Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 117854 |
| ensemblid | ENSG00000121236.21 |
| hgncid | 16277 |
| symbol | TRIM6 |
| name | tripartite motif containing 6 |
| refseq_nuc | NM_001003818.3 |
| refseq_prot | NP_001003818.1 |
| ensembl_nuc | ENST00000380097.8 |
| ensembl_prot | ENSP00000369440.3 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 5596637 |
| end | 5612952 |
| strand | + |
| ver | v1.2 |
| region | chr11:5596637-5612952 |
| region5000 | chr11:5591637-5617952 |
| regionname0 | TRIM6_chr11_5596637_5612952 |
| regionname5000 | TRIM6_chr11_5591637_5617952 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 516 | 429 | 73 | 83 | 214 | 14 | 43 | 176 | TRIM6_chr11_5591637_5617952 | TRIM6 | MCGSE others(511): Show |
chr11 | 5591637 | 5617952 |
| a0002 | 0/0 | 516 | 28 | 2 | 4 | 12 | 4 | 6 | 8 | TRIM6_chr11_5591637_5617952 | TRIM6 | MCGSE others(511): Show |
chr11 | 5591637 | 5617952 |
| a0003 | 0/0 | 516 | 14 | 13 | 1 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | MCGSE others(511): Show |
chr11 | 5591637 | 5617952 |
| a0004 | 0/0 | 516 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | MCGSE others(511): Show |
chr11 | 5591637 | 5617952 |
| a0005 | 0/0 | 516 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | MCGSE others(511): Show |
chr11 | 5591637 | 5617952 |
| a0006 | 0/0 | 516 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | MCGSE others(511): Show |
chr11 | 5591637 | 5617952 |
| a0007 | 0/0 | 516 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TRIM6_chr11_5591637_5617952 | TRIM6 | MCGSE others(511): Show |
chr11 | 5591637 | 5617952 |
| a0008 | 0/0 | 516 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TRIM6_chr11_5591637_5617952 | TRIM6 | MCGSE others(511): Show |
chr11 | 5591637 | 5617952 |
| a0009 | 0/0 | 516 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | MCGSE others(511): Show |
chr11 | 5591637 | 5617952 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1548 | 172 | 13 | 32 | 106 | 4 | 16 | TRIM6_chr11_5591637_5617952 | TRIM6 | ATGTG others(1543): Show |
chr11 | 5591637 | 5617952 | ||
| a0001c0002 | 0/0 | 1548 | 80 | 15 | 14 | 33 | 3 | 15 | TRIM6_chr11_5591637_5617952 | TRIM6 | ATGTG others(1543): Show |
chr11 | 5591637 | 5617952 | ||
| a0001c0003 | 0/0 | 1548 | 56 | 4 | 10 | 37 | 2 | 3 | TRIM6_chr11_5591637_5617952 | TRIM6 | ATGTG others(1543): Show |
chr11 | 5591637 | 5617952 | ||
| a0001c0004 | 0/0 | 1548 | 49 | 0 | 5 | 38 | 0 | 6 | TRIM6_chr11_5591637_5617952 | TRIM6 | ATGTG others(1543): Show |
chr11 | 5591637 | 5617952 | ||
| a0001c0005 | 0/0 | 1548 | 32 | 30 | 2 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | ATGTG others(1543): Show |
chr11 | 5591637 | 5617952 | ||
| a0001c0007 | 1/0 | 1548 | 20 | 2 | 12 | 0 | 4 | 1 | TRIM6_chr11_5591637_5617952 | TRIM6 | ATGTG others(1543): Show |
chr11 | 5591637 | 5617952 | ||
| a0001c0008 | 0/0 | 1548 | 9 | 6 | 3 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | ATGTG others(1543): Show |
chr11 | 5591637 | 5617952 | ||
| a0001c0011 | 0/0 | 1548 | 5 | 1 | 3 | 0 | 1 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | ATGTG others(1543): Show |
chr11 | 5591637 | 5617952 | ||
| a0001c0012 | 0/0 | 1548 | 4 | 2 | 2 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | ATGTG others(1543): Show |
chr11 | 5591637 | 5617952 | ||
| a0001c0018 | 0/0 | 1548 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM6_chr11_5591637_5617952 | TRIM6 | ATGTG others(1543): Show |
chr11 | 5591637 | 5617952 | ||
| a0001c0020 | 0/0 | 1548 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM6_chr11_5591637_5617952 | TRIM6 | ATGTG others(1543): Show |
chr11 | 5591637 | 5617952 | ||
| a0002c0006 | 0/0 | 1548 | 23 | 1 | 4 | 11 | 4 | 3 | TRIM6_chr11_5591637_5617952 | TRIM6 | ATGTG others(1543): Show |
chr11 | 5591637 | 5617952 | ||
| a0002c0015 | 0/0 | 1548 | 2 | 0 | 0 | 1 | 0 | 1 | TRIM6_chr11_5591637_5617952 | TRIM6 | ATGTG others(1543): Show |
chr11 | 5591637 | 5617952 | ||
| a0002c0016 | 0/0 | 1548 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM6_chr11_5591637_5617952 | TRIM6 | ATGTG others(1543): Show |
chr11 | 5591637 | 5617952 | ||
| a0002c0023 | 0/0 | 1548 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | ATGTG others(1543): Show |
chr11 | 5591637 | 5617952 | ||
| a0003c0009 | 0/0 | 1548 | 6 | 5 | 1 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | ATGTG others(1543): Show |
chr11 | 5591637 | 5617952 | ||
| a0003c0010 | 0/0 | 1548 | 5 | 5 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | ATGTG others(1543): Show |
chr11 | 5591637 | 5617952 | ||
| a0003c0014 | 0/0 | 1548 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | ATGTG others(1543): Show |
chr11 | 5591637 | 5617952 | ||
| a0004c0013 | 0/0 | 1548 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | ATGTG others(1543): Show |
chr11 | 5591637 | 5617952 | ||
| a0005c0017 | 0/0 | 1548 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | ATGTG others(1543): Show |
chr11 | 5591637 | 5617952 | ||
| a0006c0024 | 0/0 | 1548 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | ATGTG others(1543): Show |
chr11 | 5591637 | 5617952 | ||
| a0007c0019 | 0/0 | 1548 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | ATGTG others(1543): Show |
chr11 | 5591637 | 5617952 | ||
| a0008c0021 | 0/0 | 1548 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | ATGTG others(1543): Show |
chr11 | 5591637 | 5617952 | ||
| a0009c0022 | 0/0 | 1548 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM6_chr11_5591637_5617952 | TRIM6 | ATGTG others(1543): Show |
chr11 | 5591637 | 5617952 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3422 | 32 | 4 | 9 | 12 | 2 | 5 | TRIM6_chr11_5591637_5617952 | TRIM6 | AGAAG others(3417): Show |
chr11 | 5591637 | 5617952 |
| a0001c0001t0002 | 0/0 | 3422 | 20 | 1 | 7 | 11 | 0 | 1 | TRIM6_chr11_5591637_5617952 | TRIM6 | AGAAG others(3417): Show |
chr11 | 5591637 | 5617952 |
| a0001c0001t0003 | 0/1 | 3423 | 64 | 4 | 7 | 48 | 2 | 2 | TRIM6_chr11_5591637_5617952 | TRIM6 | AGAAG others(3418): Show |
chr11 | 5591637 | 5617952 |
| a0001c0001t0004 | 0/0 | 3422 | 28 | 4 | 4 | 17 | 0 | 3 | TRIM6_chr11_5591637_5617952 | TRIM6 | AGAAG others(3417): Show |
chr11 | 5591637 | 5617952 |
| a0001c0001t0005 | 0/0 | 3423 | 11 | 0 | 0 | 11 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | AGAAG others(3418): Show |
chr11 | 5591637 | 5617952 |
| a0001c0001t0008 | 0/0 | 3422 | 3 | 0 | 2 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | AGAAG others(3417): Show |
chr11 | 5591637 | 5617952 |
| a0001c0001t0009 | 0/0 | 3423 | 4 | 0 | 0 | 3 | 0 | 1 | TRIM6_chr11_5591637_5617952 | TRIM6 | AGAAG others(3418): Show |
chr11 | 5591637 | 5617952 |
| a0001c0001t0014 | 0/0 | 3422 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | AGAAG others(3417): Show |
chr11 | 5591637 | 5617952 |
| a0001c0001t0015 | 0/0 | 3421 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM6_chr11_5591637_5617952 | TRIM6 | AGAAG others(3416): Show |
chr11 | 5591637 | 5617952 |
| a0001c0001t0017 | 0/0 | 3421 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | AGAAG others(3416): Show |
chr11 | 5591637 | 5617952 |
| a0001c0001t0021 | 0/0 | 3422 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | AGAAG others(3417): Show |
chr11 | 5591637 | 5617952 |
| a0001c0001t0027 | 0/0 | 3422 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | AGAAG others(3417): Show |
chr11 | 5591637 | 5617952 |
| a0001c0001t0032 | 0/0 | 3422 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM6_chr11_5591637_5617952 | TRIM6 | AGAAG others(3417): Show |
chr11 | 5591637 | 5617952 |
| a0001c0001t0033 | 0/0 | 3421 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | AGAAG others(3416): Show |
chr11 | 5591637 | 5617952 |
| a0001c0001t0038 | 0/0 | 3422 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM6_chr11_5591637_5617952 | TRIM6 | AGAAG others(3417): Show |
chr11 | 5591637 | 5617952 |
| a0001c0001t0040 | 0/0 | 3422 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | AGAAG others(3417): Show |
chr11 | 5591637 | 5617952 |
| a0001c0002t0001 | 0/0 | 3422 | 20 | 2 | 5 | 9 | 1 | 3 | TRIM6_chr11_5591637_5617952 | TRIM6 | AGAAG others(3417): Show |
chr11 | 5591637 | 5617952 |
| a0001c0002t0002 | 0/0 | 3422 | 25 | 8 | 5 | 5 | 1 | 6 | TRIM6_chr11_5591637_5617952 | TRIM6 | AGAAG others(3417): Show |
chr11 | 5591637 | 5617952 |
| a0001c0002t0004 | 0/0 | 3422 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM6_chr11_5591637_5617952 | TRIM6 | AGAAG others(3417): Show |
chr11 | 5591637 | 5617952 |
| a0001c0002t0005 | 0/0 | 3423 | 3 | 0 | 0 | 2 | 0 | 1 | TRIM6_chr11_5591637_5617952 | TRIM6 | AGAAG others(3418): Show |
chr11 | 5591637 | 5617952 |
| a0001c0002t0006 | 0/0 | 3422 | 24 | 0 | 3 | 17 | 1 | 3 | TRIM6_chr11_5591637_5617952 | TRIM6 | AGAAG others(3417): Show |
chr11 | 5591637 | 5617952 |
| a0001c0002t0018 | 0/0 | 3422 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | AGAAG others(3417): Show |
chr11 | 5591637 | 5617952 |
| a0001c0002t0025 | 0/0 | 3422 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | AGAAG others(3417): Show |
chr11 | 5591637 | 5617952 |
| a0001c0002t0029 | 0/0 | 3422 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | AGAAG others(3417): Show |
chr11 | 5591637 | 5617952 |
| a0001c0002t0035 | 0/0 | 3423 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | AGAAG others(3418): Show |
chr11 | 5591637 | 5617952 |
| a0001c0002t0036 | 0/0 | 3422 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | AGAAG others(3417): Show |
chr11 | 5591637 | 5617952 |
| a0001c0003t0001 | 0/0 | 3422 | 38 | 0 | 8 | 29 | 0 | 1 | TRIM6_chr11_5591637_5617952 | TRIM6 | AGAAG others(3417): Show |
chr11 | 5591637 | 5617952 |
| a0001c0003t0002 | 0/0 | 3422 | 2 | 1 | 0 | 0 | 0 | 1 | TRIM6_chr11_5591637_5617952 | TRIM6 | AGAAG others(3417): Show |
chr11 | 5591637 | 5617952 |
| a0001c0003t0003 | 0/0 | 3423 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | AGAAG others(3418): Show |
chr11 | 5591637 | 5617952 |
| a0001c0003t0004 | 0/0 | 3422 | 4 | 3 | 1 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | AGAAG others(3417): Show |
chr11 | 5591637 | 5617952 |
| a0001c0003t0005 | 0/0 | 3423 | 3 | 0 | 1 | 0 | 1 | 1 | TRIM6_chr11_5591637_5617952 | TRIM6 | AGAAG others(3418): Show |
chr11 | 5591637 | 5617952 |
| a0001c0003t0008 | 0/0 | 3422 | 4 | 0 | 0 | 4 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | AGAAG others(3417): Show |
chr11 | 5591637 | 5617952 |
| a0001c0003t0017 | 0/0 | 3421 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | AGAAG others(3416): Show |
chr11 | 5591637 | 5617952 |
| a0001c0003t0026 | 0/0 | 3423 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | AGAAG others(3418): Show |
chr11 | 5591637 | 5617952 |
| a0001c0004t0001 | 0/0 | 3422 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | AGAAG others(3417): Show |
chr11 | 5591637 | 5617952 |
| a0001c0004t0002 | 0/0 | 3422 | 33 | 0 | 5 | 23 | 0 | 5 | TRIM6_chr11_5591637_5617952 | TRIM6 | AGAAG others(3417): Show |
chr11 | 5591637 | 5617952 |
| a0001c0004t0004 | 0/0 | 3422 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | AGAAG others(3417): Show |
chr11 | 5591637 | 5617952 |
| a0001c0004t0005 | 0/0 | 3423 | 5 | 0 | 0 | 5 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | AGAAG others(3418): Show |
chr11 | 5591637 | 5617952 |
| a0001c0004t0006 | 0/0 | 3422 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | AGAAG others(3417): Show |
chr11 | 5591637 | 5617952 |
| a0001c0004t0011 | 0/0 | 3423 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | AGAAG others(3418): Show |
chr11 | 5591637 | 5617952 |
| a0001c0004t0028 | 0/0 | 3422 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM6_chr11_5591637_5617952 | TRIM6 | AGAAG others(3417): Show |
chr11 | 5591637 | 5617952 |
| a0001c0005t0001 | 0/0 | 3422 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | AGAAG others(3417): Show |
chr11 | 5591637 | 5617952 |
| a0001c0005t0002 | 0/0 | 3422 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | AGAAG others(3417): Show |
chr11 | 5591637 | 5617952 |
| a0001c0005t0004 | 0/0 | 3422 | 16 | 15 | 1 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | AGAAG others(3417): Show |
chr11 | 5591637 | 5617952 |
| a0001c0005t0007 | 0/0 | 3421 | 7 | 7 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | AGAAG others(3416): Show |
chr11 | 5591637 | 5617952 |
| a0001c0005t0010 | 0/0 | 3422 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | AGAAG others(3417): Show |
chr11 | 5591637 | 5617952 |
| a0001c0005t0020 | 0/0 | 3422 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | AGAAG others(3417): Show |
chr11 | 5591637 | 5617952 |
| a0001c0005t0039 | 0/0 | 3422 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | AGAAG others(3417): Show |
chr11 | 5591637 | 5617952 |
| a0001c0007t0001 | 0/0 | 3422 | 13 | 1 | 9 | 0 | 2 | 1 | TRIM6_chr11_5591637_5617952 | TRIM6 | AGAAG others(3417): Show |
chr11 | 5591637 | 5617952 |
| a0001c0007t0002 | 1/0 | 3422 | 5 | 1 | 2 | 0 | 1 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | AGAAG others(3417): Show |
chr11 | 5591637 | 5617952 |
| a0001c0007t0007 | 0/0 | 3421 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | AGAAG others(3416): Show |
chr11 | 5591637 | 5617952 |
| a0001c0007t0019 | 0/0 | 3421 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | AGAAG others(3416): Show |
chr11 | 5591637 | 5617952 |
| a0001c0008t0001 | 0/0 | 3422 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | AGAAG others(3417): Show |
chr11 | 5591637 | 5617952 |
| a0001c0008t0007 | 0/0 | 3421 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | AGAAG others(3416): Show |
chr11 | 5591637 | 5617952 |
| a0001c0008t0012 | 0/0 | 3421 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | AGAAG others(3416): Show |
chr11 | 5591637 | 5617952 |
| a0001c0008t0013 | 0/0 | 3423 | 3 | 2 | 1 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | AGAAG others(3418): Show |
chr11 | 5591637 | 5617952 |
| a0001c0008t0019 | 0/0 | 3421 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | AGAAG others(3416): Show |
chr11 | 5591637 | 5617952 |
| a0001c0011t0001 | 0/0 | 3422 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | AGAAG others(3417): Show |
chr11 | 5591637 | 5617952 |
| a0001c0011t0002 | 0/0 | 3422 | 2 | 0 | 1 | 0 | 1 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | AGAAG others(3417): Show |
chr11 | 5591637 | 5617952 |
| a0001c0011t0030 | 0/0 | 3422 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | AGAAG others(3417): Show |
chr11 | 5591637 | 5617952 |
| a0001c0012t0001 | 0/0 | 3422 | 3 | 2 | 1 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | AGAAG others(3417): Show |
chr11 | 5591637 | 5617952 |
| a0001c0012t0002 | 0/0 | 3422 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | AGAAG others(3417): Show |
chr11 | 5591637 | 5617952 |
| a0001c0018t0004 | 0/0 | 3422 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM6_chr11_5591637_5617952 | TRIM6 | AGAAG others(3417): Show |
chr11 | 5591637 | 5617952 |
| a0001c0020t0008 | 0/0 | 3422 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM6_chr11_5591637_5617952 | TRIM6 | AGAAG others(3417): Show |
chr11 | 5591637 | 5617952 |
| a0002c0006t0002 | 0/0 | 3422 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | AGAAG others(3417): Show |
chr11 | 5591637 | 5617952 |
| a0002c0006t0003 | 0/0 | 3423 | 10 | 0 | 0 | 9 | 0 | 1 | TRIM6_chr11_5591637_5617952 | TRIM6 | AGAAG others(3418): Show |
chr11 | 5591637 | 5617952 |
| a0002c0006t0005 | 0/0 | 3423 | 10 | 0 | 4 | 0 | 4 | 2 | TRIM6_chr11_5591637_5617952 | TRIM6 | AGAAG others(3418): Show |
chr11 | 5591637 | 5617952 |
| a0002c0006t0014 | 0/0 | 3422 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | AGAAG others(3417): Show |
chr11 | 5591637 | 5617952 |
| a0002c0006t0022 | 0/0 | 3423 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | AGAAG others(3418): Show |
chr11 | 5591637 | 5617952 |
| a0002c0015t0005 | 0/0 | 3423 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | AGAAG others(3418): Show |
chr11 | 5591637 | 5617952 |
| a0002c0015t0009 | 0/0 | 3423 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM6_chr11_5591637_5617952 | TRIM6 | AGAAG others(3418): Show |
chr11 | 5591637 | 5617952 |
| a0002c0016t0003 | 0/0 | 3423 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM6_chr11_5591637_5617952 | TRIM6 | AGAAG others(3418): Show |
chr11 | 5591637 | 5617952 |
| a0002c0016t0005 | 0/0 | 3423 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM6_chr11_5591637_5617952 | TRIM6 | AGAAG others(3418): Show |
chr11 | 5591637 | 5617952 |
| a0002c0023t0005 | 0/0 | 3423 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | AGAAG others(3418): Show |
chr11 | 5591637 | 5617952 |
| a0003c0009t0001 | 0/0 | 3422 | 4 | 3 | 1 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | AGAAG others(3417): Show |
chr11 | 5591637 | 5617952 |
| a0003c0009t0002 | 0/0 | 3422 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | AGAAG others(3417): Show |
chr11 | 5591637 | 5617952 |
| a0003c0009t0031 | 0/0 | 3423 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | AGAAG others(3418): Show |
chr11 | 5591637 | 5617952 |
| a0003c0010t0002 | 0/0 | 3422 | 5 | 5 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | AGAAG others(3417): Show |
chr11 | 5591637 | 5617952 |
| a0003c0014t0023 | 0/0 | 3422 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | AGAAG others(3417): Show |
chr11 | 5591637 | 5617952 |
| a0003c0014t0024 | 0/0 | 3423 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | AGAAG others(3418): Show |
chr11 | 5591637 | 5617952 |
| a0003c0014t0034 | 0/0 | 3422 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | AGAAG others(3417): Show |
chr11 | 5591637 | 5617952 |
| a0004c0013t0005 | 0/0 | 3423 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | AGAAG others(3418): Show |
chr11 | 5591637 | 5617952 |
| a0005c0017t0016 | 0/0 | 3422 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | AGAAG others(3417): Show |
chr11 | 5591637 | 5617952 |
| a0006c0024t0037 | 0/0 | 3422 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | AGAAG others(3417): Show |
chr11 | 5591637 | 5617952 |
| a0007c0019t0001 | 0/0 | 3422 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | AGAAG others(3417): Show |
chr11 | 5591637 | 5617952 |
| a0008c0021t0001 | 0/0 | 3422 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | AGAAG others(3417): Show |
chr11 | 5591637 | 5617952 |
| a0009c0022t0002 | 0/0 | 3422 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM6_chr11_5591637_5617952 | TRIM6 | AGAAG others(3417): Show |
chr11 | 5591637 | 5617952 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0013 | 0/0 | 5 | 0 | 4 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0001g0022 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0001g0062 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0001g0063 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0002g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0002g0007 | 0/0 | 7 | 0 | 3 | 4 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0002g0048 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0002g0050 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0003g0004 | 0/0 | 13 | 0 | 0 | 13 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0003g0005 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0003g0009 | 0/0 | 7 | 0 | 5 | 0 | 1 | 1 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0003g0014 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0003g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0003g0037 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0003g0065 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0003g0067 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0003g0068 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0003g0070 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0003g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0003g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0003g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0003g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0003g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0003g0263 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0003g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0004g0006 | 0/0 | 7 | 0 | 0 | 6 | 0 | 1 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0004g0015 | 0/0 | 5 | 0 | 2 | 1 | 0 | 2 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0004g0026 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0004g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0004g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0004g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0004g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0004g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0004g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0004g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0004g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0004g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0004g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0004g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0004g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0005g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0005g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0005g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0005g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0005g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0005g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0005g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0008g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0008g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0008g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0009g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0009g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0009g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0014g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0015g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0015g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0017g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0021g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0027g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0032g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0033g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0038g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0001t0040g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0002t0001g0055 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0002t0001g0071 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0002t0001g0072 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0002t0001g0073 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0002t0001g0075 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0002t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0002t0002g0010 | 0/0 | 6 | 1 | 4 | 0 | 0 | 1 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0002t0002g0024 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0002t0002g0025 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0002t0002g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0002t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0002t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0002t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0002t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0002t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0002t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0002t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0002t0004g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0002t0004g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0002t0005g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0002t0005g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0002t0005g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0002t0006g0003 | 0/0 | 12 | 0 | 0 | 11 | 0 | 1 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0002t0006g0031 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0002t0006g0049 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0002t0006g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0002t0006g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0002t0006g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0002t0006g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0002t0006g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0002t0006g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0002t0006g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0002t0018g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0002t0018g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0002t0025g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0002t0029g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0002t0035g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0002t0036g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0003t0001g0002 | 0/0 | 14 | 0 | 2 | 12 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0003t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0003t0001g0012 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0003t0001g0033 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0003t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0003t0001g0057 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0003t0001g0060 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0003t0001g0077 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0003t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0003t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0003t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0003t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0003t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0003t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0003t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0003t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0003t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0003t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0003t0003g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0003t0003g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0003t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0003t0004g0056 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0003t0004g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0003t0004g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0003t0005g0016 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0003t0008g0035 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0003t0008g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0003t0017g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0003t0026g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0004t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0004t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0004t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0004t0002g0001 | 0/0 | 11 | 0 | 0 | 11 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0004t0002g0018 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0004t0002g0029 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0004t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0004t0002g0053 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0004t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0004t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0004t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0004t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0004t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0004t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0004t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0004t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0004t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0004t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0004t0002g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0004t0004g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0004t0005g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0004t0005g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0004t0005g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0004t0006g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0004t0006g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0004t0006g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0004t0011g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0004t0028g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0005t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0005t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0005t0002g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0005t0004g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0005t0004g0020 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0005t0004g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0005t0004g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0005t0004g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0005t0004g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0005t0004g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0005t0004g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0005t0004g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0005t0004g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0005t0007g0023 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0005t0007g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0005t0007g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0005t0007g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0005t0010g0054 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0005t0010g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0005t0020g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0005t0020g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0005t0039g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0007t0001g0011 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0007t0001g0058 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0007t0001g0074 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0007t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0007t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0007t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0007t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0007t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0007t0002g0011 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0007t0002g0044 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0007t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0007t0007g0008 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0007t0019g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0008t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0008t0007g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0008t0012g0030 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0008t0013g0032 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0008t0019g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0011t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0011t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0011t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0011t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0011t0030g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0012t0001g0076 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0012t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0012t0002g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0018t0004g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0001c0020t0008g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0002c0006t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0002c0006t0003g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0002c0006t0003g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0002c0006t0003g0059 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0002c0006t0003g0061 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0002c0006t0003g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0002c0006t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0002c0006t0005g0016 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0002c0006t0005g0021 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0002c0006t0005g0027 | 0/0 | 3 | 0 | 0 | 0 | 3 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0002c0006t0005g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0002c0006t0005g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0002c0006t0014g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0002c0006t0022g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0002c0015t0005g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0002c0015t0009g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0002c0016t0003g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0002c0016t0005g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0002c0023t0005g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0003c0009t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0003c0009t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0003c0009t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0003c0009t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0003c0009t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0003c0009t0031g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0003c0010t0002g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0003c0010t0002g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0003c0010t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0003c0014t0023g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0003c0014t0024g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0003c0014t0034g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0004c0013t0005g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0004c0013t0005g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0005c0017t0016g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0005c0017t0016g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0006c0024t0037g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0007c0019t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0008c0021t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| a0009c0022t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0003 | t0005 | g0016 | EUR | GBR | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG00099 | hp2 | a0001 | c0007 | t0002 | g0011 | EUR | GBR | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG00140 | hp1 | a0001 | c0007 | t0007 | g0008 | EUR | GBR | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG00140 | hp2 | a0001 | c0007 | t0001 | g0058 | EUR | GBR | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG00280 | hp1 | a0001 | c0002 | t0002 | g0119 | EUR | FIN | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG00280 | hp2 | a0001 | c0007 | t0001 | g0011 | EUR | FIN | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG00323 | hp1 | a0001 | c0011 | t0002 | g0130 | EUR | FIN | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG00323 | hp2 | a0002 | c0006 | t0005 | g0016 | EUR | FIN | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG00408 | hp1 | a0001 | c0001 | t0003 | g0213 | EAS | CHS | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG00408 | hp2 | a0001 | c0001 | t0005 | g0121 | EAS | CHS | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0190 | EAS | CHS | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG00423 | hp2 | a0002 | c0006 | t0003 | g0061 | EAS | CHS | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG00438 | hp1 | a0001 | c0003 | t0008 | g0035 | EAS | CHS | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG00438 | hp2 | a0001 | c0003 | t0001 | g0002 | EAS | CHS | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG00544 | hp1 | a0001 | c0003 | t0001 | g0002 | EAS | CHS | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG00544 | hp2 | a0001 | c0001 | t0040 | g0006 | EAS | CHS | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG00558 | hp1 | a0001 | c0003 | t0001 | g0002 | EAS | CHS | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG00558 | hp2 | a0001 | c0004 | t0002 | g0001 | EAS | CHS | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG00609 | hp1 | a0001 | c0003 | t0026 | g0002 | EAS | CHS | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG00609 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | CHS | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG00621 | hp1 | a0001 | c0002 | t0001 | g0071 | EAS | CHS | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG00621 | hp2 | a0002 | c0015 | t0005 | g0149 | EAS | CHS | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG00639 | hp1 | a0001 | c0002 | t0002 | g0024 | AMR | PUR | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG00639 | hp2 | a0001 | c0007 | t0001 | g0183 | AMR | PUR | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG00642 | hp1 | a0001 | c0003 | t0004 | g0056 | AMR | PUR | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG00642 | hp2 | a0001 | c0001 | t0008 | g0022 | AMR | PUR | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG00673 | hp1 | a0001 | c0001 | t0005 | g0153 | EAS | CHS | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG00673 | hp2 | a0001 | c0004 | t0004 | g0051 | EAS | CHS | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG00733 | hp1 | a0001 | c0001 | t0004 | g0015 | AMR | PUR | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG00733 | hp2 | a0001 | c0012 | t0001 | g0225 | AMR | PUR | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG00735 | hp1 | a0001 | c0003 | t0001 | g0077 | AMR | PUR | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG00735 | hp2 | a0001 | c0002 | t0002 | g0010 | AMR | PUR | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG00738 | hp1 | a0001 | c0002 | t0001 | g0055 | AMR | PUR | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG00738 | hp2 | a0001 | c0011 | t0001 | g0206 | AMR | PUR | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG00741 | hp1 | a0001 | c0008 | t0007 | g0038 | AMR | PUR | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG00741 | hp2 | a0001 | c0011 | t0001 | g0220 | AMR | PUR | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0009 | AMR | PUR | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG01069 | hp2 | a0002 | c0006 | t0005 | g0021 | AMR | PUR | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG01070 | hp1 | a0001 | c0007 | t0002 | g0114 | AMR | PUR | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG01070 | hp2 | a0001 | c0007 | t0001 | g0074 | AMR | PUR | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0009 | AMR | PUR | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG01071 | hp2 | a0001 | c0007 | t0001 | g0074 | AMR | PUR | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0131 | AMR | PUR | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG01081 | hp1 | a0001 | c0007 | t0001 | g0011 | AMR | PUR | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG01081 | hp2 | a0001 | c0002 | t0002 | g0010 | AMR | PUR | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG01099 | hp1 | a0001 | c0003 | t0005 | g0016 | AMR | PUR | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG01099 | hp2 | a0001 | c0001 | t0017 | g0127 | AMR | PUR | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG01106 | hp1 | a0001 | c0002 | t0001 | g0073 | AMR | PUR | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG01106 | hp2 | a0001 | c0002 | t0002 | g0010 | AMR | PUR | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG01109 | hp1 | a0001 | c0003 | t0001 | g0077 | AMR | PUR | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG01109 | hp2 | a0003 | c0009 | t0001 | g0230 | AMR | PUR | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0068 | AMR | PUR | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG01167 | hp2 | a0001 | c0008 | t0001 | g0216 | AMR | PUR | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0048 | AMR | PUR | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0009 | AMR | PUR | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0068 | AMR | PUR | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0009 | AMR | PUR | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG01175 | hp1 | a0001 | c0007 | t0002 | g0011 | AMR | PUR | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG01175 | hp2 | a0001 | c0004 | t0002 | g0018 | AMR | PUR | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG01192 | hp1 | a0001 | c0001 | t0004 | g0100 | AMR | PUR | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG01192 | hp2 | a0001 | c0012 | t0002 | g0244 | AMR | PUR | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG01243 | hp1 | a0001 | c0002 | t0035 | g0176 | AMR | PUR | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG01243 | hp2 | a0001 | c0008 | t0013 | g0032 | AMR | PUR | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG01255 | hp1 | a0001 | c0007 | t0001 | g0182 | AMR | CLM | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0246 | AMR | CLM | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG01256 | hp1 | a0001 | c0002 | t0006 | g0049 | AMR | CLM | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG01256 | hp2 | a0001 | c0002 | t0001 | g0073 | AMR | CLM | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG01257 | hp1 | a0001 | c0007 | t0001 | g0011 | AMR | CLM | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG01257 | hp2 | a0001 | c0004 | t0002 | g0018 | AMR | CLM | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG01258 | hp1 | a0001 | c0007 | t0001 | g0011 | AMR | CLM | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG01258 | hp2 | a0001 | c0002 | t0006 | g0049 | AMR | CLM | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG01261 | hp1 | a0001 | c0002 | t0002 | g0010 | AMR | CLM | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG01261 | hp2 | a0001 | c0011 | t0002 | g0124 | AMR | CLM | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0111 | AMR | CLM | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG01358 | hp1 | a0001 | c0003 | t0001 | g0188 | AMR | CLM | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG01358 | hp2 | a0001 | c0001 | t0008 | g0069 | AMR | CLM | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG01361 | hp1 | a0001 | c0002 | t0001 | g0265 | AMR | CLM | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG01361 | hp2 | a0001 | c0002 | t0001 | g0055 | AMR | CLM | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG01433 | hp1 | a0001 | c0005 | t0004 | g0020 | AMR | CLM | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG01433 | hp2 | a0001 | c0007 | t0001 | g0186 | AMR | CLM | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG01496 | hp1 | a0001 | c0007 | t0019 | g0008 | AMR | CLM | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG01515 | hp1 | a0002 | c0006 | t0005 | g0027 | EUR | IBS | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0028 | EUR | IBS | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG01516 | hp1 | a0001 | c0002 | t0006 | g0113 | EUR | IBS | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG01516 | hp2 | a0002 | c0006 | t0005 | g0027 | EUR | IBS | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG01517 | hp1 | a0002 | c0006 | t0005 | g0027 | EUR | IBS | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0028 | EUR | IBS | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG01884 | hp1 | a0001 | c0002 | t0002 | g0024 | AFR | ACB | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG01884 | hp2 | a0001 | c0007 | t0001 | g0185 | AFR | ACB | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | ACB | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG01891 | hp2 | a0003 | c0009 | t0001 | g0231 | AFR | ACB | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG01928 | hp1 | a0001 | c0003 | t0001 | g0060 | AMR | PEL | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PEL | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG01934 | hp2 | a0001 | c0001 | t0021 | g0066 | AMR | PEL | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG01943 | hp1 | a0001 | c0005 | t0002 | g0019 | AMR | PEL | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG01943 | hp2 | a0001 | c0003 | t0001 | g0193 | AMR | PEL | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | PEL | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | PEL | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG01975 | hp2 | a0001 | c0001 | t0004 | g0026 | AMR | PEL | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PEL | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG01978 | hp2 | a0002 | c0006 | t0005 | g0021 | AMR | PEL | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG01981 | hp1 | a0001 | c0003 | t0001 | g0002 | AMR | PEL | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG01981 | hp2 | a0001 | c0003 | t0001 | g0033 | AMR | PEL | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG01993 | hp2 | a0001 | c0004 | t0002 | g0018 | AMR | PEL | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PEL | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG02004 | hp2 | a0001 | c0001 | t0003 | g0009 | AMR | PEL | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG02015 | hp1 | a0001 | c0002 | t0001 | g0248 | EAS | KHV | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG02015 | hp2 | a0001 | c0003 | t0001 | g0184 | EAS | KHV | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG02040 | hp1 | a0001 | c0003 | t0001 | g0002 | EAS | KHV | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | KHV | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG02055 | hp1 | a0001 | c0002 | t0002 | g0010 | AFR | ACB | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG02055 | hp2 | a0001 | c0005 | t0004 | g0173 | AFR | ACB | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG02056 | hp1 | a0001 | c0002 | t0002 | g0158 | EAS | KHV | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG02056 | hp2 | a0001 | c0002 | t0001 | g0258 | EAS | KHV | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG02074 | hp1 | a0001 | c0003 | t0001 | g0034 | EAS | KHV | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG02074 | hp2 | a0001 | c0004 | t0002 | g0001 | EAS | KHV | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG02080 | hp1 | a0001 | c0003 | t0001 | g0002 | EAS | KHV | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG02080 | hp2 | a0001 | c0003 | t0001 | g0181 | EAS | KHV | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0239 | EAS | KHV | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG02083 | hp2 | a0001 | c0004 | t0002 | g0001 | EAS | KHV | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG02129 | hp1 | a0002 | c0006 | t0003 | g0008 | EAS | KHV | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG02129 | hp2 | a0001 | c0002 | t0005 | g0170 | EAS | KHV | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | KHV | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG02132 | hp2 | a0001 | c0002 | t0006 | g0003 | EAS | KHV | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG02135 | hp1 | a0001 | c0002 | t0002 | g0117 | EAS | KHV | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG02135 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | KHV | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG02145 | hp1 | a0001 | c0005 | t0004 | g0092 | AFR | ACB | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG02145 | hp2 | a0003 | c0009 | t0001 | g0232 | AFR | ACB | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG02148 | hp1 | a0001 | c0002 | t0006 | g0126 | AMR | PEL | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG02148 | hp2 | a0001 | c0003 | t0001 | g0002 | AMR | PEL | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG02155 | hp1 | a0001 | c0003 | t0001 | g0002 | EAS | CDX | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0070 | EAS | CDX | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | CDX | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG02165 | hp2 | a0002 | c0006 | t0003 | g0214 | EAS | CDX | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG02257 | hp1 | a0001 | c0005 | t0004 | g0019 | AFR | ACB | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG02257 | hp2 | a0001 | c0011 | t0030 | g0178 | AFR | ACB | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG02258 | hp1 | a0001 | c0001 | t0004 | g0039 | AFR | ACB | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG02258 | hp2 | a0001 | c0005 | t0004 | g0020 | AFR | ACB | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0050 | AMR | PEL | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG02273 | hp2 | a0001 | c0004 | t0002 | g0018 | AMR | PEL | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG02280 | hp1 | a0006 | c0024 | t0037 | g0175 | AFR | ACB | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0028 | AFR | ACB | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG02293 | hp1 | a0001 | c0007 | t0001 | g0058 | AMR | PEL | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG02293 | hp2 | a0002 | c0006 | t0005 | g0021 | AMR | PEL | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG02300 | hp1 | a0002 | c0006 | t0005 | g0132 | AMR | PEL | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG02300 | hp2 | a0001 | c0004 | t0002 | g0018 | AMR | PEL | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG02451 | hp1 | a0001 | c0003 | t0004 | g0093 | AFR | ACB | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0260 | AFR | ACB | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG02572 | hp1 | a0005 | c0017 | t0016 | g0242 | AFR | GWD | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG02572 | hp2 | a0001 | c0005 | t0001 | g0192 | AFR | GWD | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0253 | SAS | PJL | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG02602 | hp2 | a0001 | c0003 | t0001 | g0033 | SAS | PJL | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG02615 | hp1 | a0001 | c0005 | t0020 | g0086 | AFR | GWD | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG02615 | hp2 | a0001 | c0005 | t0007 | g0023 | AFR | GWD | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG02622 | hp1 | a0001 | c0005 | t0007 | g0243 | AFR | GWD | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG02622 | hp2 | a0001 | c0005 | t0010 | g0164 | AFR | GWD | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0259 | AFR | GWD | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG02647 | hp2 | a0003 | c0009 | t0031 | g0084 | AFR | GWD | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG02683 | hp1 | a0002 | c0006 | t0005 | g0016 | SAS | PJL | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG02683 | hp2 | a0001 | c0001 | t0003 | g0264 | SAS | PJL | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG02698 | hp1 | a0001 | c0002 | t0002 | g0115 | SAS | PJL | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG02698 | hp2 | a0002 | c0006 | t0005 | g0128 | SAS | PJL | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG02717 | hp1 | a0001 | c0005 | t0007 | g0023 | AFR | GWD | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG02717 | hp2 | a0004 | c0013 | t0005 | g0041 | AFR | GWD | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG02723 | hp1 | a0001 | c0005 | t0007 | g0023 | AFR | GWD | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG02723 | hp2 | a0001 | c0001 | t0004 | g0088 | AFR | GWD | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG02735 | hp1 | a0001 | c0002 | t0002 | g0118 | SAS | PJL | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG02735 | hp2 | a0001 | c0001 | t0003 | g0009 | SAS | PJL | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG02738 | hp1 | a0001 | c0002 | t0001 | g0257 | SAS | PJL | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG02738 | hp2 | a0001 | c0002 | t0002 | g0166 | SAS | PJL | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0209 | AFR | GWD | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG02818 | hp2 | a0001 | c0005 | t0039 | g0089 | AFR | GWD | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG02886 | hp1 | a0001 | c0005 | t0004 | g0087 | AFR | GWD | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG02886 | hp2 | a0003 | c0010 | t0002 | g0043 | AFR | GWD | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG02895 | hp1 | a0001 | c0008 | t0012 | g0030 | AFR | GWD | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG02895 | hp2 | a0001 | c0005 | t0007 | g0228 | AFR | GWD | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG02896 | hp1 | a0001 | c0008 | t0012 | g0030 | AFR | GWD | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG02896 | hp2 | a0001 | c0002 | t0002 | g0024 | AFR | GWD | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG02897 | hp1 | a0001 | c0005 | t0007 | g0023 | AFR | GWD | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG02897 | hp2 | a0001 | c0008 | t0012 | g0030 | AFR | GWD | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | ESN | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG02922 | hp2 | a0001 | c0005 | t0004 | g0080 | AFR | ESN | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG02965 | hp1 | a0005 | c0017 | t0016 | g0241 | AFR | ESN | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG02965 | hp2 | a0001 | c0005 | t0020 | g0098 | AFR | ESN | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG02970 | hp1 | a0001 | c0002 | t0018 | g0078 | AFR | ESN | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG02970 | hp2 | a0001 | c0005 | t0004 | g0090 | AFR | ESN | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG02976 | hp1 | a0003 | c0014 | t0034 | g0159 | AFR | ESN | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG02976 | hp2 | a0001 | c0008 | t0013 | g0032 | AFR | ESN | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0250 | SAS | PJL | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG03017 | hp2 | a0001 | c0001 | t0004 | g0006 | SAS | PJL | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG03041 | hp1 | a0001 | c0003 | t0004 | g0180 | AFR | GWD | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0065 | AFR | GWD | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG03098 | hp1 | a0003 | c0010 | t0002 | g0043 | AFR | MSL | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG03098 | hp2 | a0001 | c0005 | t0007 | g0219 | AFR | MSL | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG03130 | hp1 | a0003 | c0010 | t0002 | g0042 | AFR | ESN | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG03130 | hp2 | a0003 | c0009 | t0001 | g0229 | AFR | ESN | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG03139 | hp1 | a0001 | c0002 | t0025 | g0222 | AFR | ESN | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG03139 | hp2 | a0001 | c0005 | t0004 | g0019 | AFR | ESN | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG03209 | hp1 | a0001 | c0002 | t0001 | g0072 | AFR | MSL | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG03209 | hp2 | a0001 | c0008 | t0013 | g0032 | AFR | MSL | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG03225 | hp1 | a0001 | c0002 | t0002 | g0177 | AFR | MSL | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG03225 | hp2 | a0001 | c0002 | t0002 | g0104 | AFR | MSL | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG03239 | hp1 | a0002 | c0016 | t0003 | g0256 | SAS | PJL | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG03239 | hp2 | a0001 | c0002 | t0002 | g0134 | SAS | PJL | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG03453 | hp1 | a0001 | c0003 | t0004 | g0056 | AFR | MSL | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG03453 | hp2 | a0001 | c0012 | t0001 | g0076 | AFR | MSL | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG03486 | hp1 | a0001 | c0005 | t0004 | g0040 | AFR | MSL | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG03486 | hp2 | a0001 | c0001 | t0004 | g0112 | AFR | MSL | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG03490 | hp1 | a0001 | c0002 | t0005 | g0003 | SAS | PJL | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG03490 | hp2 | a0001 | c0004 | t0002 | g0053 | SAS | PJL | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG03491 | hp1 | a0001 | c0001 | t0015 | g0221 | SAS | PJL | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG03491 | hp2 | a0001 | c0004 | t0002 | g0162 | SAS | PJL | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG03492 | hp1 | a0001 | c0001 | t0015 | g0066 | SAS | PJL | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG03492 | hp2 | a0001 | c0004 | t0002 | g0053 | SAS | PJL | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG03516 | hp1 | a0004 | c0013 | t0005 | g0108 | AFR | ESN | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG03516 | hp2 | a0001 | c0005 | t0004 | g0040 | AFR | ESN | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG03540 | hp1 | a0001 | c0005 | t0001 | g0194 | AFR | GWD | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG03540 | hp2 | a0001 | c0003 | t0002 | g0110 | AFR | GWD | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0211 | AFR | MSL | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG03579 | hp2 | a0001 | c0005 | t0004 | g0020 | AFR | MSL | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG03654 | hp1 | a0001 | c0002 | t0004 | g0103 | SAS | PJL | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG03654 | hp2 | a0001 | c0002 | t0002 | g0010 | SAS | PJL | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG03669 | hp1 | a0001 | c0003 | t0002 | g0139 | SAS | PJL | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG03669 | hp2 | a0001 | c0002 | t0006 | g0003 | SAS | PJL | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG03688 | hp1 | a0001 | c0004 | t0028 | g0120 | SAS | STU | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG03688 | hp2 | a0001 | c0002 | t0001 | g0075 | SAS | STU | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG03704 | hp1 | a0001 | c0002 | t0002 | g0129 | SAS | PJL | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0251 | SAS | PJL | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG03710 | hp2 | a0001 | c0007 | t0001 | g0199 | SAS | PJL | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG03831 | hp1 | a0001 | c0001 | t0004 | g0015 | SAS | BEB | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG03831 | hp2 | a0001 | c0002 | t0006 | g0167 | SAS | BEB | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG03834 | hp1 | a0001 | c0004 | t0002 | g0163 | SAS | BEB | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG03834 | hp2 | a0001 | c0020 | t0008 | g0187 | SAS | BEB | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG03927 | hp1 | a0001 | c0001 | t0004 | g0015 | SAS | BEB | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG03927 | hp2 | a0001 | c0001 | t0009 | g0085 | SAS | BEB | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG03942 | hp1 | a0002 | c0016 | t0005 | g0169 | SAS | BEB | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG03942 | hp2 | a0001 | c0003 | t0005 | g0016 | SAS | BEB | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG04115 | hp1 | a0002 | c0006 | t0003 | g0195 | SAS | STU | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG04115 | hp2 | a0001 | c0001 | t0038 | g0245 | SAS | STU | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0252 | SAS | BEB | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG04184 | hp2 | a0001 | c0001 | t0032 | g0125 | SAS | BEB | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG04199 | hp1 | a0001 | c0002 | t0001 | g0075 | SAS | STU | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG04199 | hp2 | a0001 | c0004 | t0002 | g0122 | SAS | STU | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG04204 | hp1 | a0001 | c0002 | t0004 | g0102 | SAS | STU | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG04204 | hp2 | a0002 | c0015 | t0009 | g0157 | SAS | STU | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0048 | SAS | STU | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG04228 | hp2 | a0001 | c0002 | t0006 | g0156 | SAS | STU | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18522 | hp1 | a0001 | c0012 | t0001 | g0076 | AFR | YRI | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18522 | hp2 | a0001 | c0005 | t0010 | g0054 | AFR | YRI | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18612 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | CHB | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18612 | hp2 | a0001 | c0003 | t0001 | g0189 | EAS | CHB | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0238 | EAS | CHB | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18747 | hp2 | a0001 | c0004 | t0002 | g0001 | EAS | CHB | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18906 | hp1 | a0001 | c0002 | t0002 | g0025 | AFR | YRI | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18906 | hp2 | a0001 | c0002 | t0036 | g0174 | AFR | YRI | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18939 | hp1 | a0001 | c0001 | t0005 | g0141 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18939 | hp2 | a0001 | c0001 | t0009 | g0045 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18940 | hp1 | a0001 | c0001 | t0003 | g0037 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18940 | hp2 | a0001 | c0004 | t0002 | g0001 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18941 | hp1 | a0001 | c0004 | t0005 | g0001 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18941 | hp2 | a0001 | c0001 | t0005 | g0017 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0064 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18942 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18943 | hp2 | a0001 | c0001 | t0005 | g0154 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18944 | hp1 | a0001 | c0001 | t0003 | g0069 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18944 | hp2 | a0001 | c0001 | t0003 | g0261 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18945 | hp2 | a0001 | c0004 | t0002 | g0079 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18946 | hp1 | a0001 | c0001 | t0004 | g0091 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18946 | hp2 | a0001 | c0004 | t0002 | g0001 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18947 | hp1 | a0001 | c0002 | t0005 | g0160 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18947 | hp2 | a0001 | c0001 | t0003 | g0067 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18948 | hp1 | a0001 | c0003 | t0003 | g0012 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18948 | hp2 | a0001 | c0004 | t0002 | g0146 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18949 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18949 | hp2 | a0001 | c0004 | t0002 | g0029 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18950 | hp1 | a0001 | c0001 | t0009 | g0045 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18951 | hp1 | a0001 | c0004 | t0002 | g0001 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18951 | hp2 | a0001 | c0003 | t0001 | g0033 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18952 | hp1 | a0001 | c0004 | t0002 | g0150 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18952 | hp2 | a0001 | c0004 | t0001 | g0240 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18953 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18953 | hp2 | a0001 | c0002 | t0001 | g0218 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18954 | hp1 | a0001 | c0004 | t0006 | g0143 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18954 | hp2 | a0001 | c0001 | t0004 | g0096 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18956 | hp2 | a0001 | c0004 | t0011 | g0001 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18957 | hp1 | a0001 | c0002 | t0001 | g0212 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18957 | hp2 | a0001 | c0004 | t0001 | g0191 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18959 | hp1 | a0001 | c0004 | t0002 | g0001 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18960 | hp1 | a0001 | c0004 | t0006 | g0142 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18960 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18961 | hp2 | a0001 | c0003 | t0001 | g0002 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18963 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18963 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18964 | hp1 | a0001 | c0003 | t0008 | g0035 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18964 | hp2 | a0001 | c0001 | t0004 | g0026 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18965 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18965 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18966 | hp1 | a0002 | c0006 | t0003 | g0061 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0037 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18967 | hp1 | a0001 | c0002 | t0001 | g0226 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18968 | hp1 | a0001 | c0001 | t0008 | g0210 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18968 | hp2 | a0001 | c0004 | t0002 | g0151 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18969 | hp1 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18969 | hp2 | a0002 | c0006 | t0022 | g0197 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18970 | hp2 | a0001 | c0002 | t0006 | g0003 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18971 | hp1 | a0001 | c0003 | t0003 | g0034 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18971 | hp2 | a0001 | c0004 | t0002 | g0140 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18972 | hp1 | a0001 | c0001 | t0003 | g0037 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18972 | hp2 | a0001 | c0004 | t0005 | g0161 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18973 | hp1 | a0001 | c0003 | t0001 | g0057 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18973 | hp2 | a0001 | c0001 | t0004 | g0083 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18974 | hp1 | a0001 | c0002 | t0006 | g0031 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18974 | hp2 | a0001 | c0003 | t0001 | g0196 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18975 | hp1 | a0001 | c0003 | t0001 | g0198 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18977 | hp1 | a0001 | c0002 | t0002 | g0047 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18978 | hp1 | a0001 | c0004 | t0005 | g0001 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18978 | hp2 | a0001 | c0001 | t0003 | g0235 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18979 | hp1 | a0001 | c0004 | t0002 | g0136 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18979 | hp2 | a0002 | c0006 | t0003 | g0059 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18980 | hp1 | a0001 | c0004 | t0006 | g0147 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18980 | hp2 | a0001 | c0003 | t0001 | g0060 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18981 | hp2 | a0001 | c0001 | t0003 | g0036 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18982 | hp1 | a0001 | c0003 | t0001 | g0002 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18982 | hp2 | a0001 | c0001 | t0005 | g0017 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18983 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18983 | hp2 | a0001 | c0003 | t0001 | g0012 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18984 | hp1 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18984 | hp2 | a0001 | c0001 | t0004 | g0015 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18985 | hp1 | a0001 | c0002 | t0006 | g0171 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18985 | hp2 | a0001 | c0004 | t0005 | g0001 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18986 | hp1 | a0001 | c0003 | t0001 | g0012 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18986 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18987 | hp1 | a0001 | c0002 | t0006 | g0003 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18987 | hp2 | a0001 | c0003 | t0001 | g0012 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18988 | hp1 | a0001 | c0003 | t0001 | g0002 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18988 | hp2 | a0001 | c0003 | t0001 | g0008 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18990 | hp1 | a0001 | c0001 | t0005 | g0148 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18990 | hp2 | a0001 | c0001 | t0004 | g0097 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18991 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18992 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18992 | hp2 | a0001 | c0001 | t0004 | g0107 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18993 | hp1 | a0007 | c0019 | t0001 | g0013 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18993 | hp2 | a0001 | c0003 | t0001 | g0012 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18994 | hp2 | a0001 | c0004 | t0002 | g0029 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18995 | hp1 | a0001 | c0003 | t0001 | g0057 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18995 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18997 | hp1 | a0001 | c0002 | t0006 | g0031 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18997 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18998 | hp1 | a0001 | c0001 | t0005 | g0052 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18998 | hp2 | a0001 | c0004 | t0002 | g0001 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18999 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0036 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA19000 | hp2 | a0001 | c0004 | t0002 | g0029 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA19003 | hp1 | a0001 | c0001 | t0004 | g0099 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA19003 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA19004 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA19004 | hp2 | a0001 | c0002 | t0006 | g0003 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA19005 | hp1 | a0001 | c0004 | t0002 | g0152 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA19005 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA19007 | hp1 | a0001 | c0001 | t0003 | g0067 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA19007 | hp2 | a0001 | c0002 | t0006 | g0168 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA19009 | hp1 | a0001 | c0004 | t0011 | g0001 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA19009 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA19010 | hp1 | a0001 | c0004 | t0002 | g0001 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA19010 | hp2 | a0001 | c0001 | t0004 | g0082 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA19011 | hp1 | a0001 | c0003 | t0001 | g0002 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA19011 | hp2 | a0001 | c0002 | t0001 | g0237 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA19012 | hp1 | a0001 | c0002 | t0006 | g0003 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA19012 | hp2 | a0001 | c0002 | t0001 | g0227 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA19030 | hp1 | a0003 | c0014 | t0024 | g0233 | AFR | LWK | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA19030 | hp2 | a0001 | c0002 | t0002 | g0025 | AFR | LWK | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA19043 | hp1 | a0003 | c0014 | t0023 | g0165 | AFR | LWK | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA19043 | hp2 | a0003 | c0009 | t0002 | g0106 | AFR | LWK | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA19054 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA19056 | hp1 | a0001 | c0002 | t0006 | g0155 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA19056 | hp2 | a0001 | c0003 | t0001 | g0002 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA19057 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA19058 | hp1 | a0001 | c0001 | t0003 | g0065 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA19058 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA19062 | hp1 | a0001 | c0003 | t0008 | g0035 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA19062 | hp2 | a0001 | c0001 | t0004 | g0101 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA19063 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA19063 | hp2 | a0001 | c0002 | t0006 | g0003 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA19064 | hp1 | a0001 | c0001 | t0009 | g0095 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA19064 | hp2 | a0001 | c0002 | t0006 | g0003 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA19065 | hp1 | a0001 | c0004 | t0011 | g0001 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA19065 | hp2 | a0001 | c0002 | t0006 | g0003 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA19066 | hp1 | a0001 | c0004 | t0002 | g0001 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA19066 | hp2 | a0001 | c0003 | t0001 | g0234 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA19068 | hp1 | a0001 | c0001 | t0004 | g0026 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA19068 | hp2 | a0001 | c0001 | t0005 | g0017 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA19070 | hp2 | a0001 | c0004 | t0002 | g0051 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA19074 | hp1 | a0002 | c0006 | t0003 | g0034 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA19074 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA19075 | hp1 | a0001 | c0001 | t0033 | g0007 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA19076 | hp1 | a0001 | c0003 | t0001 | g0002 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA19076 | hp2 | a0001 | c0002 | t0006 | g0003 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA19077 | hp1 | a0001 | c0002 | t0006 | g0031 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA19077 | hp2 | a0001 | c0001 | t0005 | g0052 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA19078 | hp1 | a0001 | c0001 | t0003 | g0070 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA19078 | hp2 | a0001 | c0002 | t0006 | g0003 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA19079 | hp1 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA19079 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA19080 | hp2 | a0002 | c0006 | t0003 | g0059 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA19081 | hp1 | a0002 | c0006 | t0003 | g0008 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA19081 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA19082 | hp1 | a0001 | c0003 | t0001 | g0012 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA19083 | hp1 | a0001 | c0003 | t0003 | g0200 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA19083 | hp2 | a0002 | c0006 | t0014 | g0008 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA19084 | hp1 | a0001 | c0002 | t0002 | g0135 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA19084 | hp2 | a0001 | c0002 | t0002 | g0047 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA19085 | hp1 | a0008 | c0021 | t0001 | g0205 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA19085 | hp2 | a0001 | c0002 | t0006 | g0003 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA19087 | hp1 | a0001 | c0003 | t0008 | g0201 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA19087 | hp2 | a0001 | c0004 | t0005 | g0145 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA19088 | hp1 | a0002 | c0006 | t0003 | g0008 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA19088 | hp2 | a0001 | c0001 | t0005 | g0017 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA19090 | hp1 | a0001 | c0004 | t0002 | g0138 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA19090 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA19091 | hp1 | a0001 | c0002 | t0001 | g0071 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA19091 | hp2 | a0001 | c0004 | t0001 | g0179 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA19240 | hp1 | a0001 | c0001 | t0004 | g0039 | AFR | YRI | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA19240 | hp2 | a0003 | c0010 | t0002 | g0109 | AFR | YRI | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA20129 | hp1 | a0001 | c0007 | t0002 | g0044 | AFR | ASW | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA20129 | hp2 | a0001 | c0005 | t0010 | g0054 | AFR | ASW | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0009 | EUR | TSI | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA20752 | hp2 | a0001 | c0002 | t0001 | g0255 | EUR | TSI | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0262 | EUR | TSI | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA20805 | hp2 | a0001 | c0003 | t0017 | g0217 | EUR | TSI | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA20905 | hp1 | a0009 | c0022 | t0002 | g0123 | SAS | GIH | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA20905 | hp2 | a0001 | c0018 | t0004 | g0105 | SAS | GIH | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG01123 | hp1 | a0001 | c0001 | t0014 | g0203 | AMR | CLM | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG01123 | hp2 | a0001 | c0001 | t0004 | g0015 | AMR | CLM | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG02109 | hp1 | a0004 | c0013 | t0005 | g0041 | AFR | ACB | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG02109 | hp2 | a0001 | c0005 | t0004 | g0019 | AFR | ACB | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG02486 | hp1 | a0001 | c0002 | t0018 | g0046 | AFR | ACB | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG02486 | hp2 | a0003 | c0010 | t0002 | g0042 | AFR | ACB | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG02559 | hp1 | a0001 | c0005 | t0004 | g0094 | AFR | ACB | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG02559 | hp2 | a0001 | c0002 | t0029 | g0046 | AFR | ACB | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG03471 | hp1 | a0001 | c0002 | t0001 | g0072 | AFR | MSL | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG03471 | hp2 | a0001 | c0002 | t0002 | g0025 | AFR | MSL | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG06807 | hp1 | a0001 | c0008 | t0019 | g0038 | AFR | USA | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| HG06807 | hp2 | a0002 | c0006 | t0002 | g0021 | AFR | USA | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18955 | hp1 | a0001 | c0001 | t0003 | g0236 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA18955 | hp2 | a0001 | c0001 | t0027 | g0005 | EAS | JPT | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA20300 | hp1 | a0002 | c0023 | t0005 | g0144 | AFR | USA | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0247 | AFR | USA | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA21309 | hp1 | a0001 | c0005 | t0004 | g0020 | AFR | LWK | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| NA21309 | hp2 | a0001 | c0005 | t0004 | g0081 | AFR | LWK | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0263 | REF | REF | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| homoSapiens | grch38p0 | a0001 | c0007 | t0002 | g0044 | REF | REF | TRIM6_chr11_5591637_5617952 | TRIM6 | chr11 | 5591637 | 5617952 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:5603458 | G | T | 1 | a0006 | 1 | HG02280.hp1 | missense_variant | MODERATE | c.230G>T | p.Gly77Val | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 2/8 | 491/3422 | 230/1551 | 77/516 | chr11 | 5603458 | |||
| chr11:5604570 | G | A | 2 | a0003 a0004 |
17 | HG01109.hp2 HG01891.hp2 HG02109.hp1 others(14): Show |
missense_variant | MODERATE | c.544G>A | p.Glu182Lys | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 3/8 | 805/3422 | 544/1551 | 182/516 | chr11 | 5604570 | |||
| chr11:5604582 | G | C | 1 | a0007 | 1 | NA18993.hp1 | missense_variant | MODERATE | c.556G>C | p.Ala186Pro | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 3/8 | 817/3422 | 556/1551 | 186/516 | chr11 | 5604582 | |||
| chr11:5610240 | G | T | 1 | a0005 | 2 | HG02572.hp1 HG02965.hp1 |
missense_variant | MODERATE | c.953G>T | p.Cys318Phe | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 6/8 | 1214/3422 | 953/1551 | 318/516 | chr11 | 5610240 | |||
| chr11:5610788 | C | A | 2 | a0002 a0004 |
31 | HG00323.hp2 HG00423.hp2 HG00621.hp2 others(28): Show |
missense_variant | MODERATE | c.997C>A | p.Leu333Met | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 8/8 | 1258/3422 | 997/1551 | 333/516 | chr11 | 5610788 | |||
| chr11:5610891 | A | G | 1 | a0009 | 1 | NA20905.hp1 | missense_variant | MODERATE | c.1100A>G | p.His367Arg | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 8/8 | 1361/3422 | 1100/1551 | 367/516 | chr11 | 5610891 | |||
| chr11:5611323 | T | C | 1 | a0008 | 1 | NA19085.hp1 | missense_variant | MODERATE | c.1532T>C | p.Leu511Pro | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 8/8 | 1793/3422 | 1532/1551 | 511/516 | chr11 | 5611323 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:5603276 | C | A | 1 | a0001c0018 | 1 | NA20905.hp2 | synonymous_variant | LOW | c.48C>A | p.Ile16Ile | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 2/8 | 309/3422 | 48/1551 | 16/516 | chr11 | 5603276 | |||
| chr11:5603291 | A | C | 1 | a0001c0008 | 9 | HG00741.hp1 HG01167.hp2 HG01243.hp2 others(6): Show |
synonymous_variant | LOW | c.63A>C | p.Ala21Ala | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 2/8 | 324/3422 | 63/1551 | 21/516 | chr11 | 5603291 | |||
| chr11:5604554 | A | G | 4 | a0001c0004 a0001c0012 a0002c0023 others(1): Show |
56 | HG00558.hp2 HG00673.hp2 HG00733.hp2 others(53): Show |
synonymous_variant | LOW | c.528A>G | p.Leu176Leu | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 3/8 | 789/3422 | 528/1551 | 176/516 | chr11 | 5604554 | |||
| chr11:5604617 | A | G | 15 | a0001c0001 a0001c0002 a0001c0004 others(12): Show |
361 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(358): Show |
synonymous_variant | LOW | c.591A>G | p.Lys197Lys | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 3/8 | 852/3422 | 591/1551 | 197/516 | chr11 | 5604617 | |||
| chr11:5605543 | G | A | 1 | a0001c0020 | 1 | HG03834.hp2 | synonymous_variant | LOW | c.810G>A | p.Gln270Gln | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 4/8 | 1071/3422 | 810/1551 | 270/516 | chr11 | 5605543 | |||
| chr11:5608377 | G | A | 10 | a0001c0001 a0001c0005 a0001c0018 others(7): Show |
222 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(219): Show |
synonymous_variant | LOW | c.840G>A | p.Val280Val | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 5/8 | 1101/3422 | 840/1551 | 280/516 | chr11 | 5608377 | |||
| chr11:5610982 | G | A | 17 | a0001c0001 a0001c0002 a0001c0003 others(14): Show |
404 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(401): Show |
synonymous_variant | LOW | c.1191G>A | p.Leu397Leu | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 8/8 | 1452/3422 | 1191/1551 | 397/516 | chr11 | 5610982 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:5596661 | C | T | 1 | a0001c0001t0040 | 1 | HG00544.hp2 | 5_prime_UTR_variant | MODIFIER | c.-237C>T | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/8 | 237 | chr11 | 5596661 | ||||||
| chr11:5596666 | A | G | 11 | a0001c0001t0004 a0001c0001t0009 a0001c0001t0038 others(8): Show |
60 | HG00544.hp2 HG00609.hp2 HG00642.hp1 others(57): Show |
5_prime_UTR_variant | MODIFIER | c.-232A>G | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/8 | 232 | chr11 | 5596666 | ||||||
| chr11:5596689 | C | G | 4 | a0001c0002t0035 a0001c0002t0036 a0001c0008t0013 others(1): Show |
6 | HG01243.hp1 HG01243.hp2 HG02280.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-209C>G | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/8 | 209 | chr11 | 5596689 | ||||||
| chr11:5596698 | G | T | 3 | a0001c0005t0020 a0001c0008t0012 a0003c0014t0034 |
6 | HG02615.hp1 HG02895.hp1 HG02896.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-200G>T | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/8 | 200 | chr11 | 5596698 | ||||||
| chr11:5596728 | C | T | 1 | a0001c0001t0033 | 1 | NA19075.hp1 | 5_prime_UTR_variant | MODIFIER | c.-170C>T | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/8 | 170 | chr11 | 5596728 | ||||||
| chr11:5596757 | G | A | 38 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0008 others(35): Show |
236 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(233): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-141G>A | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/8 | chr11 | 5596757 | |||||||
| chr11:5611449 | T | G | 1 | a0001c0002t0035 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*107T>G | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 8/8 | 107 | chr11 | 5611449 | ||||||
| chr11:5611451 | T | C | 6 | a0001c0001t0008 a0001c0001t0021 a0001c0002t0006 others(3): Show |
36 | HG00438.hp1 HG00642.hp2 HG01256.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*109T>C | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 8/8 | 109 | chr11 | 5611451 | ||||||
| chr11:5611461 | G | C | 1 | a0001c0005t0039 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*119G>C | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 8/8 | 119 | chr11 | 5611461 | ||||||
| chr11:5611510 | C | G | 2 | a0001c0001t0032 a0003c0009t0031 |
2 | HG02647.hp2 HG04184.hp2 |
3_prime_UTR_variant | MODIFIER | c.*168C>G | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 8/8 | 168 | chr11 | 5611510 | ||||||
| chr11:5611637 | G | A | 24 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0009 others(21): Show |
132 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(129): Show |
3_prime_UTR_variant | MODIFIER | c.*295G>A | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 8/8 | 295 | chr11 | 5611637 | ||||||
| chr11:5611655 | G | T | 12 | a0001c0001t0015 a0001c0001t0017 a0001c0003t0017 others(9): Show |
23 | HG00140.hp1 HG00741.hp1 HG01099.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*313G>T | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 8/8 | 313 | chr11 | 5611655 | ||||||
| chr11:5611745 | G | A | 1 | a0001c0004t0011 | 3 | NA18956.hp2 NA19009.hp1 NA19065.hp1 |
3_prime_UTR_variant | MODIFIER | c.*403G>A | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 8/8 | 403 | chr11 | 5611745 | ||||||
| chr11:5611770 | C | T | 1 | a0002c0006t0022 | 1 | NA18969.hp2 | 3_prime_UTR_variant | MODIFIER | c.*428C>T | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 8/8 | 428 | chr11 | 5611770 | ||||||
| chr11:5611859 | T | C | 3 | a0001c0008t0013 a0003c0014t0023 a0003c0014t0024 |
5 | HG01243.hp2 HG02976.hp2 HG03209.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*517T>C | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 8/8 | 517 | chr11 | 5611859 | ||||||
| chr11:5611891 | G | A | 1 | a0005c0017t0016 | 2 | HG02572.hp1 HG02965.hp1 |
3_prime_UTR_variant | MODIFIER | c.*549G>A | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 8/8 | 549 | chr11 | 5611891 | ||||||
| chr11:5611932 | T | A | 1 | a0003c0009t0031 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*590T>A | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 8/8 | 590 | chr11 | 5611932 | ||||||
| chr11:5612052 | C | T | 1 | a0001c0001t0021 | 1 | HG01934.hp2 | 3_prime_UTR_variant | MODIFIER | c.*710C>T | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 8/8 | 710 | chr11 | 5612052 | ||||||
| chr11:5612186 | C | T | 1 | a0001c0002t0029 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*844C>T | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 8/8 | 844 | chr11 | 5612186 | ||||||
| chr11:5612370 | A | G | 22 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0009 others(19): Show |
131 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(128): Show |
3_prime_UTR_variant | MODIFIER | c.*1028A>G | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 8/8 | 1028 | chr11 | 5612370 | ||||||
| chr11:5612414 | T | TA | 22 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0009 others(19): Show |
131 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(128): Show |
3_prime_UTR_variant | MODIFIER | c.*1081dupA | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 8/8 | 1082 | INFO_REALIGN_3_PRIME | chr11 | 5612414 | |||||
| chr11:5612414 | TA | T | 10 | a0001c0001t0015 a0001c0001t0017 a0001c0001t0033 others(7): Show |
19 | HG00140.hp1 HG00741.hp1 HG01099.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*1081delA | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 8/8 | 1081 | INFO_REALIGN_3_PRIME | chr11 | 5612414 | |||||
| chr11:5612427 | G | A | 1 | a0003c0009t0031 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1085G>A | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 8/8 | 1085 | chr11 | 5612427 | ||||||
| chr11:5612459 | A | G | 22 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0009 others(19): Show |
131 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(128): Show |
3_prime_UTR_variant | MODIFIER | c.*1117A>G | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 8/8 | 1117 | chr11 | 5612459 | ||||||
| chr11:5612517 | C | T | 22 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0009 others(19): Show |
131 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(128): Show |
3_prime_UTR_variant | MODIFIER | c.*1175C>T | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 8/8 | 1175 | chr11 | 5612517 | ||||||
| chr11:5612558 | G | C | 1 | a0005c0017t0016 | 2 | HG02572.hp1 HG02965.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1216G>C | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 8/8 | 1216 | chr11 | 5612558 | ||||||
| chr11:5612581 | C | G | 1 | a0001c0004t0028 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1239C>G | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 8/8 | 1239 | chr11 | 5612581 | ||||||
| chr11:5612602 | G | A | 4 | a0001c0002t0018 a0001c0002t0025 a0001c0002t0029 others(1): Show |
5 | HG02486.hp1 HG02559.hp2 HG02970.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1260G>A | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 8/8 | 1260 | chr11 | 5612602 | ||||||
| chr11:5612815 | T | A | 22 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0009 others(19): Show |
131 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(128): Show |
3_prime_UTR_variant | MODIFIER | c.*1473T>A | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 8/8 | 1473 | chr11 | 5612815 | ||||||
| chr11:5612921 | A | G | 1 | a0001c0002t0035 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1579A>G | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 8/8 | 1579 | chr11 | 5612921 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:5597068 | A | ATTTTAT | 141 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0036 others(138): Show |
232 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.17+159_17+160insTT others(4): Show |
TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 5597068 | ||||||
| chr11:5597086 | A | G | 1 | a0001c0011t0030g0178 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.17+172A>G | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | chr11 | 5597086 | |||||||
| chr11:5597096 | A | G | 1 | a0001c0002t0002g0177 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.17+182A>G | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | chr11 | 5597096 | |||||||
| chr11:5597122 | C | T | 1 | a0001c0003t0001g0077 | 2 | HG00735.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.17+208C>T | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | chr11 | 5597122 | |||||||
| chr11:5597187 | T | C | 141 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0036 others(138): Show |
232 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.17+273T>C | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | chr11 | 5597187 | |||||||
| chr11:5597194 | G | A | 141 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0036 others(138): Show |
232 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.17+280G>A | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | chr11 | 5597194 | |||||||
| chr11:5597215 | C | T | 4 | a0001c0002t0035g0176 a0001c0002t0036g0174 a0001c0008t0013g0032 others(1): Show |
6 | HG01243.hp1 HG01243.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.17+301C>T | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | chr11 | 5597215 | |||||||
| chr11:5597272 | G | A | 141 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0036 others(138): Show |
232 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.17+358G>A | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | chr11 | 5597272 | |||||||
| chr11:5597340 | C | T | 1 | a0001c0002t0001g0265 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.17+426C>T | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | chr11 | 5597340 | |||||||
| chr11:5597529 | T | C | 4 | a0001c0002t0002g0024 a0001c0002t0002g0025 a0001c0002t0002g0177 others(1): Show |
8 | HG00639.hp1 HG01884.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.17+615T>C | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | chr11 | 5597529 | |||||||
| chr11:5597540 | A | T | 10 | a0001c0001t0002g0172 a0001c0002t0002g0166 a0001c0002t0005g0003 others(7): Show |
23 | HG02129.hp2 HG02132.hp2 HG02738.hp2 others(20): Show |
intron_variant | MODIFIER | c.17+626A>T | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | chr11 | 5597540 | |||||||
| chr11:5597652 | C | T | 139 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0036 others(136): Show |
229 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.17+738C>T | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | chr11 | 5597652 | |||||||
| chr11:5597664 | C | G | 139 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0036 others(136): Show |
229 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.17+750C>G | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | chr11 | 5597664 | |||||||
| chr11:5597676 | C | T | 2 | a0001c0001t0003g0262 a0001c0001t0003g0264 |
2 | HG02683.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.17+762C>T | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | chr11 | 5597676 | |||||||
| chr11:5597759 | C | G | 1 | a0001c0005t0004g0173 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.17+845C>G | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | chr11 | 5597759 | |||||||
| chr11:5597778 | G | A | 139 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0036 others(136): Show |
229 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.17+864G>A | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | chr11 | 5597778 | |||||||
| chr11:5597926 | T | TATTA | 139 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0036 others(136): Show |
229 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.17+1014_17+1017dup others(4): Show |
TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 5597926 | ||||||
| chr11:5598097 | T | A | 1 | a0001c0004t0002g0079 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.17+1183T>A | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | chr11 | 5598097 | |||||||
| chr11:5598108 | A | C | 139 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0036 others(136): Show |
229 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.17+1194A>C | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | chr11 | 5598108 | |||||||
| chr11:5598158 | A | T | 1 | a0001c0012t0001g0076 | 2 | HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.17+1244A>T | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | chr11 | 5598158 | |||||||
| chr11:5598359 | A | C | 13 | a0001c0001t0002g0172 a0001c0002t0002g0166 a0001c0002t0005g0003 others(10): Show |
27 | HG02129.hp2 HG02132.hp2 HG02622.hp2 others(24): Show |
intron_variant | MODIFIER | c.17+1445A>C | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | chr11 | 5598359 | |||||||
| chr11:5598573 | T | C | 3 | a0001c0005t0010g0054 a0001c0005t0010g0164 a0003c0014t0023g0165 |
4 | HG02622.hp2 NA18522.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.17+1659T>C | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | chr11 | 5598573 | |||||||
| chr11:5598581 | G | C | 2 | a0001c0008t0007g0038 a0001c0008t0019g0038 |
2 | HG00741.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.17+1667G>C | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | chr11 | 5598581 | |||||||
| chr11:5598612 | T | G | 2 | a0001c0003t0004g0056 a0001c0003t0004g0180 |
3 | HG00642.hp1 HG03041.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.17+1698T>G | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | chr11 | 5598612 | |||||||
| chr11:5598702 | G | T | 197 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0028 others(194): Show |
324 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(321): Show |
intron_variant | MODIFIER | c.17+1788G>T | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | chr11 | 5598702 | |||||||
| chr11:5598772 | A | G | 1 | a0001c0001t0004g0112 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.17+1858A>G | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | chr11 | 5598772 | |||||||
| chr11:5598779 | T | C | 10 | a0001c0001t0002g0172 a0001c0002t0002g0166 a0001c0002t0005g0003 others(7): Show |
23 | HG02129.hp2 HG02132.hp2 HG02738.hp2 others(20): Show |
intron_variant | MODIFIER | c.17+1865T>C | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | chr11 | 5598779 | |||||||
| chr11:5598918 | C | CT | 3 | a0001c0004t0002g0053 a0001c0004t0002g0162 a0001c0004t0002g0163 |
4 | HG03490.hp2 HG03491.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.17+2007dupT | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 5598918 | ||||||
| chr11:5599043 | C | T | 1 | a0001c0001t0009g0045 | 2 | NA18939.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.17+2129C>T | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | chr11 | 5599043 | |||||||
| chr11:5599055 | C | T | 14 | a0001c0001t0002g0111 a0001c0001t0002g0172 a0001c0002t0002g0166 others(11): Show |
28 | HG01346.hp2 HG02129.hp2 HG02132.hp2 others(25): Show |
intron_variant | MODIFIER | c.17+2141C>T | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | chr11 | 5599055 | |||||||
| chr11:5599239 | G | A | 1 | a0001c0003t0001g0181 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.17+2325G>A | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | chr11 | 5599239 | |||||||
| chr11:5599268 | G | A | 1 | a0001c0001t0009g0045 | 2 | NA18939.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.17+2354G>A | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | chr11 | 5599268 | |||||||
| chr11:5599373 | T | C | 292 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0028 others(289): Show |
476 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(473): Show |
intron_variant | MODIFIER | c.17+2459T>C | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | chr11 | 5599373 | |||||||
| chr11:5599383 | A | ATATT | 87 | a0001c0001t0001g0246 a0001c0001t0001g0247 a0001c0001t0001g0249 others(84): Show |
144 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.17+2503_17+2506dup others(4): Show |
TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 5599383 | ||||||
| chr11:5599383 | A | ATATTTAT others(1): Show |
32 | a0001c0001t0002g0111 a0001c0001t0003g0005 a0001c0001t0003g0014 others(29): Show |
51 | HG00621.hp1 HG00639.hp2 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.17+2499_17+2506dup others(8): Show |
TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 5599383 | ||||||
| chr11:5599383 | A | ATATTTAT others(5): Show |
17 | a0001c0001t0001g0022 a0001c0001t0001g0223 a0001c0001t0001g0224 others(14): Show |
26 | HG00642.hp2 HG00733.hp2 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.17+2495_17+2506dup others(12): Show |
TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 5599383 | ||||||
| chr11:5599383 | A | ATATTTAT others(9): Show |
28 | a0001c0001t0001g0013 a0001c0001t0001g0036 a0001c0001t0001g0062 others(25): Show |
54 | HG00408.hp1 HG00741.hp2 HG01069.hp1 others(51): Show |
intron_variant | MODIFIER | c.17+2491_17+2506dup others(16): Show |
TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 5599383 | ||||||
| chr11:5599383 | A | ATATTTAT others(13): Show |
5 | a0001c0001t0001g0204 a0001c0001t0001g0207 a0001c0001t0014g0203 others(2): Show |
5 | HG00738.hp2 HG01123.hp1 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.17+2487_17+2506dup others(20): Show |
TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 5599383 | ||||||
| chr11:5599383 | A | ATTTATTT others(3): Show |
1 | a0001c0001t0003g0261 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.17+2470_17+2471ins others(10): Show |
TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 5599383 | ||||||
| chr11:5599383 | ATATT | A | 85 | a0001c0001t0001g0028 a0001c0001t0002g0007 a0001c0001t0002g0017 others(82): Show |
140 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.17+2503_17+2506del others(4): Show |
TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 5599383 | ||||||
| chr11:5599383 | ATATTTAT others(1): Show |
A | 24 | a0001c0001t0001g0202 a0001c0001t0002g0172 a0001c0002t0005g0160 others(21): Show |
39 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(36): Show |
intron_variant | MODIFIER | c.17+2499_17+2506del others(8): Show |
TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 5599383 | ||||||
| chr11:5599383 | ATATTTAT others(5): Show |
A | 1 | a0001c0004t0005g0161 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.17+2495_17+2506del others(12): Show |
TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 5599383 | ||||||
| chr11:5599466 | C | T | 1 | a0001c0018t0004g0105 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.17+2552C>T | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | chr11 | 5599466 | |||||||
| chr11:5599467 | G | T | 21 | a0001c0001t0001g0246 a0001c0001t0001g0247 a0001c0001t0001g0249 others(18): Show |
25 | HG01070.hp2 HG01071.hp2 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.17+2553G>T | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | chr11 | 5599467 | |||||||
| chr11:5599505 | G | A | 138 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0036 others(135): Show |
228 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.17+2591G>A | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | chr11 | 5599505 | |||||||
| chr11:5599605 | G | A | 1 | a0001c0001t0004g0083 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.17+2691G>A | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | chr11 | 5599605 | |||||||
| chr11:5599694 | C | T | 1 | a0001c0001t0001g0260 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.17+2780C>T | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | chr11 | 5599694 | |||||||
| chr11:5599712 | A | AT | 138 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0036 others(135): Show |
228 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.17+2804dupT | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 5599712 | ||||||
| chr11:5599889 | G | C | 1 | a0001c0001t0002g0111 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.17+2975G>C | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | chr11 | 5599889 | |||||||
| chr11:5599897 | A | G | 1 | a0001c0001t0003g0259 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.17+2983A>G | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | chr11 | 5599897 | |||||||
| chr11:5599953 | C | T | 1 | a0001c0007t0002g0011 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.17+3039C>T | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | chr11 | 5599953 | |||||||
| chr11:5600008 | A | G | 1 | a0001c0002t0002g0158 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.17+3094A>G | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | chr11 | 5600008 | |||||||
| chr11:5600216 | C | T | 1 | a0001c0003t0001g0193 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.18-3030C>T | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | chr11 | 5600216 | |||||||
| chr11:5600217 | G | A | 2 | a0001c0002t0018g0046 a0001c0002t0029g0046 |
2 | HG02486.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.18-3029G>A | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | chr11 | 5600217 | |||||||
| chr11:5600233 | A | G | 244 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0028 others(241): Show |
405 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(402): Show |
intron_variant | MODIFIER | c.18-3013A>G | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | chr11 | 5600233 | |||||||
| chr11:5600380 | GAGCATCG others(9): Show |
G | 3 | a0003c0010t0002g0042 a0003c0010t0002g0043 a0003c0010t0002g0109 |
5 | HG02486.hp2 HG02886.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.18-2860_18-2845del others(16): Show |
TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 5600380 | ||||||
| chr11:5600505 | G | T | 37 | a0001c0001t0002g0017 a0001c0001t0002g0137 a0001c0001t0005g0017 others(34): Show |
62 | HG00558.hp2 HG00621.hp2 HG00673.hp1 others(59): Show |
intron_variant | MODIFIER | c.18-2741G>T | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | chr11 | 5600505 | |||||||
| chr11:5600525 | A | G | 285 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0028 others(282): Show |
467 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(464): Show |
intron_variant | MODIFIER | c.18-2721A>G | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | chr11 | 5600525 | |||||||
| chr11:5600644 | G | A | 1 | a0001c0002t0001g0072 | 2 | HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.18-2602G>A | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | chr11 | 5600644 | |||||||
| chr11:5600694 | C | CTA | 191 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0036 others(188): Show |
315 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(312): Show |
intron_variant | MODIFIER | c.18-2551_18-2550ins others(2): Show |
TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 5600694 | ||||||
| chr11:5600724 | T | G | 1 | a0002c0006t0003g0059 | 2 | NA18979.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.18-2522T>G | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | chr11 | 5600724 | |||||||
| chr11:5600821 | C | T | 2 | a0001c0002t0018g0046 a0001c0002t0029g0046 |
2 | HG02486.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.18-2425C>T | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | chr11 | 5600821 | |||||||
| chr11:5600949 | T | C | 1 | a0001c0001t0009g0085 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.18-2297T>C | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | chr11 | 5600949 | |||||||
| chr11:5600954 | A | C | 186 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0036 others(183): Show |
310 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(307): Show |
intron_variant | MODIFIER | c.18-2292A>C | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | chr11 | 5600954 | |||||||
| chr11:5600986 | C | T | 6 | a0001c0001t0001g0207 a0001c0001t0015g0066 a0001c0001t0015g0221 others(3): Show |
6 | HG00738.hp2 HG00741.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.18-2260C>T | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | chr11 | 5600986 | |||||||
| chr11:5601020 | A | G | 4 | a0001c0002t0035g0176 a0001c0002t0036g0174 a0001c0008t0013g0032 others(1): Show |
6 | HG01243.hp1 HG01243.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.18-2226A>G | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | chr11 | 5601020 | |||||||
| chr11:5601071 | C | T | 39 | a0001c0001t0002g0006 a0001c0001t0004g0006 a0001c0001t0004g0015 others(36): Show |
59 | HG00544.hp2 HG00609.hp2 HG00733.hp1 others(56): Show |
intron_variant | MODIFIER | c.18-2175C>T | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | chr11 | 5601071 | |||||||
| chr11:5601247 | T | C | 1 | a0001c0002t0002g0166 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.18-1999T>C | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | chr11 | 5601247 | |||||||
| chr11:5601404 | A | G | 4 | a0001c0005t0007g0023 a0001c0005t0007g0219 a0001c0005t0007g0228 others(1): Show |
7 | HG02615.hp2 HG02622.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.18-1842A>G | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | chr11 | 5601404 | |||||||
| chr11:5601434 | A | G | 146 | a0001c0001t0001g0028 a0001c0001t0001g0202 a0001c0001t0001g0246 others(143): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.18-1812A>G | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | chr11 | 5601434 | |||||||
| chr11:5601443 | A | G | 1 | a0001c0002t0001g0218 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.18-1803A>G | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | chr11 | 5601443 | |||||||
| chr11:5601487 | G | A | 1 | a0001c0005t0020g0086 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.18-1759G>A | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | chr11 | 5601487 | |||||||
| chr11:5601537 | C | T | 1 | a0001c0002t0001g0258 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.18-1709C>T | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | chr11 | 5601537 | |||||||
| chr11:5601560 | T | C | 193 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0036 others(190): Show |
319 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(316): Show |
intron_variant | MODIFIER | c.18-1686T>C | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | chr11 | 5601560 | |||||||
| chr11:5601626 | C | T | 1 | a0001c0002t0002g0135 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.18-1620C>T | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | chr11 | 5601626 | |||||||
| chr11:5601666 | G | A | 3 | a0001c0005t0010g0054 a0001c0005t0010g0164 a0003c0014t0023g0165 |
4 | HG02622.hp2 NA18522.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.18-1580G>A | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | chr11 | 5601666 | |||||||
| chr11:5601691 | G | C | 1 | a0001c0005t0001g0194 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.18-1555G>C | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | chr11 | 5601691 | |||||||
| chr11:5601865 | G | C | 3 | a0001c0001t0002g0137 a0001c0004t0002g0136 a0001c0004t0002g0138 |
3 | NA18959.hp2 NA18979.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.18-1381G>C | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | chr11 | 5601865 | |||||||
| chr11:5602032 | C | T | 1 | a0001c0002t0002g0134 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.18-1214C>T | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | chr11 | 5602032 | |||||||
| chr11:5602048 | T | C | 118 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0036 others(115): Show |
198 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(195): Show |
intron_variant | MODIFIER | c.18-1198T>C | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | chr11 | 5602048 | |||||||
| chr11:5602065 | T | C | 19 | a0001c0001t0002g0172 a0001c0002t0001g0055 a0001c0002t0002g0134 others(16): Show |
35 | HG00738.hp1 HG01256.hp1 HG01258.hp2 others(32): Show |
intron_variant | MODIFIER | c.18-1181T>C | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | chr11 | 5602065 | |||||||
| chr11:5602169 | A | G | 73 | a0001c0001t0001g0215 a0001c0001t0002g0006 a0001c0001t0002g0007 others(70): Show |
120 | HG00544.hp2 HG00609.hp2 HG00642.hp1 others(117): Show |
intron_variant | MODIFIER | c.18-1077A>G | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | chr11 | 5602169 | |||||||
| chr11:5602186 | G | A | 1 | a0001c0004t0002g0138 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.18-1060G>A | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | chr11 | 5602186 | |||||||
| chr11:5602207 | A | G | 181 | a0001c0001t0001g0028 a0001c0001t0001g0202 a0001c0001t0001g0215 others(178): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.18-1039A>G | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | chr11 | 5602207 | |||||||
| chr11:5602211 | C | T | 177 | a0001c0001t0001g0028 a0001c0001t0001g0202 a0001c0001t0001g0215 others(174): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.18-1035C>T | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | chr11 | 5602211 | |||||||
| chr11:5602215 | C | T | 92 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0036 others(89): Show |
154 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.18-1031C>T | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | chr11 | 5602215 | |||||||
| chr11:5602216 | G | A | 1 | a0001c0008t0001g0216 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.18-1030G>A | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | chr11 | 5602216 | |||||||
| chr11:5602222 | T | C | 272 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0028 others(269): Show |
441 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(438): Show |
intron_variant | MODIFIER | c.18-1024T>C | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | chr11 | 5602222 | |||||||
| chr11:5602234 | A | T | 1 | a0001c0001t0009g0085 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.18-1012A>T | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | chr11 | 5602234 | |||||||
| chr11:5602237 | G | A | 276 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0028 others(273): Show |
454 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(451): Show |
intron_variant | MODIFIER | c.18-1009G>A | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | chr11 | 5602237 | |||||||
| chr11:5602251 | T | C | 2 | a0001c0002t0035g0176 a0001c0008t0013g0032 |
4 | HG01243.hp1 HG01243.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.18-995T>C | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | chr11 | 5602251 | |||||||
| chr11:5602257 | A | G | 68 | a0001c0001t0001g0028 a0001c0001t0001g0249 a0001c0001t0001g0250 others(65): Show |
99 | HG00408.hp1 HG00738.hp1 HG00741.hp1 others(96): Show |
intron_variant | MODIFIER | c.18-989A>G | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | chr11 | 5602257 | |||||||
| chr11:5602266 | T | C | 14 | a0001c0002t0002g0024 a0001c0002t0002g0104 a0001c0002t0002g0115 others(11): Show |
18 | HG00280.hp1 HG00639.hp1 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.18-980T>C | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | chr11 | 5602266 | |||||||
| chr11:5602276 | TA | T | 63 | a0001c0001t0001g0202 a0001c0001t0003g0190 a0001c0001t0003g0238 others(60): Show |
108 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(105): Show |
intron_variant | MODIFIER | c.18-964delA | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 5602276 | ||||||
| chr11:5602302 | A | G | 1 | a0001c0004t0002g0140 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.18-944A>G | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | chr11 | 5602302 | |||||||
| chr11:5602309 | G | A | 1 | a0001c0001t0005g0141 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.18-937G>A | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | chr11 | 5602309 | |||||||
| chr11:5602323 | A | G | 1 | a0001c0001t0005g0121 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.18-923A>G | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | chr11 | 5602323 | |||||||
| chr11:5602357 | GGCTTGAA others(504): Show |
G | 1 | a0001c0002t0002g0115 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.18-879_18-369del | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 5602357 | ||||||
| chr11:5602370 | G | C | 3 | a0001c0008t0001g0216 a0001c0008t0007g0038 a0001c0008t0019g0038 |
3 | HG00741.hp1 HG01167.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.18-876G>C | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | chr11 | 5602370 | |||||||
| chr11:5602374 | C | T | 1 | a0001c0002t0001g0072 | 2 | HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.18-872C>T | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | chr11 | 5602374 | |||||||
| chr11:5602429 | C | A | 1 | a0002c0006t0003g0059 | 2 | NA18979.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.18-817C>A | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | chr11 | 5602429 | |||||||
| chr11:5602435 | C | T | 118 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0036 others(115): Show |
200 | HG00408.hp1 HG00558.hp2 HG00621.hp1 others(197): Show |
intron_variant | MODIFIER | c.18-811C>T | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | chr11 | 5602435 | |||||||
| chr11:5602460 | A | G | 50 | a0001c0001t0001g0036 a0001c0001t0001g0202 a0001c0001t0002g0006 others(47): Show |
83 | HG00544.hp2 HG00609.hp2 HG00733.hp1 others(80): Show |
intron_variant | MODIFIER | c.18-786A>G | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | chr11 | 5602460 | |||||||
| chr11:5602518 | G | C | 71 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0062 others(68): Show |
116 | HG00408.hp1 HG00621.hp1 HG00621.hp2 others(113): Show |
intron_variant | MODIFIER | c.18-728G>C | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | chr11 | 5602518 | |||||||
| chr11:5602585 | G | A | 1 | a0003c0014t0023g0165 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.18-661G>A | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | chr11 | 5602585 | |||||||
| chr11:5602684 | T | G | 1 | a0001c0002t0001g0257 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.18-562T>G | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | chr11 | 5602684 | |||||||
| chr11:5602741 | G | A | 1 | a0003c0014t0023g0165 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.18-505G>A | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | chr11 | 5602741 | |||||||
| chr11:5602753 | A | G | 1 | a0001c0008t0013g0032 | 3 | HG01243.hp2 HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.18-493A>G | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | chr11 | 5602753 | |||||||
| chr11:5602818 | G | C | 17 | a0001c0001t0002g0172 a0001c0002t0001g0055 a0001c0002t0002g0134 others(14): Show |
32 | HG00738.hp1 HG01243.hp1 HG01256.hp1 others(29): Show |
intron_variant | MODIFIER | c.18-428G>C | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | chr11 | 5602818 | |||||||
| chr11:5602911 | A | G | 35 | a0001c0002t0001g0071 a0001c0002t0001g0072 a0001c0002t0001g0075 others(32): Show |
48 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.18-335A>G | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | chr11 | 5602911 | |||||||
| chr11:5603037 | A | G | 11 | a0003c0009t0001g0229 a0003c0009t0001g0230 a0003c0009t0001g0231 others(8): Show |
12 | HG01109.hp2 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.18-209A>G | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 1/7 | chr11 | 5603037 | |||||||
| chr11:5603755 | T | A | 2 | a0005c0017t0016g0241 a0005c0017t0016g0242 |
2 | HG02572.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.507+20T>A | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 2/7 | chr11 | 5603755 | |||||||
| chr11:5603773 | G | A | 2 | a0001c0002t0006g0168 a0001c0002t0006g0171 |
2 | NA18985.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.507+38G>A | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 2/7 | chr11 | 5603773 | |||||||
| chr11:5604021 | C | T | 113 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0028 others(110): Show |
189 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(186): Show |
intron_variant | MODIFIER | c.507+286C>T | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 2/7 | chr11 | 5604021 | |||||||
| chr11:5604081 | C | T | 1 | a0001c0001t0002g0131 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.507+346C>T | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 2/7 | chr11 | 5604081 | |||||||
| chr11:5604100 | G | A | 146 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0028 others(143): Show |
240 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(237): Show |
intron_variant | MODIFIER | c.507+365G>A | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 2/7 | chr11 | 5604100 | |||||||
| chr11:5604162 | TTGTG | T | 5 | a0001c0001t0001g0207 a0001c0001t0015g0066 a0001c0001t0015g0221 others(2): Show |
5 | HG01934.hp2 HG03491.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.508-361_508-358del others(4): Show |
TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr11 | 5604162 | ||||||
| chr11:5604167 | TGTGTGTG others(3): Show |
T | 17 | a0001c0001t0002g0172 a0001c0002t0001g0055 a0001c0002t0002g0134 others(14): Show |
32 | HG00738.hp1 HG01243.hp1 HG01256.hp1 others(29): Show |
intron_variant | MODIFIER | c.508-357_508-348del others(10): Show |
TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr11 | 5604167 | ||||||
| chr11:5604177 | C | CGT | 4 | a0001c0001t0003g0065 a0001c0001t0003g0209 a0001c0001t0003g0211 others(1): Show |
4 | HG02647.hp1 HG02818.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.508-344_508-343dup others(2): Show |
TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr11 | 5604177 | ||||||
| chr11:5604260 | C | T | 5 | a0001c0008t0001g0216 a0001c0008t0007g0038 a0001c0008t0012g0030 others(2): Show |
9 | HG00741.hp1 HG01167.hp2 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.508-274C>T | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 2/7 | chr11 | 5604260 | |||||||
| chr11:5604334 | G | C | 1 | a0001c0002t0002g0117 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.508-200G>C | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 2/7 | chr11 | 5604334 | |||||||
| chr11:5604373 | A | G | 180 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0028 others(177): Show |
302 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(299): Show |
intron_variant | MODIFIER | c.508-161A>G | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 2/7 | chr11 | 5604373 | |||||||
| chr11:5604416 | C | T | 2 | a0001c0004t0002g0079 a0001c0004t0002g0151 |
2 | NA18945.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.508-118C>T | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 2/7 | chr11 | 5604416 | |||||||
| chr11:5604427 | A | T | 2 | a0001c0004t0001g0240 a0001c0004t0002g0150 |
2 | NA18952.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.508-107A>T | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 2/7 | chr11 | 5604427 | |||||||
| chr11:5604428 | C | T | 2 | a0001c0004t0001g0240 a0001c0004t0002g0150 |
2 | NA18952.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.508-106C>T | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 2/7 | chr11 | 5604428 | |||||||
| chr11:5604483 | C | A | 18 | a0001c0001t0001g0028 a0001c0001t0001g0246 a0001c0001t0001g0247 others(15): Show |
20 | HG01074.hp1 HG01106.hp1 HG01255.hp2 others(17): Show |
intron_variant | MODIFIER | c.508-51C>A | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 2/7 | chr11 | 5604483 | |||||||
| chr11:5604683 | A | C | 1 | a0001c0003t0001g0189 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.603+54A>C | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 3/7 | chr11 | 5604683 | |||||||
| chr11:5604758 | T | C | 37 | a0001c0002t0001g0071 a0001c0002t0001g0072 a0001c0002t0001g0075 others(34): Show |
50 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.603+129T>C | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 3/7 | chr11 | 5604758 | |||||||
| chr11:5604993 | G | C | 1 | a0001c0001t0009g0095 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.604-344G>C | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 3/7 | chr11 | 5604993 | |||||||
| chr11:5605011 | G | A | 217 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0028 others(214): Show |
354 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(351): Show |
intron_variant | MODIFIER | c.604-326G>A | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 3/7 | chr11 | 5605011 | |||||||
| chr11:5605084 | C | T | 63 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0036 others(60): Show |
115 | HG00408.hp1 HG00408.hp2 HG00621.hp2 others(112): Show |
intron_variant | MODIFIER | c.604-253C>T | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 3/7 | chr11 | 5605084 | |||||||
| chr11:5605134 | C | T | 11 | a0003c0009t0001g0229 a0003c0009t0001g0230 a0003c0009t0001g0231 others(8): Show |
12 | HG01109.hp2 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.604-203C>T | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 3/7 | chr11 | 5605134 | |||||||
| chr11:5605270 | C | T | 18 | a0001c0001t0002g0172 a0001c0001t0004g0101 a0001c0002t0001g0055 others(15): Show |
33 | HG00738.hp1 HG01243.hp1 HG01256.hp1 others(30): Show |
intron_variant | MODIFIER | c.604-67C>T | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 3/7 | chr11 | 5605270 | |||||||
| chr11:5605625 | C | T | 3 | a0003c0010t0002g0042 a0003c0010t0002g0043 a0003c0010t0002g0109 |
5 | HG02486.hp2 HG02886.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.834+58C>T | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 4/7 | chr11 | 5605625 | |||||||
| chr11:5605628 | C | T | 1 | a0001c0002t0004g0103 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.834+61C>T | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 4/7 | chr11 | 5605628 | |||||||
| chr11:5605669 | G | A | 135 | a0001c0001t0001g0202 a0001c0001t0002g0006 a0001c0001t0002g0007 others(132): Show |
217 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(214): Show |
intron_variant | MODIFIER | c.834+102G>A | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 4/7 | chr11 | 5605669 | |||||||
| chr11:5605824 | T | A | 234 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0028 others(231): Show |
376 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(373): Show |
intron_variant | MODIFIER | c.834+257T>A | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 4/7 | chr11 | 5605824 | |||||||
| chr11:5605835 | C | A | 1 | a0001c0007t0002g0114 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.834+268C>A | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 4/7 | chr11 | 5605835 | |||||||
| chr11:5605983 | A | G | 1 | a0001c0001t0001g0254 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.834+416A>G | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 4/7 | chr11 | 5605983 | |||||||
| chr11:5606126 | A | G | 1 | a0001c0001t0004g0091 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.834+559A>G | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 4/7 | chr11 | 5606126 | |||||||
| chr11:5606148 | C | G | 11 | a0003c0009t0001g0229 a0003c0009t0001g0230 a0003c0009t0001g0231 others(8): Show |
12 | HG01109.hp2 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.834+581C>G | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 4/7 | chr11 | 5606148 | |||||||
| chr11:5606177 | T | C | 39 | a0001c0002t0001g0071 a0001c0002t0001g0072 a0001c0002t0001g0073 others(36): Show |
53 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.834+610T>C | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 4/7 | chr11 | 5606177 | |||||||
| chr11:5606327 | T | G | 11 | a0003c0009t0001g0229 a0003c0009t0001g0230 a0003c0009t0001g0231 others(8): Show |
12 | HG01109.hp2 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.834+760T>G | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 4/7 | chr11 | 5606327 | |||||||
| chr11:5606444 | G | A | 76 | a0001c0001t0001g0202 a0001c0001t0002g0006 a0001c0001t0002g0007 others(73): Show |
129 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(126): Show |
intron_variant | MODIFIER | c.834+877G>A | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 4/7 | chr11 | 5606444 | |||||||
| chr11:5606766 | A | G | 11 | a0003c0009t0001g0229 a0003c0009t0001g0230 a0003c0009t0001g0231 others(8): Show |
12 | HG01109.hp2 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.834+1199A>G | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 4/7 | chr11 | 5606766 | |||||||
| chr11:5606842 | G | A | 89 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0028 others(86): Show |
143 | HG00408.hp1 HG00408.hp2 HG00621.hp2 others(140): Show |
intron_variant | MODIFIER | c.834+1275G>A | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 4/7 | chr11 | 5606842 | |||||||
| chr11:5606927 | A | G | 89 | a0001c0001t0001g0202 a0001c0001t0002g0006 a0001c0001t0002g0007 others(86): Show |
136 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.834+1360A>G | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 4/7 | chr11 | 5606927 | |||||||
| chr11:5606975 | A | G | 1 | a0001c0001t0032g0125 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.835-1397A>G | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 4/7 | chr11 | 5606975 | |||||||
| chr11:5607030 | C | T | 233 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0028 others(230): Show |
375 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(372): Show |
intron_variant | MODIFIER | c.835-1342C>T | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 4/7 | chr11 | 5607030 | |||||||
| chr11:5607064 | C | T | 292 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0028 others(289): Show |
476 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(473): Show |
intron_variant | MODIFIER | c.835-1308C>T | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 4/7 | chr11 | 5607064 | |||||||
| chr11:5607066 | T | C | 269 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0028 others(266): Show |
434 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(431): Show |
intron_variant | MODIFIER | c.835-1306T>C | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 4/7 | chr11 | 5607066 | |||||||
| chr11:5607072 | C | T | 179 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0028 others(176): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.835-1300C>T | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 4/7 | chr11 | 5607072 | |||||||
| chr11:5607121 | G | A | 1 | a0001c0001t0001g0062 | 2 | NA19075.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.835-1251G>A | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 4/7 | chr11 | 5607121 | |||||||
| chr11:5607158 | C | T | 1 | a0001c0020t0008g0187 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.835-1214C>T | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 4/7 | chr11 | 5607158 | |||||||
| chr11:5607169 | A | G | 1 | a0001c0008t0012g0030 | 3 | HG02895.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.835-1203A>G | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 4/7 | chr11 | 5607169 | |||||||
| chr11:5607170 | C | G | 1 | a0001c0004t0028g0120 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.835-1202C>G | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 4/7 | chr11 | 5607170 | |||||||
| chr11:5607203 | C | CA | 33 | a0001c0003t0001g0057 a0001c0004t0001g0179 a0001c0004t0001g0191 others(30): Show |
56 | HG00558.hp2 HG00673.hp2 HG00733.hp2 others(53): Show |
intron_variant | MODIFIER | c.835-1157dupA | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr11 | 5607203 | ||||||
| chr11:5607206 | A | C | 93 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0028 others(90): Show |
147 | HG00408.hp1 HG00408.hp2 HG00621.hp2 others(144): Show |
intron_variant | MODIFIER | c.835-1166A>C | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 4/7 | chr11 | 5607206 | |||||||
| chr11:5607208 | A | C | 68 | a0001c0001t0001g0202 a0001c0001t0002g0006 a0001c0001t0002g0007 others(65): Show |
118 | HG00423.hp1 HG00544.hp2 HG00609.hp2 others(115): Show |
intron_variant | MODIFIER | c.835-1164A>C | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 4/7 | chr11 | 5607208 | |||||||
| chr11:5607265 | T | G | 43 | a0001c0002t0001g0071 a0001c0002t0001g0072 a0001c0002t0001g0073 others(40): Show |
59 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.835-1107T>G | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 4/7 | chr11 | 5607265 | |||||||
| chr11:5607416 | T | G | 1 | a0001c0002t0002g0129 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.835-956T>G | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 4/7 | chr11 | 5607416 | |||||||
| chr11:5607433 | G | T | 1 | a0001c0005t0004g0090 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.835-939G>T | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 4/7 | chr11 | 5607433 | |||||||
| chr11:5607482 | G | A | 216 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0028 others(213): Show |
339 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(336): Show |
intron_variant | MODIFIER | c.835-890G>A | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 4/7 | chr11 | 5607482 | |||||||
| chr11:5607712 | T | A | 2 | a0005c0017t0016g0241 a0005c0017t0016g0242 |
2 | HG02572.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.835-660T>A | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 4/7 | chr11 | 5607712 | |||||||
| chr11:5607715 | G | C | 47 | a0001c0001t0001g0202 a0001c0001t0002g0006 a0001c0001t0002g0007 others(44): Show |
78 | HG00423.hp1 HG00544.hp2 HG00609.hp2 others(75): Show |
intron_variant | MODIFIER | c.835-657G>C | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 4/7 | chr11 | 5607715 | |||||||
| chr11:5607796 | G | A | 1 | a0001c0003t0001g0196 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.835-576G>A | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 4/7 | chr11 | 5607796 | |||||||
| chr11:5607820 | T | C | 186 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0028 others(183): Show |
287 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(284): Show |
intron_variant | MODIFIER | c.835-552T>C | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 4/7 | chr11 | 5607820 | |||||||
| chr11:5607860 | G | T | 1 | a0001c0001t0032g0125 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.835-512G>T | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 4/7 | chr11 | 5607860 | |||||||
| chr11:5607946 | A | G | 21 | a0001c0002t0001g0055 a0001c0002t0002g0134 a0001c0002t0002g0166 others(18): Show |
40 | HG00738.hp1 HG00741.hp1 HG01167.hp2 others(37): Show |
intron_variant | MODIFIER | c.835-426A>G | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 4/7 | chr11 | 5607946 | |||||||
| chr11:5607975 | G | A | 238 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0028 others(235): Show |
380 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(377): Show |
intron_variant | MODIFIER | c.835-397G>A | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 4/7 | chr11 | 5607975 | |||||||
| chr11:5608084 | A | C | 47 | a0001c0001t0001g0202 a0001c0001t0002g0006 a0001c0001t0002g0007 others(44): Show |
78 | HG00423.hp1 HG00544.hp2 HG00609.hp2 others(75): Show |
intron_variant | MODIFIER | c.835-288A>C | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 4/7 | chr11 | 5608084 | |||||||
| chr11:5608095 | A | G | 21 | a0001c0002t0001g0055 a0001c0002t0002g0134 a0001c0002t0002g0166 others(18): Show |
40 | HG00738.hp1 HG00741.hp1 HG01167.hp2 others(37): Show |
intron_variant | MODIFIER | c.835-277A>G | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 4/7 | chr11 | 5608095 | |||||||
| chr11:5608105 | G | A | 32 | a0001c0004t0001g0179 a0001c0004t0001g0191 a0001c0004t0001g0240 others(29): Show |
54 | HG00558.hp2 HG00673.hp2 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.835-267G>A | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 4/7 | chr11 | 5608105 | |||||||
| chr11:5608129 | C | A | 5 | a0001c0001t0003g0009 a0001c0001t0003g0068 a0001c0001t0003g0262 others(2): Show |
12 | HG01069.hp1 HG01071.hp1 HG01123.hp1 others(9): Show |
intron_variant | MODIFIER | c.835-243C>A | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 4/7 | chr11 | 5608129 | |||||||
| chr11:5608455 | G | A | 1 | a0001c0004t0001g0240 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.857+61G>A | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 5/7 | chr11 | 5608455 | |||||||
| chr11:5608517 | C | T | 13 | a0001c0001t0001g0028 a0001c0001t0001g0246 a0001c0001t0001g0247 others(10): Show |
14 | HG01074.hp1 HG01255.hp2 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.857+123C>T | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 5/7 | chr11 | 5608517 | |||||||
| chr11:5608574 | A | G | 1 | a0001c0002t0006g0167 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.857+180A>G | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 5/7 | chr11 | 5608574 | |||||||
| chr11:5608747 | C | T | 1 | a0002c0006t0003g0061 | 2 | HG00423.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.857+353C>T | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 5/7 | chr11 | 5608747 | |||||||
| chr11:5608847 | A | AT | 39 | a0001c0002t0001g0257 a0001c0002t0005g0160 a0001c0002t0018g0046 others(36): Show |
60 | HG00558.hp2 HG00673.hp2 HG00733.hp2 others(57): Show |
intron_variant | MODIFIER | c.857+474dupT | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr11 | 5608847 | ||||||
| chr11:5608847 | A | ATTTTT | 5 | a0001c0001t0001g0215 a0001c0001t0002g0116 a0001c0001t0003g0070 others(2): Show |
6 | HG01952.hp2 HG02155.hp2 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.857+470_857+474dup others(5): Show |
TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr11 | 5608847 | ||||||
| chr11:5608847 | A | ATTTTTT | 60 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0028 others(57): Show |
108 | HG00408.hp1 HG00408.hp2 HG00621.hp2 others(105): Show |
intron_variant | MODIFIER | c.857+469_857+474dup others(6): Show |
TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr11 | 5608847 | ||||||
| chr11:5608847 | A | ATTTTTTT | 37 | a0001c0001t0001g0036 a0001c0001t0001g0247 a0001c0001t0001g0251 others(34): Show |
53 | HG00741.hp2 HG01123.hp1 HG01243.hp2 others(50): Show |
intron_variant | MODIFIER | c.857+468_857+474dup others(7): Show |
TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr11 | 5608847 | ||||||
| chr11:5608847 | A | ATTTTTTT others(1): Show |
35 | a0001c0001t0001g0202 a0001c0001t0001g0252 a0001c0001t0001g0253 others(32): Show |
61 | HG00544.hp2 HG00609.hp2 HG00741.hp1 others(58): Show |
intron_variant | MODIFIER | c.857+467_857+474dup others(8): Show |
TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr11 | 5608847 | ||||||
| chr11:5608847 | A | ATTTTTTT others(2): Show |
16 | a0001c0001t0002g0007 a0001c0001t0004g0015 a0001c0001t0004g0100 others(13): Show |
28 | HG00733.hp1 HG00738.hp1 HG01123.hp2 others(25): Show |
intron_variant | MODIFIER | c.857+466_857+474dup others(9): Show |
TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr11 | 5608847 | ||||||
| chr11:5608847 | A | ATTTTTTT others(3): Show |
4 | a0001c0001t0002g0048 a0001c0001t0002g0133 a0001c0001t0004g0091 others(1): Show |
5 | HG01168.hp1 HG01243.hp1 HG04228.hp1 others(2): Show |
intron_variant | MODIFIER | c.857+465_857+474dup others(10): Show |
TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr11 | 5608847 | ||||||
| chr11:5608847 | A | ATTTTTTT others(7): Show |
1 | a0001c0005t0004g0173 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.857+461_857+474dup others(14): Show |
TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr11 | 5608847 | ||||||
| chr11:5608847 | AT | A | 9 | a0001c0001t0001g0204 a0001c0001t0001g0208 a0001c0002t0001g0237 others(6): Show |
13 | HG00639.hp1 HG01884.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.857+474delT | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr11 | 5608847 | ||||||
| chr11:5608958 | T | C | 40 | a0001c0002t0001g0071 a0001c0002t0001g0072 a0001c0002t0001g0073 others(37): Show |
54 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.857+564T>C | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 5/7 | chr11 | 5608958 | |||||||
| chr11:5609075 | C | G | 4 | a0001c0002t0002g0024 a0001c0002t0002g0025 a0001c0002t0002g0104 others(1): Show |
8 | HG00639.hp1 HG01884.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.857+681C>G | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 5/7 | chr11 | 5609075 | |||||||
| chr11:5609104 | G | A | 1 | a0001c0001t0004g0097 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.857+710G>A | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 5/7 | chr11 | 5609104 | |||||||
| chr11:5609159 | C | T | 156 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0028 others(153): Show |
260 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(257): Show |
intron_variant | MODIFIER | c.857+765C>T | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 5/7 | chr11 | 5609159 | |||||||
| chr11:5609182 | G | A | 214 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0028 others(211): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.857+788G>A | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 5/7 | chr11 | 5609182 | |||||||
| chr11:5609405 | T | C | 211 | a0001c0001t0001g0028 a0001c0001t0001g0036 a0001c0001t0001g0063 others(208): Show |
353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.858-740T>C | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 5/7 | chr11 | 5609405 | |||||||
| chr11:5609451 | G | C | 1 | a0002c0006t0022g0197 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.858-694G>C | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 5/7 | chr11 | 5609451 | |||||||
| chr11:5609635 | A | G | 12 | a0001c0002t0002g0166 a0001c0002t0005g0003 a0001c0002t0006g0003 others(9): Show |
26 | HG01256.hp1 HG01258.hp2 HG01516.hp1 others(23): Show |
intron_variant | MODIFIER | c.858-510A>G | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 5/7 | chr11 | 5609635 | |||||||
| chr11:5609649 | G | A | 29 | a0001c0001t0001g0028 a0001c0001t0001g0246 a0001c0001t0001g0247 others(26): Show |
31 | HG01074.hp1 HG01109.hp2 HG01255.hp2 others(28): Show |
intron_variant | MODIFIER | c.858-496G>A | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 5/7 | chr11 | 5609649 | |||||||
| chr11:5609650 | C | T | 1 | a0001c0004t0005g0161 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.858-495C>T | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 5/7 | chr11 | 5609650 | |||||||
| chr11:5609715 | G | T | 34 | a0001c0001t0001g0036 a0001c0001t0001g0064 a0001c0001t0001g0207 others(31): Show |
52 | HG00408.hp1 HG00408.hp2 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.858-430G>T | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 5/7 | chr11 | 5609715 | |||||||
| chr11:5609733 | T | C | 2 | a0001c0002t0002g0010 a0001c0002t0002g0129 |
7 | HG00735.hp2 HG01081.hp2 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.858-412T>C | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 5/7 | chr11 | 5609733 | |||||||
| chr11:5609787 | G | T | 2 | a0003c0009t0001g0230 a0003c0009t0001g0232 |
2 | HG01109.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.858-358G>T | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 5/7 | chr11 | 5609787 | |||||||
| chr11:5609796 | G | A | 1 | a0001c0005t0004g0173 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.858-349G>A | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 5/7 | chr11 | 5609796 | |||||||
| chr11:5609797 | C | T | 2 | a0003c0014t0023g0165 a0003c0014t0024g0233 |
2 | NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.858-348C>T | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 5/7 | chr11 | 5609797 | |||||||
| chr11:5609850 | G | C | 1 | a0001c0003t0001g0198 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.858-295G>C | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 5/7 | chr11 | 5609850 | |||||||
| chr11:5609909 | C | T | 40 | a0001c0001t0001g0063 a0001c0001t0001g0223 a0001c0001t0002g0137 others(37): Show |
67 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.858-236C>T | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 5/7 | chr11 | 5609909 | |||||||
| chr11:5609910 | G | T | 11 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0002t0001g0073 others(8): Show |
13 | HG00280.hp1 HG01106.hp1 HG01256.hp2 others(10): Show |
intron_variant | MODIFIER | c.858-235G>T | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 5/7 | chr11 | 5609910 | |||||||
| chr11:5609913 | A | C | 3 | a0001c0007t0001g0058 a0001c0007t0001g0183 a0001c0007t0002g0114 |
4 | HG00140.hp2 HG00639.hp2 HG01070.hp1 others(1): Show |
intron_variant | MODIFIER | c.858-232A>C | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 5/7 | chr11 | 5609913 | |||||||
| chr11:5609922 | C | CA | 17 | a0001c0001t0008g0210 a0001c0002t0002g0166 a0001c0002t0005g0003 others(14): Show |
33 | HG00438.hp1 HG01256.hp1 HG01258.hp2 others(30): Show |
intron_variant | MODIFIER | c.858-213dupA | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr11 | 5609922 | ||||||
| chr11:5609938 | A | G | 2 | a0005c0017t0016g0241 a0005c0017t0016g0242 |
2 | HG02572.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.858-207A>G | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 5/7 | chr11 | 5609938 | |||||||
| chr11:5610049 | T | C | 2 | a0005c0017t0016g0241 a0005c0017t0016g0242 |
2 | HG02572.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.858-96T>C | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 5/7 | chr11 | 5610049 | |||||||
| chr11:5610248 | A | C | 1 | a0001c0008t0012g0030 | 3 | HG02895.hp1 HG02896.hp1 HG02897.hp2 |
splice_region_variant&intron_variant | LOW | c.958+3A>C | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 6/7 | chr11 | 5610248 | |||||||
| chr11:5610249 | A | C | 65 | a0001c0001t0001g0207 a0001c0001t0001g0250 a0001c0001t0001g0252 others(62): Show |
91 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(88): Show |
splice_region_variant&intron_variant | LOW | c.958+4A>C | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 6/7 | chr11 | 5610249 | |||||||
| chr11:5610366 | G | T | 1 | a0001c0001t0001g0253 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.958+121G>T | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 6/7 | chr11 | 5610366 | |||||||
| chr11:5610390 | C | T | 4 | a0001c0005t0007g0023 a0001c0005t0007g0219 a0001c0005t0007g0228 others(1): Show |
7 | HG02615.hp2 HG02622.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.958+145C>T | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 6/7 | chr11 | 5610390 | |||||||
| chr11:5610391 | G | A | 1 | a0001c0001t0003g0264 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.959-144G>A | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 6/7 | chr11 | 5610391 | |||||||
| chr11:5610392 | G | T | 265 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0028 others(262): Show |
440 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(437): Show |
intron_variant | MODIFIER | c.959-143G>T | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 6/7 | chr11 | 5610392 | |||||||
| chr11:5610426 | A | C | 1 | a0001c0008t0001g0216 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.959-109A>C | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 6/7 | chr11 | 5610426 | |||||||
| chr11:5610459 | A | G | 3 | a0001c0008t0013g0032 a0003c0014t0023g0165 a0003c0014t0024g0233 |
5 | HG01243.hp2 HG02976.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.959-76A>G | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 6/7 | chr11 | 5610459 | |||||||
| chr11:5610629 | A | G | 1 | a0001c0002t0001g0072 | 2 | HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.985+68A>G | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 7/7 | chr11 | 5610629 | |||||||
| chr11:5610729 | G | A | 1 | a0001c0007t0001g0186 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.986-48G>A | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 7/7 | chr11 | 5610729 | |||||||
| chr11:5610742 | G | A | 29 | a0001c0001t0001g0063 a0001c0001t0001g0223 a0001c0001t0002g0137 others(26): Show |
50 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.986-35G>A | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 7/7 | chr11 | 5610742 | |||||||
| chr11:5610742 | G | C | 1 | a0001c0001t0002g0111 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.986-35G>C | TRIM6 | ENSG00000121236.21 | transcript | ENST00000380097.8 | protein_coding | 7/7 | chr11 | 5610742 |