Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 120824 |
| ensemblid | ENSG00000220948.6 |
| hgncid | 43972 |
| symbol | TRIM51G |
| name | tripartite motif-containing 51G |
| refseq_nuc | NM_001396075.1 |
| refseq_prot | NP_001383004.1 |
| ensembl_nuc | ENST00000534741.3 |
| ensembl_prot | ENSP00000497050.1 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 48975498 |
| end | 48983885 |
| strand | - |
| ver | v1.2 |
| region | chr11:48975498-48983885 |
| region5000 | chr11:48970498-48988885 |
| regionname0 | TRIM51G_chr11_48975498_48983885 |
| regionname5000 | TRIM51G_chr11_48970498_48988885 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 452 | 189 | 43 | 42 | 75 | 11 | 18 | 62 | TRIM51G_chr11_48970498_48988885 | TRIM51G | MNSGI others(447): Show |
chr11 | 48970498 | 48988885 |
| a0002 | 0/0 | 201 | 137 | 19 | 16 | 78 | 5 | 19 | 55 | TRIM51G_chr11_48970498_48988885 | TRIM51G | MNSGI others(196): Show |
chr11 | 48970498 | 48988885 |
| a0003 | 0/1 | 452 | 76 | 23 | 12 | 37 | 0 | 3 | 29 | TRIM51G_chr11_48970498_48988885 | TRIM51G | MNSGI others(447): Show |
chr11 | 48970498 | 48988885 |
| a0004 | 1/0 | 452 | 10 | 9 | 0 | 0 | 0 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | MNSGI others(447): Show |
chr11 | 48970498 | 48988885 |
| a0005 | 0/0 | 452 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | MNSGI others(447): Show |
chr11 | 48970498 | 48988885 |
| a0006 | 0/0 | 342 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | TRIM51G_chr11_48970498_48988885 | TRIM51G | MNSGI others(337): Show |
chr11 | 48970498 | 48988885 |
| a0007 | 0/0 | 452 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | MNSGI others(447): Show |
chr11 | 48970498 | 48988885 |
| a0008 | 0/0 | 452 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | MNSGI others(447): Show |
chr11 | 48970498 | 48988885 |
| a0009 | 0/0 | 452 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | MNSGI others(447): Show |
chr11 | 48970498 | 48988885 |
| a0010 | 0/0 | 452 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TRIM51G_chr11_48970498_48988885 | TRIM51G | MNSGI others(447): Show |
chr11 | 48970498 | 48988885 |
| a0011 | 0/0 | 201 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TRIM51G_chr11_48970498_48988885 | TRIM51G | MNSGI others(196): Show |
chr11 | 48970498 | 48988885 |
| a0012 | 0/0 | 201 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TRIM51G_chr11_48970498_48988885 | TRIM51G | MNSGI others(196): Show |
chr11 | 48970498 | 48988885 |
| a0013 | 0/0 | 452 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | MNSGI others(447): Show |
chr11 | 48970498 | 48988885 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1356 | 181 | 38 | 41 | 74 | 10 | 18 | TRIM51G_chr11_48970498_48988885 | TRIM51G | ATGAA others(1351): Show |
chr11 | 48970498 | 48988885 | ||
| a0001c0006 | 0/0 | 1356 | 7 | 5 | 1 | 0 | 1 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | ATGAA others(1351): Show |
chr11 | 48970498 | 48988885 | ||
| a0001c0011 | 0/0 | 1356 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | ATGAA others(1351): Show |
chr11 | 48970498 | 48988885 | ||
| a0002c0002 | 0/0 | 1356 | 106 | 18 | 14 | 54 | 4 | 16 | TRIM51G_chr11_48970498_48988885 | TRIM51G | ATGAA others(1351): Show |
chr11 | 48970498 | 48988885 | ||
| a0002c0004 | 0/0 | 1356 | 29 | 0 | 2 | 23 | 1 | 3 | TRIM51G_chr11_48970498_48988885 | TRIM51G | ATGAA others(1351): Show |
chr11 | 48970498 | 48988885 | ||
| a0002c0015 | 0/0 | 1356 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | ATGAA others(1351): Show |
chr11 | 48970498 | 48988885 | ||
| a0002c0016 | 0/0 | 1356 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | ATGAA others(1351): Show |
chr11 | 48970498 | 48988885 | ||
| a0003c0003 | 0/1 | 1356 | 76 | 23 | 12 | 37 | 0 | 3 | TRIM51G_chr11_48970498_48988885 | TRIM51G | ATGAA others(1351): Show |
chr11 | 48970498 | 48988885 | ||
| a0004c0005 | 1/0 | 1356 | 10 | 9 | 0 | 0 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | ATGAA others(1351): Show |
chr11 | 48970498 | 48988885 | ||
| a0005c0007 | 0/0 | 1356 | 3 | 2 | 1 | 0 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | ATGAA others(1351): Show |
chr11 | 48970498 | 48988885 | ||
| a0006c0008 | 0/0 | 1356 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | ATGAA others(1351): Show |
chr11 | 48970498 | 48988885 | ||
| a0007c0009 | 0/0 | 1356 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | ATGAA others(1351): Show |
chr11 | 48970498 | 48988885 | ||
| a0008c0017 | 0/0 | 1356 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | ATGAA others(1351): Show |
chr11 | 48970498 | 48988885 | ||
| a0009c0014 | 0/0 | 1356 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | ATGAA others(1351): Show |
chr11 | 48970498 | 48988885 | ||
| a0010c0012 | 0/0 | 1356 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | ATGAA others(1351): Show |
chr11 | 48970498 | 48988885 | ||
| a0011c0018 | 0/0 | 1356 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | ATGAA others(1351): Show |
chr11 | 48970498 | 48988885 | ||
| a0012c0010 | 0/0 | 1356 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | ATGAA others(1351): Show |
chr11 | 48970498 | 48988885 | ||
| a0013c0013 | 0/0 | 1356 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | ATGAA others(1351): Show |
chr11 | 48970498 | 48988885 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1510 | 180 | 38 | 41 | 74 | 10 | 17 | TRIM51G_chr11_48970498_48988885 | TRIM51G | CCAGA others(1505): Show |
chr11 | 48970498 | 48988885 |
| a0001c0001t0004 | 0/0 | 1510 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM51G_chr11_48970498_48988885 | TRIM51G | CCAGA others(1505): Show |
chr11 | 48970498 | 48988885 |
| a0001c0006t0003 | 0/0 | 1510 | 7 | 5 | 1 | 0 | 1 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | CCAGA others(1505): Show |
chr11 | 48970498 | 48988885 |
| a0001c0011t0001 | 0/0 | 1510 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | CCAGA others(1505): Show |
chr11 | 48970498 | 48988885 |
| a0002c0002t0002 | 0/0 | 1510 | 106 | 18 | 14 | 54 | 4 | 16 | TRIM51G_chr11_48970498_48988885 | TRIM51G | CCAGA others(1505): Show |
chr11 | 48970498 | 48988885 |
| a0002c0004t0002 | 0/0 | 1510 | 29 | 0 | 2 | 23 | 1 | 3 | TRIM51G_chr11_48970498_48988885 | TRIM51G | CCAGA others(1505): Show |
chr11 | 48970498 | 48988885 |
| a0002c0015t0002 | 0/0 | 1510 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | CCAGA others(1505): Show |
chr11 | 48970498 | 48988885 |
| a0002c0016t0002 | 0/0 | 1510 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | CCAGA others(1505): Show |
chr11 | 48970498 | 48988885 |
| a0003c0003t0001 | 0/1 | 1510 | 76 | 23 | 12 | 37 | 0 | 3 | TRIM51G_chr11_48970498_48988885 | TRIM51G | CCAGA others(1505): Show |
chr11 | 48970498 | 48988885 |
| a0004c0005t0002 | 1/0 | 1510 | 10 | 9 | 0 | 0 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | CCAGA others(1505): Show |
chr11 | 48970498 | 48988885 |
| a0005c0007t0001 | 0/0 | 1510 | 3 | 2 | 1 | 0 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | CCAGA others(1505): Show |
chr11 | 48970498 | 48988885 |
| a0006c0008t0001 | 0/0 | 1510 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | CCAGA others(1505): Show |
chr11 | 48970498 | 48988885 |
| a0007c0009t0001 | 0/0 | 1510 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | CCAGA others(1505): Show |
chr11 | 48970498 | 48988885 |
| a0008c0017t0001 | 0/0 | 1510 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | CCAGA others(1505): Show |
chr11 | 48970498 | 48988885 |
| a0009c0014t0002 | 0/0 | 1510 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | CCAGA others(1505): Show |
chr11 | 48970498 | 48988885 |
| a0010c0012t0001 | 0/0 | 1510 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | CCAGA others(1505): Show |
chr11 | 48970498 | 48988885 |
| a0011c0018t0002 | 0/0 | 1510 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | CCAGA others(1505): Show |
chr11 | 48970498 | 48988885 |
| a0012c0010t0002 | 0/0 | 1510 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | CCAGA others(1505): Show |
chr11 | 48970498 | 48988885 |
| a0013c0013t0001 | 0/0 | 1510 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | CCAGA others(1505): Show |
chr11 | 48970498 | 48988885 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 39 | 0 | 6 | 30 | 0 | 3 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0001c0001t0001g0003 | 0/0 | 35 | 0 | 10 | 21 | 2 | 2 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0001c0001t0001g0004 | 0/0 | 20 | 5 | 0 | 14 | 0 | 1 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0001c0001t0001g0008 | 0/0 | 10 | 0 | 5 | 1 | 2 | 2 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0001c0001t0001g0011 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0001c0001t0001g0015 | 0/0 | 5 | 0 | 0 | 3 | 0 | 2 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0001c0001t0001g0024 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0001c0001t0001g0025 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0001c0001t0001g0026 | 0/0 | 4 | 1 | 2 | 0 | 0 | 1 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0001c0001t0001g0027 | 0/0 | 4 | 0 | 1 | 0 | 2 | 1 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0001c0001t0001g0034 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0001c0001t0001g0035 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0001c0001t0001g0047 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0001c0001t0001g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0001c0001t0001g0051 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0001c0001t0001g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0001c0001t0001g0053 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0001c0001t0001g0054 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0001c0001t0001g0055 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0001c0001t0004g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0001c0006t0003g0032 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0001c0006t0003g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0001c0006t0003g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0001c0006t0003g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0001c0011t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0002c0002t0002g0005 | 0/0 | 14 | 2 | 3 | 4 | 2 | 3 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0002c0002t0002g0007 | 0/0 | 11 | 1 | 1 | 8 | 0 | 1 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0002c0002t0002g0009 | 0/0 | 7 | 0 | 1 | 6 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0002c0002t0002g0012 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0002c0002t0002g0013 | 0/0 | 5 | 0 | 2 | 0 | 0 | 3 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0002c0002t0002g0014 | 0/0 | 5 | 0 | 0 | 3 | 0 | 2 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0002c0002t0002g0017 | 0/0 | 4 | 2 | 0 | 1 | 1 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0002c0002t0002g0019 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0002c0002t0002g0020 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0002c0002t0002g0021 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0002c0002t0002g0028 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0002c0002t0002g0029 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0002c0002t0002g0030 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0002c0002t0002g0031 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0002c0002t0002g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0002c0002t0002g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0002c0002t0002g0042 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0002c0002t0002g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0002c0002t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0002c0002t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0002c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0002c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0002c0002t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0002c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0002c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0002c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0002c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0002c0002t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0002c0002t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0002c0002t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0002c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0002c0002t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0002c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0002c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0002c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0002c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0002c0002t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0002c0002t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0002c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0002c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0002c0004t0002g0010 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0002c0004t0002g0018 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0002c0004t0002g0040 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0002c0004t0002g0041 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0002c0004t0002g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0002c0004t0002g0045 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0002c0004t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0002c0004t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0002c0004t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0002c0004t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0002c0004t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0002c0004t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0002c0004t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0002c0004t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0002c0004t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0002c0004t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0002c0015t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0002c0016t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0003c0003t0001g0001 | 0/0 | 42 | 10 | 9 | 21 | 0 | 2 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0003c0003t0001g0006 | 0/0 | 13 | 5 | 1 | 7 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0003c0003t0001g0022 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0003c0003t0001g0023 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0003c0003t0001g0033 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0003c0003t0001g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0003c0003t0001g0049 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0003c0003t0001g0098 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0003c0003t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0003c0003t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0003c0003t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0003c0003t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0003c0003t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0004c0005t0002g0016 | 1/0 | 4 | 3 | 0 | 0 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0004c0005t0002g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0004c0005t0002g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0004c0005t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0004c0005t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0005c0007t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0005c0007t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0005c0007t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0006c0008t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0006c0008t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0007c0009t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0008c0017t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0009c0014t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0010c0012t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0011c0018t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0012c0010t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| a0013c0013t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0002 | g0017 | EUR | GBR | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | GBR | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0035 | EUR | GBR | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | GBR | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0025 | EUR | FIN | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0116 | EUR | FIN | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | FIN | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0128 | EUR | FIN | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG00408 | hp1 | a0002 | c0002 | t0002 | g0021 | EAS | CHS | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG00408 | hp2 | a0003 | c0003 | t0001 | g0001 | EAS | CHS | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG00423 | hp1 | a0003 | c0003 | t0001 | g0001 | EAS | CHS | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG00438 | hp1 | a0002 | c0004 | t0002 | g0057 | EAS | CHS | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG00438 | hp2 | a0002 | c0002 | t0002 | g0012 | EAS | CHS | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG00544 | hp1 | a0002 | c0002 | t0002 | g0007 | EAS | CHS | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG00558 | hp1 | a0001 | c0011 | t0001 | g0119 | EAS | CHS | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG00558 | hp2 | a0003 | c0003 | t0001 | g0006 | EAS | CHS | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG00597 | hp1 | a0002 | c0004 | t0002 | g0044 | EAS | CHS | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG00597 | hp2 | a0003 | c0003 | t0001 | g0001 | EAS | CHS | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG00609 | hp1 | a0002 | c0004 | t0002 | g0018 | EAS | CHS | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG00609 | hp2 | a0003 | c0003 | t0001 | g0102 | EAS | CHS | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG00621 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | CHS | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG00621 | hp2 | a0002 | c0002 | t0002 | g0043 | EAS | CHS | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG00673 | hp1 | a0002 | c0002 | t0002 | g0019 | EAS | CHS | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG00733 | hp1 | a0002 | c0002 | t0002 | g0005 | AMR | PUR | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG00733 | hp2 | a0003 | c0003 | t0001 | g0001 | AMR | PUR | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG01070 | hp2 | a0002 | c0002 | t0002 | g0013 | AMR | PUR | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG01071 | hp1 | a0002 | c0002 | t0002 | g0013 | AMR | PUR | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG01071 | hp2 | a0002 | c0004 | t0002 | g0045 | AMR | PUR | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG01081 | hp2 | a0003 | c0003 | t0001 | g0006 | AMR | PUR | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG01099 | hp1 | a0003 | c0003 | t0001 | g0001 | AMR | PUR | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG01099 | hp2 | a0002 | c0004 | t0002 | g0040 | AMR | PUR | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG01167 | hp1 | a0002 | c0002 | t0002 | g0076 | AMR | PUR | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG01168 | hp2 | a0002 | c0002 | t0002 | g0065 | AMR | PUR | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG01175 | hp2 | a0007 | c0009 | t0001 | g0123 | AMR | PUR | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG01192 | hp1 | a0001 | c0006 | t0003 | g0032 | AMR | PUR | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG01243 | hp1 | a0003 | c0003 | t0001 | g0001 | AMR | PUR | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG01243 | hp2 | a0005 | c0007 | t0001 | g0108 | AMR | PUR | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG01255 | hp1 | a0003 | c0003 | t0001 | g0001 | AMR | CLM | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | CLM | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | CLM | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG01257 | hp2 | a0003 | c0003 | t0001 | g0099 | AMR | CLM | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | CLM | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG01258 | hp2 | a0002 | c0002 | t0002 | g0088 | AMR | CLM | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG01261 | hp2 | a0003 | c0003 | t0001 | g0001 | AMR | CLM | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG01346 | hp1 | a0003 | c0003 | t0001 | g0001 | AMR | CLM | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG01346 | hp2 | a0003 | c0003 | t0001 | g0033 | AMR | CLM | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG01358 | hp1 | a0002 | c0002 | t0002 | g0075 | AMR | CLM | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG01358 | hp2 | a0003 | c0003 | t0001 | g0001 | AMR | CLM | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG01361 | hp1 | a0002 | c0002 | t0002 | g0009 | AMR | CLM | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG01433 | hp2 | a0002 | c0002 | t0002 | g0061 | AMR | CLM | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG01515 | hp1 | a0001 | c0006 | t0003 | g0032 | EUR | IBS | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0027 | EUR | IBS | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG01516 | hp1 | a0002 | c0002 | t0002 | g0005 | EUR | IBS | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG01516 | hp2 | a0002 | c0002 | t0002 | g0042 | EUR | IBS | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG01517 | hp1 | a0002 | c0002 | t0002 | g0005 | EUR | IBS | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0027 | EUR | IBS | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG01884 | hp1 | a0005 | c0007 | t0001 | g0109 | AFR | ACB | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | ACB | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PEL | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG01952 | hp2 | a0002 | c0002 | t0002 | g0007 | AMR | PEL | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG01978 | hp1 | a0002 | c0002 | t0002 | g0005 | AMR | PEL | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG01978 | hp2 | a0003 | c0003 | t0001 | g0001 | AMR | PEL | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG01993 | hp1 | a0002 | c0002 | t0002 | g0030 | AMR | PEL | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG02004 | hp2 | a0002 | c0002 | t0002 | g0042 | AMR | PEL | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG02015 | hp1 | a0002 | c0002 | t0002 | g0017 | EAS | KHV | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG02015 | hp2 | a0002 | c0004 | t0002 | g0079 | EAS | KHV | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG02027 | hp1 | a0002 | c0002 | t0002 | g0043 | EAS | KHV | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG02040 | hp1 | a0002 | c0004 | t0002 | g0041 | EAS | KHV | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG02040 | hp2 | a0003 | c0003 | t0001 | g0023 | EAS | KHV | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG02055 | hp1 | a0002 | c0002 | t0002 | g0074 | AFR | ACB | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | ACB | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG02056 | hp1 | a0003 | c0003 | t0001 | g0001 | EAS | KHV | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG02056 | hp2 | a0008 | c0017 | t0001 | g0125 | EAS | KHV | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG02071 | hp1 | a0002 | c0002 | t0002 | g0021 | EAS | KHV | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG02074 | hp1 | a0003 | c0003 | t0001 | g0049 | EAS | KHV | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG02074 | hp2 | a0002 | c0002 | t0002 | g0020 | EAS | KHV | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG02083 | hp1 | a0006 | c0008 | t0001 | g0124 | EAS | KHV | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG02129 | hp1 | a0002 | c0002 | t0002 | g0029 | EAS | KHV | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG02132 | hp1 | a0002 | c0002 | t0002 | g0007 | EAS | KHV | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG02132 | hp2 | a0002 | c0002 | t0002 | g0071 | EAS | KHV | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG02135 | hp1 | a0002 | c0002 | t0002 | g0014 | EAS | KHV | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | ACB | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG02155 | hp1 | a0002 | c0004 | t0002 | g0040 | EAS | CDX | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG02155 | hp2 | a0002 | c0002 | t0002 | g0066 | EAS | CDX | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG02165 | hp1 | a0002 | c0002 | t0002 | g0007 | EAS | CDX | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG02165 | hp2 | a0002 | c0002 | t0002 | g0063 | EAS | CDX | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG02257 | hp1 | a0005 | c0007 | t0001 | g0113 | AFR | ACB | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG02258 | hp1 | a0002 | c0002 | t0002 | g0058 | AFR | ACB | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG02258 | hp2 | a0003 | c0003 | t0001 | g0001 | AFR | ACB | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG02273 | hp2 | a0003 | c0003 | t0001 | g0001 | AMR | PEL | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | ACB | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG02280 | hp2 | a0002 | c0002 | t0002 | g0005 | AFR | ACB | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG02293 | hp2 | a0002 | c0002 | t0002 | g0005 | AMR | PEL | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | ACB | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG02451 | hp2 | a0003 | c0003 | t0001 | g0006 | AFR | ACB | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | KHV | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG02572 | hp1 | a0002 | c0002 | t0002 | g0031 | AFR | GWD | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG02602 | hp2 | a0002 | c0004 | t0002 | g0070 | SAS | PJL | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG02615 | hp1 | a0004 | c0005 | t0002 | g0037 | AFR | GWD | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG02615 | hp2 | a0003 | c0003 | t0001 | g0022 | AFR | GWD | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG02622 | hp2 | a0004 | c0005 | t0002 | g0036 | AFR | GWD | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG02630 | hp2 | a0002 | c0002 | t0002 | g0028 | AFR | GWD | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG02647 | hp1 | a0003 | c0003 | t0001 | g0001 | AFR | GWD | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG02683 | hp1 | a0002 | c0002 | t0002 | g0080 | SAS | PJL | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG02698 | hp1 | a0003 | c0003 | t0001 | g0001 | SAS | PJL | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG02698 | hp2 | a0002 | c0004 | t0002 | g0086 | SAS | PJL | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG02717 | hp2 | a0004 | c0005 | t0002 | g0036 | AFR | GWD | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG02723 | hp2 | a0002 | c0002 | t0002 | g0007 | AFR | GWD | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG02735 | hp1 | a0003 | c0003 | t0001 | g0033 | SAS | PJL | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG02738 | hp1 | a0002 | c0002 | t0002 | g0007 | SAS | PJL | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG02809 | hp1 | a0001 | c0006 | t0003 | g0032 | AFR | GWD | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG02809 | hp2 | a0002 | c0002 | t0002 | g0078 | AFR | GWD | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG02818 | hp2 | a0003 | c0003 | t0001 | g0022 | AFR | GWD | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG02886 | hp1 | a0003 | c0003 | t0001 | g0001 | AFR | GWD | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG02886 | hp2 | a0003 | c0003 | t0001 | g0022 | AFR | GWD | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG02895 | hp1 | a0002 | c0002 | t0002 | g0028 | AFR | GWD | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG02895 | hp2 | a0003 | c0003 | t0001 | g0006 | AFR | GWD | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG02896 | hp1 | a0003 | c0003 | t0001 | g0006 | AFR | GWD | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG02897 | hp1 | a0002 | c0002 | t0002 | g0028 | AFR | GWD | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG02897 | hp2 | a0003 | c0003 | t0001 | g0006 | AFR | GWD | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG02922 | hp1 | a0001 | c0006 | t0003 | g0097 | AFR | ESN | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | ESN | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | ESN | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG02965 | hp2 | a0004 | c0005 | t0002 | g0016 | AFR | ESN | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG02970 | hp1 | a0003 | c0003 | t0001 | g0001 | AFR | ESN | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG02970 | hp2 | a0002 | c0002 | t0002 | g0031 | AFR | ESN | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG02976 | hp1 | a0001 | c0006 | t0003 | g0096 | AFR | ESN | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | ESN | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG03017 | hp1 | a0002 | c0002 | t0002 | g0013 | SAS | PJL | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG03017 | hp2 | a0002 | c0004 | t0002 | g0084 | SAS | PJL | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG03041 | hp1 | a0004 | c0005 | t0002 | g0016 | AFR | GWD | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | MSL | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | MSL | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG03130 | hp1 | a0004 | c0005 | t0002 | g0016 | AFR | ESN | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ESN | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | ESN | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | ESN | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG03209 | hp1 | a0002 | c0002 | t0002 | g0017 | AFR | MSL | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG03209 | hp2 | a0003 | c0003 | t0001 | g0006 | AFR | MSL | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | MSL | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG03225 | hp2 | a0003 | c0003 | t0001 | g0001 | AFR | MSL | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG03239 | hp1 | a0002 | c0002 | t0002 | g0029 | SAS | PJL | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG03239 | hp2 | a0002 | c0002 | t0002 | g0005 | SAS | PJL | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG03453 | hp1 | a0002 | c0015 | t0002 | g0069 | AFR | MSL | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG03453 | hp2 | a0009 | c0014 | t0002 | g0059 | AFR | MSL | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | MSL | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG03486 | hp2 | a0003 | c0003 | t0001 | g0001 | AFR | MSL | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG03492 | hp1 | a0002 | c0002 | t0002 | g0014 | SAS | PJL | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG03492 | hp2 | a0003 | c0003 | t0001 | g0001 | SAS | PJL | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | ESN | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG03516 | hp2 | a0003 | c0003 | t0001 | g0103 | AFR | ESN | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG03540 | hp2 | a0002 | c0002 | t0002 | g0039 | AFR | GWD | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG03579 | hp1 | a0004 | c0005 | t0002 | g0060 | AFR | MSL | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG03579 | hp2 | a0002 | c0002 | t0002 | g0089 | AFR | MSL | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG03654 | hp2 | a0002 | c0002 | t0002 | g0077 | SAS | PJL | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG03704 | hp2 | a0002 | c0002 | t0002 | g0005 | SAS | PJL | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG03831 | hp1 | a0002 | c0002 | t0002 | g0068 | SAS | BEB | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG03834 | hp1 | a0002 | c0002 | t0002 | g0014 | SAS | BEB | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG03927 | hp1 | a0002 | c0002 | t0002 | g0085 | SAS | BEB | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | BEB | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG03942 | hp1 | a0001 | c0001 | t0004 | g0056 | SAS | BEB | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG03942 | hp2 | a0002 | c0002 | t0002 | g0013 | SAS | BEB | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG04115 | hp1 | a0002 | c0002 | t0002 | g0030 | SAS | STU | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | STU | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG04199 | hp1 | a0002 | c0002 | t0002 | g0005 | SAS | STU | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG04199 | hp2 | a0002 | c0002 | t0002 | g0013 | SAS | STU | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG04204 | hp1 | a0002 | c0002 | t0002 | g0029 | SAS | STU | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | STU | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA18522 | hp1 | a0002 | c0002 | t0002 | g0039 | AFR | YRI | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA18522 | hp2 | a0003 | c0003 | t0001 | g0049 | AFR | YRI | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA18906 | hp1 | a0003 | c0003 | t0001 | g0022 | AFR | YRI | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | YRI | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA18939 | hp1 | a0002 | c0002 | t0002 | g0064 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA18940 | hp2 | a0003 | c0003 | t0001 | g0006 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA18941 | hp1 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA18942 | hp1 | a0003 | c0003 | t0001 | g0006 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA18943 | hp2 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA18944 | hp1 | a0003 | c0003 | t0001 | g0048 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA18944 | hp2 | a0002 | c0004 | t0002 | g0010 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA18945 | hp2 | a0002 | c0004 | t0002 | g0082 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA18946 | hp1 | a0003 | c0003 | t0001 | g0100 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA18947 | hp1 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA18947 | hp2 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA18948 | hp2 | a0002 | c0004 | t0002 | g0010 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA18951 | hp2 | a0002 | c0004 | t0002 | g0045 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA18953 | hp1 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA18954 | hp1 | a0003 | c0003 | t0001 | g0023 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA18954 | hp2 | a0002 | c0002 | t0002 | g0073 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA18959 | hp1 | a0002 | c0004 | t0002 | g0010 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA18959 | hp2 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA18960 | hp1 | a0002 | c0002 | t0002 | g0083 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA18960 | hp2 | a0002 | c0002 | t0002 | g0091 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA18962 | hp1 | a0002 | c0004 | t0002 | g0092 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA18963 | hp1 | a0002 | c0004 | t0002 | g0010 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA18963 | hp2 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA18964 | hp1 | a0002 | c0002 | t0002 | g0020 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA18964 | hp2 | a0010 | c0012 | t0001 | g0132 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA18965 | hp1 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA18966 | hp1 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA18967 | hp1 | a0011 | c0018 | t0002 | g0072 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA18970 | hp1 | a0003 | c0003 | t0001 | g0006 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA18971 | hp2 | a0002 | c0004 | t0002 | g0018 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA18972 | hp2 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA18973 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA18973 | hp2 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA18974 | hp1 | a0003 | c0003 | t0001 | g0023 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA18974 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA18975 | hp2 | a0002 | c0002 | t0002 | g0081 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA18977 | hp1 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA18977 | hp2 | a0002 | c0004 | t0002 | g0062 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA18978 | hp1 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA18978 | hp2 | a0002 | c0002 | t0002 | g0012 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA18979 | hp1 | a0002 | c0002 | t0002 | g0012 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA18981 | hp1 | a0002 | c0004 | t0002 | g0010 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA18981 | hp2 | a0003 | c0003 | t0001 | g0006 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA18984 | hp1 | a0006 | c0008 | t0001 | g0118 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA18985 | hp2 | a0002 | c0002 | t0002 | g0019 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA18986 | hp1 | a0002 | c0004 | t0002 | g0010 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA18986 | hp2 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA18987 | hp2 | a0012 | c0010 | t0002 | g0067 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA18988 | hp2 | a0002 | c0004 | t0002 | g0018 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA18990 | hp1 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA18993 | hp1 | a0003 | c0003 | t0001 | g0048 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA18999 | hp1 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA19000 | hp1 | a0002 | c0002 | t0002 | g0020 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA19005 | hp2 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA19007 | hp1 | a0002 | c0002 | t0002 | g0019 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA19007 | hp2 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA19009 | hp1 | a0002 | c0004 | t0002 | g0010 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA19009 | hp2 | a0002 | c0002 | t0002 | g0019 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA19010 | hp1 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA19010 | hp2 | a0002 | c0004 | t0002 | g0018 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA19011 | hp2 | a0003 | c0003 | t0001 | g0006 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA19030 | hp1 | a0013 | c0013 | t0001 | g0129 | AFR | LWK | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | LWK | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | LWK | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA19043 | hp2 | a0003 | c0003 | t0001 | g0001 | AFR | LWK | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA19055 | hp1 | a0002 | c0002 | t0002 | g0021 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA19056 | hp2 | a0002 | c0002 | t0002 | g0038 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA19057 | hp2 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA19059 | hp1 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA19059 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA19062 | hp1 | a0003 | c0003 | t0001 | g0006 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA19062 | hp2 | a0002 | c0002 | t0002 | g0038 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA19065 | hp1 | a0002 | c0002 | t0002 | g0012 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA19066 | hp1 | a0002 | c0004 | t0002 | g0090 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA19066 | hp2 | a0002 | c0002 | t0002 | g0014 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA19070 | hp1 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA19074 | hp2 | a0002 | c0002 | t0002 | g0093 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA19076 | hp1 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA19076 | hp2 | a0002 | c0002 | t0002 | g0020 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA19077 | hp1 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA19078 | hp2 | a0002 | c0002 | t0002 | g0021 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA19081 | hp1 | a0002 | c0004 | t0002 | g0094 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA19082 | hp1 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA19083 | hp1 | a0002 | c0002 | t0002 | g0012 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA19084 | hp1 | a0002 | c0004 | t0002 | g0044 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA19084 | hp2 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA19086 | hp1 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA19088 | hp1 | a0003 | c0003 | t0001 | g0023 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA19089 | hp1 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA19090 | hp2 | a0002 | c0016 | t0002 | g0087 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | YRI | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA19240 | hp2 | a0001 | c0006 | t0003 | g0046 | AFR | YRI | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA20129 | hp1 | a0003 | c0003 | t0001 | g0033 | AFR | ASW | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA20129 | hp2 | a0002 | c0002 | t0002 | g0005 | AFR | ASW | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA20752 | hp2 | a0002 | c0004 | t0002 | g0041 | EUR | TSI | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | GIH | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | GIH | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | CLM | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG02109 | hp1 | a0003 | c0003 | t0001 | g0001 | AFR | ACB | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG02109 | hp2 | a0002 | c0002 | t0002 | g0031 | AFR | ACB | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG02486 | hp1 | a0003 | c0003 | t0001 | g0001 | AFR | ACB | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG02559 | hp1 | a0001 | c0006 | t0003 | g0046 | AFR | ACB | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG03471 | hp1 | a0003 | c0003 | t0001 | g0001 | AFR | MSL | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG03471 | hp2 | a0004 | c0005 | t0002 | g0037 | AFR | MSL | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | USA | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| HG06807 | hp2 | a0004 | c0005 | t0002 | g0095 | AFR | USA | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA18955 | hp1 | a0002 | c0002 | t0002 | g0012 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA18955 | hp2 | a0002 | c0002 | t0002 | g0014 | EAS | JPT | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA20300 | hp1 | a0003 | c0003 | t0001 | g0101 | AFR | USA | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA20300 | hp2 | a0002 | c0002 | t0002 | g0017 | AFR | USA | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA21309 | hp1 | a0002 | c0002 | t0002 | g0030 | AFR | LWK | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | LWK | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| homoSapiens | chm13v2 | a0003 | c0003 | t0001 | g0098 | REF | REF | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| homoSapiens | grch38p0 | a0004 | c0005 | t0002 | g0016 | REF | REF | TRIM51G_chr11_48970498_48988885 | TRIM51G | chr11 | 48970498 | 48988885 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:48975562 | T | C | 1 | a0002 | 1 | HG03453.hp1 | missense_variant | MODERATE | c.1295A>G | p.Tyr432Cys | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 7/7 | 1446/1510 | 1295/1359 | 432/452 | chr11 | 48975562 | |||
| chr11:48975782 | T | G | 3 | a0002 a0011 a0012 |
139 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(136): Show |
missense_variant | MODERATE | c.1075A>C | p.Asn359His | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 7/7 | 1226/1510 | 1075/1359 | 359/452 | chr11 | 48975782 | |||
| chr11:48975829 | C | T | 1 | a0006 | 2 | HG02083.hp1 NA18984.hp1 |
stop_gained | HIGH | c.1028G>A | p.Trp343* | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 7/7 | 1179/1510 | 1028/1359 | 343/452 | chr11 | 48975829 | |||
| chr11:48975949 | T | C | 1 | a0010 | 1 | NA18964.hp2 | missense_variant | MODERATE | c.908A>G | p.His303Arg | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 7/7 | 1059/1510 | 908/1359 | 303/452 | chr11 | 48975949 | |||
| chr11:48977136 | A | G | 1 | a0003 | 75 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(72): Show |
missense_variant | MODERATE | c.808T>C | p.Phe270Leu | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 6/7 | 959/1510 | 808/1359 | 270/452 | chr11 | 48977136 | |||
| chr11:48977151 | G | C | 1 | a0013 | 1 | NA19030.hp1 | missense_variant | MODERATE | c.793C>G | p.Pro265Ala | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 6/7 | 944/1510 | 793/1359 | 265/452 | chr11 | 48977151 | |||
| chr11:48978951 | T | G | 1 | a0002 | 29 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(26): Show |
missense_variant | MODERATE | c.659A>C | p.Glu220Ala | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 4/7 | 810/1510 | 659/1359 | 220/452 | chr11 | 48978951 | |||
| chr11:48978970 | C | T | 8 | a0001 a0003 a0005 others(5): Show |
273 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(270): Show |
missense_variant | MODERATE | c.640G>A | p.Glu214Lys | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 4/7 | 791/1510 | 640/1359 | 214/452 | chr11 | 48978970 | |||
| chr11:48979005 | T | C | 1 | a0009 | 1 | HG03453.hp2 | missense_variant | MODERATE | c.605A>G | p.Gln202Arg | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 4/7 | 756/1510 | 605/1359 | 202/452 | chr11 | 48979005 | |||
| chr11:48979006 | G | A | 3 | a0002 a0011 a0012 |
139 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(136): Show |
stop_gained | HIGH | c.604C>T | p.Gln202* | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 4/7 | 755/1510 | 604/1359 | 202/452 | chr11 | 48979006 | |||
| chr11:48979011 | C | A | 1 | a0008 | 1 | HG02056.hp2 | missense_variant | MODERATE | c.599G>T | p.Arg200Met | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 4/7 | 750/1510 | 599/1359 | 200/452 | chr11 | 48979011 | |||
| chr11:48981449 | G | A | 1 | a0005 | 3 | HG01243.hp2 HG01884.hp1 HG02257.hp1 |
missense_variant | MODERATE | c.247C>T | p.Arg83Trp | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 2/7 | 398/1510 | 247/1359 | 83/452 | chr11 | 48981449 | |||
| chr11:48981460 | T | C | 1 | a0011 | 1 | NA18967.hp1 | missense_variant | MODERATE | c.236A>G | p.Lys79Arg | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 2/7 | 387/1510 | 236/1359 | 79/452 | chr11 | 48981460 | |||
| chr11:48981466 | G | A | 1 | a0005 | 3 | HG01243.hp2 HG01884.hp1 HG02257.hp1 |
missense_variant | MODERATE | c.230C>T | p.Ala77Val | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 2/7 | 381/1510 | 230/1359 | 77/452 | chr11 | 48981466 | |||
| chr11:48981470 | T | A | 1 | a0005 | 3 | HG01243.hp2 HG01884.hp1 HG02257.hp1 |
missense_variant | MODERATE | c.226A>T | p.Ile76Phe | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 2/7 | 377/1510 | 226/1359 | 76/452 | chr11 | 48981470 | |||
| chr11:48981609 | G | T | 1 | a0012 | 1 | NA18987.hp2 | missense_variant | MODERATE | c.87C>A | p.Asp29Glu | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 2/7 | 238/1510 | 87/1359 | 29/452 | chr11 | 48981609 | |||
| chr11:48981664 | C | T | 1 | a0007 | 1 | HG01175.hp2 | missense_variant | MODERATE | c.32G>A | p.Arg11Lys | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 2/7 | 183/1510 | 32/1359 | 11/452 | chr11 | 48981664 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:48975555 | G | A | 6 | a0002c0002 a0002c0004 a0002c0015 others(3): Show |
139 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(136): Show |
synonymous_variant | LOW | c.1302C>T | p.Ile434Ile | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 7/7 | 1453/1510 | 1302/1359 | 434/452 | chr11 | 48975555 | |||
| chr11:48975600 | G | A | 1 | a0001c0011 | 1 | HG00558.hp1 | synonymous_variant | LOW | c.1257C>T | p.Thr419Thr | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 7/7 | 1408/1510 | 1257/1359 | 419/452 | chr11 | 48975600 | |||
| chr11:48975726 | G | C | 1 | a0001c0006 | 7 | HG01192.hp1 HG01515.hp1 HG02559.hp1 others(4): Show |
synonymous_variant | LOW | c.1131C>G | p.Leu377Leu | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 7/7 | 1282/1510 | 1131/1359 | 377/452 | chr11 | 48975726 | |||
| chr11:48975974 | T | G | 1 | a0002c0016 | 1 | NA19090.hp2 | synonymous_variant | LOW | c.883A>C | p.Arg295Arg | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 7/7 | 1034/1510 | 883/1359 | 295/452 | chr11 | 48975974 | |||
| chr11:48981456 | G | A | 1 | a0005c0007 | 3 | HG01243.hp2 HG01884.hp1 HG02257.hp1 |
synonymous_variant | LOW | c.240C>T | p.Ala80Ala | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 2/7 | 391/1510 | 240/1359 | 80/452 | chr11 | 48981456 | |||
| chr11:48981465 | G | A | 1 | a0005c0007 | 3 | HG01243.hp2 HG01884.hp1 HG02257.hp1 |
synonymous_variant | LOW | c.231C>T | p.Ala77Ala | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 2/7 | 382/1510 | 231/1359 | 77/452 | chr11 | 48981465 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:48983783 | A | G | 1 | a0001c0006t0003 | 7 | HG01192.hp1 HG01515.hp1 HG02559.hp1 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-49T>C | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/7 | 2088 | chr11 | 48983783 | ||||||
| chr11:48983840 | C | A | 11 | a0001c0001t0001 a0001c0001t0004 a0001c0006t0003 others(8): Show |
273 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(270): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-106G>T | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/7 | chr11 | 48983840 | |||||||
| chr11:48983868 | A | T | 1 | a0001c0001t0004 | 1 | HG03942.hp1 | 5_prime_UTR_variant | MODIFIER | c.-134T>A | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/7 | 2173 | chr11 | 48983868 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:48976040 | C | T | 134 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(131): Show |
412 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(409): Show |
intron_variant | MODIFIER | c.860-43G>A | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 6/6 | chr11 | 48976040 | |||||||
| chr11:48976058 | A | G | 1 | a0002c0002t0002g0074 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.860-61T>C | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 6/6 | chr11 | 48976058 | |||||||
| chr11:48976086 | C | G | 6 | a0001c0001t0001g0027 a0001c0001t0001g0055 a0001c0001t0001g0116 others(3): Show |
10 | HG00280.hp2 HG01123.hp2 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.860-89G>C | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 6/6 | chr11 | 48976086 | |||||||
| chr11:48976171 | T | C | 1 | a0002c0002t0002g0080 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.860-174A>G | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 6/6 | chr11 | 48976171 | |||||||
| chr11:48976464 | G | T | 1 | a0003c0003t0001g0023 | 4 | HG02040.hp2 NA18954.hp1 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.860-467C>A | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 6/6 | chr11 | 48976464 | |||||||
| chr11:48976592 | A | C | 1 | a0003c0003t0001g0103 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.859+493T>G | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 6/6 | chr11 | 48976592 | |||||||
| chr11:48976689 | A | G | 2 | a0001c0001t0001g0117 a0001c0001t0001g0131 |
2 | HG03669.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.859+396T>C | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 6/6 | chr11 | 48976689 | |||||||
| chr11:48976704 | C | T | 2 | a0001c0001t0001g0034 a0001c0001t0001g0107 |
4 | HG01891.hp1 HG02896.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.859+381G>A | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 6/6 | chr11 | 48976704 | |||||||
| chr11:48976721 | G | C | 2 | a0001c0001t0001g0034 a0001c0001t0001g0107 |
4 | HG01891.hp1 HG02896.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.859+364C>G | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 6/6 | chr11 | 48976721 | |||||||
| chr11:48976754 | A | T | 1 | a0003c0003t0001g0099 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.859+331T>A | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 6/6 | chr11 | 48976754 | |||||||
| chr11:48976825 | T | G | 1 | a0003c0003t0001g0103 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.859+260A>C | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 6/6 | chr11 | 48976825 | |||||||
| chr11:48976897 | CTA | C | 1 | a0003c0003t0001g0033 | 3 | HG01346.hp2 HG02735.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.859+186_859+187del others(2): Show |
TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 6/6 | chr11 | 48976897 | |||||||
| chr11:48976964 | G | A | 1 | a0001c0001t0001g0114 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.859+121C>T | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 6/6 | chr11 | 48976964 | |||||||
| chr11:48977007 | G | A | 3 | a0002c0002t0002g0081 a0002c0002t0002g0091 a0011c0018t0002g0072 |
3 | NA18960.hp2 NA18967.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.859+78C>T | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 6/6 | chr11 | 48977007 | |||||||
| chr11:48977387 | T | C | 74 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(71): Show |
273 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(270): Show |
intron_variant | MODIFIER | c.762-205A>G | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 5/6 | chr11 | 48977387 | |||||||
| chr11:48977578 | G | A | 2 | a0001c0001t0001g0025 a0001c0001t0001g0128 |
5 | HG00280.hp1 HG00323.hp2 HG00741.hp1 others(2): Show |
intron_variant | MODIFIER | c.762-396C>T | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 5/6 | chr11 | 48977578 | |||||||
| chr11:48977646 | C | A | 1 | a0001c0001t0001g0130 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.762-464G>T | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 5/6 | chr11 | 48977646 | |||||||
| chr11:48977766 | T | G | 74 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(71): Show |
273 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(270): Show |
intron_variant | MODIFIER | c.761+372A>C | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 5/6 | chr11 | 48977766 | |||||||
| chr11:48977775 | T | C | 26 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(23): Show |
137 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.761+363A>G | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 5/6 | chr11 | 48977775 | |||||||
| chr11:48977800 | G | T | 2 | a0001c0001t0001g0034 a0001c0001t0001g0107 |
4 | HG01891.hp1 HG02896.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.761+338C>A | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 5/6 | chr11 | 48977800 | |||||||
| chr11:48977843 | A | G | 1 | a0001c0001t0001g0024 | 4 | HG02723.hp1 HG03130.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.761+295T>C | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 5/6 | chr11 | 48977843 | |||||||
| chr11:48977858 | C | T | 1 | a0002c0004t0002g0070 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.761+280G>A | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 5/6 | chr11 | 48977858 | |||||||
| chr11:48977898 | T | G | 1 | a0003c0003t0001g0103 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.761+240A>C | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 5/6 | chr11 | 48977898 | |||||||
| chr11:48977898 | T | TTTTATTT others(1): Show |
4 | a0004c0005t0002g0036 a0004c0005t0002g0037 a0004c0005t0002g0060 others(1): Show |
6 | HG02615.hp1 HG02622.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.761+232_761+239dup others(8): Show |
TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 5/6 | chr11 | 48977898 | |||||||
| chr11:48977898 | TTTTA | T | 72 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(69): Show |
271 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.761+236_761+239del others(4): Show |
TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 5/6 | chr11 | 48977898 | |||||||
| chr11:48977931 | T | G | 1 | a0003c0003t0001g0103 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.761+207A>C | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 5/6 | chr11 | 48977931 | |||||||
| chr11:48977933 | G | T | 1 | a0003c0003t0001g0103 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.761+205C>A | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 5/6 | chr11 | 48977933 | |||||||
| chr11:48977975 | G | C | 74 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(71): Show |
273 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(270): Show |
intron_variant | MODIFIER | c.761+163C>G | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 5/6 | chr11 | 48977975 | |||||||
| chr11:48977993 | T | A | 3 | a0001c0001t0001g0050 a0001c0001t0001g0112 a0001c0001t0001g0114 |
4 | HG01109.hp1 HG02965.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.761+145A>T | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 5/6 | chr11 | 48977993 | |||||||
| chr11:48977999 | C | A | 1 | a0001c0001t0001g0111 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.761+139G>T | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 5/6 | chr11 | 48977999 | |||||||
| chr11:48978010 | G | A | 1 | a0003c0003t0001g0048 | 2 | NA18944.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.761+128C>T | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 5/6 | chr11 | 48978010 | |||||||
| chr11:48978118 | A | C | 1 | a0002c0015t0002g0069 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.761+20T>G | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 5/6 | chr11 | 48978118 | |||||||
| chr11:48978185 | G | C | 5 | a0002c0002t0002g0028 a0002c0002t0002g0039 a0002c0002t0002g0078 others(2): Show |
8 | HG02630.hp2 HG02809.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.739-25C>G | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 4/6 | chr11 | 48978185 | |||||||
| chr11:48978216 | T | A | 1 | a0003c0003t0001g0103 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.739-56A>T | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 4/6 | chr11 | 48978216 | |||||||
| chr11:48978281 | G | A | 60 | a0002c0002t0002g0005 a0002c0002t0002g0007 a0002c0002t0002g0009 others(57): Show |
139 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.739-121C>T | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 4/6 | chr11 | 48978281 | |||||||
| chr11:48978414 | G | T | 2 | a0001c0001t0001g0052 a0002c0004t0002g0079 |
3 | HG01884.hp2 HG02015.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.739-254C>A | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 4/6 | chr11 | 48978414 | |||||||
| chr11:48978526 | C | T | 20 | a0001c0001t0001g0011 a0001c0001t0001g0034 a0001c0001t0001g0104 others(17): Show |
91 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.738+346G>A | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 4/6 | chr11 | 48978526 | |||||||
| chr11:48978674 | G | A | 1 | a0002c0002t0002g0038 | 2 | NA19056.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.738+198C>T | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 4/6 | chr11 | 48978674 | |||||||
| chr11:48978753 | A | C | 74 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(71): Show |
273 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(270): Show |
intron_variant | MODIFIER | c.738+119T>G | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 4/6 | chr11 | 48978753 | |||||||
| chr11:48978761 | GT | G | 54 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(51): Show |
182 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.738+110delA | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 4/6 | chr11 | 48978761 | |||||||
| chr11:48978867 | C | T | 2 | a0005c0007t0001g0108 a0005c0007t0001g0109 |
2 | HG01243.hp2 HG01884.hp1 |
splice_region_variant&intron_variant | LOW | c.738+5G>A | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 4/6 | chr11 | 48978867 | |||||||
| chr11:48978871 | C | G | 74 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(71): Show |
273 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(270): Show |
splice_donor_variant&intron_variant | HIGH | c.738+1G>C | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 4/6 | chr11 | 48978871 | |||||||
| chr11:48979121 | A | C | 3 | a0005c0007t0001g0108 a0005c0007t0001g0109 a0005c0007t0001g0113 |
3 | HG01243.hp2 HG01884.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.508-19T>G | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 3/6 | chr11 | 48979121 | |||||||
| chr11:48979179 | G | C | 1 | a0009c0014t0002g0059 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.508-77C>G | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 3/6 | chr11 | 48979179 | |||||||
| chr11:48979202 | G | A | 74 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(71): Show |
273 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(270): Show |
intron_variant | MODIFIER | c.508-100C>T | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 3/6 | chr11 | 48979202 | |||||||
| chr11:48979258 | A | G | 6 | a0001c0001t0001g0011 a0001c0001t0001g0104 a0001c0001t0001g0105 others(3): Show |
12 | HG01109.hp2 HG02280.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.508-156T>C | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 3/6 | chr11 | 48979258 | |||||||
| chr11:48979335 | G | T | 1 | a0005c0007t0001g0113 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.508-233C>A | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 3/6 | chr11 | 48979335 | |||||||
| chr11:48979409 | G | A | 134 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(131): Show |
412 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(409): Show |
intron_variant | MODIFIER | c.508-307C>T | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 3/6 | chr11 | 48979409 | |||||||
| chr11:48979448 | T | G | 1 | a0002c0004t0002g0090 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.508-346A>C | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 3/6 | chr11 | 48979448 | |||||||
| chr11:48979452 | G | A | 1 | a0002c0002t0002g0073 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.508-350C>T | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 3/6 | chr11 | 48979452 | |||||||
| chr11:48979454 | C | A | 60 | a0002c0002t0002g0005 a0002c0002t0002g0007 a0002c0002t0002g0009 others(57): Show |
139 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.508-352G>T | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 3/6 | chr11 | 48979454 | |||||||
| chr11:48979538 | C | G | 74 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(71): Show |
273 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(270): Show |
intron_variant | MODIFIER | c.508-436G>C | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 3/6 | chr11 | 48979538 | |||||||
| chr11:48979619 | C | T | 74 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(71): Show |
273 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(270): Show |
intron_variant | MODIFIER | c.508-517G>A | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 3/6 | chr11 | 48979619 | |||||||
| chr11:48979692 | C | T | 25 | a0002c0002t0002g0012 a0002c0002t0002g0013 a0002c0002t0002g0019 others(22): Show |
47 | HG00408.hp1 HG00438.hp2 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.508-590G>A | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 3/6 | chr11 | 48979692 | |||||||
| chr11:48979699 | C | T | 1 | a0003c0003t0001g0101 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.508-597G>A | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 3/6 | chr11 | 48979699 | |||||||
| chr11:48979720 | A | G | 2 | a0001c0001t0001g0110 a0001c0001t0001g0111 |
2 | HG02145.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.508-618T>C | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 3/6 | chr11 | 48979720 | |||||||
| chr11:48979751 | G | C | 1 | a0004c0005t0002g0036 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.508-649C>G | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 3/6 | chr11 | 48979751 | |||||||
| chr11:48979802 | C | CAT | 60 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(57): Show |
249 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(246): Show |
intron_variant | MODIFIER | c.508-702_508-701dup others(2): Show |
TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 3/6 | chr11 | 48979802 | |||||||
| chr11:48979802 | C | CATAT | 8 | a0001c0001t0001g0050 a0001c0001t0001g0104 a0001c0001t0001g0105 others(5): Show |
9 | HG01109.hp1 HG02145.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.508-704_508-701dup others(4): Show |
TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 3/6 | chr11 | 48979802 | |||||||
| chr11:48979802 | C | CATATAT | 3 | a0001c0001t0001g0011 a0001c0001t0001g0140 a0001c0001t0001g0141 |
9 | HG01109.hp2 HG02486.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.508-706_508-701dup others(6): Show |
TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 3/6 | chr11 | 48979802 | |||||||
| chr11:48979802 | CAT | C | 60 | a0002c0002t0002g0005 a0002c0002t0002g0007 a0002c0002t0002g0009 others(57): Show |
139 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.508-702_508-701del others(2): Show |
TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 3/6 | chr11 | 48979802 | |||||||
| chr11:48979858 | AT | A | 26 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(23): Show |
137 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.508-757delA | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 3/6 | chr11 | 48979858 | |||||||
| chr11:48979861 | T | A | 26 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(23): Show |
137 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.508-759A>T | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 3/6 | chr11 | 48979861 | |||||||
| chr11:48979971 | C | G | 4 | a0001c0006t0003g0032 a0001c0006t0003g0046 a0001c0006t0003g0096 others(1): Show |
7 | HG01192.hp1 HG01515.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.508-869G>C | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 3/6 | chr11 | 48979971 | |||||||
| chr11:48980027 | G | C | 1 | a0002c0004t0002g0086 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.507+879C>G | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 3/6 | chr11 | 48980027 | |||||||
| chr11:48980071 | A | G | 134 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(131): Show |
412 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(409): Show |
intron_variant | MODIFIER | c.507+835T>C | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 3/6 | chr11 | 48980071 | |||||||
| chr11:48980090 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.507+816C>T | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 3/6 | chr11 | 48980090 | |||||||
| chr11:48980111 | A | C | 1 | a0001c0001t0001g0141 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.507+795T>G | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 3/6 | chr11 | 48980111 | |||||||
| chr11:48980213 | A | T | 3 | a0005c0007t0001g0108 a0005c0007t0001g0109 a0005c0007t0001g0113 |
3 | HG01243.hp2 HG01884.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.507+693T>A | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 3/6 | chr11 | 48980213 | |||||||
| chr11:48980261 | C | A | 1 | a0001c0001t0001g0126 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.507+645G>T | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 3/6 | chr11 | 48980261 | |||||||
| chr11:48980299 | C | T | 1 | a0001c0001t0001g0134 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.507+607G>A | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 3/6 | chr11 | 48980299 | |||||||
| chr11:48980340 | C | A | 1 | a0004c0005t0002g0060 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.507+566G>T | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 3/6 | chr11 | 48980340 | |||||||
| chr11:48980590 | A | T | 134 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(131): Show |
412 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(409): Show |
intron_variant | MODIFIER | c.507+316T>A | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 3/6 | chr11 | 48980590 | |||||||
| chr11:48980599 | G | C | 2 | a0001c0001t0001g0034 a0001c0001t0001g0107 |
4 | HG01891.hp1 HG02896.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.507+307C>G | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 3/6 | chr11 | 48980599 | |||||||
| chr11:48980694 | G | T | 3 | a0005c0007t0001g0108 a0005c0007t0001g0109 a0005c0007t0001g0113 |
3 | HG01243.hp2 HG01884.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.507+212C>A | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 3/6 | chr11 | 48980694 | |||||||
| chr11:48980695 | C | T | 11 | a0003c0003t0001g0001 a0003c0003t0001g0006 a0003c0003t0001g0022 others(8): Show |
72 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.507+211G>A | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 3/6 | chr11 | 48980695 | |||||||
| chr11:48980755 | T | C | 60 | a0002c0002t0002g0005 a0002c0002t0002g0007 a0002c0002t0002g0009 others(57): Show |
139 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.507+151A>G | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 3/6 | chr11 | 48980755 | |||||||
| chr11:48980756 | A | G | 1 | a0004c0005t0002g0036 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.507+150T>C | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 3/6 | chr11 | 48980756 | |||||||
| chr11:48980771 | G | A | 1 | a0003c0003t0001g0022 | 4 | HG02615.hp2 HG02818.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.507+135C>T | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 3/6 | chr11 | 48980771 | |||||||
| chr11:48980791 | T | G | 74 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(71): Show |
273 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(270): Show |
intron_variant | MODIFIER | c.507+115A>C | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 3/6 | chr11 | 48980791 | |||||||
| chr11:48980902 | T | C | 1 | a0001c0001t0001g0120 | 1 | HG03710.hp2 | splice_region_variant&intron_variant | LOW | c.507+4A>G | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 3/6 | chr11 | 48980902 | |||||||
| chr11:48981107 | T | G | 1 | a0001c0001t0001g0121 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.412-106A>C | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 2/6 | chr11 | 48981107 | |||||||
| chr11:48981191 | G | A | 134 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(131): Show |
412 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(409): Show |
intron_variant | MODIFIER | c.411+94C>T | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 2/6 | chr11 | 48981191 | |||||||
| chr11:48981732 | T | G | 133 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(130): Show |
411 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(408): Show |
intron_variant | MODIFIER | c.-4-33A>C | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48981732 | |||||||
| chr11:48981738 | G | C | 1 | a0003c0003t0001g0033 | 3 | HG01346.hp2 HG02735.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-4-39C>G | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48981738 | |||||||
| chr11:48981760 | A | G | 3 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0106 |
3 | HG02280.hp1 HG02818.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-4-61T>C | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48981760 | |||||||
| chr11:48981762 | C | G | 3 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0106 |
3 | HG02280.hp1 HG02818.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-4-63G>C | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48981762 | |||||||
| chr11:48981763 | A | G | 3 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0106 |
3 | HG02280.hp1 HG02818.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-4-64T>C | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48981763 | |||||||
| chr11:48981764 | C | T | 3 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0106 |
3 | HG02280.hp1 HG02818.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-4-65G>A | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48981764 | |||||||
| chr11:48981765 | C | G | 3 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0106 |
3 | HG02280.hp1 HG02818.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-4-66G>C | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48981765 | |||||||
| chr11:48981810 | G | A | 60 | a0002c0002t0002g0005 a0002c0002t0002g0007 a0002c0002t0002g0009 others(57): Show |
139 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.-4-111C>T | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48981810 | |||||||
| chr11:48981833 | C | T | 1 | a0001c0001t0001g0122 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-4-134G>A | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48981833 | |||||||
| chr11:48981917 | T | C | 1 | a0003c0003t0001g0102 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-4-218A>G | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48981917 | |||||||
| chr11:48981965 | C | A | 1 | a0003c0003t0001g0033 | 3 | HG01346.hp2 HG02735.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-4-266G>T | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48981965 | |||||||
| chr11:48981969 | G | A | 42 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(39): Show |
166 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.-4-270C>T | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48981969 | |||||||
| chr11:48982003 | G | C | 2 | a0002c0002t0002g0065 a0002c0002t0002g0076 |
2 | HG01167.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.-4-304C>G | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48982003 | |||||||
| chr11:48982026 | G | A | 3 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0106 |
3 | HG02280.hp1 HG02818.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-4-327C>T | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48982026 | |||||||
| chr11:48982087 | C | T | 73 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(70): Show |
272 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(269): Show |
intron_variant | MODIFIER | c.-4-388G>A | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48982087 | |||||||
| chr11:48982089 | G | T | 1 | a0003c0003t0001g0103 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-4-390C>A | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48982089 | |||||||
| chr11:48982294 | T | C | 11 | a0002c0002t0002g0012 a0002c0002t0002g0019 a0002c0002t0002g0020 others(8): Show |
26 | HG00408.hp1 HG00438.hp2 HG00621.hp2 others(23): Show |
intron_variant | MODIFIER | c.-4-595A>G | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48982294 | |||||||
| chr11:48982308 | G | T | 7 | a0002c0002t0002g0042 a0002c0002t0002g0058 a0002c0002t0002g0065 others(4): Show |
8 | HG01167.hp1 HG01168.hp2 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.-4-609C>A | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48982308 | |||||||
| chr11:48982369 | T | C | 74 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(71): Show |
273 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(270): Show |
intron_variant | MODIFIER | c.-4-670A>G | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48982369 | |||||||
| chr11:48982389 | G | A | 74 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(71): Show |
273 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(270): Show |
intron_variant | MODIFIER | c.-4-690C>T | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48982389 | |||||||
| chr11:48982449 | A | G | 1 | a0001c0001t0001g0115 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-4-750T>C | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48982449 | |||||||
| chr11:48982473 | G | A | 12 | a0003c0003t0001g0001 a0003c0003t0001g0006 a0003c0003t0001g0022 others(9): Show |
75 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.-4-774C>T | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48982473 | |||||||
| chr11:48982477 | G | C | 7 | a0002c0002t0002g0042 a0002c0002t0002g0058 a0002c0002t0002g0065 others(4): Show |
8 | HG01167.hp1 HG01168.hp2 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.-4-778C>G | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48982477 | |||||||
| chr11:48982484 | G | A | 7 | a0002c0002t0002g0042 a0002c0002t0002g0058 a0002c0002t0002g0065 others(4): Show |
8 | HG01167.hp1 HG01168.hp2 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.-4-785C>T | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48982484 | |||||||
| chr11:48982495 | T | G | 1 | a0001c0001t0001g0112 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-4-796A>C | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48982495 | |||||||
| chr11:48982600 | T | C | 60 | a0002c0002t0002g0005 a0002c0002t0002g0007 a0002c0002t0002g0009 others(57): Show |
139 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.-4-901A>G | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48982600 | |||||||
| chr11:48982685 | A | G | 1 | a0002c0004t0002g0084 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-4-986T>C | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48982685 | |||||||
| chr11:48982755 | A | C | 1 | a0011c0018t0002g0072 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-5+984T>G | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48982755 | |||||||
| chr11:48982772 | C | T | 134 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(131): Show |
412 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(409): Show |
intron_variant | MODIFIER | c.-5+967G>A | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48982772 | |||||||
| chr11:48982788 | C | T | 60 | a0002c0002t0002g0005 a0002c0002t0002g0007 a0002c0002t0002g0009 others(57): Show |
139 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.-5+951G>A | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48982788 | |||||||
| chr11:48982792 | C | T | 60 | a0002c0002t0002g0005 a0002c0002t0002g0007 a0002c0002t0002g0009 others(57): Show |
139 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.-5+947G>A | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48982792 | |||||||
| chr11:48982813 | T | A | 1 | a0003c0003t0001g0103 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-5+926A>T | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48982813 | |||||||
| chr11:48982814 | A | T | 1 | a0003c0003t0001g0103 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-5+925T>A | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48982814 | |||||||
| chr11:48982815 | G | A | 1 | a0003c0003t0001g0103 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-5+924C>T | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48982815 | |||||||
| chr11:48982929 | G | C | 134 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(131): Show |
412 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(409): Show |
intron_variant | MODIFIER | c.-5+810C>G | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48982929 | |||||||
| chr11:48982946 | G | GGTGT | 9 | a0001c0001t0001g0002 a0001c0001t0001g0052 a0001c0001t0001g0053 others(6): Show |
50 | HG00423.hp2 HG00642.hp1 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.-5+792_-5+793insAC others(2): Show |
TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48982946 | |||||||
| chr11:48982946 | G | GGTGTGT | 8 | a0001c0001t0001g0003 a0001c0001t0001g0025 a0001c0001t0001g0051 others(5): Show |
46 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.-5+792_-5+793insAC others(4): Show |
TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48982946 | |||||||
| chr11:48982946 | G | GGTGTGTG others(1): Show |
4 | a0001c0001t0001g0004 a0001c0001t0001g0115 a0001c0001t0001g0116 others(1): Show |
23 | HG00280.hp2 HG01934.hp1 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.-5+792_-5+793insAC others(6): Show |
TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48982946 | |||||||
| chr11:48982947 | G | GTGTA | 2 | a0001c0001t0001g0140 a0002c0002t0002g0013 |
6 | HG01070.hp2 HG01071.hp1 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.-5+791_-5+792insTA others(2): Show |
TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48982947 | |||||||
| chr11:48982947 | G | GTGTATA | 4 | a0001c0001t0001g0104 a0002c0002t0002g0017 a0002c0002t0002g0064 others(1): Show |
7 | HG00099.hp1 HG01168.hp2 HG02015.hp1 others(4): Show |
intron_variant | MODIFIER | c.-5+791_-5+792insTA others(4): Show |
TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48982947 | |||||||
| chr11:48982947 | G | GTGTATAT others(1): Show |
9 | a0001c0001t0001g0141 a0002c0002t0002g0007 a0002c0002t0002g0028 others(6): Show |
25 | HG00544.hp1 HG00609.hp1 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.-5+791_-5+792insTA others(6): Show |
TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48982947 | |||||||
| chr11:48982947 | G | GTGTATAT others(3): Show |
10 | a0001c0001t0001g0105 a0002c0002t0002g0005 a0002c0002t0002g0029 others(7): Show |
27 | HG00621.hp1 HG00733.hp1 HG01099.hp2 others(24): Show |
intron_variant | MODIFIER | c.-5+791_-5+792insTA others(8): Show |
TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48982947 | |||||||
| chr11:48982947 | G | GTGTATAT others(5): Show |
6 | a0002c0002t0002g0009 a0002c0002t0002g0042 a0002c0002t0002g0077 others(3): Show |
14 | HG01361.hp1 HG01516.hp2 HG02004.hp2 others(11): Show |
intron_variant | MODIFIER | c.-5+791_-5+792insTA others(10): Show |
TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48982947 | |||||||
| chr11:48982947 | G | GTGTATAT others(7): Show |
6 | a0001c0001t0001g0106 a0002c0002t0002g0014 a0002c0002t0002g0080 others(3): Show |
10 | HG02135.hp1 HG02683.hp1 HG03225.hp1 others(7): Show |
intron_variant | MODIFIER | c.-5+791_-5+792insTA others(12): Show |
TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48982947 | |||||||
| chr11:48982947 | G | GTGTATAT others(9): Show |
8 | a0002c0002t0002g0020 a0002c0002t0002g0030 a0002c0002t0002g0085 others(5): Show |
14 | HG00597.hp1 HG01258.hp2 HG01993.hp1 others(11): Show |
intron_variant | MODIFIER | c.-5+791_-5+792insTA others(14): Show |
TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48982947 | |||||||
| chr11:48982947 | G | GTGTATAT others(11): Show |
4 | a0002c0002t0002g0012 a0002c0002t0002g0089 a0002c0004t0002g0010 others(1): Show |
15 | HG00438.hp2 HG03579.hp2 NA18944.hp2 others(12): Show |
intron_variant | MODIFIER | c.-5+791_-5+792insTA others(16): Show |
TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48982947 | |||||||
| chr11:48982947 | G | GTGTATAT others(13): Show |
1 | a0002c0004t0002g0045 | 2 | HG01071.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.-5+791_-5+792insTA others(18): Show |
TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48982947 | |||||||
| chr11:48982947 | G | GTGTATAT others(15): Show |
3 | a0002c0002t0002g0091 a0002c0002t0002g0093 a0002c0004t0002g0092 |
3 | NA18960.hp2 NA18962.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.-5+791_-5+792insTA others(20): Show |
TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48982947 | |||||||
| chr11:48982947 | G | GTGTATAT others(19): Show |
1 | a0002c0004t0002g0094 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.-5+791_-5+792insTA others(24): Show |
TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48982947 | |||||||
| chr11:48982947 | G | GTGTGTAT others(3): Show |
1 | a0002c0002t0002g0066 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-5+791_-5+792insTA others(8): Show |
TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48982947 | |||||||
| chr11:48982947 | G | GTGTGTAT others(5): Show |
1 | a0002c0002t0002g0071 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-5+791_-5+792insTA others(10): Show |
TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48982947 | |||||||
| chr11:48982947 | G | GTGTGTAT others(9): Show |
1 | a0002c0002t0002g0043 | 2 | HG00621.hp2 HG02027.hp1 |
intron_variant | MODIFIER | c.-5+791_-5+792insTA others(14): Show |
TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48982947 | |||||||
| chr11:48982947 | G | GTGTGTAT others(11): Show |
1 | a0002c0002t0002g0019 | 4 | HG00673.hp1 NA18985.hp2 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.-5+791_-5+792insTA others(16): Show |
TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48982947 | |||||||
| chr11:48982947 | G | GTGTGTAT others(13): Show |
1 | a0002c0002t0002g0021 | 4 | HG00408.hp1 HG02071.hp1 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.-5+791_-5+792insTA others(18): Show |
TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48982947 | |||||||
| chr11:48982947 | G | GTGTGTGT others(1): Show |
3 | a0001c0001t0001g0130 a0001c0006t0003g0096 a0013c0013t0001g0129 |
3 | HG00642.hp2 HG02976.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-5+791_-5+792insTA others(6): Show |
TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48982947 | |||||||
| chr11:48982947 | G | GTGTGTGT others(3): Show |
6 | a0001c0001t0001g0035 a0001c0001t0001g0110 a0001c0001t0001g0111 others(3): Show |
10 | HG00140.hp1 HG00738.hp2 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.-5+791_-5+792insTA others(8): Show |
TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48982947 | |||||||
| chr11:48982947 | G | GTGTGTGT others(5): Show |
5 | a0001c0001t0001g0015 a0001c0001t0001g0027 a0001c0001t0001g0050 others(2): Show |
13 | HG01515.hp2 HG01517.hp2 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.-5+791_-5+792insTA others(10): Show |
TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48982947 | |||||||
| chr11:48982947 | G | GTGTGTGT others(7): Show |
1 | a0001c0001t0001g0136 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-5+791_-5+792insTA others(12): Show |
TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48982947 | |||||||
| chr11:48982947 | G | GTGTGTGT others(9): Show |
1 | a0001c0006t0003g0097 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-5+791_-5+792insTA others(14): Show |
TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48982947 | |||||||
| chr11:48982947 | G | GTGTGTGT others(11): Show |
1 | a0001c0001t0001g0055 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-5+791_-5+792insTA others(16): Show |
TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48982947 | |||||||
| chr11:48982947 | G | GTGTGTGT others(15): Show |
1 | a0001c0001t0001g0137 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-5+791_-5+792insTA others(20): Show |
TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48982947 | |||||||
| chr11:48982947 | G | GTGTGTGT others(17): Show |
1 | a0001c0001t0001g0139 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-5+791_-5+792insTA others(22): Show |
TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48982947 | |||||||
| chr11:48982947 | G | GTGTGTGT others(3): Show |
3 | a0001c0001t0001g0008 a0001c0001t0001g0128 a0005c0007t0001g0108 |
12 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(9): Show |
intron_variant | MODIFIER | c.-5+791_-5+792insTA others(8): Show |
TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48982947 | |||||||
| chr11:48982947 | G | GTGTGTGT others(5): Show |
4 | a0001c0001t0001g0026 a0001c0001t0001g0047 a0001c0001t0001g0131 others(1): Show |
8 | HG01168.hp1 HG01169.hp2 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.-5+791_-5+792insTA others(10): Show |
TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48982947 | |||||||
| chr11:48982947 | G | GTGTGTGT others(7): Show |
2 | a0001c0001t0001g0133 a0005c0007t0001g0113 |
2 | HG02257.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-5+791_-5+792insTA others(12): Show |
TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48982947 | |||||||
| chr11:48982947 | G | GTGTGTGT others(9): Show |
1 | a0001c0001t0001g0135 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-5+791_-5+792insTA others(14): Show |
TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48982947 | |||||||
| chr11:48982947 | G | GTGTGTGT others(19): Show |
1 | a0001c0001t0001g0138 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-5+791_-5+792insTA others(24): Show |
TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48982947 | |||||||
| chr11:48982947 | GTATATAT others(3): Show |
G | 7 | a0002c0002t0002g0031 a0002c0002t0002g0058 a0003c0003t0001g0006 others(4): Show |
25 | HG00558.hp2 HG00609.hp2 HG01081.hp2 others(22): Show |
intron_variant | MODIFIER | c.-5+782_-5+791delTG others(8): Show |
TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48982947 | |||||||
| chr11:48982947 | GTATATAT others(5): Show |
G | 5 | a0001c0001t0001g0034 a0003c0003t0001g0001 a0003c0003t0001g0022 others(2): Show |
51 | HG00408.hp2 HG00423.hp1 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.-5+780_-5+791delTA others(10): Show |
TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48982947 | |||||||
| chr11:48982947 | GTATATAT others(7): Show |
G | 1 | a0001c0001t0001g0107 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-5+778_-5+791delTA others(12): Show |
TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48982947 | |||||||
| chr11:48982948 | TATATATA others(1): Show |
T | 2 | a0003c0003t0001g0033 a0003c0003t0001g0049 |
3 | HG01346.hp2 HG02074.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-5+783_-5+790delGT others(6): Show |
TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48982948 | |||||||
| chr11:48982949 | A | G | 27 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(24): Show |
116 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.-5+790T>C | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48982949 | |||||||
| chr11:48982950 | TATATAC | T | 5 | a0001c0001t0001g0024 a0001c0001t0001g0127 a0002c0004t0002g0062 others(2): Show |
8 | HG01943.hp1 HG02723.hp1 HG02735.hp1 others(5): Show |
intron_variant | MODIFIER | c.-5+783_-5+788delGT others(4): Show |
TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48982950 | |||||||
| chr11:48982951 | A | G | 8 | a0001c0001t0001g0002 a0001c0001t0001g0054 a0001c0001t0001g0122 others(5): Show |
47 | HG00423.hp2 HG00642.hp1 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.-5+788T>C | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48982951 | |||||||
| chr11:48982951 | A | T | 1 | a0003c0003t0001g0103 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-5+788T>A | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48982951 | |||||||
| chr11:48982952 | TATAC | T | 2 | a0001c0001t0001g0011 a0001c0001t0001g0054 |
5 | HG02630.hp1 HG03041.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.-5+783_-5+786delGT others(2): Show |
TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48982952 | |||||||
| chr11:48982955 | A | ATATATAT others(4): Show |
1 | a0002c0004t0002g0057 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-5+783_-5+784insAT others(9): Show |
TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48982955 | |||||||
| chr11:48982956 | C | A | 1 | a0002c0004t0002g0057 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-5+783G>T | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48982956 | |||||||
| chr11:48982956 | C | T | 113 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(110): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.-5+783G>A | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48982956 | |||||||
| chr11:48982956 | CAT | C | 3 | a0004c0005t0002g0036 a0004c0005t0002g0037 a0004c0005t0002g0060 |
4 | HG02622.hp2 HG02717.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-5+781_-5+782delAT | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48982956 | |||||||
| chr11:48982957 | A | G | 5 | a0001c0001t0001g0024 a0001c0001t0001g0054 a0001c0001t0001g0127 others(2): Show |
10 | HG01346.hp2 HG01943.hp1 HG02074.hp1 others(7): Show |
intron_variant | MODIFIER | c.-5+782T>C | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48982957 | |||||||
| chr11:48982958 | TATATATA others(6): Show |
T | 1 | a0003c0003t0001g0103 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-5+768_-5+780delTA others(11): Show |
TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48982958 | |||||||
| chr11:48982959 | A | G | 9 | a0001c0001t0001g0024 a0001c0001t0001g0127 a0002c0002t0002g0031 others(6): Show |
30 | HG00558.hp2 HG00609.hp2 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.-5+780T>C | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48982959 | |||||||
| chr11:48982961 | A | G | 6 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0003c0003t0001g0001 others(3): Show |
55 | HG00408.hp2 HG00423.hp1 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.-5+778T>C | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48982961 | |||||||
| chr11:48982962 | T | C | 1 | a0001c0001t0001g0050 | 2 | HG02965.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-5+777A>G | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48982962 | |||||||
| chr11:48982963 | A | G | 1 | a0001c0001t0001g0107 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-5+776T>C | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48982963 | |||||||
| chr11:48982964 | T | C | 4 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 others(1): Show |
4 | HG01109.hp1 HG02145.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.-5+775A>G | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48982964 | |||||||
| chr11:48982966 | T | C | 3 | a0002c0004t0002g0044 a0002c0004t0002g0092 a0002c0004t0002g0094 |
3 | HG00597.hp1 NA18962.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.-5+773A>G | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48982966 | |||||||
| chr11:48982981 | A | T | 1 | a0002c0004t0002g0057 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-5+758T>A | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48982981 | |||||||
| chr11:48983101 | G | A | 1 | a0002c0002t0002g0031 | 3 | HG02109.hp2 HG02572.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.-5+638C>T | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48983101 | |||||||
| chr11:48983205 | C | T | 1 | a0001c0006t0003g0046 | 2 | HG02559.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-5+534G>A | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48983205 | |||||||
| chr11:48983239 | A | T | 1 | a0002c0004t0002g0057 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-5+500T>A | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48983239 | |||||||
| chr11:48983278 | T | C | 6 | a0001c0001t0001g0011 a0001c0001t0001g0104 a0001c0001t0001g0105 others(3): Show |
12 | HG01109.hp2 HG02280.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.-5+461A>G | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48983278 | |||||||
| chr11:48983378 | G | C | 1 | a0004c0005t0002g0095 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-5+361C>G | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48983378 | |||||||
| chr11:48983460 | C | T | 18 | a0001c0001t0001g0011 a0001c0001t0001g0104 a0001c0001t0001g0105 others(15): Show |
87 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.-5+279G>A | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48983460 | |||||||
| chr11:48983471 | G | A | 42 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(39): Show |
166 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.-5+268C>T | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48983471 | |||||||
| chr11:48983503 | A | T | 1 | a0001c0001t0001g0047 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-5+236T>A | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48983503 | |||||||
| chr11:48983545 | C | T | 1 | a0002c0004t0002g0057 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-5+194G>A | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48983545 | |||||||
| chr11:48983546 | A | C | 1 | a0002c0004t0002g0057 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-5+193T>G | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48983546 | |||||||
| chr11:48983728 | G | A | 3 | a0001c0001t0001g0011 a0001c0001t0001g0140 a0001c0001t0001g0141 |
9 | HG01109.hp2 HG02486.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.-5+11C>T | TRIM51G | ENSG00000220948.6 | transcript | ENST00000534741.3 | protein_coding | 1/6 | chr11 | 48983728 |