t0001g0221 |
2 | NA19000.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.261+654C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 3/12 | chr4 | 71767647 | |||||||
| chr4:71767678 | T | A | 1 | a0001c0001t0001g0036 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.261+623A>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 3/12 | chr4 | 71767678 | |||||||
| chr4:71767696 | A | G | 1 | a0001c0001t0002g0253 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.261+605T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 3/12 | chr4 | 71767696 | |||||||
| chr4:71767714 | T | C | 7 | a0001c0001t0001g0186 a0002c0002t0001g0024 a0002c0002t0001g0025 others(4): Show |
9 | HG01071.hp1 HG01123.hp1 HG01928.hp2 others(6): Show |
intron_variant | MODIFIER | c.261+587A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 3/12 | chr4 | 71767714 | |||||||
| chr4:71767869 | C | A | 4 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0009t0001g0191 others(1): Show |
4 | HG02280.hp2 HG02922.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.261+432G>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 3/12 | chr4 | 71767869 | |||||||
| chr4:71767952 | T | C | 59 | a0001c0001t0001g0026 a0001c0001t0001g0035 a0001c0001t0001g0051 others(56): Show |
71 | HG00423.hp2 HG00597.hp1 HG00621.hp2 others(68): Show |
intron_variant | MODIFIER | c.261+349A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 3/12 | chr4 | 71767952 | |||||||
| chr4:71768055 | T | A | 43 | a0001c0001t0001g0013 a0001c0001t0001g0050 a0001c0001t0001g0052 others(40): Show |
48 | HG00423.hp1 HG00544.hp2 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.261+246A>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 3/12 | chr4 | 71768055 | |||||||
| chr4:71768116 | A | G | 1 | a0002c0002t0001g0153 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.261+185T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 3/12 | chr4 | 71768116 | |||||||
| chr4:71768117 | T | A | 1 | a0001c0001t0001g0237 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.261+184A>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 3/12 | chr4 | 71768117 | |||||||
| chr4:71768491 | C | G | 1 | a0001c0005t0001g0014 | 3 | HG02451.hp2 HG02970.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.129-58G>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 2/12 | chr4 | 71768491 | |||||||
| chr4:71768503 | C | G | 3 | a0003c0003t0001g0041 a0003c0003t0001g0064 a0003c0003t0001g0097 |
3 | NA18947.hp1 NA18988.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.129-70G>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 2/12 | chr4 | 71768503 | |||||||
| chr4:71768559 | C | A | 21 | a0001c0001t0001g0013 a0001c0001t0001g0050 a0001c0001t0001g0112 others(18): Show |
28 | HG01167.hp1 HG01243.hp1 HG02109.hp2 others(25): Show |
intron_variant | MODIFIER | c.129-126G>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 2/12 | chr4 | 71768559 | |||||||
| chr4:71768626 | C | T | 56 | a0001c0001t0001g0035 a0001c0001t0001g0051 a0001c0001t0001g0096 others(53): Show |
67 | HG00423.hp2 HG00597.hp1 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.129-193G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 2/12 | chr4 | 71768626 | |||||||
| chr4:71768666 | A | G | 55 | a0001c0001t0001g0035 a0001c0001t0001g0051 a0001c0001t0001g0096 others(52): Show |
66 | HG00423.hp2 HG00597.hp1 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.129-233T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 2/12 | chr4 | 71768666 | |||||||
| chr4:71768966 | G | A | 1 | a0001c0001t0002g0253 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.128+365C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 2/12 | chr4 | 71768966 | |||||||
| chr4:71769001 | C | T | 1 | a0001c0004t0001g0205 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.128+330G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 2/12 | chr4 | 71769001 | |||||||
| chr4:71769081 | C | T | 1 | a0001c0001t0001g0036 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.128+250G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 2/12 | chr4 | 71769081 | |||||||
| chr4:71769131 | C | A | 1 | a0002c0002t0001g0133 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.128+200G>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 2/12 | chr4 | 71769131 | |||||||
| chr4:71769183 | C | T | 1 | a0001c0001t0002g0242 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.128+148G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 2/12 | chr4 | 71769183 | |||||||
| chr4:71769253 | G | A | 6 | a0001c0001t0001g0050 a0001c0001t0001g0112 a0001c0001t0002g0030 others(3): Show |
8 | HG02809.hp1 HG03209.hp1 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.128+78C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 2/12 | chr4 | 71769253 | |||||||
| chr4:71769258 | G | A | 192 | a0001c0001t0001g0026 a0001c0001t0001g0036 a0001c0001t0001g0043 others(189): Show |
230 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.128+73C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 2/12 | chr4 | 71769258 | |||||||
| chr4:71769645 | C | T | 39 | a0001c0004t0001g0003 a0001c0004t0001g0007 a0001c0004t0001g0029 others(36): Show |
48 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.59-245G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71769645 | |||||||
| chr4:71769646 | G | A | 6 | a0001c0001t0001g0050 a0001c0001t0001g0112 a0001c0001t0002g0030 others(3): Show |
8 | HG02809.hp1 HG03209.hp1 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.59-246C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71769646 | |||||||
| chr4:71769668 | G | A | 3 | a0001c0008t0001g0018 a0001c0008t0001g0105 a0001c0020t0001g0104 |
4 | HG01884.hp2 HG02717.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.59-268C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71769668 | |||||||
| chr4:71769766 | C | A | 1 | a0001c0004t0001g0222 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.59-366G>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71769766 | |||||||
| chr4:71769795 | A | T | 305 | a0001c0001t0001g0013 a0001c0001t0001g0026 a0001c0001t0001g0035 others(302): Show |
363 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(360): Show |
intron_variant | MODIFIER | c.59-395T>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71769795 | |||||||
| chr4:71769844 | A | G | 1 | a0003c0003t0001g0152 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.59-444T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71769844 | |||||||
| chr4:71769978 | TTCAGCTG others(76): Show |
T | 1 | a0001c0001t0002g0318 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.59-661_59-579delGG others(81): Show |
GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71769978 | |||||||
| chr4:71770042 | G | C | 34 | a0001c0001t0001g0052 a0001c0001t0001g0196 a0001c0001t0002g0033 others(31): Show |
35 | HG00423.hp1 HG00544.hp2 HG00597.hp2 others(32): Show |
intron_variant | MODIFIER | c.59-642C>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71770042 | |||||||
| chr4:71770063 | T | G | 1 | a0001c0001t0002g0318 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.59-663A>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71770063 | |||||||
| chr4:71770222 | G | A | 1 | a0001c0001t0001g0036 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.59-822C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71770222 | |||||||
| chr4:71770440 | A | G | 3 | a0001c0001t0002g0241 a0001c0005t0001g0124 a0001c0005t0001g0125 |
3 | HG01167.hp1 HG01243.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.59-1040T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71770440 | |||||||
| chr4:71770555 | C | T | 192 | a0001c0001t0001g0026 a0001c0001t0001g0036 a0001c0001t0001g0043 others(189): Show |
230 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.59-1155G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71770555 | |||||||
| chr4:71770570 | GC | G | 3 | a0001c0001t0001g0013 a0001c0001t0001g0138 a0001c0001t0001g0237 |
5 | HG02145.hp1 HG02258.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.59-1171delG | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71770570 | |||||||
| chr4:71770589 | T | G | 1 | a0002c0002t0001g0134 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.59-1189A>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71770589 | |||||||
| chr4:71770907 | G | A | 33 | a0001c0001t0001g0052 a0001c0001t0001g0196 a0001c0001t0002g0033 others(30): Show |
34 | HG00423.hp1 HG00544.hp2 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.59-1507C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71770907 | |||||||
| chr4:71771260 | T | C | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | NA18951.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.59-1860A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71771260 | |||||||
| chr4:71771335 | A | AT | 33 | a0001c0001t0001g0052 a0001c0001t0001g0196 a0001c0001t0002g0033 others(30): Show |
34 | HG00423.hp1 HG00544.hp2 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.59-1936dupA | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71771335 | |||||||
| chr4:71771363 | A | G | 207 | a0001c0001t0001g0026 a0001c0001t0001g0043 a0001c0001t0001g0055 others(204): Show |
250 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.59-1963T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71771363 | |||||||
| chr4:71771627 | C | T | 9 | a0001c0001t0001g0050 a0001c0001t0001g0112 a0001c0001t0002g0030 others(6): Show |
11 | HG01167.hp1 HG01243.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.59-2227G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71771627 | |||||||
| chr4:71771833 | T | C | 1 | a0001c0001t0001g0036 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.59-2433A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71771833 | |||||||
| chr4:71772397 | C | T | 1 | a0003c0003t0001g0139 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.59-2997G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71772397 | |||||||
| chr4:71772467 | A | G | 3 | a0001c0004t0001g0007 a0001c0004t0001g0203 a0001c0004t0001g0204 |
6 | HG00438.hp2 NA18988.hp1 NA18989.hp2 others(3): Show |
intron_variant | MODIFIER | c.59-3067T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71772467 | |||||||
| chr4:71772797 | T | A | 3 | a0001c0001t0002g0241 a0001c0005t0001g0124 a0001c0005t0001g0125 |
3 | HG01167.hp1 HG01243.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.59-3397A>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71772797 | |||||||
| chr4:71773029 | T | A | 1 | a0002c0002t0001g0187 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.59-3629A>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71773029 | |||||||
| chr4:71773085 | T | C | 1 | a0001c0004t0001g0232 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.59-3685A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71773085 | |||||||
| chr4:71773107 | C | A | 58 | a0001c0001t0001g0035 a0001c0001t0001g0051 a0001c0001t0001g0096 others(55): Show |
70 | HG00423.hp2 HG00597.hp1 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.59-3707G>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71773107 | |||||||
| chr4:71773107 | C | T | 4 | a0001c0001t0002g0033 a0001c0001t0002g0254 a0001c0001t0002g0263 others(1): Show |
5 | HG00597.hp2 HG00609.hp2 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.59-3707G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71773107 | |||||||
| chr4:71773108 | G | T | 9 | a0001c0005t0001g0014 a0001c0005t0001g0021 a0001c0005t0001g0126 others(6): Show |
12 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.59-3708C>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71773108 | |||||||
| chr4:71773285 | G | A | 12 | a0001c0001t0001g0013 a0001c0001t0001g0138 a0001c0001t0001g0237 others(9): Show |
17 | HG02109.hp2 HG02145.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.59-3885C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71773285 | |||||||
| chr4:71773302 | T | A | 1 | a0001c0001t0002g0276 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.59-3902A>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71773302 | |||||||
| chr4:71773337 | A | T | 1 | a0001c0001t0002g0262 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.59-3937T>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71773337 | |||||||
| chr4:71773343 | A | T | 1 | a0001c0001t0002g0261 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.59-3943T>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71773343 | |||||||
| chr4:71773485 | A | G | 1 | a0001c0001t0001g0144 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.59-4085T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71773485 | |||||||
| chr4:71773490 | T | G | 1 | a0003c0003t0001g0093 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.59-4090A>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71773490 | |||||||
| chr4:71773565 | C | T | 69 | a0001c0001t0001g0043 a0001c0001t0001g0055 a0001c0001t0001g0069 others(66): Show |
84 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.59-4165G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71773565 | |||||||
| chr4:71773673 | C | T | 1 | a0003c0003t0001g0139 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.59-4273G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71773673 | |||||||
| chr4:71773674 | G | A | 9 | a0001c0001t0001g0050 a0001c0001t0001g0112 a0001c0001t0002g0030 others(6): Show |
11 | HG01167.hp1 HG01243.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.59-4274C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71773674 | |||||||
| chr4:71773767 | A | G | 1 | a0001c0020t0001g0104 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.59-4367T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71773767 | |||||||
| chr4:71773872 | C | T | 4 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0009t0001g0191 others(1): Show |
4 | HG02280.hp2 HG02922.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-4472G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71773872 | |||||||
| chr4:71774028 | G | T | 4 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0009t0001g0191 others(1): Show |
4 | HG02280.hp2 HG02922.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-4628C>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71774028 | |||||||
| chr4:71774226 | G | A | 2 | a0001c0001t0001g0121 a0001c0001t0002g0289 |
2 | HG02630.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.59-4826C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71774226 | |||||||
| chr4:71774255 | A | C | 4 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0009t0001g0191 others(1): Show |
4 | HG02280.hp2 HG02922.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-4855T>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71774255 | |||||||
| chr4:71774426 | A | C | 1 | a0001c0005t0001g0014 | 3 | HG02451.hp2 HG02970.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.59-5026T>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71774426 | |||||||
| chr4:71774432 | T | C | 321 | a0001c0001t0001g0013 a0001c0001t0001g0026 a0001c0001t0001g0035 others(318): Show |
384 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(381): Show |
intron_variant | MODIFIER | c.59-5032A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71774432 | |||||||
| chr4:71774507 | A | AG | 69 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0148 others(66): Show |
82 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.59-5108dupC | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71774507 | |||||||
| chr4:71774681 | T | A | 1 | a0001c0001t0002g0277 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.59-5281A>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71774681 | |||||||
| chr4:71774726 | T | G | 16 | a0001c0001t0001g0115 a0001c0001t0001g0118 a0001c0001t0002g0253 others(13): Show |
21 | HG00735.hp2 HG01109.hp2 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.59-5326A>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71774726 | |||||||
| chr4:71774859 | AC | A | 9 | a0001c0005t0001g0014 a0001c0005t0001g0021 a0001c0005t0001g0126 others(6): Show |
12 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.59-5460delG | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71774859 | |||||||
| chr4:71774861 | T | A | 9 | a0001c0005t0001g0014 a0001c0005t0001g0021 a0001c0005t0001g0126 others(6): Show |
12 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.59-5461A>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71774861 | |||||||
| chr4:71774927 | T | C | 1 | a0003c0003t0001g0095 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.59-5527A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71774927 | |||||||
| chr4:71774992 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.59-5592C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71774992 | |||||||
| chr4:71775032 | CT | C | 288 | a0001c0001t0001g0013 a0001c0001t0001g0026 a0001c0001t0001g0035 others(285): Show |
345 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(342): Show |
intron_variant | MODIFIER | c.59-5633delA | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71775032 | |||||||
| chr4:71775032 | CTT | C | 9 | a0001c0001t0001g0036 a0001c0001t0001g0202 a0001c0001t0002g0277 others(6): Show |
10 | HG03540.hp2 NA18963.hp1 NA18969.hp1 others(7): Show |
intron_variant | MODIFIER | c.59-5634_59-5633del others(2): Show |
GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71775032 | |||||||
| chr4:71775033 | T | C | 16 | a0001c0001t0001g0115 a0001c0001t0001g0118 a0001c0004t0001g0020 others(13): Show |
20 | HG00735.hp2 HG01243.hp2 HG01515.hp1 others(17): Show |
intron_variant | MODIFIER | c.59-5633A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71775033 | |||||||
| chr4:71775034 | T | C | 71 | a0001c0001t0001g0043 a0001c0001t0001g0055 a0001c0001t0001g0069 others(68): Show |
86 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.59-5634A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71775034 | |||||||
| chr4:71775119 | C | T | 7 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0148 others(4): Show |
9 | HG03834.hp1 NA18950.hp1 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.59-5719G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71775119 | |||||||
| chr4:71775155 | T | C | 1 | a0003c0003t0002g0287 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.59-5755A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71775155 | |||||||
| chr4:71775261 | T | A | 1 | a0001c0001t0002g0278 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.59-5861A>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71775261 | |||||||
| chr4:71775557 | A | AAACATAG others(45): Show |
1 | a0001c0001t0002g0324 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.59-6209_59-6158dup others(52): Show |
GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71775557 | |||||||
| chr4:71775559 | A | C | 1 | a0001c0001t0002g0257 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.59-6159T>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71775559 | |||||||
| chr4:71775562 | T | C | 15 | a0001c0001t0001g0115 a0001c0001t0001g0118 a0001c0004t0001g0019 others(12): Show |
20 | HG00735.hp2 HG01243.hp2 HG01515.hp1 others(17): Show |
intron_variant | MODIFIER | c.59-6162A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71775562 | |||||||
| chr4:71775647 | G | T | 1 | a0001c0001t0002g0256 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.59-6247C>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71775647 | |||||||
| chr4:71775701 | A | G | 1 | a0001c0001t0002g0253 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.59-6301T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71775701 | |||||||
| chr4:71775789 | A | G | 58 | a0001c0001t0001g0035 a0001c0001t0001g0051 a0001c0001t0001g0096 others(55): Show |
70 | HG00423.hp2 HG00597.hp1 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.59-6389T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71775789 | |||||||
| chr4:71775824 | G | A | 1 | a0001c0001t0002g0310 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.59-6424C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71775824 | |||||||
| chr4:71776331 | A | G | 9 | a0001c0005t0001g0014 a0001c0005t0001g0021 a0001c0005t0001g0126 others(6): Show |
12 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.59-6931T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71776331 | |||||||
| chr4:71776451 | A | G | 1 | a0001c0001t0002g0253 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.59-7051T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71776451 | |||||||
| chr4:71776586 | G | A | 2 | a0001c0001t0002g0280 a0001c0001t0002g0281 |
2 | NA18960.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.59-7186C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71776586 | |||||||
| chr4:71776650 | C | T | 1 | a0002c0002t0001g0236 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.59-7250G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71776650 | |||||||
| chr4:71776718 | A | G | 2 | a0002c0002t0001g0142 a0002c0002t0001g0143 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.58+7243T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71776718 | |||||||
| chr4:71776766 | T | C | 1 | a0003c0003t0001g0139 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.58+7195A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71776766 | |||||||
| chr4:71776931 | T | C | 33 | a0001c0001t0001g0052 a0001c0001t0001g0196 a0001c0001t0002g0033 others(30): Show |
34 | HG00423.hp1 HG00544.hp2 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.58+7030A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71776931 | |||||||
| chr4:71777237 | T | C | 16 | a0001c0001t0001g0115 a0001c0001t0001g0118 a0001c0001t0002g0253 others(13): Show |
21 | HG00735.hp2 HG01109.hp2 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.58+6724A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71777237 | |||||||
| chr4:71777313 | C | G | 1 | a0001c0001t0002g0255 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.58+6648G>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71777313 | |||||||
| chr4:71777380 | C | T | 1 | a0002c0002t0001g0059 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.58+6581G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71777380 | |||||||
| chr4:71777762 | AT | A | 9 | a0001c0004t0001g0223 a0001c0004t0001g0224 a0001c0004t0001g0225 others(6): Show |
9 | HG02145.hp2 HG02280.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.58+6198delA | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71777762 | |||||||
| chr4:71777771 | T | C | 77 | a0001c0001t0001g0043 a0001c0001t0001g0055 a0001c0001t0001g0069 others(74): Show |
93 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.58+6190A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71777771 | |||||||
| chr4:71777806 | T | G | 1 | a0001c0001t0001g0202 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.58+6155A>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71777806 | |||||||
| chr4:71777830 | G | A | 1 | a0002c0002t0002g0251 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.58+6131C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71777830 | |||||||
| chr4:71777847 | G | A | 3 | a0001c0001t0002g0241 a0001c0005t0001g0124 a0001c0005t0001g0125 |
3 | HG01167.hp1 HG01243.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.58+6114C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71777847 | |||||||
| chr4:71777876 | G | C | 1 | a0001c0001t0002g0279 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.58+6085C>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71777876 | |||||||
| chr4:71778041 | T | A | 1 | a0002c0002t0002g0251 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.58+5920A>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71778041 | |||||||
| chr4:71778041 | TA | T | 64 | a0001c0001t0001g0035 a0001c0001t0001g0050 a0001c0001t0001g0051 others(61): Show |
77 | HG00423.hp2 HG00597.hp1 HG00621.hp2 others(74): Show |
intron_variant | MODIFIER | c.58+5919delT | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71778041 | |||||||
| chr4:71778043 | A | T | 191 | a0001c0001t0001g0026 a0001c0001t0001g0043 a0001c0001t0001g0055 others(188): Show |
229 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.58+5918T>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71778043 | |||||||
| chr4:71778075 | C | T | 1 | a0001c0001t0002g0254 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.58+5886G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71778075 | |||||||
| chr4:71778319 | T | C | 9 | a0001c0001t0001g0050 a0001c0001t0001g0112 a0001c0001t0002g0030 others(6): Show |
11 | HG01167.hp1 HG01243.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.58+5642A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71778319 | |||||||
| chr4:71778580 | A | G | 16 | a0001c0001t0001g0115 a0001c0001t0001g0118 a0001c0001t0002g0253 others(13): Show |
21 | HG00735.hp2 HG01109.hp2 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.58+5381T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71778580 | |||||||
| chr4:71778886 | T | C | 319 | a0001c0001t0001g0013 a0001c0001t0001g0026 a0001c0001t0001g0035 others(316): Show |
382 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(379): Show |
intron_variant | MODIFIER | c.58+5075A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71778886 | |||||||
| chr4:71778887 | G | A | 33 | a0001c0001t0001g0052 a0001c0001t0001g0196 a0001c0001t0002g0033 others(30): Show |
34 | HG00423.hp1 HG00544.hp2 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.58+5074C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71778887 | |||||||
| chr4:71778891 | G | GTTA | 41 | a0001c0001t0001g0052 a0001c0001t0001g0112 a0001c0001t0001g0196 others(38): Show |
46 | HG00423.hp1 HG00544.hp2 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.58+5067_58+5069dup others(3): Show |
GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71778891 | |||||||
| chr4:71778891 | G | GTTATTA | 53 | a0001c0001t0001g0013 a0001c0001t0001g0035 a0001c0001t0001g0051 others(50): Show |
65 | HG00423.hp2 HG00597.hp1 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.58+5064_58+5069dup others(6): Show |
GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71778891 | |||||||
| chr4:71778891 | G | GTTATTAT others(2): Show |
47 | a0001c0001t0001g0036 a0001c0001t0002g0008 a0001c0001t0002g0252 others(44): Show |
59 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.58+5061_58+5069dup others(9): Show |
GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71778891 | |||||||
| chr4:71778891 | G | GTTATTAT others(5): Show |
14 | a0001c0001t0002g0321 a0001c0004t0001g0230 a0001c0004t0001g0231 others(11): Show |
16 | HG01243.hp1 HG01884.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.58+5058_58+5069dup others(12): Show |
GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71778891 | |||||||
| chr4:71778891 | G | GTTATTGT others(2): Show |
74 | a0001c0001t0001g0026 a0001c0001t0001g0055 a0001c0001t0001g0144 others(71): Show |
85 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.58+5069_58+5070ins others(9): Show |
GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71778891 | |||||||
| chr4:71778891 | G | GTTATTGT others(5): Show |
62 | a0001c0001t0001g0043 a0001c0001t0001g0069 a0001c0001t0001g0083 others(59): Show |
78 | HG00438.hp1 HG00558.hp1 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.58+5069_58+5070ins others(12): Show |
GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71778891 | |||||||
| chr4:71778891 | G | GTTATTGT others(8): Show |
9 | a0002c0002t0001g0027 a0002c0002t0002g0251 a0003c0003t0001g0047 others(6): Show |
10 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.58+5069_58+5070ins others(15): Show |
GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71778891 | |||||||
| chr4:71778891 | G | GTTATTGT others(11): Show |
1 | a0003c0003t0001g0103 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.58+5069_58+5070ins others(18): Show |
GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71778891 | |||||||
| chr4:71778921 | ATTG | A | 8 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0002g0241 others(5): Show |
9 | HG01167.hp1 HG01884.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.58+5037_58+5039del others(3): Show |
GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71778921 | |||||||
| chr4:71778924 | G | A | 311 | a0001c0001t0001g0013 a0001c0001t0001g0026 a0001c0001t0001g0035 others(308): Show |
373 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(370): Show |
intron_variant | MODIFIER | c.58+5037C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71778924 | |||||||
| chr4:71779141 | A | G | 38 | a0001c0001t0001g0052 a0001c0001t0001g0193 a0001c0001t0001g0194 others(35): Show |
39 | HG00423.hp1 HG00544.hp2 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.58+4820T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71779141 | |||||||
| chr4:71779245 | G | A | 228 | a0001c0001t0001g0026 a0001c0001t0001g0043 a0001c0001t0001g0052 others(225): Show |
267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.58+4716C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71779245 | |||||||
| chr4:71779540 | A | C | 4 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0009t0001g0191 others(1): Show |
4 | HG02280.hp2 HG02922.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.58+4421T>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71779540 | |||||||
| chr4:71779569 | G | A | 51 | a0001c0001t0001g0121 a0001c0001t0002g0001 a0001c0001t0002g0008 others(48): Show |
62 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.58+4392C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71779569 | |||||||
| chr4:71779760 | A | G | 1 | a0003c0003t0001g0049 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.58+4201T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71779760 | |||||||
| chr4:71779945 | A | T | 1 | a0002c0002t0001g0140 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.58+4016T>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71779945 | |||||||
| chr4:71780021 | C | G | 1 | a0003c0003t0003g0048 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.58+3940G>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71780021 | |||||||
| chr4:71780089 | G | A | 92 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0030 others(89): Show |
106 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.58+3872C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71780089 | |||||||
| chr4:71780170 | T | C | 4 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0009t0001g0191 others(1): Show |
4 | HG02280.hp2 HG02922.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.58+3791A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71780170 | |||||||
| chr4:71780423 | A | G | 92 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0030 others(89): Show |
106 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.58+3538T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71780423 | |||||||
| chr4:71780537 | G | GAA | 48 | a0001c0001t0001g0196 a0001c0001t0001g0200 a0001c0001t0001g0201 others(45): Show |
57 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.58+3422_58+3423dup others(2): Show |
GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71780537 | |||||||
| chr4:71780693 | T | A | 1 | a0001c0001t0002g0324 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.58+3268A>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71780693 | |||||||
| chr4:71780724 | G | A | 54 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0246 others(51): Show |
65 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.58+3237C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71780724 | |||||||
| chr4:71780739 | G | C | 1 | a0001c0001t0002g0324 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.58+3222C>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71780739 | |||||||
| chr4:71780752 | T | A | 1 | a0001c0001t0002g0324 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.58+3209A>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71780752 | |||||||
| chr4:71780754 | T | A | 1 | a0001c0001t0002g0324 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.58+3207A>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71780754 | |||||||
| chr4:71780765 | G | A | 1 | a0001c0001t0002g0324 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.58+3196C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71780765 | |||||||
| chr4:71780767 | A | G | 1 | a0001c0001t0002g0324 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.58+3194T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71780767 | |||||||
| chr4:71780773 | C | G | 1 | a0001c0001t0002g0324 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.58+3188G>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71780773 | |||||||
| chr4:71780774 | T | G | 1 | a0001c0001t0002g0324 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.58+3187A>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71780774 | |||||||
| chr4:71780776 | C | G | 1 | a0001c0001t0002g0324 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.58+3185G>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71780776 | |||||||
| chr4:71780779 | T | A | 1 | a0001c0001t0002g0324 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.58+3182A>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71780779 | |||||||
| chr4:71780785 | T | A | 1 | a0001c0001t0002g0324 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.58+3176A>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71780785 | |||||||
| chr4:71780787 | G | A | 1 | a0001c0001t0002g0324 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.58+3174C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71780787 | |||||||
| chr4:71780788 | G | C | 1 | a0001c0001t0002g0324 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.58+3173C>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71780788 | |||||||
| chr4:71780794 | A | C | 1 | a0001c0001t0002g0324 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.58+3167T>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71780794 | |||||||
| chr4:71780799 | A | G | 1 | a0001c0001t0002g0324 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.58+3162T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71780799 | |||||||
| chr4:71780807 | C | T | 1 | a0001c0001t0002g0324 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.58+3154G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71780807 | |||||||
| chr4:71780821 | G | A | 8 | a0001c0005t0001g0021 a0001c0005t0001g0124 a0001c0005t0001g0125 others(5): Show |
9 | HG01243.hp1 HG02486.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.58+3140C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71780821 | |||||||
| chr4:71780829 | A | C | 1 | a0003c0003t0001g0047 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.58+3132T>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71780829 | |||||||
| chr4:71780844 | AGAACTGG others(11): Show |
A | 1 | a0001c0001t0002g0324 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.58+3099_58+3116del others(18): Show |
GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71780844 | |||||||
| chr4:71780876 | T | C | 317 | a0001c0001t0001g0026 a0001c0001t0001g0035 a0001c0001t0001g0036 others(314): Show |
378 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(375): Show |
intron_variant | MODIFIER | c.58+3085A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71780876 | |||||||
| chr4:71781008 | G | A | 202 | a0001c0001t0001g0026 a0001c0001t0001g0035 a0001c0001t0001g0036 others(199): Show |
243 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.58+2953C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71781008 | |||||||
| chr4:71781042 | A | G | 1 | a0002c0002t0001g0136 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.58+2919T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71781042 | |||||||
| chr4:71781046 | T | C | 49 | a0001c0001t0001g0196 a0001c0001t0001g0200 a0001c0001t0001g0201 others(46): Show |
58 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.58+2915A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71781046 | |||||||
| chr4:71781090 | A | G | 5 | a0002c0002t0001g0131 a0002c0002t0001g0133 a0002c0002t0001g0134 others(2): Show |
5 | NA18972.hp1 NA18982.hp2 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.58+2871T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71781090 | |||||||
| chr4:71781151 | C | T | 1 | a0001c0001t0002g0252 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.58+2810G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71781151 | |||||||
| chr4:71781290 | C | T | 1 | a0002c0002t0001g0046 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.58+2671G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71781290 | |||||||
| chr4:71781410 | C | A | 2 | a0002c0002t0001g0235 a0002c0002t0001g0236 |
2 | HG00280.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.58+2551G>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71781410 | |||||||
| chr4:71781410 | C | T | 1 | a0002c0002t0002g0251 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.58+2551G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71781410 | |||||||
| chr4:71781428 | A | G | 2 | a0001c0004t0002g0250 a0001c0011t0002g0032 |
3 | HG02818.hp2 HG03209.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.58+2533T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71781428 | |||||||
| chr4:71781475 | T | A | 1 | a0001c0001t0001g0237 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.58+2486A>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71781475 | |||||||
| chr4:71781718 | G | C | 1 | a0001c0001t0001g0238 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.58+2243C>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71781718 | |||||||
| chr4:71781871 | C | G | 1 | a0003c0003t0001g0045 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.58+2090G>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71781871 | |||||||
| chr4:71781925 | A | G | 5 | a0001c0001t0002g0246 a0001c0001t0002g0247 a0001c0001t0002g0248 others(2): Show |
5 | HG01106.hp2 HG01943.hp1 HG02080.hp1 others(2): Show |
intron_variant | MODIFIER | c.58+2036T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71781925 | |||||||
| chr4:71782031 | A | T | 1 | a0001c0001t0002g0241 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.58+1930T>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71782031 | |||||||
| chr4:71782032 | C | T | 22 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0115 others(19): Show |
28 | HG00735.hp2 HG01243.hp2 HG01358.hp1 others(25): Show |
intron_variant | MODIFIER | c.58+1929G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71782032 | |||||||
| chr4:71782045 | A | G | 115 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0115 others(112): Show |
135 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(132): Show |
intron_variant | MODIFIER | c.58+1916T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71782045 | |||||||
| chr4:71782283 | T | G | 1 | a0001c0004t0001g0020 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.58+1678A>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71782283 | |||||||
| chr4:71782288 | A | G | 5 | a0001c0001t0002g0030 a0001c0001t0002g0031 a0001c0001t0002g0242 others(2): Show |
7 | HG02109.hp2 HG02809.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.58+1673T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71782288 | |||||||
| chr4:71782304 | C | T | 1 | a0001c0001t0002g0241 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.58+1657G>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71782304 | |||||||
| chr4:71782571 | A | G | 2 | a0001c0005t0001g0124 a0001c0005t0001g0125 |
2 | HG01243.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.58+1390T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71782571 | |||||||
| chr4:71782723 | T | G | 1 | a0003c0003t0001g0239 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.58+1238A>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71782723 | |||||||
| chr4:71782739 | G | T | 1 | a0001c0005t0001g0124 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.58+1222C>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71782739 | |||||||
| chr4:71782843 | TGGCCTAT others(5): Show |
T | 6 | a0001c0001t0001g0043 a0002c0002t0001g0040 a0002c0002t0001g0042 others(3): Show |
10 | NA18941.hp1 NA18943.hp2 NA18950.hp2 others(7): Show |
intron_variant | MODIFIER | c.58+1106_58+1117del others(12): Show |
GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71782843 | |||||||
| chr4:71782848 | T | C | 1 | a0002c0002t0001g0005 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.58+1113A>G | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71782848 | |||||||
| chr4:71783006 | A | G | 8 | a0001c0005t0001g0021 a0001c0005t0001g0124 a0001c0005t0001g0125 others(5): Show |
9 | HG01243.hp1 HG02486.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.58+955T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71783006 | |||||||
| chr4:71783134 | A | G | 115 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0115 others(112): Show |
135 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(132): Show |
intron_variant | MODIFIER | c.58+827T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71783134 | |||||||
| chr4:71783215 | C | A | 1 | a0001c0001t0001g0240 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.58+746G>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71783215 | |||||||
| chr4:71783222 | A | G | 3 | a0003c0003t0001g0037 a0003c0003t0001g0038 a0003c0003t0001g0039 |
3 | HG00642.hp1 HG00741.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.58+739T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71783222 | |||||||
| chr4:71783331 | A | G | 74 | a0001c0001t0001g0043 a0001c0001t0001g0050 a0001c0001t0001g0051 others(71): Show |
90 | HG00140.hp1 HG00544.hp1 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.58+630T>C | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71783331 | |||||||
| chr4:71783345 | A | T | 2 | a0001c0001t0001g0035 a0001c0001t0001g0036 |
2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.58+616T>A | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71783345 | |||||||
| chr4:71783682 | G | A | 1 | a0002c0002t0002g0325 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.58+279C>T | GC | ENSG00000145321.13 | transcript | ENST00000273951.13 | protein_coding | 1/12 | chr4 | 71783682 |