Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 5225 |
| ensemblid | ENSG00000096088.16 |
| hgncid | 8890 |
| symbol | PGC |
| name | progastricsin |
| refseq_nuc | NM_002630.4 |
| refseq_prot | NP_002621.1 |
| ensembl_nuc | ENST00000373025.7 |
| ensembl_prot | ENSP00000362116.3 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 41736711 |
| end | 41747397 |
| strand | - |
| ver | v1.2 |
| region | chr6:41736711-41747397 |
| region5000 | chr6:41731711-41752397 |
| regionname0 | PGC_chr6_41736711_41747397 |
| regionname5000 | PGC_chr6_41731711_41752397 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 388 | 458 | 97 | 84 | 207 | 18 | 50 | 157 | PGC_chr6_41731711_41752397 | PGC | MKWMV others(383): Show |
chr6 | 41731711 | 41752397 |
| a0002 | 0/0 | 388 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | MKWMV others(383): Show |
chr6 | 41731711 | 41752397 |
| a0003 | 0/0 | 166 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | MKWMV others(161): Show |
chr6 | 41731711 | 41752397 |
| a0004 | 0/0 | 388 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PGC_chr6_41731711_41752397 | PGC | MKWMV others(383): Show |
chr6 | 41731711 | 41752397 |
| a0005 | 0/0 | 388 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | MKWMV others(383): Show |
chr6 | 41731711 | 41752397 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1164 | 451 | 91 | 84 | 206 | 18 | 50 | PGC_chr6_41731711_41752397 | PGC | ATGAA others(1159): Show |
chr6 | 41731711 | 41752397 | ||
| a0001c0002 | 0/0 | 1164 | 5 | 5 | 0 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | ATGAA others(1159): Show |
chr6 | 41731711 | 41752397 | ||
| a0001c0007 | 0/0 | 1164 | 1 | 0 | 0 | 1 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | ATGAA others(1159): Show |
chr6 | 41731711 | 41752397 | ||
| a0001c0008 | 0/0 | 1164 | 1 | 1 | 0 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | ATGAA others(1159): Show |
chr6 | 41731711 | 41752397 | ||
| a0002c0003 | 0/0 | 1164 | 3 | 2 | 1 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | ATGAA others(1159): Show |
chr6 | 41731711 | 41752397 | ||
| a0003c0005 | 0/0 | 1174 | 1 | 0 | 1 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | ATGAA others(1169): Show |
chr6 | 41731711 | 41752397 | ||
| a0004c0006 | 0/0 | 1164 | 1 | 0 | 0 | 1 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | ATGAA others(1159): Show |
chr6 | 41731711 | 41752397 | ||
| a0005c0004 | 0/0 | 1164 | 1 | 1 | 0 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | ATGAA others(1159): Show |
chr6 | 41731711 | 41752397 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1371 | 444 | 88 | 83 | 206 | 17 | 48 | PGC_chr6_41731711_41752397 | PGC | ACTCC others(1366): Show |
chr6 | 41731711 | 41752397 |
| a0001c0001t0002 | 0/0 | 1371 | 4 | 0 | 1 | 0 | 1 | 2 | PGC_chr6_41731711_41752397 | PGC | ACTCC others(1366): Show |
chr6 | 41731711 | 41752397 |
| a0001c0001t0003 | 0/0 | 1371 | 2 | 2 | 0 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | ACTCC others(1366): Show |
chr6 | 41731711 | 41752397 |
| a0001c0001t0004 | 0/0 | 1371 | 1 | 1 | 0 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | ACTCC others(1366): Show |
chr6 | 41731711 | 41752397 |
| a0001c0002t0001 | 0/0 | 1371 | 5 | 5 | 0 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | ACTCC others(1366): Show |
chr6 | 41731711 | 41752397 |
| a0001c0007t0001 | 0/0 | 1371 | 1 | 0 | 0 | 1 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | ACTCC others(1366): Show |
chr6 | 41731711 | 41752397 |
| a0001c0008t0001 | 0/0 | 1371 | 1 | 1 | 0 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | ACTCC others(1366): Show |
chr6 | 41731711 | 41752397 |
| a0002c0003t0001 | 0/0 | 1371 | 3 | 2 | 1 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | ACTCC others(1366): Show |
chr6 | 41731711 | 41752397 |
| a0003c0005t0001 | 0/0 | 1381 | 1 | 0 | 1 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | ACTCC others(1376): Show |
chr6 | 41731711 | 41752397 |
| a0004c0006t0001 | 0/0 | 1371 | 1 | 0 | 0 | 1 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | ACTCC others(1366): Show |
chr6 | 41731711 | 41752397 |
| a0005c0004t0001 | 0/0 | 1371 | 1 | 1 | 0 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | ACTCC others(1366): Show |
chr6 | 41731711 | 41752397 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 47 | 1 | 3 | 31 | 2 | 10 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0002 | 0/0 | 16 | 0 | 3 | 5 | 2 | 6 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0003 | 0/0 | 16 | 2 | 1 | 12 | 0 | 1 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0004 | 0/0 | 14 | 0 | 13 | 1 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0005 | 0/0 | 13 | 0 | 0 | 13 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0006 | 0/0 | 10 | 2 | 0 | 2 | 3 | 3 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0007 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0008 | 0/0 | 9 | 0 | 3 | 6 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0009 | 0/0 | 9 | 1 | 0 | 8 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0010 | 0/0 | 8 | 0 | 3 | 5 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0011 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0012 | 0/0 | 8 | 0 | 1 | 7 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0013 | 0/0 | 7 | 0 | 6 | 0 | 1 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0014 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0015 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0016 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0017 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0018 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0022 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0023 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0025 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0026 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0027 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0028 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0029 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0034 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0041 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0042 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0044 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0046 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0050 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0053 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0054 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0055 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0057 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0058 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0059 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0086 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0002g0060 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0003g0056 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0001t0004g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0002t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0002t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0002t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0002t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0002t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0007t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0001c0008t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0002c0003t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0002c0003t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0003c0005t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0004c0006t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| a0005c0004t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | GBR | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | GBR | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0040 | EUR | GBR | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0062 | EUR | FIN | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0037 | EUR | FIN | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0046 | EUR | FIN | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | CHS | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | CHS | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | CHS | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | CHS | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | CHS | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | CHS | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | CHS | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | CHS | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | CHS | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | CHS | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG01070 | hp2 | a0003 | c0005 | t0001 | g0079 | AMR | PUR | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | CLM | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | CLM | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | CLM | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | CLM | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0060 | AMR | CLM | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG01361 | hp1 | a0002 | c0003 | t0001 | g0064 | AMR | CLM | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | CLM | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | CLM | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0020 | EUR | IBS | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0013 | EUR | IBS | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0016 | EUR | IBS | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0016 | EUR | IBS | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0020 | EUR | IBS | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | ACB | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG01891 | hp1 | a0001 | c0002 | t0001 | g0167 | AFR | ACB | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | ACB | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PEL | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | PEL | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PEL | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PEL | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | KHV | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | KHV | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | KHV | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | KHV | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | KHV | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | KHV | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | ACB | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PEL | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | PEL | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CDX | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | CDX | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | CDX | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | CDX | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | ACB | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | ACB | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PEL | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | ACB | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02280 | hp2 | a0001 | c0002 | t0001 | g0202 | AFR | ACB | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PEL | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | PEL | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | ACB | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | KHV | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | GWD | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | GWD | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | GWD | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02622 | hp2 | a0001 | c0008 | t0001 | g0192 | AFR | GWD | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | GWD | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02647 | hp1 | a0001 | c0001 | t0004 | g0230 | AFR | GWD | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0056 | AFR | GWD | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | GWD | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | GWD | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | GWD | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | GWD | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | GWD | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02895 | hp2 | a0001 | c0001 | t0003 | g0056 | AFR | GWD | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02896 | hp1 | a0002 | c0003 | t0001 | g0033 | AFR | GWD | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | GWD | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02897 | hp1 | a0002 | c0003 | t0001 | g0033 | AFR | GWD | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02922 | hp1 | a0001 | c0002 | t0001 | g0082 | AFR | ESN | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | ESN | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | ESN | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | ESN | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | ESN | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02970 | hp2 | a0001 | c0002 | t0001 | g0084 | AFR | ESN | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | ESN | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | ESN | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | GWD | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | MSL | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | MSL | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG03130 | hp1 | a0001 | c0002 | t0001 | g0119 | AFR | ESN | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | ESN | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | ESN | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | ESN | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | ESN | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | ESN | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | MSL | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | MSL | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | MSL | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | MSL | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | MSL | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | MSL | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | MSL | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | MSL | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0057 | SAS | PJL | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0057 | SAS | PJL | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | ESN | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | ESN | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | GWD | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | MSL | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | MSL | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | STU | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0195 | SAS | STU | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | BEB | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0232 | SAS | BEB | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0225 | SAS | BEB | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0148 | SAS | BEB | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | BEB | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0231 | SAS | BEB | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | BEB | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | STU | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0212 | SAS | STU | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0040 | SAS | STU | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0228 | SAS | STU | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0154 | SAS | STU | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | YRI | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | YRI | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | CHB | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | CHB | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHB | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | CHB | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | YRI | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | YRI | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA18981 | hp2 | a0004 | c0006 | t0001 | g0182 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA18999 | hp2 | a0001 | c0007 | t0001 | g0157 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | LWK | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | LWK | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA19043 | hp1 | a0005 | c0004 | t0001 | g0087 | AFR | LWK | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | LWK | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA19059 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA19059 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | YRI | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | YRI | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | ASW | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | ASW | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | TSI | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0060 | EUR | TSI | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0120 | EUR | TSI | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0076 | SAS | GIH | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | CLM | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | ACB | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | ACB | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | ACB | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | MSL | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | MSL | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | USA | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | USA | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | USA | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | USA | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | LWK | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | LWK | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0086 | REF | REF | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0044 | REF | REF | PGC_chr6_41731711_41752397 | PGC | chr6 | 41731711 | 41752397 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:41737773 | T | C | 1 | a0004 | 1 | NA18981.hp2 | missense_variant | MODERATE | c.971A>G | p.Asn324Ser | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 8/9 | 1034/1371 | 971/1167 | 324/388 | chr6 | 41737773 | |||
| chr6:41742456 | C | CGAACTCC others(3): Show |
1 | a0003 | 1 | HG01070.hp2 | frameshift_variant | HIGH | c.471_480dupCCAGGAGT others(2): Show |
p.Gly161fs | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 5/9 | 543/1371 | 480/1167 | 160/388 | chr6 | 41742456 | |||
| chr6:41743311 | C | G | 1 | a0002 | 3 | HG01361.hp1 HG02896.hp1 HG02897.hp1 |
missense_variant | MODERATE | c.407G>C | p.Ser136Thr | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 4/9 | 470/1371 | 407/1167 | 136/388 | chr6 | 41743311 | |||
| chr6:41744687 | C | T | 1 | a0005 | 1 | NA19043.hp1 | missense_variant | MODERATE | c.181G>A | p.Val61Met | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 2/9 | 244/1371 | 181/1167 | 61/388 | chr6 | 41744687 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:41736888 | C | T | 1 | a0001c0002 | 5 | HG01891.hp1 HG02280.hp2 HG02922.hp1 others(2): Show |
synonymous_variant | LOW | c.1131G>A | p.Leu377Leu | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 9/9 | 1194/1371 | 1131/1167 | 377/388 | chr6 | 41736888 | |||
| chr6:41742313 | G | C | 1 | a0001c0007 | 1 | NA18999.hp2 | synonymous_variant | LOW | c.624C>G | p.Pro208Pro | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 5/9 | 687/1371 | 624/1167 | 208/388 | chr6 | 41742313 | |||
| chr6:41742328 | G | A | 1 | a0001c0008 | 1 | HG02622.hp2 | synonymous_variant | LOW | c.609C>T | p.Gly203Gly | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 5/9 | 672/1371 | 609/1167 | 203/388 | chr6 | 41742328 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:41736718 | G | T | 1 | a0001c0001t0003 | 2 | HG02647.hp2 HG02895.hp2 |
3_prime_UTR_variant | MODIFIER | c.*134C>A | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 9/9 | 134 | chr6 | 41736718 | ||||||
| chr6:41747368 | C | A | 1 | a0001c0001t0004 | 1 | HG02647.hp1 | 5_prime_UTR_variant | MODIFIER | c.-34G>T | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 1/9 | 34 | chr6 | 41747368 | ||||||
| chr6:41747388 | G | A | 1 | a0001c0001t0002 | 4 | HG01358.hp1 HG03834.hp1 HG04184.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-54C>T | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 1/9 | 54 | chr6 | 41747388 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:41737034 | C | G | 56 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(53): Show |
117 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.1015-30G>C | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 8/8 | chr6 | 41737034 | |||||||
| chr6:41737034 | C | T | 1 | a0001c0001t0001g0089 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1015-30G>A | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 8/8 | chr6 | 41737034 | |||||||
| chr6:41737202 | G | A | 1 | a0001c0001t0001g0161 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1015-198C>T | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 8/8 | chr6 | 41737202 | |||||||
| chr6:41737266 | T | C | 1 | a0001c0001t0003g0056 | 2 | HG02647.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.1015-262A>G | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 8/8 | chr6 | 41737266 | |||||||
| chr6:41737274 | A | G | 1 | a0001c0001t0001g0217 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1015-270T>C | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 8/8 | chr6 | 41737274 | |||||||
| chr6:41737489 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1014+241G>A | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 8/8 | chr6 | 41737489 | |||||||
| chr6:41737537 | C | A | 2 | a0001c0001t0001g0028 a0001c0001t0001g0156 |
4 | HG02257.hp1 HG02451.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1014+193G>T | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 8/8 | chr6 | 41737537 | |||||||
| chr6:41737657 | A | G | 3 | a0001c0001t0001g0096 a0001c0001t0001g0117 a0001c0001t0001g0127 |
3 | HG02630.hp2 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1014+73T>C | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 8/8 | chr6 | 41737657 | |||||||
| chr6:41737715 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1014+15C>T | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 8/8 | chr6 | 41737715 | |||||||
| chr6:41737720 | C | A | 2 | a0001c0002t0001g0167 a0001c0002t0001g0202 |
2 | HG01891.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1014+10G>T | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 8/8 | chr6 | 41737720 | |||||||
| chr6:41737874 | G | A | 71 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(68): Show |
134 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(131): Show |
intron_variant | MODIFIER | c.916-46C>T | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41737874 | |||||||
| chr6:41737901 | C | T | 1 | a0001c0001t0001g0011 | 8 | HG02027.hp2 NA18959.hp1 NA18978.hp2 others(5): Show |
intron_variant | MODIFIER | c.916-73G>A | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41737901 | |||||||
| chr6:41737906 | A | T | 1 | a0001c0001t0001g0117 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.916-78T>A | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41737906 | |||||||
| chr6:41738089 | G | A | 1 | a0001c0001t0001g0019 | 3 | HG00558.hp1 HG00673.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.916-261C>T | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738089 | |||||||
| chr6:41738123 | C | CATATATA others(53): Show |
1 | a0001c0001t0001g0096 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.916-296_916-295ins others(60): Show |
PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738123 | |||||||
| chr6:41738132 | G | GCATATAT others(3): Show |
4 | a0001c0001t0001g0051 a0001c0001t0001g0083 a0001c0001t0001g0110 others(1): Show |
5 | HG01081.hp1 HG02257.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.916-314_916-305dup others(10): Show |
PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738132 | |||||||
| chr6:41738132 | G | GCATATAT others(5): Show |
1 | a0001c0001t0001g0198 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.916-305_916-304ins others(12): Show |
PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738132 | |||||||
| chr6:41738132 | G | GCATATAT others(99): Show |
1 | a0001c0001t0001g0127 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.916-305_916-304ins others(106): Show |
PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738132 | |||||||
| chr6:41738133 | C | T | 57 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(54): Show |
118 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.916-305G>A | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738133 | |||||||
| chr6:41738135 | T | TATATATA others(285): Show |
1 | a0001c0001t0001g0115 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.916-308_916-307ins others(292): Show |
PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738135 | |||||||
| chr6:41738135 | T | TATATATA others(261): Show |
1 | a0001c0001t0001g0177 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.916-308_916-307ins others(268): Show |
PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738135 | |||||||
| chr6:41738135 | T | TATATATA others(263): Show |
1 | a0001c0001t0001g0129 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.916-308_916-307ins others(270): Show |
PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738135 | |||||||
| chr6:41738143 | TGCATATA others(41): Show |
T | 1 | a0001c0001t0001g0126 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.916-363_916-316del others(48): Show |
PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738143 | |||||||
| chr6:41738144 | G | A | 121 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(118): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.916-316C>T | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738144 | |||||||
| chr6:41738145 | CATATATA others(101): Show |
C | 1 | a0001c0001t0001g0068 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.916-425_916-318del | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738145 | |||||||
| chr6:41738146 | A | ATATATAT others(3): Show |
1 | a0001c0001t0001g0095 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.916-319_916-318ins others(10): Show |
PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738146 | |||||||
| chr6:41738146 | A | G | 2 | a0001c0001t0001g0129 a0001c0001t0001g0177 |
2 | HG00642.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.916-318T>C | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738146 | |||||||
| chr6:41738149 | TATATATA others(95): Show |
T | 1 | a0001c0001t0001g0139 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.916-423_916-322del | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738149 | |||||||
| chr6:41738155 | T | C | 3 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0003g0056 |
9 | HG00544.hp1 HG00673.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.916-327A>G | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738155 | |||||||
| chr6:41738155 | T | TGCATATA others(53): Show |
1 | a0001c0001t0001g0173 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.916-328_916-327ins others(60): Show |
PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738155 | |||||||
| chr6:41738155 | TACATATA others(103): Show |
T | 56 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(53): Show |
117 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.916-437_916-328del | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738155 | |||||||
| chr6:41738156 | A | ACATATAT others(359): Show |
1 | a0001c0001t0001g0117 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.916-329_916-328ins others(366): Show |
PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738156 | |||||||
| chr6:41738156 | A | G | 5 | a0001c0001t0001g0051 a0001c0001t0001g0083 a0001c0001t0001g0110 others(2): Show |
6 | HG01081.hp1 HG02257.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.916-328T>C | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738156 | |||||||
| chr6:41738156 | ACATATAT others(3): Show |
A | 8 | a0001c0001t0001g0037 a0001c0001t0001g0078 a0001c0001t0001g0093 others(5): Show |
10 | HG00280.hp2 HG00642.hp2 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.916-338_916-329del others(10): Show |
PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738156 | |||||||
| chr6:41738156 | ACATATAT others(39): Show |
A | 6 | a0001c0001t0001g0200 a0001c0002t0001g0082 a0001c0002t0001g0084 others(3): Show |
6 | HG01891.hp1 HG01891.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.916-374_916-329del others(46): Show |
PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738156 | |||||||
| chr6:41738157 | C | CAT | 97 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(94): Show |
217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.916-331_916-330dup others(2): Show |
PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738157 | |||||||
| chr6:41738157 | C | CATATATA others(7): Show |
3 | a0001c0001t0001g0113 a0001c0001t0001g0172 a0002c0003t0001g0064 |
3 | HG01361.hp1 HG02280.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.916-330_916-329ins others(14): Show |
PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738157 | |||||||
| chr6:41738157 | C | T | 4 | a0001c0001t0001g0001 a0001c0001t0001g0173 a0001c0001t0001g0212 others(1): Show |
6 | HG00544.hp1 HG00673.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.916-329G>A | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738157 | |||||||
| chr6:41738166 | G | A | 6 | a0001c0001t0001g0051 a0001c0001t0001g0083 a0001c0001t0001g0110 others(3): Show |
7 | HG01081.hp1 HG02257.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.916-338C>T | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738166 | |||||||
| chr6:41738167 | C | CAT | 3 | a0001c0001t0001g0026 a0001c0001t0001g0132 a0001c0001t0001g0172 |
4 | HG03654.hp1 HG03942.hp1 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.916-341_916-340dup others(2): Show |
PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738167 | |||||||
| chr6:41738168 | A | G | 5 | a0001c0001t0001g0051 a0001c0001t0001g0083 a0001c0001t0001g0110 others(2): Show |
6 | HG01081.hp1 HG02257.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.916-340T>C | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738168 | |||||||
| chr6:41738169 | T | TATATATA others(3): Show |
11 | a0001c0001t0001g0006 a0001c0001t0001g0025 a0001c0001t0001g0040 others(8): Show |
22 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(19): Show |
intron_variant | MODIFIER | c.916-351_916-342dup others(10): Show |
PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738169 | |||||||
| chr6:41738176 | ATACATAT others(31): Show |
A | 2 | a0001c0001t0001g0028 a0001c0001t0001g0156 |
4 | HG02257.hp1 HG02451.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.916-386_916-349del others(38): Show |
PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738176 | |||||||
| chr6:41738178 | A | ACATATAT others(29): Show |
2 | a0001c0001t0001g0003 a0001c0001t0001g0010 |
3 | NA18955.hp1 NA18972.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.916-386_916-351dup others(36): Show |
PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738178 | |||||||
| chr6:41738178 | A | ACATATAT others(41): Show |
1 | a0001c0001t0001g0003 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.916-398_916-351dup others(48): Show |
PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738178 | |||||||
| chr6:41738178 | A | ACATATAT others(3): Show |
1 | a0001c0001t0001g0148 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.916-351_916-350ins others(10): Show |
PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738178 | |||||||
| chr6:41738178 | A | G | 70 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(67): Show |
175 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.916-350T>C | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738178 | |||||||
| chr6:41738180 | A | G | 2 | a0001c0001t0001g0129 a0001c0001t0001g0177 |
2 | HG00642.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.916-352T>C | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738180 | |||||||
| chr6:41738181 | T | TATATATA others(69): Show |
2 | a0001c0001t0001g0140 a0005c0004t0001g0087 |
2 | HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.916-354_916-353ins others(76): Show |
PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738181 | |||||||
| chr6:41738181 | T | TATATATA others(3): Show |
1 | a0001c0001t0001g0073 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-354_916-353ins others(10): Show |
PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738181 | |||||||
| chr6:41738181 | T | TATATATA others(35): Show |
1 | a0001c0001t0001g0155 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.916-354_916-353ins others(42): Show |
PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738181 | |||||||
| chr6:41738181 | T | TATATATA others(35): Show |
1 | a0001c0001t0001g0162 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.916-354_916-353ins others(42): Show |
PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738181 | |||||||
| chr6:41738188 | ATG | A | 13 | a0001c0001t0001g0037 a0001c0001t0001g0049 a0001c0001t0001g0078 others(10): Show |
16 | HG00280.hp2 HG00642.hp2 HG01358.hp1 others(13): Show |
intron_variant | MODIFIER | c.916-362_916-361del others(2): Show |
PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738188 | |||||||
| chr6:41738189 | TGC | T | 5 | a0001c0001t0001g0058 a0001c0001t0001g0067 a0001c0001t0001g0112 others(2): Show |
6 | HG01346.hp1 HG01993.hp1 HG02148.hp1 others(3): Show |
intron_variant | MODIFIER | c.916-363_916-362del others(2): Show |
PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738189 | |||||||
| chr6:41738190 | G | A | 52 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(49): Show |
134 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.916-362C>T | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738190 | |||||||
| chr6:41738190 | G | GCATATAT others(41): Show |
1 | a0001c0001t0001g0210 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.916-363_916-362ins others(48): Show |
PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738190 | |||||||
| chr6:41738191 | CAT | C | 2 | a0001c0001t0001g0014 a0003c0005t0001g0079 |
6 | HG00639.hp1 HG01069.hp2 HG01070.hp2 others(3): Show |
intron_variant | MODIFIER | c.916-365_916-364del others(2): Show |
PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738191 | |||||||
| chr6:41738193 | T | C | 6 | a0001c0001t0001g0058 a0001c0001t0001g0067 a0001c0001t0001g0112 others(3): Show |
7 | HG01346.hp1 HG01993.hp1 HG02148.hp1 others(4): Show |
intron_variant | MODIFIER | c.916-365A>G | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738193 | |||||||
| chr6:41738193 | T | TATATATG others(1): Show |
48 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(45): Show |
145 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.916-366_916-365ins others(8): Show |
PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738193 | |||||||
| chr6:41738193 | T | TATATATG others(11): Show |
1 | a0001c0001t0001g0085 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.916-366_916-365ins others(18): Show |
PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738193 | |||||||
| chr6:41738201 | TGC | T | 7 | a0001c0001t0001g0037 a0001c0001t0001g0078 a0001c0001t0001g0093 others(4): Show |
9 | HG00280.hp2 HG00642.hp2 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.916-375_916-374del others(2): Show |
PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738201 | |||||||
| chr6:41738202 | G | A | 71 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(68): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.916-374C>T | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738202 | |||||||
| chr6:41738205 | T | C | 9 | a0001c0001t0001g0037 a0001c0001t0001g0078 a0001c0001t0001g0085 others(6): Show |
11 | HG00280.hp2 HG00642.hp2 HG01358.hp1 others(8): Show |
intron_variant | MODIFIER | c.916-377A>G | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738205 | |||||||
| chr6:41738205 | T | TATATATA others(47): Show |
3 | a0001c0001t0001g0049 a0001c0001t0001g0080 a0001c0001t0001g0109 |
4 | HG02258.hp1 HG02809.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.916-378_916-377ins others(54): Show |
PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738205 | |||||||
| chr6:41738205 | T | TATATATA others(3): Show |
61 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(58): Show |
170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.916-378_916-377ins others(10): Show |
PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738205 | |||||||
| chr6:41738205 | T | TATATATA others(49): Show |
10 | a0001c0001t0001g0012 a0001c0001t0001g0058 a0001c0001t0001g0067 others(7): Show |
18 | HG00597.hp2 HG01346.hp1 HG01981.hp1 others(15): Show |
intron_variant | MODIFIER | c.916-378_916-377ins others(56): Show |
PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738205 | |||||||
| chr6:41738205 | T | TATATATA others(15): Show |
1 | a0001c0001t0003g0056 | 2 | HG02647.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.916-378_916-377ins others(22): Show |
PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738205 | |||||||
| chr6:41738205 | T | TATATATA others(61): Show |
1 | a0001c0001t0001g0090 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.916-378_916-377ins others(68): Show |
PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738205 | |||||||
| chr6:41738205 | T | TATATATA others(37): Show |
1 | a0001c0001t0001g0154 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.916-378_916-377ins others(44): Show |
PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738205 | |||||||
| chr6:41738205 | T | TATATATA others(45): Show |
1 | a0001c0001t0001g0188 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.916-378_916-377ins others(52): Show |
PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738205 | |||||||
| chr6:41738205 | T | TATATATA others(3): Show |
2 | a0001c0001t0001g0113 a0002c0003t0001g0064 |
2 | HG01361.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.916-387_916-378dup others(10): Show |
PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738205 | |||||||
| chr6:41738205 | T | TATATATA others(45): Show |
1 | a0001c0001t0001g0102 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.916-378_916-377ins others(52): Show |
PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738205 | |||||||
| chr6:41738205 | T | TATATATA others(47): Show |
3 | a0001c0001t0001g0101 a0001c0001t0001g0176 a0001c0001t0001g0181 |
3 | HG02129.hp2 HG02717.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.916-378_916-377ins others(54): Show |
PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738205 | |||||||
| chr6:41738214 | G | A | 5 | a0001c0001t0001g0095 a0001c0001t0001g0117 a0001c0001t0001g0129 others(2): Show |
5 | HG00642.hp1 HG02723.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.916-386C>T | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738214 | |||||||
| chr6:41738215 | C | CATATATA others(379): Show |
4 | a0001c0001t0001g0051 a0001c0001t0001g0083 a0001c0001t0001g0110 others(1): Show |
5 | HG01081.hp1 HG02257.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.916-388_916-387ins others(386): Show |
PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738215 | |||||||
| chr6:41738215 | CATATATA others(17): Show |
C | 1 | a0001c0001t0001g0196 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.916-411_916-388del others(24): Show |
PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738215 | |||||||
| chr6:41738216 | A | G | 2 | a0001c0001t0001g0095 a0001c0001t0001g0173 |
2 | HG03098.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.916-388T>C | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738216 | |||||||
| chr6:41738222 | A | G | 1 | a0001c0001t0003g0056 | 2 | HG02647.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.916-394T>C | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738222 | |||||||
| chr6:41738226 | G | A | 109 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(106): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.916-398C>T | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738226 | |||||||
| chr6:41738226 | G | GCATATAT others(77): Show |
2 | a0001c0001t0001g0165 a0001c0001t0001g0207 |
2 | HG02559.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.916-399_916-398ins others(84): Show |
PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738226 | |||||||
| chr6:41738226 | G | GCATATAT others(53): Show |
1 | a0001c0001t0001g0124 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.916-399_916-398ins others(60): Show |
PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738226 | |||||||
| chr6:41738226 | G | GCATATAT others(51): Show |
1 | a0002c0003t0001g0033 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.916-399_916-398ins others(58): Show |
PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738226 | |||||||
| chr6:41738226 | G | GCATATAT others(47): Show |
2 | a0001c0001t0001g0014 a0003c0005t0001g0079 |
6 | HG00639.hp1 HG01069.hp2 HG01070.hp2 others(3): Show |
intron_variant | MODIFIER | c.916-399_916-398ins others(54): Show |
PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738226 | |||||||
| chr6:41738227 | CATATATA others(5): Show |
C | 3 | a0001c0001t0001g0029 a0001c0001t0001g0183 a0001c0001t0001g0226 |
5 | HG00733.hp2 HG02109.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.916-411_916-400del others(12): Show |
PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738227 | |||||||
| chr6:41738237 | T | C | 9 | a0001c0001t0001g0037 a0001c0001t0001g0078 a0001c0001t0001g0093 others(6): Show |
11 | HG00280.hp2 HG00642.hp2 HG01358.hp1 others(8): Show |
intron_variant | MODIFIER | c.916-409A>G | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738237 | |||||||
| chr6:41738238 | G | A | 13 | a0001c0001t0001g0037 a0001c0001t0001g0051 a0001c0001t0001g0078 others(10): Show |
16 | HG00280.hp2 HG00642.hp2 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.916-410C>T | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738238 | |||||||
| chr6:41738238 | G | GCATATAT others(119): Show |
2 | a0001c0001t0001g0129 a0001c0001t0001g0177 |
2 | HG00642.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.916-411_916-410ins others(126): Show |
PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738238 | |||||||
| chr6:41738238 | G | GCGTATAT others(289): Show |
1 | a0001c0001t0001g0173 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.916-411_916-410ins others(296): Show |
PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738238 | |||||||
| chr6:41738239 | T | C | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(160): Show |
328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.916-411A>G | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738239 | |||||||
| chr6:41738239 | T | TATATATA others(41): Show |
1 | a0001c0001t0001g0115 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.916-412_916-411ins others(48): Show |
PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738239 | |||||||
| chr6:41738240 | A | ATATATAT others(281): Show |
1 | a0001c0001t0001g0096 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.916-413_916-412ins others(288): Show |
PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738240 | |||||||
| chr6:41738240 | A | ATATATAT others(257): Show |
1 | a0001c0001t0001g0127 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.916-413_916-412ins others(264): Show |
PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738240 | |||||||
| chr6:41738241 | T | C | 2 | a0001c0001t0001g0100 a0001c0001t0001g0173 |
2 | HG03098.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.916-413A>G | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738241 | |||||||
| chr6:41738241 | T | TATATATA others(267): Show |
1 | a0001c0001t0001g0095 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.916-414_916-413ins others(274): Show |
PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738241 | |||||||
| chr6:41738241 | T | TATATATG others(401): Show |
1 | a0001c0001t0001g0198 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.916-414_916-413ins others(408): Show |
PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738241 | |||||||
| chr6:41738250 | G | A | 3 | a0001c0001t0001g0054 a0001c0001t0001g0168 a0001c0008t0001g0192 |
4 | HG02572.hp1 HG02622.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.916-422C>T | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738250 | |||||||
| chr6:41738253 | T | TATATATA others(3): Show |
12 | a0001c0001t0001g0027 a0001c0001t0001g0034 a0001c0001t0001g0053 others(9): Show |
17 | HG01070.hp1 HG01071.hp1 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.916-426_916-425ins others(10): Show |
PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738253 | |||||||
| chr6:41738264 | G | GCA | 3 | a0001c0001t0001g0126 a0001c0002t0001g0167 a0001c0002t0001g0202 |
3 | HG01891.hp1 HG02280.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.916-438_916-437dup others(2): Show |
PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738264 | |||||||
| chr6:41738264 | GCA | G | 145 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(142): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.916-438_916-437del others(2): Show |
PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738264 | |||||||
| chr6:41738264 | GCACA | G | 5 | a0001c0001t0001g0049 a0001c0001t0001g0080 a0001c0001t0001g0109 others(2): Show |
6 | HG02258.hp1 HG02809.hp1 HG06807.hp2 others(3): Show |
intron_variant | MODIFIER | c.916-440_916-437del others(4): Show |
PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738264 | |||||||
| chr6:41738266 | A | ATATATAT others(5): Show |
12 | a0001c0001t0001g0027 a0001c0001t0001g0034 a0001c0001t0001g0053 others(9): Show |
17 | HG01070.hp1 HG01071.hp1 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.916-439_916-438ins others(12): Show |
PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738266 | |||||||
| chr6:41738266 | A | G | 57 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(54): Show |
118 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.916-438T>C | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738266 | |||||||
| chr6:41738268 | A | G | 1 | a0001c0001t0001g0159 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.916-440T>C | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738268 | |||||||
| chr6:41738281 | C | T | 1 | a0001c0001t0001g0038 | 2 | NA18985.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.916-453G>A | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738281 | |||||||
| chr6:41738297 | T | G | 1 | a0001c0001t0001g0200 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.916-469A>C | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738297 | |||||||
| chr6:41738354 | A | C | 1 | a0001c0001t0001g0103 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.916-526T>G | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738354 | |||||||
| chr6:41738366 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.916-538C>T | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738366 | |||||||
| chr6:41738453 | C | T | 91 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(88): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.916-625G>A | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738453 | |||||||
| chr6:41738554 | G | C | 1 | a0001c0001t0001g0105 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.916-726C>G | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738554 | |||||||
| chr6:41738667 | A | G | 1 | a0001c0001t0001g0099 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.916-839T>C | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738667 | |||||||
| chr6:41738782 | C | A | 1 | a0001c0001t0002g0060 | 2 | HG01358.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.916-954G>T | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738782 | |||||||
| chr6:41738807 | A | G | 2 | a0001c0001t0001g0107 a0001c0001t0002g0231 |
2 | HG02738.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.916-979T>C | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738807 | |||||||
| chr6:41738891 | T | C | 4 | a0001c0001t0001g0037 a0001c0001t0001g0078 a0001c0001t0001g0093 others(1): Show |
5 | HG00280.hp2 HG00642.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.915+908A>G | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738891 | |||||||
| chr6:41738952 | T | A | 56 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(53): Show |
117 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.915+847A>T | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738952 | |||||||
| chr6:41738980 | C | A | 1 | a0001c0001t0001g0150 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.915+819G>T | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41738980 | |||||||
| chr6:41739097 | G | A | 7 | a0001c0001t0001g0037 a0001c0001t0001g0078 a0001c0001t0001g0093 others(4): Show |
9 | HG00280.hp2 HG00642.hp2 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.915+702C>T | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41739097 | |||||||
| chr6:41739314 | C | T | 1 | a0001c0001t0001g0057 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.915+485G>A | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41739314 | |||||||
| chr6:41739360 | G | A | 1 | a0001c0001t0001g0106 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.915+439C>T | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41739360 | |||||||
| chr6:41739405 | G | C | 7 | a0001c0001t0001g0037 a0001c0001t0001g0078 a0001c0001t0001g0093 others(4): Show |
9 | HG00280.hp2 HG00642.hp2 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.915+394C>G | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41739405 | |||||||
| chr6:41739406 | G | A | 2 | a0001c0001t0001g0078 a0001c0001t0001g0097 |
2 | HG00642.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.915+393C>T | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41739406 | |||||||
| chr6:41739422 | C | CT | 6 | a0001c0001t0001g0072 a0001c0001t0001g0098 a0001c0001t0001g0147 others(3): Show |
6 | HG00621.hp2 HG03710.hp2 HG04228.hp2 others(3): Show |
intron_variant | MODIFIER | c.915+376dupA | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41739422 | |||||||
| chr6:41739445 | G | A | 12 | a0001c0001t0001g0051 a0001c0001t0001g0083 a0001c0001t0001g0095 others(9): Show |
13 | HG00642.hp1 HG01081.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.915+354C>T | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41739445 | |||||||
| chr6:41739645 | C | T | 1 | a0001c0001t0001g0162 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.915+154G>A | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41739645 | |||||||
| chr6:41739662 | G | A | 1 | a0001c0001t0001g0090 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.915+137C>T | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41739662 | |||||||
| chr6:41739711 | G | A | 2 | a0001c0001t0001g0091 a0001c0001t0001g0126 |
2 | NA18969.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.915+88C>T | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 7/8 | chr6 | 41739711 | |||||||
| chr6:41740232 | T | C | 5 | a0001c0002t0001g0082 a0001c0002t0001g0084 a0001c0002t0001g0119 others(2): Show |
5 | HG01891.hp1 HG02280.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.767+259A>G | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 6/8 | chr6 | 41740232 | |||||||
| chr6:41740252 | G | T | 3 | a0001c0001t0001g0065 a0001c0001t0001g0145 a0001c0001t0001g0211 |
3 | HG01168.hp2 HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.767+239C>A | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 6/8 | chr6 | 41740252 | |||||||
| chr6:41740360 | C | CTT | 5 | a0001c0001t0001g0065 a0001c0001t0001g0145 a0001c0001t0001g0186 others(2): Show |
5 | HG01168.hp2 HG02809.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.767+129_767+130dup others(2): Show |
PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 6/8 | chr6 | 41740360 | |||||||
| chr6:41740636 | G | A | 51 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(48): Show |
111 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.648-26C>T | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 5/8 | chr6 | 41740636 | |||||||
| chr6:41740755 | C | A | 1 | a0001c0001t0001g0135 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.648-145G>T | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 5/8 | chr6 | 41740755 | |||||||
| chr6:41740819 | C | G | 1 | a0002c0003t0001g0033 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.648-209G>C | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 5/8 | chr6 | 41740819 | |||||||
| chr6:41740884 | G | T | 5 | a0001c0001t0001g0065 a0001c0001t0001g0145 a0001c0001t0001g0186 others(2): Show |
5 | HG01168.hp2 HG02809.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.648-274C>A | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 5/8 | chr6 | 41740884 | |||||||
| chr6:41740915 | G | A | 1 | a0001c0001t0001g0185 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.648-305C>T | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 5/8 | chr6 | 41740915 | |||||||
| chr6:41740926 | C | T | 28 | a0001c0001t0001g0037 a0001c0001t0001g0054 a0001c0001t0001g0078 others(25): Show |
32 | HG00280.hp2 HG00642.hp2 HG01358.hp1 others(29): Show |
intron_variant | MODIFIER | c.648-316G>A | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 5/8 | chr6 | 41740926 | |||||||
| chr6:41740982 | C | T | 1 | a0001c0001t0001g0126 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.648-372G>A | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 5/8 | chr6 | 41740982 | |||||||
| chr6:41741059 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.648-449C>T | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 5/8 | chr6 | 41741059 | |||||||
| chr6:41741200 | C | G | 66 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(63): Show |
127 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.648-590G>C | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 5/8 | chr6 | 41741200 | |||||||
| chr6:41741371 | C | T | 1 | a0001c0001t0001g0176 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.648-761G>A | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 5/8 | chr6 | 41741371 | |||||||
| chr6:41741501 | C | G | 1 | a0001c0001t0001g0122 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.647+789G>C | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 5/8 | chr6 | 41741501 | |||||||
| chr6:41741610 | C | T | 5 | a0001c0002t0001g0082 a0001c0002t0001g0084 a0001c0002t0001g0119 others(2): Show |
5 | HG01891.hp1 HG02280.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.647+680G>A | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 5/8 | chr6 | 41741610 | |||||||
| chr6:41741799 | C | A | 4 | a0001c0001t0001g0048 a0001c0001t0001g0133 a0001c0001t0001g0160 others(1): Show |
5 | HG00597.hp1 NA18939.hp1 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.647+491G>T | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 5/8 | chr6 | 41741799 | |||||||
| chr6:41741816 | A | G | 1 | a0001c0001t0003g0056 | 2 | HG02647.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.647+474T>C | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 5/8 | chr6 | 41741816 | |||||||
| chr6:41741878 | A | T | 12 | a0001c0001t0001g0017 a0001c0001t0001g0022 a0001c0001t0001g0030 others(9): Show |
21 | HG00323.hp1 HG00597.hp1 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.647+412T>A | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 5/8 | chr6 | 41741878 | |||||||
| chr6:41741976 | G | C | 2 | a0001c0001t0001g0038 a0001c0001t0001g0092 |
3 | NA18985.hp1 NA19003.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.647+314C>G | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 5/8 | chr6 | 41741976 | |||||||
| chr6:41742043 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.647+247G>A | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 5/8 | chr6 | 41742043 | |||||||
| chr6:41742109 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.647+181C>T | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 5/8 | chr6 | 41742109 | |||||||
| chr6:41742245 | G | A | 5 | a0001c0002t0001g0082 a0001c0002t0001g0084 a0001c0002t0001g0119 others(2): Show |
5 | HG01891.hp1 HG02280.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.647+45C>T | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 5/8 | chr6 | 41742245 | |||||||
| chr6:41742258 | G | A | 12 | a0001c0001t0001g0054 a0001c0001t0001g0113 a0001c0001t0001g0124 others(9): Show |
14 | HG01361.hp1 HG02258.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.647+32C>T | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 5/8 | chr6 | 41742258 | |||||||
| chr6:41742679 | C | T | 3 | a0001c0001t0001g0113 a0002c0003t0001g0033 a0002c0003t0001g0064 |
4 | HG01361.hp1 HG02280.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.448-190G>A | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 4/8 | chr6 | 41742679 | |||||||
| chr6:41742686 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.448-197C>T | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 4/8 | chr6 | 41742686 | |||||||
| chr6:41742703 | C | T | 1 | a0001c0001t0001g0094 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.448-214G>A | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 4/8 | chr6 | 41742703 | |||||||
| chr6:41742709 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.448-220G>A | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 4/8 | chr6 | 41742709 | |||||||
| chr6:41742716 | C | A | 1 | a0001c0001t0001g0107 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.448-227G>T | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 4/8 | chr6 | 41742716 | |||||||
| chr6:41742717 | C | G | 1 | a0001c0001t0001g0107 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.448-228G>C | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 4/8 | chr6 | 41742717 | |||||||
| chr6:41742718 | T | A | 1 | a0001c0001t0001g0107 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.448-229A>T | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 4/8 | chr6 | 41742718 | |||||||
| chr6:41742733 | T | C | 1 | a0001c0001t0001g0195 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.448-244A>G | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 4/8 | chr6 | 41742733 | |||||||
| chr6:41742741 | C | T | 1 | a0001c0001t0001g0200 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.448-252G>A | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 4/8 | chr6 | 41742741 | |||||||
| chr6:41742906 | G | C | 1 | a0001c0001t0001g0047 | 2 | HG00408.hp2 HG00621.hp1 |
intron_variant | MODIFIER | c.447+365C>G | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 4/8 | chr6 | 41742906 | |||||||
| chr6:41742916 | A | G | 54 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(51): Show |
106 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(103): Show |
intron_variant | MODIFIER | c.447+355T>C | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 4/8 | chr6 | 41742916 | |||||||
| chr6:41742937 | G | T | 1 | a0001c0001t0001g0126 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.447+334C>A | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 4/8 | chr6 | 41742937 | |||||||
| chr6:41743117 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.447+154C>T | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 4/8 | chr6 | 41743117 | |||||||
| chr6:41743219 | C | G | 1 | a0001c0001t0001g0092 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.447+52G>C | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 4/8 | chr6 | 41743219 | |||||||
| chr6:41743478 | C | T | 2 | a0001c0001t0001g0134 a0001c0001t0001g0135 |
2 | HG00741.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.329-89G>A | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 3/8 | chr6 | 41743478 | |||||||
| chr6:41743584 | C | G | 19 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(16): Show |
50 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(47): Show |
intron_variant | MODIFIER | c.329-195G>C | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 3/8 | chr6 | 41743584 | |||||||
| chr6:41743790 | C | A | 2 | a0001c0001t0001g0080 a0001c0001t0001g0139 |
2 | HG03130.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.329-401G>T | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 3/8 | chr6 | 41743790 | |||||||
| chr6:41743826 | A | G | 1 | a0001c0001t0001g0172 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.329-437T>C | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 3/8 | chr6 | 41743826 | |||||||
| chr6:41744032 | T | C | 11 | a0001c0001t0001g0054 a0001c0001t0001g0065 a0001c0001t0001g0108 others(8): Show |
12 | HG02258.hp2 HG02572.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.328+365A>G | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 3/8 | chr6 | 41744032 | |||||||
| chr6:41744045 | A | AATGGAGT others(3): Show |
4 | a0001c0001t0001g0034 a0001c0001t0001g0140 a0001c0001t0001g0147 others(1): Show |
5 | HG01255.hp2 HG03579.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.328+342_328+351dup others(10): Show |
PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 3/8 | chr6 | 41744045 | |||||||
| chr6:41744259 | G | A | 1 | a0001c0001t0001g0159 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.328+138C>T | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 3/8 | chr6 | 41744259 | |||||||
| chr6:41744320 | T | C | 5 | a0001c0001t0001g0048 a0001c0001t0001g0133 a0001c0001t0001g0160 others(2): Show |
6 | HG00597.hp1 NA18939.hp1 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.328+77A>G | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 3/8 | chr6 | 41744320 | |||||||
| chr6:41744820 | T | C | 1 | a0001c0001t0001g0038 | 2 | NA18985.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.60-12A>G | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 1/8 | chr6 | 41744820 | |||||||
| chr6:41744823 | C | A | 1 | a0001c0002t0001g0167 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.60-15G>T | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 1/8 | chr6 | 41744823 | |||||||
| chr6:41744930 | C | T | 1 | a0001c0001t0001g0229 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.60-122G>A | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 1/8 | chr6 | 41744930 | |||||||
| chr6:41744971 | C | T | 1 | a0001c0001t0001g0024 | 3 | NA18979.hp1 NA19003.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.60-163G>A | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 1/8 | chr6 | 41744971 | |||||||
| chr6:41744977 | CTCTG | C | 31 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0022 others(28): Show |
58 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.60-173_60-170delCA others(2): Show |
PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 1/8 | chr6 | 41744977 | |||||||
| chr6:41744985 | GTCTGTC | G | 54 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(51): Show |
145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
intron_variant | MODIFIER | c.60-183_60-178delGA others(4): Show |
PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 1/8 | chr6 | 41744985 | |||||||
| chr6:41744989 | GTC | G | 39 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(36): Show |
69 | HG00423.hp1 HG00438.hp2 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.60-183_60-182delGA | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 1/8 | chr6 | 41744989 | |||||||
| chr6:41744993 | C | CTGTG | 3 | a0001c0001t0002g0060 a0001c0001t0002g0231 a0001c0001t0002g0232 |
4 | HG01358.hp1 HG03834.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.60-186_60-185insCA others(2): Show |
PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 1/8 | chr6 | 41744993 | |||||||
| chr6:41744993 | C | G | 3 | a0001c0001t0001g0209 a0001c0001t0001g0214 a0003c0005t0001g0079 |
3 | HG01070.hp2 HG02071.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.60-185G>C | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 1/8 | chr6 | 41744993 | |||||||
| chr6:41744993 | CTCTG | C | 32 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0049 others(29): Show |
40 | HG00741.hp2 HG01891.hp1 HG02109.hp1 others(37): Show |
intron_variant | MODIFIER | c.60-189_60-186delCA others(2): Show |
PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 1/8 | chr6 | 41744993 | |||||||
| chr6:41744993 | CTCTGTG | C | 40 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0010 others(37): Show |
95 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(92): Show |
intron_variant | MODIFIER | c.60-191_60-186delCA others(4): Show |
PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 1/8 | chr6 | 41744993 | |||||||
| chr6:41744995 | C | G | 50 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0014 others(47): Show |
93 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.60-187G>C | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 1/8 | chr6 | 41744995 | |||||||
| chr6:41744997 | G | C | 28 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(25): Show |
76 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.60-189C>G | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 1/8 | chr6 | 41744997 | |||||||
| chr6:41745012 | TGTGC | T | 8 | a0001c0001t0001g0023 a0001c0001t0001g0077 a0001c0001t0001g0078 others(5): Show |
10 | HG00642.hp2 HG00735.hp1 HG00738.hp1 others(7): Show |
intron_variant | MODIFIER | c.60-208_60-205delGC others(2): Show |
PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 1/8 | chr6 | 41745012 | |||||||
| chr6:41745014 | T | C | 1 | a0001c0001t0001g0173 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.60-206A>G | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 1/8 | chr6 | 41745014 | |||||||
| chr6:41745014 | T | TGTGCGC | 3 | a0001c0001t0001g0004 a0001c0001t0001g0057 a0001c0001t0001g0217 |
16 | HG01106.hp2 HG01257.hp1 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.60-207_60-206insGC others(4): Show |
PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 1/8 | chr6 | 41745014 | |||||||
| chr6:41745014 | T | TGTGTGC | 3 | a0001c0001t0001g0168 a0001c0001t0001g0200 a0001c0001t0001g0201 |
3 | HG01891.hp2 HG03139.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.60-207_60-206insGC others(4): Show |
PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 1/8 | chr6 | 41745014 | |||||||
| chr6:41745016 | C | T | 120 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(117): Show |
214 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(211): Show |
intron_variant | MODIFIER | c.60-208G>A | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 1/8 | chr6 | 41745016 | |||||||
| chr6:41745025 | G | A | 3 | a0001c0001t0001g0065 a0001c0001t0001g0121 a0001c0001t0001g0122 |
3 | HG02818.hp2 HG02976.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.60-217C>T | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 1/8 | chr6 | 41745025 | |||||||
| chr6:41745191 | C | T | 4 | a0001c0001t0001g0083 a0001c0002t0001g0082 a0001c0002t0001g0084 others(1): Show |
5 | HG02896.hp1 HG02897.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.60-383G>A | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 1/8 | chr6 | 41745191 | |||||||
| chr6:41745243 | CT | C | 166 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(163): Show |
339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.60-436delA | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 1/8 | chr6 | 41745243 | |||||||
| chr6:41745248 | T | A | 1 | a0001c0001t0001g0015 | 5 | NA18939.hp2 NA18941.hp1 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.60-440A>T | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 1/8 | chr6 | 41745248 | |||||||
| chr6:41745308 | C | T | 1 | a0001c0001t0001g0076 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.60-500G>A | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 1/8 | chr6 | 41745308 | |||||||
| chr6:41745332 | G | A | 3 | a0001c0001t0002g0060 a0001c0001t0002g0231 a0001c0001t0002g0232 |
4 | HG01358.hp1 HG03834.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.60-524C>T | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 1/8 | chr6 | 41745332 | |||||||
| chr6:41745473 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.60-665G>A | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 1/8 | chr6 | 41745473 | |||||||
| chr6:41745474 | G | A | 3 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0128 |
3 | HG02109.hp2 HG02630.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.60-666C>T | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 1/8 | chr6 | 41745474 | |||||||
| chr6:41745527 | C | T | 1 | a0001c0001t0001g0061 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.60-719G>A | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 1/8 | chr6 | 41745527 | |||||||
| chr6:41745547 | T | C | 1 | a0001c0001t0001g0065 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.60-739A>G | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 1/8 | chr6 | 41745547 | |||||||
| chr6:41745548 | A | AC | 4 | a0001c0001t0001g0196 a0001c0001t0001g0209 a0001c0001t0001g0210 others(1): Show |
4 | HG01168.hp2 HG02615.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.60-741_60-740insG | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 1/8 | chr6 | 41745548 | |||||||
| chr6:41745548 | A | ACT | 33 | a0001c0001t0001g0003 a0001c0001t0001g0027 a0001c0001t0001g0051 others(30): Show |
54 | HG00423.hp1 HG00642.hp1 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.60-741_60-740insAG | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 1/8 | chr6 | 41745548 | |||||||
| chr6:41745548 | A | ACTT | 3 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0001g0171 |
3 | NA18978.hp1 NA19010.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.60-741_60-740insAA others(1): Show |
PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 1/8 | chr6 | 41745548 | |||||||
| chr6:41745548 | AG | A | 16 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0168 others(13): Show |
21 | HG01891.hp1 HG01891.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.60-741delC | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 1/8 | chr6 | 41745548 | |||||||
| chr6:41745549 | G | C | 26 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0017 others(23): Show |
57 | HG00438.hp2 HG00597.hp2 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.60-741C>G | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 1/8 | chr6 | 41745549 | |||||||
| chr6:41745549 | G | GT | 12 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(9): Show |
15 | HG00621.hp2 HG02486.hp1 HG02970.hp1 others(12): Show |
intron_variant | MODIFIER | c.60-742dupA | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 1/8 | chr6 | 41745549 | |||||||
| chr6:41745549 | G | T | 40 | a0001c0001t0001g0003 a0001c0001t0001g0027 a0001c0001t0001g0051 others(37): Show |
61 | HG00423.hp1 HG00642.hp1 HG00733.hp2 others(58): Show |
intron_variant | MODIFIER | c.60-741C>A | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 1/8 | chr6 | 41745549 | |||||||
| chr6:41745550 | T | C | 16 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0168 others(13): Show |
21 | HG01891.hp1 HG01891.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.60-742A>G | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 1/8 | chr6 | 41745550 | |||||||
| chr6:41745709 | C | T | 1 | a0002c0003t0001g0064 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.60-901G>A | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 1/8 | chr6 | 41745709 | |||||||
| chr6:41745791 | C | T | 1 | a0001c0001t0001g0070 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.60-983G>A | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 1/8 | chr6 | 41745791 | |||||||
| chr6:41745838 | T | G | 3 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0128 |
3 | HG02109.hp2 HG02630.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.60-1030A>C | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 1/8 | chr6 | 41745838 | |||||||
| chr6:41745900 | C | T | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(162): Show |
337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.60-1092G>A | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 1/8 | chr6 | 41745900 | |||||||
| chr6:41745965 | C | T | 6 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0066 others(3): Show |
21 | HG01069.hp1 HG01081.hp2 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.60-1157G>A | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 1/8 | chr6 | 41745965 | |||||||
| chr6:41745974 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.60-1166G>A | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 1/8 | chr6 | 41745974 | |||||||
| chr6:41746019 | G | A | 1 | a0002c0003t0001g0064 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.60-1211C>T | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 1/8 | chr6 | 41746019 | |||||||
| chr6:41746030 | C | T | 1 | a0001c0001t0001g0016 | 4 | HG01192.hp2 HG01361.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.60-1222G>A | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 1/8 | chr6 | 41746030 | |||||||
| chr6:41746059 | G | C | 1 | a0001c0001t0001g0050 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.59+1217C>G | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 1/8 | chr6 | 41746059 | |||||||
| chr6:41746114 | A | G | 1 | a0001c0001t0001g0168 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.59+1162T>C | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 1/8 | chr6 | 41746114 | |||||||
| chr6:41746118 | C | T | 1 | a0002c0003t0001g0064 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.59+1158G>A | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 1/8 | chr6 | 41746118 | |||||||
| chr6:41746162 | C | CA | 54 | a0001c0001t0001g0003 a0001c0001t0001g0027 a0001c0001t0001g0028 others(51): Show |
81 | HG00423.hp1 HG00642.hp1 HG00733.hp2 others(78): Show |
intron_variant | MODIFIER | c.59+1113dupT | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 1/8 | chr6 | 41746162 | |||||||
| chr6:41746381 | C | A | 3 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 |
3 | HG01168.hp2 HG02615.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.59+895G>T | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 1/8 | chr6 | 41746381 | |||||||
| chr6:41746445 | G | A | 1 | a0001c0001t0001g0212 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.59+831C>T | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 1/8 | chr6 | 41746445 | |||||||
| chr6:41746596 | C | A | 19 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0017 others(16): Show |
48 | HG00438.hp2 HG00597.hp2 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.59+680G>T | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 1/8 | chr6 | 41746596 | |||||||
| chr6:41746762 | G | A | 1 | a0001c0001t0001g0224 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.59+514C>T | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 1/8 | chr6 | 41746762 | |||||||
| chr6:41746824 | G | A | 2 | a0001c0001t0001g0225 a0001c0001t0001g0226 |
2 | HG00733.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.59+452C>T | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 1/8 | chr6 | 41746824 | |||||||
| chr6:41746908 | G | A | 1 | a0001c0001t0001g0227 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.59+368C>T | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 1/8 | chr6 | 41746908 | |||||||
| chr6:41746913 | T | C | 1 | a0001c0001t0001g0228 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.59+363A>G | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 1/8 | chr6 | 41746913 | |||||||
| chr6:41746942 | G | C | 1 | a0001c0001t0001g0229 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.59+334C>G | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 1/8 | chr6 | 41746942 | |||||||
| chr6:41746952 | C | T | 1 | a0001c0001t0001g0063 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.59+324G>A | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 1/8 | chr6 | 41746952 | |||||||
| chr6:41747054 | A | G | 1 | a0001c0001t0001g0062 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.59+222T>C | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 1/8 | chr6 | 41747054 | |||||||
| chr6:41747107 | C | T | 1 | a0001c0001t0001g0061 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.59+169G>A | PGC | ENSG00000096088.16 | transcript | ENST00000373025.7 | protein_coding | 1/8 | chr6 | 41747107 |