Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 7706 |
| ensemblid | ENSG00000121060.19 |
| hgncid | 12932 |
| symbol | TRIM25 |
| name | tripartite motif containing 25 |
| refseq_nuc | NM_005082.5 |
| refseq_prot | NP_005073.2 |
| ensembl_nuc | ENST00000316881.9 |
| ensembl_prot | ENSP00000323889.4 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 56887909 |
| end | 56914049 |
| strand | - |
| ver | v1.2 |
| region | chr17:56887909-56914049 |
| region5000 | chr17:56882909-56919049 |
| regionname0 | TRIM25_chr17_56887909_56914049 |
| regionname5000 | TRIM25_chr17_56882909_56919049 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 630 | 263 | 68 | 45 | 101 | 13 | 36 | 68 | TRIM25_chr17_56882909_56919049 | TRIM25 | MAELC others(625): Show |
chr17 | 56882909 | 56919049 |
| a0002 | 1/1 | 630 | 96 | 10 | 27 | 44 | 2 | 11 | 39 | TRIM25_chr17_56882909_56919049 | TRIM25 | MAELC others(625): Show |
chr17 | 56882909 | 56919049 |
| a0003 | 0/0 | 630 | 12 | 12 | 0 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | MAELC others(625): Show |
chr17 | 56882909 | 56919049 |
| a0004 | 0/0 | 630 | 6 | 0 | 0 | 6 | 0 | 0 | 6 | TRIM25_chr17_56882909_56919049 | TRIM25 | MAELC others(625): Show |
chr17 | 56882909 | 56919049 |
| a0005 | 0/0 | 630 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | MAELC others(625): Show |
chr17 | 56882909 | 56919049 |
| a0006 | 0/0 | 630 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | MAELC others(625): Show |
chr17 | 56882909 | 56919049 |
| a0007 | 0/0 | 630 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | MAELC others(625): Show |
chr17 | 56882909 | 56919049 |
| a0008 | 0/0 | 73 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | MRRGQ others(68): Show |
chr17 | 56882909 | 56919049 |
| a0009 | 0/0 | 630 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | MAELC others(625): Show |
chr17 | 56882909 | 56919049 |
| a0010 | 0/0 | 630 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | MAELC others(625): Show |
chr17 | 56882909 | 56919049 |
| a0011 | 0/0 | 630 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | MAELC others(625): Show |
chr17 | 56882909 | 56919049 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1890 | 259 | 66 | 44 | 100 | 13 | 36 | TRIM25_chr17_56882909_56919049 | TRIM25 | ATGGC others(1885): Show |
chr17 | 56882909 | 56919049 | ||
| a0001c0008 | 0/0 | 1890 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | ATGGC others(1885): Show |
chr17 | 56882909 | 56919049 | ||
| a0001c0011 | 0/0 | 1890 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | ATGGC others(1885): Show |
chr17 | 56882909 | 56919049 | ||
| a0001c0012 | 0/0 | 1890 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | ATGGC others(1885): Show |
chr17 | 56882909 | 56919049 | ||
| a0001c0014 | 0/0 | 1890 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | ATGGC others(1885): Show |
chr17 | 56882909 | 56919049 | ||
| a0002c0002 | 1/1 | 1890 | 96 | 10 | 27 | 44 | 2 | 11 | TRIM25_chr17_56882909_56919049 | TRIM25 | ATGGC others(1885): Show |
chr17 | 56882909 | 56919049 | ||
| a0003c0003 | 0/0 | 1890 | 11 | 11 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | ATGGC others(1885): Show |
chr17 | 56882909 | 56919049 | ||
| a0003c0007 | 0/0 | 1890 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | ATGGC others(1885): Show |
chr17 | 56882909 | 56919049 | ||
| a0004c0004 | 0/0 | 1890 | 6 | 0 | 0 | 6 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | ATGGC others(1885): Show |
chr17 | 56882909 | 56919049 | ||
| a0005c0013 | 0/0 | 1890 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | ATGGC others(1885): Show |
chr17 | 56882909 | 56919049 | ||
| a0006c0006 | 0/0 | 1890 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | ATGGC others(1885): Show |
chr17 | 56882909 | 56919049 | ||
| a0007c0010 | 0/0 | 1890 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | ATGGC others(1885): Show |
chr17 | 56882909 | 56919049 | ||
| a0008c0005 | 0/0 | 1890 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | AGGGC others(1885): Show |
chr17 | 56882909 | 56919049 | ||
| a0009c0016 | 0/0 | 1890 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | ATGGC others(1885): Show |
chr17 | 56882909 | 56919049 | ||
| a0010c0015 | 0/0 | 1890 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | ATGGC others(1885): Show |
chr17 | 56882909 | 56919049 | ||
| a0011c0009 | 0/0 | 1890 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | ATGGC others(1885): Show |
chr17 | 56882909 | 56919049 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5745 | 146 | 16 | 18 | 84 | 3 | 25 | TRIM25_chr17_56882909_56919049 | TRIM25 | CGTTT others(5740): Show |
chr17 | 56882909 | 56919049 |
| a0001c0001t0002 | 0/0 | 5744 | 43 | 19 | 13 | 3 | 3 | 5 | TRIM25_chr17_56882909_56919049 | TRIM25 | CGTTT others(5739): Show |
chr17 | 56882909 | 56919049 |
| a0001c0001t0003 | 0/0 | 5744 | 23 | 5 | 11 | 3 | 4 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | CGTTT others(5739): Show |
chr17 | 56882909 | 56919049 |
| a0001c0001t0004 | 0/0 | 5745 | 10 | 6 | 1 | 1 | 0 | 2 | TRIM25_chr17_56882909_56919049 | TRIM25 | CGTTT others(5740): Show |
chr17 | 56882909 | 56919049 |
| a0001c0001t0005 | 0/0 | 5745 | 8 | 8 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | CGTTT others(5740): Show |
chr17 | 56882909 | 56919049 |
| a0001c0001t0006 | 0/0 | 5744 | 3 | 2 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | CGTTT others(5739): Show |
chr17 | 56882909 | 56919049 |
| a0001c0001t0008 | 0/0 | 5745 | 4 | 1 | 0 | 0 | 3 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | CGTTT others(5740): Show |
chr17 | 56882909 | 56919049 |
| a0001c0001t0009 | 0/0 | 5745 | 4 | 0 | 0 | 4 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | CGTTT others(5740): Show |
chr17 | 56882909 | 56919049 |
| a0001c0001t0011 | 0/0 | 5744 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | CGTTT others(5739): Show |
chr17 | 56882909 | 56919049 |
| a0001c0001t0012 | 0/0 | 5745 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | CGTTT others(5740): Show |
chr17 | 56882909 | 56919049 |
| a0001c0001t0015 | 0/0 | 5745 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | CGTTT others(5740): Show |
chr17 | 56882909 | 56919049 |
| a0001c0001t0023 | 0/0 | 5744 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | CGTTT others(5739): Show |
chr17 | 56882909 | 56919049 |
| a0001c0001t0024 | 0/0 | 5744 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | CGTTT others(5739): Show |
chr17 | 56882909 | 56919049 |
| a0001c0001t0026 | 0/0 | 5745 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | CGTTT others(5740): Show |
chr17 | 56882909 | 56919049 |
| a0001c0001t0027 | 0/0 | 5745 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | CGTTT others(5740): Show |
chr17 | 56882909 | 56919049 |
| a0001c0001t0029 | 0/0 | 5744 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | CGTTT others(5739): Show |
chr17 | 56882909 | 56919049 |
| a0001c0001t0030 | 0/0 | 5744 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | CGTTT others(5739): Show |
chr17 | 56882909 | 56919049 |
| a0001c0001t0032 | 0/0 | 5744 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | CGTTT others(5739): Show |
chr17 | 56882909 | 56919049 |
| a0001c0001t0034 | 0/0 | 5745 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | CGTTT others(5740): Show |
chr17 | 56882909 | 56919049 |
| a0001c0001t0035 | 0/0 | 5745 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | CGTTT others(5740): Show |
chr17 | 56882909 | 56919049 |
| a0001c0001t0037 | 0/0 | 5745 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | CGTTT others(5740): Show |
chr17 | 56882909 | 56919049 |
| a0001c0001t0038 | 0/0 | 5745 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | CGTTT others(5740): Show |
chr17 | 56882909 | 56919049 |
| a0001c0001t0039 | 0/0 | 5744 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | CGTTT others(5739): Show |
chr17 | 56882909 | 56919049 |
| a0001c0001t0041 | 0/0 | 5745 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | CGTTT others(5740): Show |
chr17 | 56882909 | 56919049 |
| a0001c0008t0006 | 0/0 | 5744 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | CGTTT others(5739): Show |
chr17 | 56882909 | 56919049 |
| a0001c0011t0003 | 0/0 | 5744 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | CGTTT others(5739): Show |
chr17 | 56882909 | 56919049 |
| a0001c0012t0013 | 0/0 | 5748 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | CGTTT others(5743): Show |
chr17 | 56882909 | 56919049 |
| a0001c0014t0025 | 0/0 | 5745 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | CGTTT others(5740): Show |
chr17 | 56882909 | 56919049 |
| a0002c0002t0001 | 1/0 | 5745 | 34 | 2 | 4 | 23 | 0 | 4 | TRIM25_chr17_56882909_56919049 | TRIM25 | CGTTT others(5740): Show |
chr17 | 56882909 | 56919049 |
| a0002c0002t0002 | 0/0 | 5744 | 29 | 4 | 4 | 18 | 1 | 2 | TRIM25_chr17_56882909_56919049 | TRIM25 | CGTTT others(5739): Show |
chr17 | 56882909 | 56919049 |
| a0002c0002t0003 | 0/1 | 5744 | 18 | 1 | 12 | 0 | 0 | 4 | TRIM25_chr17_56882909_56919049 | TRIM25 | CGTTT others(5739): Show |
chr17 | 56882909 | 56919049 |
| a0002c0002t0004 | 0/0 | 5745 | 3 | 0 | 3 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | CGTTT others(5740): Show |
chr17 | 56882909 | 56919049 |
| a0002c0002t0006 | 0/0 | 5744 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | CGTTT others(5739): Show |
chr17 | 56882909 | 56919049 |
| a0002c0002t0011 | 0/0 | 5744 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | CGTTT others(5739): Show |
chr17 | 56882909 | 56919049 |
| a0002c0002t0012 | 0/0 | 5745 | 2 | 0 | 1 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | CGTTT others(5740): Show |
chr17 | 56882909 | 56919049 |
| a0002c0002t0014 | 0/0 | 5744 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | CGTTT others(5739): Show |
chr17 | 56882909 | 56919049 |
| a0002c0002t0022 | 0/0 | 5744 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | CGTTT others(5739): Show |
chr17 | 56882909 | 56919049 |
| a0002c0002t0028 | 0/0 | 5744 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | CGTTT others(5739): Show |
chr17 | 56882909 | 56919049 |
| a0002c0002t0031 | 0/0 | 5744 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | CGTTT others(5739): Show |
chr17 | 56882909 | 56919049 |
| a0002c0002t0033 | 0/0 | 5745 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | CGTTT others(5740): Show |
chr17 | 56882909 | 56919049 |
| a0002c0002t0036 | 0/0 | 5745 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | CGTTT others(5740): Show |
chr17 | 56882909 | 56919049 |
| a0002c0002t0040 | 0/0 | 5744 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | CGTTT others(5739): Show |
chr17 | 56882909 | 56919049 |
| a0003c0003t0007 | 0/0 | 5744 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | CGTTT others(5739): Show |
chr17 | 56882909 | 56919049 |
| a0003c0003t0010 | 0/0 | 5744 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | CGTTT others(5739): Show |
chr17 | 56882909 | 56919049 |
| a0003c0003t0017 | 0/0 | 5745 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | CGTTT others(5740): Show |
chr17 | 56882909 | 56919049 |
| a0003c0003t0018 | 0/0 | 5744 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | CGTTT others(5739): Show |
chr17 | 56882909 | 56919049 |
| a0003c0003t0019 | 0/0 | 5744 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | CGTTT others(5739): Show |
chr17 | 56882909 | 56919049 |
| a0003c0003t0020 | 0/0 | 5745 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | CGTTT others(5740): Show |
chr17 | 56882909 | 56919049 |
| a0003c0003t0021 | 0/0 | 5744 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | CGTTT others(5739): Show |
chr17 | 56882909 | 56919049 |
| a0003c0007t0016 | 0/0 | 5749 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | CGTTT others(5744): Show |
chr17 | 56882909 | 56919049 |
| a0004c0004t0001 | 0/0 | 5745 | 6 | 0 | 0 | 6 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | CGTTT others(5740): Show |
chr17 | 56882909 | 56919049 |
| a0005c0013t0003 | 0/0 | 5744 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | CGTTT others(5739): Show |
chr17 | 56882909 | 56919049 |
| a0006c0006t0007 | 0/0 | 5744 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | CGTTT others(5739): Show |
chr17 | 56882909 | 56919049 |
| a0007c0010t0013 | 0/0 | 5748 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | CGTTT others(5743): Show |
chr17 | 56882909 | 56919049 |
| a0008c0005t0001 | 0/0 | 5745 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | CGTTT others(5740): Show |
chr17 | 56882909 | 56919049 |
| a0009c0016t0001 | 0/0 | 5745 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | CGTTT others(5740): Show |
chr17 | 56882909 | 56919049 |
| a0010c0015t0002 | 0/0 | 5744 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | CGTTT others(5739): Show |
chr17 | 56882909 | 56919049 |
| a0011c0009t0001 | 0/0 | 5745 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | CGTTT others(5740): Show |
chr17 | 56882909 | 56919049 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 36 | 2 | 4 | 19 | 1 | 10 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0001g0006 | 0/0 | 12 | 1 | 2 | 6 | 0 | 3 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0001g0007 | 0/0 | 7 | 0 | 1 | 6 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0001g0010 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0002g0003 | 0/0 | 13 | 2 | 7 | 1 | 0 | 3 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0002g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0002g0019 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0002g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0002g0030 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0003g0009 | 0/0 | 5 | 0 | 4 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0003g0026 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0003g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0003g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0003g0042 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0003g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0003g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0003g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0003g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0003g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0003g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0004g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0004g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0004g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0004g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0004g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0004g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0004g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0004g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0004g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0005g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0005g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0005g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0005g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0005g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0005g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0005g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0006g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0006g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0006g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0008g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0008g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0008g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0008g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0009g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0011g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0011g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0012g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0015g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0023g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0024g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0026g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0027g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0029g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0030g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0032g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0034g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0035g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0037g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0038g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0039g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0001t0041g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0008t0006g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0011t0003g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0012t0013g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0001c0014t0025g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0002c0002t0001g0004 | 0/0 | 13 | 0 | 0 | 11 | 0 | 2 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0002c0002t0001g0008 | 0/0 | 5 | 1 | 3 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0002c0002t0001g0011 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0002c0002t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0002c0002t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0002c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0002c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0002c0002t0001g0168 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0002c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0002c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0002c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0002c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0002c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0002c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0002c0002t0002g0005 | 0/0 | 12 | 1 | 3 | 8 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0002c0002t0002g0012 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0002c0002t0002g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0002c0002t0002g0044 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0002c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0002c0002t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0002c0002t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0002c0002t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0002c0002t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0002c0002t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0002c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0002c0002t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0002c0002t0003g0002 | 0/1 | 15 | 1 | 12 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0002c0002t0003g0023 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0002c0002t0003g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0002c0002t0004g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0002c0002t0004g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0002c0002t0006g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0002c0002t0011g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0002c0002t0012g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0002c0002t0012g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0002c0002t0014g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0002c0002t0022g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0002c0002t0028g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0002c0002t0031g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0002c0002t0033g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0002c0002t0036g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0002c0002t0040g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0003c0003t0007g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0003c0003t0007g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0003c0003t0010g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0003c0003t0017g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0003c0003t0018g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0003c0003t0019g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0003c0003t0020g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0003c0003t0021g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0003c0007t0016g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0004c0004t0001g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0004c0004t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0004c0004t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0005c0013t0003g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0006c0006t0007g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0007c0010t0013g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0008c0005t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0009c0016t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0010c0015t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| a0011c0009t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0157 | EUR | GBR | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG00099 | hp2 | a0002 | c0002 | t0028 | g0182 | EUR | GBR | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0156 | EUR | GBR | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG00140 | hp2 | a0005 | c0013 | t0003 | g0129 | EUR | GBR | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0037 | EUR | FIN | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0028 | EUR | FIN | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | CHS | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | CHS | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG00438 | hp2 | a0001 | c0001 | t0034 | g0128 | EAS | CHS | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG00558 | hp1 | a0001 | c0001 | t0009 | g0013 | EAS | CHS | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | CHS | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | CHS | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | CHS | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG00639 | hp1 | a0002 | c0002 | t0004 | g0067 | AMR | PUR | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG00639 | hp2 | a0002 | c0002 | t0004 | g0043 | AMR | PUR | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0193 | AMR | PUR | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG00673 | hp2 | a0001 | c0001 | t0015 | g0033 | EAS | CHS | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG00735 | hp2 | a0002 | c0002 | t0003 | g0002 | AMR | PUR | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0009 | AMR | PUR | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG01069 | hp1 | a0002 | c0002 | t0006 | g0066 | AMR | PUR | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG01070 | hp1 | a0002 | c0002 | t0001 | g0062 | AMR | PUR | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0019 | AMR | PUR | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0019 | AMR | PUR | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0192 | AMR | PUR | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0075 | AMR | PUR | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0095 | AMR | PUR | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0092 | AMR | PUR | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG01168 | hp1 | a0002 | c0002 | t0003 | g0002 | AMR | PUR | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG01169 | hp1 | a0002 | c0002 | t0003 | g0002 | AMR | PUR | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG01175 | hp1 | a0002 | c0002 | t0002 | g0005 | AMR | PUR | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0009 | AMR | PUR | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG01192 | hp1 | a0002 | c0002 | t0001 | g0008 | AMR | PUR | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG01192 | hp2 | a0002 | c0002 | t0004 | g0043 | AMR | PUR | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0030 | AMR | PUR | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG01255 | hp1 | a0002 | c0002 | t0003 | g0002 | AMR | CLM | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | CLM | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG01256 | hp1 | a0001 | c0011 | t0003 | g0191 | AMR | CLM | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG01256 | hp2 | a0002 | c0002 | t0003 | g0002 | AMR | CLM | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG01257 | hp1 | a0002 | c0002 | t0002 | g0005 | AMR | CLM | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG01257 | hp2 | a0002 | c0002 | t0014 | g0025 | AMR | CLM | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG01258 | hp1 | a0002 | c0002 | t0002 | g0005 | AMR | CLM | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG01258 | hp2 | a0002 | c0002 | t0003 | g0002 | AMR | CLM | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | CLM | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG01346 | hp1 | a0001 | c0001 | t0003 | g0032 | AMR | CLM | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG01358 | hp1 | a0001 | c0001 | t0004 | g0145 | AMR | CLM | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG01358 | hp2 | a0002 | c0002 | t0012 | g0064 | AMR | CLM | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG01361 | hp1 | a0001 | c0001 | t0003 | g0160 | AMR | CLM | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG01361 | hp2 | a0002 | c0002 | t0003 | g0002 | AMR | CLM | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0032 | AMR | CLM | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG01496 | hp1 | a0001 | c0001 | t0029 | g0161 | AMR | CLM | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG01496 | hp2 | a0002 | c0002 | t0014 | g0025 | AMR | CLM | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG01515 | hp1 | a0001 | c0001 | t0003 | g0042 | EUR | IBS | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG01515 | hp2 | a0001 | c0001 | t0008 | g0211 | EUR | IBS | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG01516 | hp1 | a0001 | c0001 | t0003 | g0026 | EUR | IBS | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG01516 | hp2 | a0001 | c0001 | t0008 | g0127 | EUR | IBS | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG01517 | hp1 | a0001 | c0001 | t0003 | g0042 | EUR | IBS | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG01517 | hp2 | a0001 | c0001 | t0008 | g0120 | EUR | IBS | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG01884 | hp1 | a0001 | c0001 | t0005 | g0163 | AFR | ACB | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG01884 | hp2 | a0001 | c0001 | t0004 | g0119 | AFR | ACB | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0151 | AFR | ACB | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG01891 | hp2 | a0001 | c0001 | t0024 | g0085 | AFR | ACB | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG01934 | hp1 | a0002 | c0002 | t0001 | g0008 | AMR | PEL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG01934 | hp2 | a0002 | c0002 | t0002 | g0044 | AMR | PEL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG01943 | hp1 | a0002 | c0002 | t0003 | g0002 | AMR | PEL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0164 | AMR | PEL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG01975 | hp2 | a0002 | c0002 | t0003 | g0002 | AMR | PEL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG01978 | hp2 | a0002 | c0002 | t0003 | g0002 | AMR | PEL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG01993 | hp1 | a0002 | c0002 | t0003 | g0002 | AMR | PEL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG01993 | hp2 | a0001 | c0001 | t0003 | g0009 | AMR | PEL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG02004 | hp1 | a0002 | c0002 | t0001 | g0008 | AMR | PEL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PEL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG02040 | hp2 | a0002 | c0002 | t0036 | g0169 | EAS | KHV | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0106 | AFR | ACB | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG02055 | hp2 | a0002 | c0002 | t0002 | g0005 | AFR | ACB | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG02056 | hp2 | a0002 | c0002 | t0012 | g0167 | EAS | KHV | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG02071 | hp1 | a0001 | c0001 | t0038 | g0185 | EAS | KHV | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | KHV | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | KHV | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG02135 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | KHV | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0208 | AFR | ACB | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PEL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG02148 | hp2 | a0001 | c0001 | t0003 | g0009 | AMR | PEL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG02155 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | CDX | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG02165 | hp1 | a0001 | c0001 | t0015 | g0033 | EAS | CDX | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CDX | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG02257 | hp1 | a0003 | c0007 | t0016 | g0049 | AFR | ACB | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG02257 | hp2 | a0002 | c0002 | t0002 | g0040 | AFR | ACB | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | ACB | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | ACB | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG02273 | hp1 | a0002 | c0002 | t0003 | g0002 | AMR | PEL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PEL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG02280 | hp2 | a0001 | c0001 | t0006 | g0076 | AFR | ACB | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG02300 | hp1 | a0001 | c0001 | t0003 | g0188 | AMR | PEL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0047 | AFR | ACB | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG02451 | hp2 | a0003 | c0003 | t0007 | g0022 | AFR | ACB | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | KHV | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | KHV | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG02572 | hp1 | a0002 | c0002 | t0002 | g0040 | AFR | GWD | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0078 | AFR | GWD | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0030 | AFR | GWD | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0098 | AFR | GWD | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG02622 | hp2 | a0002 | c0002 | t0031 | g0140 | AFR | GWD | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0047 | AFR | GWD | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG02630 | hp2 | a0001 | c0001 | t0005 | g0046 | AFR | GWD | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0029 | AFR | GWD | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG02647 | hp2 | a0003 | c0003 | t0020 | g0054 | AFR | GWD | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0213 | SAS | PJL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG02683 | hp2 | a0001 | c0001 | t0004 | g0126 | SAS | PJL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG02698 | hp1 | a0002 | c0002 | t0003 | g0002 | SAS | PJL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG02717 | hp1 | a0001 | c0001 | t0004 | g0060 | AFR | GWD | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG02723 | hp1 | a0001 | c0001 | t0012 | g0099 | AFR | GWD | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | GWD | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | PJL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG02735 | hp2 | a0002 | c0002 | t0001 | g0172 | SAS | PJL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG02809 | hp1 | a0001 | c0001 | t0005 | g0097 | AFR | GWD | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG02809 | hp2 | a0002 | c0002 | t0001 | g0063 | AFR | GWD | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG02818 | hp1 | a0001 | c0001 | t0004 | g0061 | AFR | GWD | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0029 | AFR | GWD | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG02886 | hp1 | a0001 | c0001 | t0011 | g0084 | AFR | GWD | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG02886 | hp2 | a0001 | c0001 | t0006 | g0109 | AFR | GWD | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG02895 | hp1 | a0003 | c0003 | t0010 | g0015 | AFR | GWD | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0150 | AFR | GWD | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG02896 | hp1 | a0003 | c0003 | t0021 | g0055 | AFR | GWD | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | GWD | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG02922 | hp1 | a0003 | c0003 | t0007 | g0022 | AFR | ESN | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG02922 | hp2 | a0003 | c0003 | t0017 | g0052 | AFR | ESN | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0118 | AFR | ESN | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | ESN | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | ESN | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG02970 | hp2 | a0001 | c0001 | t0004 | g0149 | AFR | ESN | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | ESN | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG02976 | hp2 | a0001 | c0001 | t0037 | g0088 | AFR | ESN | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG03017 | hp1 | a0001 | c0001 | t0004 | g0086 | SAS | PJL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0048 | AFR | GWD | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG03098 | hp1 | a0003 | c0003 | t0010 | g0015 | AFR | MSL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | MSL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG03130 | hp1 | a0003 | c0003 | t0019 | g0051 | AFR | ESN | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG03130 | hp2 | a0001 | c0001 | t0005 | g0207 | AFR | ESN | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG03139 | hp1 | a0006 | c0006 | t0007 | g0056 | AFR | ESN | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | ESN | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG03195 | hp1 | a0002 | c0002 | t0022 | g0091 | AFR | ESN | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG03195 | hp2 | a0001 | c0001 | t0005 | g0214 | AFR | ESN | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG03209 | hp1 | a0001 | c0001 | t0027 | g0108 | AFR | MSL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG03209 | hp2 | a0001 | c0001 | t0005 | g0102 | AFR | MSL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG03225 | hp1 | a0007 | c0010 | t0013 | g0107 | AFR | MSL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0048 | AFR | MSL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG03239 | hp1 | a0002 | c0002 | t0033 | g0165 | SAS | PJL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG03453 | hp1 | a0001 | c0001 | t0008 | g0083 | AFR | MSL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG03453 | hp2 | a0001 | c0001 | t0005 | g0110 | AFR | MSL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0100 | AFR | MSL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG03486 | hp2 | a0001 | c0001 | t0004 | g0024 | AFR | MSL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG03490 | hp1 | a0002 | c0002 | t0001 | g0004 | SAS | PJL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG03491 | hp2 | a0002 | c0002 | t0003 | g0023 | SAS | PJL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG03492 | hp1 | a0002 | c0002 | t0003 | g0023 | SAS | PJL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG03492 | hp2 | a0002 | c0002 | t0001 | g0004 | SAS | PJL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0077 | AFR | ESN | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | ESN | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0071 | AFR | GWD | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG03654 | hp1 | a0001 | c0001 | t0039 | g0199 | SAS | PJL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | STU | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG03704 | hp2 | a0001 | c0001 | t0035 | g0200 | SAS | PJL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0136 | SAS | PJL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG03831 | hp1 | a0001 | c0001 | t0032 | g0158 | SAS | BEB | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG03834 | hp1 | a0008 | c0005 | t0001 | g0057 | SAS | BEB | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0148 | SAS | BEB | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG03927 | hp1 | a0002 | c0002 | t0003 | g0170 | SAS | BEB | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG03942 | hp2 | a0001 | c0001 | t0041 | g0101 | SAS | BEB | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | STU | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG04115 | hp2 | a0002 | c0002 | t0001 | g0181 | SAS | STU | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0074 | SAS | BEB | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | STU | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | STU | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | STU | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG04228 | hp2 | a0002 | c0002 | t0002 | g0173 | SAS | STU | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA18522 | hp1 | a0001 | c0001 | t0005 | g0046 | AFR | YRI | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA18522 | hp2 | a0002 | c0002 | t0011 | g0154 | AFR | YRI | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA18612 | hp2 | a0002 | c0002 | t0001 | g0171 | EAS | CHB | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | CHB | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | CHB | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA18906 | hp1 | a0003 | c0003 | t0018 | g0050 | AFR | YRI | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | YRI | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA18940 | hp1 | a0002 | c0002 | t0001 | g0176 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA18943 | hp1 | a0002 | c0002 | t0002 | g0203 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA18944 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA18944 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA18946 | hp1 | a0001 | c0001 | t0006 | g0133 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA18946 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA18948 | hp1 | a0009 | c0016 | t0001 | g0216 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA18948 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA18951 | hp1 | a0004 | c0004 | t0001 | g0183 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA18951 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA18952 | hp1 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA18962 | hp1 | a0002 | c0002 | t0002 | g0174 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA18963 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA18964 | hp2 | a0002 | c0002 | t0040 | g0179 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA18965 | hp1 | a0002 | c0002 | t0002 | g0175 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA18965 | hp2 | a0002 | c0002 | t0002 | g0012 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA18966 | hp2 | a0002 | c0002 | t0002 | g0141 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA18967 | hp2 | a0002 | c0002 | t0002 | g0012 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA18968 | hp1 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA18970 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA18970 | hp2 | a0002 | c0002 | t0002 | g0012 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA18971 | hp2 | a0001 | c0001 | t0009 | g0013 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA18972 | hp1 | a0004 | c0004 | t0001 | g0187 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA18980 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA18982 | hp1 | a0004 | c0004 | t0001 | g0014 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA18983 | hp2 | a0001 | c0001 | t0003 | g0034 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA18984 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA18990 | hp1 | a0002 | c0002 | t0001 | g0177 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA18990 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA18992 | hp2 | a0002 | c0002 | t0001 | g0178 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA18995 | hp1 | a0002 | c0002 | t0002 | g0012 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA18999 | hp1 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0034 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA19000 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA19003 | hp1 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA19004 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA19005 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA19006 | hp1 | a0002 | c0002 | t0002 | g0012 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA19006 | hp2 | a0001 | c0001 | t0009 | g0013 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA19009 | hp1 | a0001 | c0001 | t0009 | g0013 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA19009 | hp2 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA19030 | hp1 | a0003 | c0003 | t0010 | g0015 | AFR | LWK | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | LWK | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA19043 | hp1 | a0003 | c0003 | t0007 | g0053 | AFR | LWK | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA19043 | hp2 | a0010 | c0015 | t0002 | g0215 | AFR | LWK | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA19056 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA19057 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA19058 | hp1 | a0004 | c0004 | t0001 | g0014 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA19058 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA19062 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA19062 | hp2 | a0002 | c0002 | t0001 | g0166 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA19065 | hp1 | a0001 | c0014 | t0025 | g0087 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA19068 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA19075 | hp2 | a0002 | c0002 | t0002 | g0180 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA19077 | hp1 | a0001 | c0001 | t0004 | g0131 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA19077 | hp2 | a0002 | c0002 | t0001 | g0068 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA19085 | hp1 | a0004 | c0004 | t0001 | g0014 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA19088 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA19091 | hp2 | a0004 | c0004 | t0001 | g0014 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | YRI | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA19240 | hp2 | a0001 | c0012 | t0013 | g0089 | AFR | YRI | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA20129 | hp1 | a0002 | c0002 | t0003 | g0002 | AFR | ASW | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0162 | AFR | ASW | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA20752 | hp2 | a0002 | c0002 | t0002 | g0044 | EUR | TSI | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0026 | EUR | TSI | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0155 | EUR | TSI | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0194 | SAS | GIH | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA20905 | hp2 | a0002 | c0002 | t0002 | g0065 | SAS | GIH | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0152 | AFR | ACB | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG02109 | hp2 | a0002 | c0002 | t0001 | g0008 | AFR | ACB | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG02486 | hp1 | a0001 | c0008 | t0006 | g0058 | AFR | ACB | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG02486 | hp2 | a0001 | c0001 | t0011 | g0111 | AFR | ACB | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG03471 | hp1 | a0001 | c0001 | t0004 | g0024 | AFR | MSL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG03471 | hp2 | a0001 | c0001 | t0023 | g0206 | AFR | MSL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG06807 | hp1 | a0001 | c0001 | t0026 | g0059 | AFR | USA | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| HG06807 | hp2 | a0001 | c0001 | t0030 | g0153 | AFR | USA | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA20300 | hp1 | a0002 | c0002 | t0002 | g0069 | AFR | USA | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | USA | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| NA21309 | hp2 | a0011 | c0009 | t0001 | g0115 | AFR | LWK | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0003 | g0002 | REF | REF | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0001 | g0168 | REF | REF | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:56891791 | T | C | 1 | a0007 | 1 | HG03225.hp1 | missense_variant | MODERATE | c.1802A>G | p.Tyr601Cys | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 9/9 | 1863/5745 | 1802/1893 | 601/630 | chr17 | 56891791 | |||
| chr17:56891819 | C | T | 1 | a0005 | 1 | HG00140.hp2 | missense_variant | MODERATE | c.1774G>A | p.Ala592Thr | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 9/9 | 1835/5745 | 1774/1893 | 592/630 | chr17 | 56891819 | |||
| chr17:56901433 | G | A | 7 | a0001 a0003 a0004 others(4): Show |
285 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(282): Show |
missense_variant | MODERATE | c.1073C>T | p.Pro358Leu | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 4/9 | 1134/5745 | 1073/1893 | 358/630 | chr17 | 56901433 | |||
| chr17:56904409 | G | T | 1 | a0004 | 6 | NA18951.hp1 NA18972.hp1 NA18982.hp1 others(3): Show |
missense_variant | MODERATE | c.773C>A | p.Thr258Asn | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 3/9 | 834/5745 | 773/1893 | 258/630 | chr17 | 56904409 | |||
| chr17:56904475 | C | T | 1 | a0011 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.707G>A | p.Arg236Lys | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 3/9 | 768/5745 | 707/1893 | 236/630 | chr17 | 56904475 | |||
| chr17:56913436 | T | C | 3 | a0003 a0006 a0010 |
14 | HG02257.hp1 HG02451.hp2 HG02647.hp2 others(11): Show |
missense_variant | MODERATE | c.553A>G | p.Thr185Ala | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/9 | 614/5745 | 553/1893 | 185/630 | chr17 | 56913436 | |||
| chr17:56913723 | A | C | 2 | a0003 a0006 |
13 | HG02257.hp1 HG02451.hp2 HG02647.hp2 others(10): Show |
missense_variant | MODERATE | c.266T>G | p.Val89Gly | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/9 | 327/5745 | 266/1893 | 89/630 | chr17 | 56913723 | |||
| chr17:56913796 | T | G | 1 | a0009 | 1 | NA18948.hp1 | missense_variant | MODERATE | c.193A>C | p.Lys65Gln | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/9 | 254/5745 | 193/1893 | 65/630 | chr17 | 56913796 | |||
| chr17:56913987 | A | C | 1 | a0008 | 1 | HG03834.hp1 | start_lost | HIGH | c.2T>G | p.Met1? | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/9 | 63/5745 | 2/1893 | 1/630 | chr17 | 56913987 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:56891868 | C | T | 2 | a0001c0012 a0007c0010 |
2 | HG03225.hp1 NA19240.hp2 |
synonymous_variant | LOW | c.1725G>A | p.Thr575Thr | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 9/9 | 1786/5745 | 1725/1893 | 575/630 | chr17 | 56891868 | |||
| chr17:56891955 | G | A | 1 | a0003c0007 | 1 | HG02257.hp1 | synonymous_variant | LOW | c.1638C>T | p.Ser546Ser | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 9/9 | 1699/5745 | 1638/1893 | 546/630 | chr17 | 56891955 | |||
| chr17:56899167 | C | T | 1 | a0001c0011 | 1 | HG01256.hp1 | synonymous_variant | LOW | c.1101G>A | p.Glu367Glu | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 5/9 | 1162/5745 | 1101/1893 | 367/630 | chr17 | 56899167 | |||
| chr17:56904402 | T | C | 1 | a0001c0014 | 1 | NA19065.hp1 | synonymous_variant | LOW | c.780A>G | p.Thr260Thr | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 3/9 | 841/5745 | 780/1893 | 260/630 | chr17 | 56904402 | |||
| chr17:56908513 | C | T | 1 | a0001c0008 | 1 | HG02486.hp1 | synonymous_variant | LOW | c.648G>A | p.Ala216Ala | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 2/9 | 709/5745 | 648/1893 | 216/630 | chr17 | 56908513 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:56887993 | T | C | 3 | a0001c0012t0013 a0003c0007t0016 a0007c0010t0013 |
3 | HG02257.hp1 HG03225.hp1 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3707A>G | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 9/9 | 3707 | chr17 | 56887993 | ||||||
| chr17:56888022 | G | A | 2 | a0001c0001t0011 a0002c0002t0011 |
3 | HG02486.hp2 HG02886.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3678C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 9/9 | 3678 | chr17 | 56888022 | ||||||
| chr17:56888047 | C | T | 1 | a0002c0002t0014 | 2 | HG01257.hp2 HG01496.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3653G>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 9/9 | 3653 | chr17 | 56888047 | ||||||
| chr17:56888115 | T | C | 1 | a0001c0001t0035 | 1 | HG03704.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3585A>G | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 9/9 | 3585 | chr17 | 56888115 | ||||||
| chr17:56888174 | G | A | 1 | a0002c0002t0036 | 1 | HG02040.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3526C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 9/9 | 3526 | chr17 | 56888174 | ||||||
| chr17:56888498 | CT | C | 31 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0006 others(28): Show |
147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
3_prime_UTR_variant | MODIFIER | c.*3201delA | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 9/9 | 3201 | chr17 | 56888498 | ||||||
| chr17:56888511 | A | T | 1 | a0001c0001t0034 | 1 | HG00438.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3189T>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 9/9 | 3189 | chr17 | 56888511 | ||||||
| chr17:56888571 | A | G | 6 | a0001c0001t0003 a0001c0001t0024 a0001c0011t0003 others(3): Show |
45 | HG00140.hp2 HG00735.hp2 HG00741.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*3129T>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 9/9 | 3129 | chr17 | 56888571 | ||||||
| chr17:56888584 | C | T | 2 | a0001c0001t0030 a0003c0003t0010 |
4 | HG02895.hp1 HG03098.hp1 HG06807.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3116G>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 9/9 | 3116 | chr17 | 56888584 | ||||||
| chr17:56888606 | G | T | 1 | a0002c0002t0033 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3094C>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 9/9 | 3094 | chr17 | 56888606 | ||||||
| chr17:56888672 | G | A | 1 | a0002c0002t0031 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3028C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 9/9 | 3028 | chr17 | 56888672 | ||||||
| chr17:56888743 | A | G | 1 | a0001c0001t0032 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2957T>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 9/9 | 2957 | chr17 | 56888743 | ||||||
| chr17:56888879 | C | T | 1 | a0001c0001t0041 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2821G>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 9/9 | 2821 | chr17 | 56888879 | ||||||
| chr17:56888921 | C | T | 1 | a0003c0003t0018 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2779G>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 9/9 | 2779 | chr17 | 56888921 | ||||||
| chr17:56889133 | A | G | 3 | a0001c0012t0013 a0003c0007t0016 a0007c0010t0013 |
3 | HG02257.hp1 HG03225.hp1 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2567T>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 9/9 | 2567 | chr17 | 56889133 | ||||||
| chr17:56889176 | T | TAAAA | 3 | a0001c0012t0013 a0003c0007t0016 a0007c0010t0013 |
3 | HG02257.hp1 HG03225.hp1 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2523_*2524insTTTT | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 9/9 | 2523 | chr17 | 56889176 | ||||||
| chr17:56889177 | G | A | 3 | a0001c0012t0013 a0003c0007t0016 a0007c0010t0013 |
3 | HG02257.hp1 HG03225.hp1 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2523C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 9/9 | 2523 | chr17 | 56889177 | ||||||
| chr17:56889183 | T | A | 3 | a0001c0012t0013 a0003c0007t0016 a0007c0010t0013 |
3 | HG02257.hp1 HG03225.hp1 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2517A>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 9/9 | 2517 | chr17 | 56889183 | ||||||
| chr17:56889223 | C | T | 1 | a0003c0007t0016 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2477G>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 9/9 | 2477 | chr17 | 56889223 | ||||||
| chr17:56889224 | G | A | 1 | a0001c0001t0032 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2476C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 9/9 | 2476 | chr17 | 56889224 | ||||||
| chr17:56889329 | T | G | 1 | a0001c0001t0009 | 4 | HG00558.hp1 NA18971.hp2 NA19006.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2371A>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 9/9 | 2371 | chr17 | 56889329 | ||||||
| chr17:56889339 | C | A | 1 | a0001c0001t0015 | 2 | HG00673.hp2 HG02165.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2361G>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 9/9 | 2361 | chr17 | 56889339 | ||||||
| chr17:56889444 | A | G | 8 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0026 others(5): Show |
26 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*2256T>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 9/9 | 2256 | chr17 | 56889444 | ||||||
| chr17:56889576 | G | A | 1 | a0001c0001t0037 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2124C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 9/9 | 2124 | chr17 | 56889576 | ||||||
| chr17:56889788 | G | A | 1 | a0003c0003t0019 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1912C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 9/9 | 1912 | chr17 | 56889788 | ||||||
| chr17:56889895 | A | G | 1 | a0001c0001t0029 | 1 | HG01496.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1805T>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 9/9 | 1805 | chr17 | 56889895 | ||||||
| chr17:56889959 | C | T | 1 | a0001c0001t0027 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1741G>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 9/9 | 1741 | chr17 | 56889959 | ||||||
| chr17:56889994 | G | C | 1 | a0001c0001t0038 | 1 | HG02071.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1706C>G | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 9/9 | 1706 | chr17 | 56889994 | ||||||
| chr17:56890043 | T | C | 24 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0012 others(21): Show |
138 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(135): Show |
3_prime_UTR_variant | MODIFIER | c.*1657A>G | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 9/9 | 1657 | chr17 | 56890043 | ||||||
| chr17:56890117 | G | T | 1 | a0001c0001t0026 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1583C>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 9/9 | 1583 | chr17 | 56890117 | ||||||
| chr17:56890167 | A | G | 38 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(35): Show |
174 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(171): Show |
3_prime_UTR_variant | MODIFIER | c.*1533T>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 9/9 | 1533 | chr17 | 56890167 | ||||||
| chr17:56890258 | A | T | 2 | a0001c0001t0023 a0002c0002t0022 |
2 | HG03195.hp1 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1442T>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 9/9 | 1442 | chr17 | 56890258 | ||||||
| chr17:56890297 | C | T | 1 | a0001c0014t0025 | 1 | NA19065.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1403G>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 9/9 | 1403 | chr17 | 56890297 | ||||||
| chr17:56890482 | A | G | 3 | a0001c0012t0013 a0003c0007t0016 a0007c0010t0013 |
3 | HG02257.hp1 HG03225.hp1 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1218T>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 9/9 | 1218 | chr17 | 56890482 | ||||||
| chr17:56890535 | C | T | 1 | a0001c0001t0024 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1165G>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 9/9 | 1165 | chr17 | 56890535 | ||||||
| chr17:56890538 | G | A | 1 | a0001c0001t0039 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1162C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 9/9 | 1162 | chr17 | 56890538 | ||||||
| chr17:56890588 | G | A | 1 | a0001c0001t0005 | 8 | HG01884.hp1 HG02630.hp2 HG02809.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1112C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 9/9 | 1112 | chr17 | 56890588 | ||||||
| chr17:56890746 | T | C | 1 | a0002c0002t0040 | 1 | NA18964.hp2 | 3_prime_UTR_variant | MODIFIER | c.*954A>G | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 9/9 | 954 | chr17 | 56890746 | ||||||
| chr17:56890747 | T | C | 1 | a0001c0001t0041 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*953A>G | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 9/9 | 953 | chr17 | 56890747 | ||||||
| chr17:56890826 | T | C | 2 | a0001c0001t0023 a0002c0002t0022 |
2 | HG03195.hp1 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*874A>G | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 9/9 | 874 | chr17 | 56890826 | ||||||
| chr17:56890968 | A | G | 7 | a0001c0001t0011 a0001c0001t0023 a0001c0012t0013 others(4): Show |
8 | HG02257.hp1 HG02486.hp2 HG02886.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*732T>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 9/9 | 732 | chr17 | 56890968 | ||||||
| chr17:56891579 | C | T | 1 | a0002c0002t0022 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*121G>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 9/9 | 121 | chr17 | 56891579 | ||||||
| chr17:56914010 | A | G | 9 | a0003c0003t0007 a0003c0003t0010 a0003c0003t0017 others(6): Show |
13 | HG02257.hp1 HG02451.hp2 HG02647.hp2 others(10): Show |
5_prime_UTR_variant | MODIFIER | c.-22T>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/9 | 22 | chr17 | 56914010 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:56892373 | C | A | 8 | a0001c0001t0004g0024 a0001c0001t0004g0060 a0001c0001t0004g0061 others(5): Show |
9 | HG00639.hp1 HG02717.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.1364-144G>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 8/8 | chr17 | 56892373 | |||||||
| chr17:56892374 | CATCT | C | 8 | a0001c0001t0005g0046 a0001c0001t0005g0097 a0001c0001t0005g0102 others(5): Show |
9 | HG01884.hp1 HG02630.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1364-149_1364-146d others(6): Show |
TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 8/8 | chr17 | 56892374 | |||||||
| chr17:56892453 | C | G | 1 | a0001c0001t0001g0204 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1364-224G>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 8/8 | chr17 | 56892453 | |||||||
| chr17:56892626 | C | T | 1 | a0001c0001t0001g0079 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1364-397G>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 8/8 | chr17 | 56892626 | |||||||
| chr17:56892717 | G | A | 1 | a0003c0003t0007g0053 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1364-488C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 8/8 | chr17 | 56892717 | |||||||
| chr17:56892768 | C | G | 3 | a0001c0001t0011g0084 a0001c0001t0011g0111 a0002c0002t0011g0154 |
3 | HG02486.hp2 HG02886.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1364-539G>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 8/8 | chr17 | 56892768 | |||||||
| chr17:56892820 | G | T | 110 | a0001c0001t0001g0041 a0001c0001t0001g0117 a0001c0001t0001g0159 others(107): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.1364-591C>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 8/8 | chr17 | 56892820 | |||||||
| chr17:56892839 | C | T | 1 | a0001c0001t0001g0027 | 2 | NA18947.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.1364-610G>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 8/8 | chr17 | 56892839 | |||||||
| chr17:56893220 | G | A | 1 | a0001c0001t0001g0198 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1364-991C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 8/8 | chr17 | 56893220 | |||||||
| chr17:56893223 | G | GTCTGTAA others(268): Show |
2 | a0001c0012t0013g0089 a0007c0010t0013g0107 |
2 | HG03225.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1364-995_1364-994i others(277): Show |
TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 8/8 | chr17 | 56893223 | |||||||
| chr17:56893224 | C | T | 2 | a0001c0012t0013g0089 a0007c0010t0013g0107 |
2 | HG03225.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1364-995G>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 8/8 | chr17 | 56893224 | |||||||
| chr17:56893230 | T | C | 2 | a0001c0012t0013g0089 a0007c0010t0013g0107 |
2 | HG03225.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1364-1001A>G | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 8/8 | chr17 | 56893230 | |||||||
| chr17:56893401 | G | A | 3 | a0001c0001t0006g0109 a0001c0008t0006g0058 a0003c0003t0021g0055 |
3 | HG02486.hp1 HG02886.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1364-1172C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 8/8 | chr17 | 56893401 | |||||||
| chr17:56893501 | A | T | 1 | a0002c0002t0031g0140 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1364-1272T>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 8/8 | chr17 | 56893501 | |||||||
| chr17:56893729 | G | A | 1 | a0001c0001t0001g0096 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1364-1500C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 8/8 | chr17 | 56893729 | |||||||
| chr17:56893782 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1364-1553C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 8/8 | chr17 | 56893782 | |||||||
| chr17:56893803 | A | G | 4 | a0001c0001t0001g0041 a0001c0001t0001g0117 a0001c0001t0001g0205 others(1): Show |
5 | HG02717.hp2 HG02809.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1363+1540T>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 8/8 | chr17 | 56893803 | |||||||
| chr17:56893880 | C | A | 165 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0018 others(162): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.1363+1463G>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 8/8 | chr17 | 56893880 | |||||||
| chr17:56894093 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1363+1250G>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 8/8 | chr17 | 56894093 | |||||||
| chr17:56894177 | T | G | 1 | a0001c0001t0027g0108 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1363+1166A>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 8/8 | chr17 | 56894177 | |||||||
| chr17:56894384 | G | A | 1 | a0001c0001t0001g0134 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1363+959C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 8/8 | chr17 | 56894384 | |||||||
| chr17:56894409 | C | T | 1 | a0001c0001t0002g0150 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1363+934G>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 8/8 | chr17 | 56894409 | |||||||
| chr17:56894576 | C | T | 2 | a0001c0001t0001g0027 a0001c0014t0025g0087 |
3 | NA18947.hp1 NA18952.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.1363+767G>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 8/8 | chr17 | 56894576 | |||||||
| chr17:56894651 | T | C | 1 | a0001c0001t0001g0130 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1363+692A>G | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 8/8 | chr17 | 56894651 | |||||||
| chr17:56894842 | T | C | 1 | a0001c0001t0004g0131 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1363+501A>G | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 8/8 | chr17 | 56894842 | |||||||
| chr17:56895003 | A | G | 2 | a0001c0001t0002g0078 a0003c0007t0016g0049 |
2 | HG02257.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1363+340T>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 8/8 | chr17 | 56895003 | |||||||
| chr17:56895032 | C | G | 1 | a0001c0001t0002g0078 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1363+311G>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 8/8 | chr17 | 56895032 | |||||||
| chr17:56895040 | G | A | 26 | a0001c0001t0001g0018 a0001c0001t0001g0070 a0001c0001t0001g0072 others(23): Show |
42 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.1363+303C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 8/8 | chr17 | 56895040 | |||||||
| chr17:56895045 | C | T | 1 | a0007c0010t0013g0107 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1363+298G>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 8/8 | chr17 | 56895045 | |||||||
| chr17:56895120 | C | T | 1 | a0002c0002t0001g0178 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1363+223G>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 8/8 | chr17 | 56895120 | |||||||
| chr17:56895121 | G | T | 1 | a0001c0001t0004g0149 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1363+222C>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 8/8 | chr17 | 56895121 | |||||||
| chr17:56895696 | G | A | 1 | a0001c0008t0006g0058 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1181-92C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 6/8 | chr17 | 56895696 | |||||||
| chr17:56895750 | T | A | 2 | a0001c0001t0006g0109 a0003c0003t0021g0055 |
2 | HG02886.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1181-146A>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 6/8 | chr17 | 56895750 | |||||||
| chr17:56895850 | G | A | 2 | a0002c0002t0022g0091 a0010c0015t0002g0215 |
2 | HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1180+76C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 6/8 | chr17 | 56895850 | |||||||
| chr17:56895981 | T | C | 1 | a0002c0002t0022g0091 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1154-29A>G | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 5/8 | chr17 | 56895981 | |||||||
| chr17:56896029 | T | C | 1 | a0001c0001t0001g0105 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1154-77A>G | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 5/8 | chr17 | 56896029 | |||||||
| chr17:56896061 | G | A | 1 | a0001c0001t0004g0060 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1154-109C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 5/8 | chr17 | 56896061 | |||||||
| chr17:56896160 | A | C | 1 | a0001c0001t0002g0118 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1154-208T>G | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 5/8 | chr17 | 56896160 | |||||||
| chr17:56896180 | A | G | 70 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0027 others(67): Show |
100 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(97): Show |
intron_variant | MODIFIER | c.1154-228T>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 5/8 | chr17 | 56896180 | |||||||
| chr17:56896322 | A | G | 2 | a0001c0001t0001g0116 a0001c0001t0001g0117 |
2 | HG02717.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1154-370T>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 5/8 | chr17 | 56896322 | |||||||
| chr17:56896347 | G | GA | 209 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(206): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.1154-396dupT | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 5/8 | chr17 | 56896347 | |||||||
| chr17:56896381 | T | C | 4 | a0002c0002t0022g0091 a0002c0002t0031g0140 a0007c0010t0013g0107 others(1): Show |
4 | HG02622.hp2 HG03195.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1154-429A>G | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 5/8 | chr17 | 56896381 | |||||||
| chr17:56896498 | C | CA | 5 | a0001c0001t0001g0073 a0001c0001t0002g0030 a0001c0001t0002g0136 others(2): Show |
6 | HG01243.hp1 HG02109.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1154-547dupT | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 5/8 | chr17 | 56896498 | |||||||
| chr17:56896518 | A | T | 3 | a0002c0002t0002g0040 a0002c0002t0002g0069 a0002c0002t0011g0154 |
4 | HG02257.hp2 HG02572.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1154-566T>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 5/8 | chr17 | 56896518 | |||||||
| chr17:56896661 | C | G | 1 | a0006c0006t0007g0056 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1154-709G>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 5/8 | chr17 | 56896661 | |||||||
| chr17:56896668 | C | CA | 62 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0017 others(59): Show |
129 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.1154-717dupT | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 5/8 | chr17 | 56896668 | |||||||
| chr17:56896752 | G | A | 1 | a0001c0001t0002g0118 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1154-800C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 5/8 | chr17 | 56896752 | |||||||
| chr17:56897049 | G | A | 1 | a0001c0001t0001g0196 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1154-1097C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 5/8 | chr17 | 56897049 | |||||||
| chr17:56897099 | C | T | 4 | a0002c0002t0022g0091 a0002c0002t0031g0140 a0007c0010t0013g0107 others(1): Show |
4 | HG02622.hp2 HG03195.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1154-1147G>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 5/8 | chr17 | 56897099 | |||||||
| chr17:56897174 | G | T | 1 | a0007c0010t0013g0107 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1154-1222C>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 5/8 | chr17 | 56897174 | |||||||
| chr17:56897298 | C | T | 14 | a0001c0001t0001g0113 a0001c0001t0001g0125 a0001c0001t0003g0032 others(11): Show |
34 | HG00639.hp1 HG00735.hp2 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.1154-1346G>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 5/8 | chr17 | 56897298 | |||||||
| chr17:56897299 | G | A | 1 | a0002c0002t0002g0173 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1154-1347C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 5/8 | chr17 | 56897299 | |||||||
| chr17:56897345 | C | A | 4 | a0002c0002t0022g0091 a0002c0002t0031g0140 a0007c0010t0013g0107 others(1): Show |
4 | HG02622.hp2 HG03195.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1154-1393G>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 5/8 | chr17 | 56897345 | |||||||
| chr17:56897346 | A | G | 4 | a0002c0002t0022g0091 a0002c0002t0031g0140 a0007c0010t0013g0107 others(1): Show |
4 | HG02622.hp2 HG03195.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1154-1394T>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 5/8 | chr17 | 56897346 | |||||||
| chr17:56897456 | G | A | 4 | a0002c0002t0022g0091 a0002c0002t0031g0140 a0007c0010t0013g0107 others(1): Show |
4 | HG02622.hp2 HG03195.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1154-1504C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 5/8 | chr17 | 56897456 | |||||||
| chr17:56897662 | G | A | 3 | a0001c0001t0001g0134 a0001c0001t0003g0034 a0001c0001t0006g0133 |
4 | NA18946.hp1 NA18983.hp2 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.1153+1453C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 5/8 | chr17 | 56897662 | |||||||
| chr17:56897817 | C | T | 4 | a0002c0002t0022g0091 a0002c0002t0031g0140 a0007c0010t0013g0107 others(1): Show |
4 | HG02622.hp2 HG03195.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1153+1298G>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 5/8 | chr17 | 56897817 | |||||||
| chr17:56897872 | C | T | 1 | a0001c0001t0001g0124 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1153+1243G>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 5/8 | chr17 | 56897872 | |||||||
| chr17:56897944 | G | A | 4 | a0002c0002t0022g0091 a0002c0002t0031g0140 a0007c0010t0013g0107 others(1): Show |
4 | HG02622.hp2 HG03195.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1153+1171C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 5/8 | chr17 | 56897944 | |||||||
| chr17:56898147 | G | A | 1 | a0001c0001t0011g0111 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1153+968C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 5/8 | chr17 | 56898147 | |||||||
| chr17:56898204 | G | A | 1 | a0001c0001t0003g0160 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1153+911C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 5/8 | chr17 | 56898204 | |||||||
| chr17:56898223 | A | AGTATATG others(12): Show |
4 | a0002c0002t0022g0091 a0002c0002t0031g0140 a0007c0010t0013g0107 others(1): Show |
4 | HG02622.hp2 HG03195.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1153+873_1153+891d others(21): Show |
TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 5/8 | chr17 | 56898223 | |||||||
| chr17:56898261 | A | G | 1 | a0001c0001t0002g0078 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1153+854T>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 5/8 | chr17 | 56898261 | |||||||
| chr17:56898298 | CGGTATAT others(12): Show |
C | 1 | a0001c0001t0001g0135 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1153+798_1153+816d others(21): Show |
TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 5/8 | chr17 | 56898298 | |||||||
| chr17:56898317 | T | TGGTATAT others(12): Show |
1 | a0001c0001t0002g0078 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1153+797_1153+798i others(21): Show |
TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 5/8 | chr17 | 56898317 | |||||||
| chr17:56898318 | G | A | 1 | a0001c0001t0001g0197 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1153+797C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 5/8 | chr17 | 56898318 | |||||||
| chr17:56898414 | C | T | 1 | a0001c0001t0001g0121 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1153+701G>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 5/8 | chr17 | 56898414 | |||||||
| chr17:56898502 | A | G | 1 | a0001c0001t0004g0149 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1153+613T>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 5/8 | chr17 | 56898502 | |||||||
| chr17:56898708 | C | CA | 21 | a0001c0001t0001g0103 a0001c0001t0001g0146 a0001c0001t0001g0190 others(18): Show |
27 | HG01099.hp1 HG01109.hp1 HG01934.hp2 others(24): Show |
intron_variant | MODIFIER | c.1153+406dupT | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 5/8 | chr17 | 56898708 | |||||||
| chr17:56898770 | T | G | 4 | a0002c0002t0022g0091 a0002c0002t0031g0140 a0007c0010t0013g0107 others(1): Show |
4 | HG02622.hp2 HG03195.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1153+345A>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 5/8 | chr17 | 56898770 | |||||||
| chr17:56898912 | G | A | 1 | a0001c0001t0008g0083 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1153+203C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 5/8 | chr17 | 56898912 | |||||||
| chr17:56898943 | C | G | 180 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(177): Show |
295 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(292): Show |
intron_variant | MODIFIER | c.1153+172G>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 5/8 | chr17 | 56898943 | |||||||
| chr17:56898973 | C | T | 4 | a0002c0002t0022g0091 a0002c0002t0031g0140 a0007c0010t0013g0107 others(1): Show |
4 | HG02622.hp2 HG03195.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1153+142G>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 5/8 | chr17 | 56898973 | |||||||
| chr17:56898976 | A | G | 180 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(177): Show |
295 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(292): Show |
intron_variant | MODIFIER | c.1153+139T>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 5/8 | chr17 | 56898976 | |||||||
| chr17:56898980 | G | C | 1 | a0002c0002t0002g0141 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1153+135C>G | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 5/8 | chr17 | 56898980 | |||||||
| chr17:56899039 | C | T | 1 | a0001c0001t0002g0029 | 2 | HG02647.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1153+76G>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 5/8 | chr17 | 56899039 | |||||||
| chr17:56899294 | C | T | 2 | a0001c0001t0001g0082 a0001c0001t0008g0083 |
2 | HG02723.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1088-114G>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 4/8 | chr17 | 56899294 | |||||||
| chr17:56899295 | G | A | 1 | a0010c0015t0002g0215 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1088-115C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 4/8 | chr17 | 56899295 | |||||||
| chr17:56899309 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1088-129G>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 4/8 | chr17 | 56899309 | |||||||
| chr17:56899315 | T | C | 1 | a0001c0001t0002g0136 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1088-135A>G | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 4/8 | chr17 | 56899315 | |||||||
| chr17:56899528 | G | A | 1 | a0001c0001t0004g0060 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1088-348C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 4/8 | chr17 | 56899528 | |||||||
| chr17:56899561 | C | A | 174 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(171): Show |
289 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(286): Show |
intron_variant | MODIFIER | c.1088-381G>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 4/8 | chr17 | 56899561 | |||||||
| chr17:56899603 | C | G | 1 | a0006c0006t0007g0056 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1088-423G>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 4/8 | chr17 | 56899603 | |||||||
| chr17:56899687 | G | A | 4 | a0002c0002t0022g0091 a0002c0002t0031g0140 a0007c0010t0013g0107 others(1): Show |
4 | HG02622.hp2 HG03195.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1088-507C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 4/8 | chr17 | 56899687 | |||||||
| chr17:56899794 | G | A | 1 | a0001c0001t0001g0198 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1088-614C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 4/8 | chr17 | 56899794 | |||||||
| chr17:56899858 | T | C | 1 | a0002c0002t0002g0174 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1088-678A>G | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 4/8 | chr17 | 56899858 | |||||||
| chr17:56900201 | G | A | 2 | a0001c0001t0001g0045 a0001c0001t0001g0209 |
3 | NA18998.hp1 NA19003.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1088-1021C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 4/8 | chr17 | 56900201 | |||||||
| chr17:56900208 | C | T | 1 | a0003c0003t0020g0054 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1088-1028G>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 4/8 | chr17 | 56900208 | |||||||
| chr17:56900209 | G | A | 6 | a0002c0002t0001g0176 a0002c0002t0001g0177 a0002c0002t0001g0178 others(3): Show |
10 | NA18940.hp1 NA18964.hp2 NA18965.hp1 others(7): Show |
intron_variant | MODIFIER | c.1088-1029C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 4/8 | chr17 | 56900209 | |||||||
| chr17:56900213 | C | CA | 72 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0021 others(69): Show |
103 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.1088-1034dupT | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 4/8 | chr17 | 56900213 | |||||||
| chr17:56900213 | CA | C | 13 | a0002c0002t0001g0008 a0002c0002t0001g0062 a0002c0002t0001g0063 others(10): Show |
32 | HG00639.hp1 HG00735.hp2 HG01069.hp1 others(29): Show |
intron_variant | MODIFIER | c.1088-1034delT | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 4/8 | chr17 | 56900213 | |||||||
| chr17:56900244 | G | A | 4 | a0001c0001t0001g0070 a0001c0001t0001g0072 a0001c0001t0001g0073 others(1): Show |
4 | HG02258.hp1 HG02976.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1088-1064C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 4/8 | chr17 | 56900244 | |||||||
| chr17:56900270 | C | T | 1 | a0002c0002t0001g0062 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1088-1090G>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 4/8 | chr17 | 56900270 | |||||||
| chr17:56900302 | A | G | 4 | a0002c0002t0022g0091 a0002c0002t0031g0140 a0007c0010t0013g0107 others(1): Show |
4 | HG02622.hp2 HG03195.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1087+1117T>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 4/8 | chr17 | 56900302 | |||||||
| chr17:56900356 | C | T | 1 | a0001c0001t0005g0097 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1087+1063G>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 4/8 | chr17 | 56900356 | |||||||
| chr17:56900403 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1087+1016C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 4/8 | chr17 | 56900403 | |||||||
| chr17:56900419 | C | T | 178 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(175): Show |
293 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.1087+1000G>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 4/8 | chr17 | 56900419 | |||||||
| chr17:56900746 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1087+673C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 4/8 | chr17 | 56900746 | |||||||
| chr17:56900938 | G | A | 1 | a0001c0001t0004g0119 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1087+481C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 4/8 | chr17 | 56900938 | |||||||
| chr17:56901020 | C | T | 4 | a0002c0002t0022g0091 a0002c0002t0031g0140 a0007c0010t0013g0107 others(1): Show |
4 | HG02622.hp2 HG03195.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1087+399G>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 4/8 | chr17 | 56901020 | |||||||
| chr17:56901110 | A | G | 10 | a0001c0001t0001g0028 a0001c0001t0001g0081 a0001c0001t0001g0093 others(7): Show |
11 | HG00280.hp2 HG01099.hp2 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.1087+309T>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 4/8 | chr17 | 56901110 | |||||||
| chr17:56901193 | A | C | 4 | a0002c0002t0022g0091 a0002c0002t0031g0140 a0007c0010t0013g0107 others(1): Show |
4 | HG02622.hp2 HG03195.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1087+226T>G | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 4/8 | chr17 | 56901193 | |||||||
| chr17:56901275 | G | A | 1 | a0002c0002t0040g0179 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1087+144C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 4/8 | chr17 | 56901275 | |||||||
| chr17:56901332 | G | A | 3 | a0002c0002t0022g0091 a0007c0010t0013g0107 a0010c0015t0002g0215 |
3 | HG03195.hp1 HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1087+87C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 4/8 | chr17 | 56901332 | |||||||
| chr17:56901358 | T | G | 4 | a0002c0002t0022g0091 a0002c0002t0031g0140 a0007c0010t0013g0107 others(1): Show |
4 | HG02622.hp2 HG03195.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1087+61A>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 4/8 | chr17 | 56901358 | |||||||
| chr17:56901393 | G | T | 4 | a0002c0002t0022g0091 a0002c0002t0031g0140 a0007c0010t0013g0107 others(1): Show |
4 | HG02622.hp2 HG03195.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1087+26C>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 4/8 | chr17 | 56901393 | |||||||
| chr17:56901767 | G | A | 178 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(175): Show |
293 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.928-189C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 3/8 | chr17 | 56901767 | |||||||
| chr17:56901787 | A | G | 1 | a0001c0001t0001g0143 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.928-209T>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 3/8 | chr17 | 56901787 | |||||||
| chr17:56901873 | G | A | 1 | a0001c0001t0001g0138 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.928-295C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 3/8 | chr17 | 56901873 | |||||||
| chr17:56901900 | T | C | 1 | a0001c0001t0002g0078 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.928-322A>G | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 3/8 | chr17 | 56901900 | |||||||
| chr17:56901990 | G | A | 1 | a0001c0001t0001g0204 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.928-412C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 3/8 | chr17 | 56901990 | |||||||
| chr17:56902007 | G | C | 1 | a0001c0001t0003g0026 | 2 | HG01516.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.928-429C>G | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 3/8 | chr17 | 56902007 | |||||||
| chr17:56902165 | T | C | 2 | a0001c0001t0001g0035 a0001c0001t0001g0036 |
4 | HG00621.hp2 HG02129.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.928-587A>G | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 3/8 | chr17 | 56902165 | |||||||
| chr17:56902171 | T | C | 1 | a0001c0001t0005g0163 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.928-593A>G | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 3/8 | chr17 | 56902171 | |||||||
| chr17:56902497 | G | A | 1 | a0010c0015t0002g0215 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.928-919C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 3/8 | chr17 | 56902497 | |||||||
| chr17:56902519 | C | T | 1 | a0001c0001t0005g0046 | 2 | HG02630.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.928-941G>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 3/8 | chr17 | 56902519 | |||||||
| chr17:56902642 | TGCTGGCA others(3): Show |
T | 1 | a0001c0001t0001g0142 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.928-1074_928-1065d others(12): Show |
TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 3/8 | chr17 | 56902642 | |||||||
| chr17:56902654 | C | T | 1 | a0001c0001t0003g0188 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.928-1076G>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 3/8 | chr17 | 56902654 | |||||||
| chr17:56902776 | C | T | 1 | a0001c0001t0001g0122 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.928-1198G>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 3/8 | chr17 | 56902776 | |||||||
| chr17:56902874 | A | G | 1 | a0001c0001t0001g0142 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.928-1296T>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 3/8 | chr17 | 56902874 | |||||||
| chr17:56903026 | A | C | 4 | a0002c0002t0022g0091 a0002c0002t0031g0140 a0007c0010t0013g0107 others(1): Show |
4 | HG02622.hp2 HG03195.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.927+1229T>G | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 3/8 | chr17 | 56903026 | |||||||
| chr17:56903034 | G | A | 4 | a0002c0002t0022g0091 a0002c0002t0031g0140 a0007c0010t0013g0107 others(1): Show |
4 | HG02622.hp2 HG03195.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.927+1221C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 3/8 | chr17 | 56903034 | |||||||
| chr17:56903126 | C | T | 1 | a0001c0001t0027g0108 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.927+1129G>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 3/8 | chr17 | 56903126 | |||||||
| chr17:56903219 | G | A | 2 | a0002c0002t0031g0140 a0010c0015t0002g0215 |
2 | HG02622.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.927+1036C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 3/8 | chr17 | 56903219 | |||||||
| chr17:56903272 | C | T | 4 | a0001c0001t0001g0082 a0001c0001t0008g0083 a0001c0001t0011g0084 others(1): Show |
4 | HG01891.hp2 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.927+983G>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 3/8 | chr17 | 56903272 | |||||||
| chr17:56903361 | A | G | 4 | a0002c0002t0022g0091 a0002c0002t0031g0140 a0007c0010t0013g0107 others(1): Show |
4 | HG02622.hp2 HG03195.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.927+894T>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 3/8 | chr17 | 56903361 | |||||||
| chr17:56903376 | C | G | 11 | a0002c0002t0001g0008 a0002c0002t0001g0062 a0002c0002t0001g0063 others(8): Show |
30 | HG00639.hp1 HG00735.hp2 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.927+879G>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 3/8 | chr17 | 56903376 | |||||||
| chr17:56903620 | C | T | 85 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0021 others(82): Show |
122 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.927+635G>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 3/8 | chr17 | 56903620 | |||||||
| chr17:56904210 | C | CA | 8 | a0001c0001t0001g0105 a0001c0001t0002g0077 a0001c0001t0002g0139 others(5): Show |
8 | HG02071.hp2 HG03516.hp1 HG03654.hp1 others(5): Show |
intron_variant | MODIFIER | c.927+44dupT | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 3/8 | chr17 | 56904210 | |||||||
| chr17:56904235 | A | C | 2 | a0002c0002t0031g0140 a0010c0015t0002g0215 |
2 | HG02622.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.927+20T>G | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 3/8 | chr17 | 56904235 | |||||||
| chr17:56904557 | G | T | 13 | a0001c0001t0002g0016 a0001c0001t0002g0075 a0001c0001t0002g0077 others(10): Show |
18 | HG01099.hp1 HG01109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.694-69C>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 2/8 | chr17 | 56904557 | |||||||
| chr17:56904608 | A | G | 2 | a0002c0002t0031g0140 a0010c0015t0002g0215 |
2 | HG02622.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.694-120T>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 2/8 | chr17 | 56904608 | |||||||
| chr17:56904988 | A | G | 1 | a0011c0009t0001g0115 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.694-500T>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 2/8 | chr17 | 56904988 | |||||||
| chr17:56905227 | G | A | 1 | a0001c0001t0029g0161 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.694-739C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 2/8 | chr17 | 56905227 | |||||||
| chr17:56905442 | G | A | 69 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0021 others(66): Show |
100 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.694-954C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 2/8 | chr17 | 56905442 | |||||||
| chr17:56905569 | A | G | 2 | a0001c0001t0001g0018 a0009c0016t0001g0216 |
4 | NA18945.hp2 NA18948.hp1 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.694-1081T>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 2/8 | chr17 | 56905569 | |||||||
| chr17:56905820 | G | A | 16 | a0001c0001t0002g0016 a0001c0001t0002g0075 a0001c0001t0002g0077 others(13): Show |
21 | HG01099.hp1 HG01109.hp1 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.694-1332C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 2/8 | chr17 | 56905820 | |||||||
| chr17:56905869 | A | C | 1 | a0001c0001t0001g0121 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.694-1381T>G | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 2/8 | chr17 | 56905869 | |||||||
| chr17:56906218 | A | AG | 178 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(175): Show |
293 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.694-1731dupC | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 2/8 | chr17 | 56906218 | |||||||
| chr17:56906245 | G | A | 2 | a0001c0001t0037g0088 a0001c0012t0013g0089 |
2 | HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.694-1757C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 2/8 | chr17 | 56906245 | |||||||
| chr17:56906271 | A | G | 1 | a0001c0001t0002g0157 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.694-1783T>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 2/8 | chr17 | 56906271 | |||||||
| chr17:56906327 | A | AC | 12 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0159 others(9): Show |
25 | HG00099.hp1 HG00140.hp1 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.694-1840dupG | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 2/8 | chr17 | 56906327 | |||||||
| chr17:56906498 | A | AT | 33 | a0001c0001t0001g0031 a0001c0001t0001g0070 a0001c0001t0001g0072 others(30): Show |
48 | HG00099.hp1 HG00140.hp1 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.693+1969dupA | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 2/8 | chr17 | 56906498 | |||||||
| chr17:56906605 | T | C | 1 | a0002c0002t0001g0181 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.693+1863A>G | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 2/8 | chr17 | 56906605 | |||||||
| chr17:56906648 | C | T | 87 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0017 others(84): Show |
165 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.693+1820G>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 2/8 | chr17 | 56906648 | |||||||
| chr17:56907029 | A | G | 1 | a0001c0001t0001g0142 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.693+1439T>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 2/8 | chr17 | 56907029 | |||||||
| chr17:56907030 | G | A | 1 | a0001c0001t0001g0142 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.693+1438C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 2/8 | chr17 | 56907030 | |||||||
| chr17:56907570 | T | C | 6 | a0001c0001t0001g0037 a0001c0001t0001g0143 a0001c0001t0001g0144 others(3): Show |
7 | HG00280.hp1 HG00735.hp1 HG01074.hp1 others(4): Show |
intron_variant | MODIFIER | c.693+898A>G | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 2/8 | chr17 | 56907570 | |||||||
| chr17:56907809 | A | G | 15 | a0001c0001t0002g0016 a0001c0001t0002g0075 a0001c0001t0002g0077 others(12): Show |
20 | HG01099.hp1 HG01109.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.693+659T>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 2/8 | chr17 | 56907809 | |||||||
| chr17:56907915 | G | A | 1 | a0001c0001t0001g0020 | 3 | HG02129.hp2 NA18966.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.693+553C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 2/8 | chr17 | 56907915 | |||||||
| chr17:56907977 | G | T | 2 | a0002c0002t0022g0091 a0007c0010t0013g0107 |
2 | HG03195.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.693+491C>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 2/8 | chr17 | 56907977 | |||||||
| chr17:56908372 | A | G | 1 | a0010c0015t0002g0215 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.693+96T>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 2/8 | chr17 | 56908372 | |||||||
| chr17:56908411 | G | A | 2 | a0001c0001t0001g0038 a0001c0001t0001g0039 |
4 | NA18947.hp2 NA18985.hp1 NA19085.hp2 others(1): Show |
intron_variant | MODIFIER | c.693+57C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 2/8 | chr17 | 56908411 | |||||||
| chr17:56909238 | G | C | 1 | a0001c0001t0002g0106 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.598-675C>G | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56909238 | |||||||
| chr17:56909471 | T | G | 169 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(166): Show |
281 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.598-908A>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56909471 | |||||||
| chr17:56909483 | G | A | 1 | a0001c0001t0001g0201 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.598-920C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56909483 | |||||||
| chr17:56909606 | T | A | 169 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(166): Show |
281 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.598-1043A>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56909606 | |||||||
| chr17:56909610 | G | A | 155 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(152): Show |
262 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.598-1047C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56909610 | |||||||
| chr17:56909645 | A | C | 3 | a0001c0001t0001g0017 a0001c0001t0001g0112 a0001c0001t0009g0013 |
8 | HG00558.hp1 HG00673.hp1 HG02523.hp1 others(5): Show |
intron_variant | MODIFIER | c.598-1082T>G | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56909645 | |||||||
| chr17:56909684 | C | CA | 163 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(160): Show |
275 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.598-1122dupT | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56909684 | |||||||
| chr17:56909919 | G | A | 13 | a0001c0001t0002g0016 a0001c0001t0002g0075 a0001c0001t0002g0077 others(10): Show |
18 | HG01099.hp1 HG02257.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.598-1356C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56909919 | |||||||
| chr17:56909964 | T | C | 1 | a0001c0001t0001g0148 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.598-1401A>G | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56909964 | |||||||
| chr17:56910022 | C | T | 1 | a0002c0002t0003g0023 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.598-1459G>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56910022 | |||||||
| chr17:56910159 | GA | G | 4 | a0001c0001t0001g0041 a0001c0001t0030g0153 a0002c0002t0002g0040 others(1): Show |
6 | HG02257.hp2 HG02572.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.598-1597delT | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56910159 | |||||||
| chr17:56910168 | A | AAC | 12 | a0001c0001t0002g0016 a0001c0001t0002g0075 a0001c0001t0002g0077 others(9): Show |
17 | HG01099.hp1 HG02257.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.598-1606_598-1605i others(4): Show |
TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56910168 | |||||||
| chr17:56910168 | A | AC | 3 | a0001c0001t0002g0078 a0006c0006t0007g0056 a0010c0015t0002g0215 |
3 | HG02615.hp1 HG03139.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.598-1606_598-1605i others(3): Show |
TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56910168 | |||||||
| chr17:56910180 | G | T | 1 | a0001c0001t0001g0204 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.598-1617C>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56910180 | |||||||
| chr17:56910257 | C | T | 1 | a0001c0001t0002g0155 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.598-1694G>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56910257 | |||||||
| chr17:56910349 | G | A | 1 | a0001c0001t0001g0090 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.598-1786C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56910349 | |||||||
| chr17:56910470 | C | T | 1 | a0001c0001t0003g0026 | 2 | HG01516.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.598-1907G>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56910470 | |||||||
| chr17:56910727 | G | C | 2 | a0002c0002t0022g0091 a0007c0010t0013g0107 |
2 | HG03195.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.598-2164C>G | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56910727 | |||||||
| chr17:56910789 | G | A | 32 | a0001c0001t0001g0028 a0001c0001t0001g0093 a0001c0001t0001g0094 others(29): Show |
38 | HG00280.hp2 HG00738.hp2 HG01099.hp2 others(35): Show |
intron_variant | MODIFIER | c.598-2226C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56910789 | |||||||
| chr17:56910790 | A | C | 191 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(188): Show |
325 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(322): Show |
intron_variant | MODIFIER | c.598-2227T>G | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56910790 | |||||||
| chr17:56910821 | C | T | 170 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(167): Show |
282 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.598-2258G>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56910821 | |||||||
| chr17:56910880 | G | A | 15 | a0001c0001t0001g0070 a0001c0001t0001g0072 a0001c0001t0001g0073 others(12): Show |
28 | HG00099.hp1 HG00140.hp1 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.598-2317C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56910880 | |||||||
| chr17:56911140 | G | A | 1 | a0001c0001t0003g0164 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.597+2252C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56911140 | |||||||
| chr17:56911347 | C | T | 14 | a0001c0001t0002g0016 a0001c0001t0002g0075 a0001c0001t0002g0077 others(11): Show |
19 | HG01099.hp1 HG02257.hp1 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.597+2045G>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56911347 | |||||||
| chr17:56911398 | G | A | 1 | a0002c0002t0028g0182 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.597+1994C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56911398 | |||||||
| chr17:56911472 | C | T | 1 | a0006c0006t0007g0056 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.597+1920G>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56911472 | |||||||
| chr17:56911494 | C | T | 19 | a0001c0001t0002g0016 a0001c0001t0002g0075 a0001c0001t0002g0077 others(16): Show |
24 | HG01099.hp1 HG02257.hp1 HG02280.hp2 others(21): Show |
intron_variant | MODIFIER | c.597+1898G>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56911494 | |||||||
| chr17:56911515 | G | A | 1 | a0007c0010t0013g0107 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.597+1877C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56911515 | |||||||
| chr17:56911578 | C | CA | 107 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0017 others(104): Show |
206 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.597+1813dupT | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56911578 | |||||||
| chr17:56911617 | A | G | 191 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(188): Show |
325 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(322): Show |
intron_variant | MODIFIER | c.597+1775T>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56911617 | |||||||
| chr17:56911705 | T | C | 2 | a0006c0006t0007g0056 a0010c0015t0002g0215 |
2 | HG03139.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.597+1687A>G | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56911705 | |||||||
| chr17:56912002 | G | A | 27 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0021 others(24): Show |
50 | HG00408.hp1 HG00438.hp1 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.597+1390C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912002 | |||||||
| chr17:56912046 | G | A | 12 | a0001c0001t0002g0016 a0001c0001t0002g0075 a0001c0001t0002g0077 others(9): Show |
17 | HG01099.hp1 HG02257.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.597+1346C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912046 | |||||||
| chr17:56912046 | GA | G | 2 | a0001c0001t0001g0017 a0001c0001t0009g0013 |
5 | HG00558.hp1 NA18971.hp2 NA19006.hp2 others(2): Show |
intron_variant | MODIFIER | c.597+1345delT | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912046 | |||||||
| chr17:56912143 | G | A | 1 | a0002c0002t0002g0203 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.597+1249C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912143 | |||||||
| chr17:56912249 | G | A | 9 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0002g0208 others(6): Show |
12 | HG00738.hp2 HG02145.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.597+1143C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912249 | |||||||
| chr17:56912370 | C | G | 1 | a0001c0001t0001g0209 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.597+1022G>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912370 | |||||||
| chr17:56912372 | A | C | 1 | a0001c0001t0001g0209 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.597+1020T>G | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912372 | |||||||
| chr17:56912374 | A | C | 1 | a0001c0001t0001g0209 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.597+1018T>G | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912374 | |||||||
| chr17:56912376 | C | G | 1 | a0001c0001t0001g0209 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.597+1016G>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912376 | |||||||
| chr17:56912378 | C | G | 1 | a0001c0001t0001g0209 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.597+1014G>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912378 | |||||||
| chr17:56912379 | A | G | 1 | a0001c0001t0001g0209 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.597+1013T>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912379 | |||||||
| chr17:56912380 | T | G | 1 | a0001c0001t0001g0209 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.597+1012A>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912380 | |||||||
| chr17:56912382 | C | G | 1 | a0001c0001t0001g0209 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.597+1010G>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912382 | |||||||
| chr17:56912384 | C | G | 1 | a0001c0001t0001g0209 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.597+1008G>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912384 | |||||||
| chr17:56912385 | A | G | 1 | a0001c0001t0001g0209 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.597+1007T>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912385 | |||||||
| chr17:56912386 | A | G | 1 | a0001c0001t0001g0209 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.597+1006T>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912386 | |||||||
| chr17:56912387 | A | G | 1 | a0001c0001t0001g0209 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.597+1005T>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912387 | |||||||
| chr17:56912389 | T | G | 1 | a0001c0001t0001g0209 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.597+1003A>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912389 | |||||||
| chr17:56912390 | C | G | 1 | a0001c0001t0001g0209 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.597+1002G>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912390 | |||||||
| chr17:56912391 | A | G | 1 | a0001c0001t0001g0209 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.597+1001T>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912391 | |||||||
| chr17:56912392 | C | G | 1 | a0001c0001t0001g0209 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.597+1000G>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912392 | |||||||
| chr17:56912393 | A | G | 1 | a0001c0001t0001g0209 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.597+999T>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912393 | |||||||
| chr17:56912394 | C | G | 1 | a0001c0001t0001g0209 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.597+998G>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912394 | |||||||
| chr17:56912397 | C | G | 1 | a0001c0001t0001g0209 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.597+995G>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912397 | |||||||
| chr17:56912398 | C | G | 1 | a0001c0001t0001g0209 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.597+994G>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912398 | |||||||
| chr17:56912399 | A | G | 1 | a0001c0001t0001g0209 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.597+993T>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912399 | |||||||
| chr17:56912402 | A | G | 1 | a0001c0001t0001g0209 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.597+990T>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912402 | |||||||
| chr17:56912403 | C | G | 1 | a0001c0001t0001g0209 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.597+989G>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912403 | |||||||
| chr17:56912406 | A | G | 1 | a0001c0001t0001g0209 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.597+986T>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912406 | |||||||
| chr17:56912409 | A | G | 1 | a0001c0001t0001g0209 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.597+983T>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912409 | |||||||
| chr17:56912410 | C | G | 1 | a0001c0001t0001g0209 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.597+982G>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912410 | |||||||
| chr17:56912411 | A | G | 1 | a0001c0001t0001g0209 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.597+981T>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912411 | |||||||
| chr17:56912412 | C | G | 1 | a0001c0001t0001g0209 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.597+980G>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912412 | |||||||
| chr17:56912413 | T | G | 1 | a0001c0001t0001g0209 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.597+979A>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912413 | |||||||
| chr17:56912414 | A | G | 1 | a0001c0001t0001g0209 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.597+978T>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912414 | |||||||
| chr17:56912415 | T | G | 1 | a0001c0001t0001g0209 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.597+977A>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912415 | |||||||
| chr17:56912458 | T | G | 1 | a0001c0001t0001g0210 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.597+934A>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912458 | |||||||
| chr17:56912467 | C | T | 14 | a0001c0001t0002g0016 a0001c0001t0002g0075 a0001c0001t0002g0077 others(11): Show |
19 | HG01099.hp1 HG02257.hp1 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.597+925G>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912467 | |||||||
| chr17:56912509 | C | G | 1 | a0001c0001t0002g0074 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.597+883G>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912509 | |||||||
| chr17:56912530 | C | T | 4 | a0001c0001t0001g0070 a0001c0001t0001g0072 a0001c0001t0001g0073 others(1): Show |
4 | HG02258.hp1 HG02976.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.597+862G>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912530 | |||||||
| chr17:56912813 | T | G | 1 | a0001c0001t0008g0211 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.597+579A>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912813 | |||||||
| chr17:56912838 | A | ATTTGAAT others(3): Show |
1 | a0001c0001t0005g0214 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.597+553_597+554ins others(10): Show |
TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912838 | |||||||
| chr17:56912842 | A | T | 1 | a0001c0001t0005g0214 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.597+550T>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912842 | |||||||
| chr17:56912844 | C | A | 1 | a0001c0001t0005g0214 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.597+548G>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912844 | |||||||
| chr17:56912845 | A | T | 1 | a0001c0001t0005g0214 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.597+547T>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912845 | |||||||
| chr17:56912846 | T | G | 1 | a0001c0001t0005g0214 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.597+546A>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912846 | |||||||
| chr17:56912850 | A | T | 1 | a0001c0001t0005g0214 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.597+542T>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912850 | |||||||
| chr17:56912857 | G | T | 1 | a0001c0001t0005g0214 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.597+535C>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912857 | |||||||
| chr17:56912858 | G | T | 1 | a0001c0001t0005g0214 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.597+534C>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912858 | |||||||
| chr17:56912859 | C | A | 1 | a0001c0001t0005g0214 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.597+533G>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912859 | |||||||
| chr17:56912859 | C | T | 1 | a0001c0001t0003g0026 | 2 | HG01516.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.597+533G>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912859 | |||||||
| chr17:56912860 | G | A | 2 | a0001c0001t0001g0212 a0001c0001t0001g0213 |
2 | HG01099.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.597+532C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912860 | |||||||
| chr17:56912860 | G | C | 1 | a0001c0001t0005g0214 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.597+532C>G | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912860 | |||||||
| chr17:56912862 | A | T | 1 | a0001c0001t0005g0214 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.597+530T>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912862 | |||||||
| chr17:56912863 | G | C | 1 | a0001c0001t0005g0214 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.597+529C>G | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912863 | |||||||
| chr17:56912866 | G | T | 1 | a0001c0001t0005g0214 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.597+526C>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912866 | |||||||
| chr17:56912872 | G | C | 1 | a0001c0001t0005g0214 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.597+520C>G | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912872 | |||||||
| chr17:56912876 | T | C | 1 | a0001c0001t0005g0214 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.597+516A>G | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912876 | |||||||
| chr17:56912877 | T | C | 1 | a0001c0001t0005g0214 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.597+515A>G | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912877 | |||||||
| chr17:56912878 | A | G | 1 | a0001c0001t0005g0214 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.597+514T>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912878 | |||||||
| chr17:56912882 | A | T | 1 | a0001c0001t0005g0214 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.597+510T>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912882 | |||||||
| chr17:56912888 | T | G | 1 | a0001c0001t0005g0214 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.597+504A>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912888 | |||||||
| chr17:56913008 | T | C | 9 | a0003c0003t0007g0022 a0003c0003t0007g0053 a0003c0003t0010g0015 others(6): Show |
12 | HG02257.hp1 HG02451.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.597+384A>G | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56913008 | |||||||
| chr17:56913258 | T | C | 1 | a0002c0002t0002g0069 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.597+134A>G | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56913258 | |||||||
| chr17:56913291 | C | CT | 17 | a0001c0001t0004g0024 a0001c0001t0004g0060 a0001c0001t0004g0061 others(14): Show |
37 | HG00639.hp1 HG00735.hp2 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.597+100dupA | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56913291 | |||||||
| chr17:56913343 | C | A | 2 | a0006c0006t0007g0056 a0010c0015t0002g0215 |
2 | HG03139.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.597+49G>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56913343 |