Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 7726 |
| ensemblid | ENSG00000234127.9 |
| hgncid | 12962 |
| symbol | TRIM26 |
| name | tripartite motif containing 26 |
| refseq_nuc | NM_003449.5 |
| refseq_prot | NP_003440.1 |
| ensembl_nuc | ENST00000454678.7 |
| ensembl_prot | ENSP00000410446.2 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 30184455 |
| end | 30213406 |
| strand | - |
| ver | v1.2 |
| region | chr6:30184455-30213406 |
| region5000 | chr6:30179455-30218406 |
| regionname0 | TRIM26_chr6_30184455_30213406 |
| regionname5000 | TRIM26_chr6_30179455_30218406 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 539 | 410 | 96 | 74 | 183 | 15 | 41 | 139 | TRIM26_chr6_30179455_30218406 | TRIM26 | MATSA others(534): Show |
chr6 | 30179455 | 30218406 |
| a0002 | 0/0 | 539 | 22 | 0 | 6 | 15 | 0 | 1 | 12 | TRIM26_chr6_30179455_30218406 | TRIM26 | MATSA others(534): Show |
chr6 | 30179455 | 30218406 |
| a0003 | 0/0 | 539 | 7 | 0 | 0 | 1 | 0 | 6 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | MATSA others(534): Show |
chr6 | 30179455 | 30218406 |
| a0004 | 0/0 | 539 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TRIM26_chr6_30179455_30218406 | TRIM26 | MATSA others(534): Show |
chr6 | 30179455 | 30218406 |
| a0005 | 0/0 | 539 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | MATSA others(534): Show |
chr6 | 30179455 | 30218406 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1617 | 230 | 35 | 37 | 123 | 9 | 25 | TRIM26_chr6_30179455_30218406 | TRIM26 | ATGGC others(1612): Show |
chr6 | 30179455 | 30218406 | ||
| a0001c0002 | 0/0 | 1617 | 86 | 42 | 13 | 23 | 3 | 5 | TRIM26_chr6_30179455_30218406 | TRIM26 | ATGGC others(1612): Show |
chr6 | 30179455 | 30218406 | ||
| a0001c0003 | 0/0 | 1617 | 70 | 8 | 21 | 29 | 3 | 9 | TRIM26_chr6_30179455_30218406 | TRIM26 | ATGGC others(1612): Show |
chr6 | 30179455 | 30218406 | ||
| a0001c0005 | 0/0 | 1617 | 18 | 9 | 0 | 7 | 0 | 2 | TRIM26_chr6_30179455_30218406 | TRIM26 | ATGGC others(1612): Show |
chr6 | 30179455 | 30218406 | ||
| a0001c0007 | 0/0 | 1617 | 3 | 0 | 3 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | ATGGC others(1612): Show |
chr6 | 30179455 | 30218406 | ||
| a0001c0008 | 0/0 | 1617 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | ATGGC others(1612): Show |
chr6 | 30179455 | 30218406 | ||
| a0001c0009 | 0/0 | 1617 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | ATGGC others(1612): Show |
chr6 | 30179455 | 30218406 | ||
| a0001c0010 | 0/0 | 1617 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | ATGGC others(1612): Show |
chr6 | 30179455 | 30218406 | ||
| a0002c0004 | 0/0 | 1617 | 22 | 0 | 6 | 15 | 0 | 1 | TRIM26_chr6_30179455_30218406 | TRIM26 | ATGGC others(1612): Show |
chr6 | 30179455 | 30218406 | ||
| a0003c0006 | 0/0 | 1617 | 7 | 0 | 0 | 1 | 0 | 6 | TRIM26_chr6_30179455_30218406 | TRIM26 | ATGGC others(1612): Show |
chr6 | 30179455 | 30218406 | ||
| a0004c0011 | 0/0 | 1617 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | ATGGC others(1612): Show |
chr6 | 30179455 | 30218406 | ||
| a0005c0012 | 0/0 | 1617 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | ATGGC others(1612): Show |
chr6 | 30179455 | 30218406 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3518 | 97 | 31 | 24 | 35 | 2 | 5 | TRIM26_chr6_30179455_30218406 | TRIM26 | GAGCT others(3513): Show |
chr6 | 30179455 | 30218406 |
| a0001c0001t0002 | 0/0 | 3518 | 81 | 0 | 9 | 60 | 3 | 9 | TRIM26_chr6_30179455_30218406 | TRIM26 | GAGCT others(3513): Show |
chr6 | 30179455 | 30218406 |
| a0001c0001t0003 | 0/0 | 3518 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | GAGCT others(3513): Show |
chr6 | 30179455 | 30218406 |
| a0001c0001t0004 | 0/1 | 3518 | 46 | 2 | 4 | 26 | 4 | 9 | TRIM26_chr6_30179455_30218406 | TRIM26 | GAGCT others(3513): Show |
chr6 | 30179455 | 30218406 |
| a0001c0001t0012 | 0/0 | 3518 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM26_chr6_30179455_30218406 | TRIM26 | GAGCT others(3513): Show |
chr6 | 30179455 | 30218406 |
| a0001c0001t0014 | 0/0 | 3518 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | GAGCT others(3513): Show |
chr6 | 30179455 | 30218406 |
| a0001c0001t0022 | 0/0 | 3518 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | GAGCT others(3513): Show |
chr6 | 30179455 | 30218406 |
| a0001c0002t0005 | 0/0 | 3518 | 25 | 18 | 3 | 1 | 0 | 3 | TRIM26_chr6_30179455_30218406 | TRIM26 | GAGCT others(3513): Show |
chr6 | 30179455 | 30218406 |
| a0001c0002t0006 | 0/0 | 3518 | 21 | 0 | 0 | 21 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | GAGCT others(3513): Show |
chr6 | 30179455 | 30218406 |
| a0001c0002t0007 | 0/0 | 3518 | 17 | 9 | 6 | 0 | 2 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | GAGCT others(3513): Show |
chr6 | 30179455 | 30218406 |
| a0001c0002t0008 | 0/0 | 3518 | 12 | 9 | 1 | 0 | 0 | 2 | TRIM26_chr6_30179455_30218406 | TRIM26 | GAGCT others(3513): Show |
chr6 | 30179455 | 30218406 |
| a0001c0002t0010 | 0/0 | 3518 | 6 | 2 | 3 | 0 | 1 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | GAGCT others(3513): Show |
chr6 | 30179455 | 30218406 |
| a0001c0002t0015 | 0/0 | 3518 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | GAGCT others(3513): Show |
chr6 | 30179455 | 30218406 |
| a0001c0002t0017 | 0/0 | 3518 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | GAGCT others(3513): Show |
chr6 | 30179455 | 30218406 |
| a0001c0002t0018 | 0/0 | 3518 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | GAGCT others(3513): Show |
chr6 | 30179455 | 30218406 |
| a0001c0002t0019 | 0/0 | 3518 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | GAGCT others(3513): Show |
chr6 | 30179455 | 30218406 |
| a0001c0002t0020 | 0/0 | 3518 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | GAGCT others(3513): Show |
chr6 | 30179455 | 30218406 |
| a0001c0003t0002 | 0/0 | 3518 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | GAGCT others(3513): Show |
chr6 | 30179455 | 30218406 |
| a0001c0003t0003 | 0/0 | 3518 | 52 | 2 | 16 | 28 | 3 | 3 | TRIM26_chr6_30179455_30218406 | TRIM26 | GAGCT others(3513): Show |
chr6 | 30179455 | 30218406 |
| a0001c0003t0009 | 0/0 | 3517 | 8 | 0 | 3 | 0 | 0 | 5 | TRIM26_chr6_30179455_30218406 | TRIM26 | GAGCT others(3512): Show |
chr6 | 30179455 | 30218406 |
| a0001c0003t0011 | 0/0 | 3518 | 5 | 4 | 1 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | GAGCT others(3513): Show |
chr6 | 30179455 | 30218406 |
| a0001c0003t0013 | 0/0 | 3518 | 2 | 1 | 1 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | GAGCT others(3513): Show |
chr6 | 30179455 | 30218406 |
| a0001c0003t0021 | 0/0 | 3517 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM26_chr6_30179455_30218406 | TRIM26 | GAGCT others(3512): Show |
chr6 | 30179455 | 30218406 |
| a0001c0003t0025 | 0/0 | 3518 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | GAGCT others(3513): Show |
chr6 | 30179455 | 30218406 |
| a0001c0005t0001 | 0/0 | 3518 | 18 | 9 | 0 | 7 | 0 | 2 | TRIM26_chr6_30179455_30218406 | TRIM26 | GAGCT others(3513): Show |
chr6 | 30179455 | 30218406 |
| a0001c0007t0001 | 0/0 | 3518 | 3 | 0 | 3 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | GAGCT others(3513): Show |
chr6 | 30179455 | 30218406 |
| a0001c0008t0016 | 0/0 | 3518 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | GAGCT others(3513): Show |
chr6 | 30179455 | 30218406 |
| a0001c0009t0001 | 0/0 | 3518 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | GAGCT others(3513): Show |
chr6 | 30179455 | 30218406 |
| a0001c0010t0024 | 0/0 | 3518 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | GAGCT others(3513): Show |
chr6 | 30179455 | 30218406 |
| a0002c0004t0001 | 0/0 | 3518 | 21 | 0 | 6 | 14 | 0 | 1 | TRIM26_chr6_30179455_30218406 | TRIM26 | GAGCT others(3513): Show |
chr6 | 30179455 | 30218406 |
| a0002c0004t0023 | 0/0 | 3518 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | GAGCT others(3513): Show |
chr6 | 30179455 | 30218406 |
| a0003c0006t0005 | 0/0 | 3518 | 7 | 0 | 0 | 1 | 0 | 6 | TRIM26_chr6_30179455_30218406 | TRIM26 | GAGCT others(3513): Show |
chr6 | 30179455 | 30218406 |
| a0004c0011t0002 | 0/0 | 3518 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | GAGCT others(3513): Show |
chr6 | 30179455 | 30218406 |
| a0005c0012t0004 | 0/0 | 3518 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | GAGCT others(3513): Show |
chr6 | 30179455 | 30218406 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0001g0013 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0001g0036 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0001g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0001g0362 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0001g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0001g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0002g0006 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0002g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0002g0014 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0002g0015 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0002g0016 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0002g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0002g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0002g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0002g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0004g0001 | 0/0 | 7 | 1 | 0 | 3 | 1 | 2 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0004g0018 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0004g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0004g0041 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0004g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0004g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0004g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0004g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0004g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0004g0318 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0004g0335 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0004g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0004g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0004g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0004g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0004g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0004g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0004g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0004g0343 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0004g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0004g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0004g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0004g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0004g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0004g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0004g0352 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0004g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0004g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0004g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0004g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0004g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0004g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0004g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0004g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0012g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0012g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0014g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0014g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0001t0022g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0002t0005g0002 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0002t0005g0005 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0002t0005g0011 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0002t0005g0027 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0002t0005g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0002t0005g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0002t0005g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0002t0005g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0002t0005g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0002t0005g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0002t0005g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0002t0005g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0002t0005g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0002t0005g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0002t0006g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0002t0006g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0002t0006g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0002t0006g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0002t0006g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0002t0006g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0002t0006g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0002t0006g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0002t0006g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0002t0006g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0002t0006g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0002t0006g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0002t0006g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0002t0006g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0002t0006g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0002t0006g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0002t0007g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0002t0007g0012 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0002t0007g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0002t0007g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0002t0007g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0002t0007g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0002t0007g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0002t0007g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0002t0007g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0002t0007g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0002t0007g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0002t0008g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0002t0008g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0002t0008g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0002t0008g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0002t0008g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0002t0008g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0002t0008g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0002t0008g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0002t0008g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0002t0008g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0002t0008g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0002t0008g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0002t0010g0004 | 0/0 | 5 | 2 | 2 | 0 | 1 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0002t0010g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0002t0015g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0002t0017g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0002t0018g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0002t0019g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0002t0020g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0003t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0003t0003g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0003t0003g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0003t0003g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0003t0003g0025 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0003t0003g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0003t0003g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0003t0003g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0003t0003g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0003t0003g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0003t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0003t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0003t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0003t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0003t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0003t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0003t0003g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0003t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0003t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0003t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0003t0003g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0003t0003g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0003t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0003t0003g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0003t0003g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0003t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0003t0003g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0003t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0003t0003g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0003t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0003t0003g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0003t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0003t0003g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0003t0003g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0003t0003g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0003t0003g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0003t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0003t0003g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0003t0003g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0003t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0003t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0003t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0003t0003g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0003t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0003t0003g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0003t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0003t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0003t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0003t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0003t0009g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0003t0009g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0003t0009g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0003t0009g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0003t0009g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0003t0009g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0003t0009g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0003t0011g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0003t0011g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0003t0011g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0003t0011g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0003t0011g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0003t0013g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0003t0013g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0003t0021g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0003t0025g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0005t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0005t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0005t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0005t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0005t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0005t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0005t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0005t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0005t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0005t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0005t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0005t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0005t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0005t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0005t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0007t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0007t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0007t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0008t0016g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0009t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0001c0010t0024g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0002c0004t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0002c0004t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0002c0004t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0002c0004t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0002c0004t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0002c0004t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0002c0004t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0002c0004t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0002c0004t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0002c0004t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0002c0004t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0002c0004t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0002c0004t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0002c0004t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0002c0004t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0002c0004t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0002c0004t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0002c0004t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0002c0004t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0002c0004t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0002c0004t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0002c0004t0023g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0003c0006t0005g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0003c0006t0005g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0003c0006t0005g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0003c0006t0005g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0003c0006t0005g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0003c0006t0005g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0003c0006t0005g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0004c0011t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| a0005c0012t0004g0346 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0004 | g0335 | EUR | GBR | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG00099 | hp2 | a0001 | c0002 | t0010 | g0004 | EUR | GBR | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG00140 | hp1 | a0001 | c0001 | t0004 | g0001 | EUR | GBR | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG00140 | hp2 | a0001 | c0003 | t0003 | g0025 | EUR | GBR | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0014 | EUR | FIN | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG00280 | hp2 | a0001 | c0003 | t0003 | g0123 | EUR | FIN | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0015 | EUR | FIN | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG00323 | hp2 | a0001 | c0003 | t0003 | g0101 | EUR | FIN | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | CHS | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0213 | EAS | CHS | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | CHS | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG00423 | hp2 | a0001 | c0001 | t0004 | g0339 | EAS | CHS | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0262 | EAS | CHS | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG00438 | hp2 | a0001 | c0003 | t0003 | g0112 | EAS | CHS | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG00544 | hp1 | a0001 | c0001 | t0004 | g0337 | EAS | CHS | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0266 | EAS | CHS | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG00558 | hp1 | a0001 | c0003 | t0003 | g0104 | EAS | CHS | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG00558 | hp2 | a0001 | c0001 | t0004 | g0353 | EAS | CHS | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0240 | EAS | CHS | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0204 | EAS | CHS | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG00609 | hp1 | a0001 | c0001 | t0004 | g0356 | EAS | CHS | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG00609 | hp2 | a0001 | c0003 | t0003 | g0134 | EAS | CHS | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG00621 | hp1 | a0001 | c0003 | t0003 | g0022 | EAS | CHS | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | CHS | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG00639 | hp1 | a0001 | c0007 | t0001 | g0165 | AMR | PUR | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG00673 | hp1 | a0002 | c0004 | t0001 | g0216 | EAS | CHS | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG00673 | hp2 | a0001 | c0003 | t0003 | g0122 | EAS | CHS | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0253 | AMR | PUR | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0296 | AMR | PUR | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG00735 | hp1 | a0001 | c0001 | t0004 | g0348 | AMR | PUR | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG00738 | hp1 | a0001 | c0003 | t0009 | g0147 | AMR | PUR | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG00738 | hp2 | a0001 | c0002 | t0010 | g0004 | AMR | PUR | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0250 | AMR | PUR | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG00741 | hp2 | a0001 | c0002 | t0005 | g0071 | AMR | PUR | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0015 | AMR | PUR | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG01069 | hp2 | a0001 | c0002 | t0010 | g0082 | AMR | PUR | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0331 | AMR | PUR | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG01070 | hp2 | a0001 | c0002 | t0010 | g0004 | AMR | PUR | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0015 | AMR | PUR | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0332 | AMR | PUR | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG01074 | hp1 | a0001 | c0002 | t0007 | g0020 | AMR | PUR | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG01074 | hp2 | a0001 | c0001 | t0004 | g0354 | AMR | PUR | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0292 | AMR | PUR | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0256 | AMR | PUR | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG01099 | hp1 | a0001 | c0002 | t0007 | g0072 | AMR | PUR | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0222 | AMR | PUR | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG01106 | hp2 | a0001 | c0002 | t0005 | g0011 | AMR | PUR | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | PUR | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG01109 | hp2 | a0001 | c0003 | t0009 | g0145 | AMR | PUR | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG01167 | hp1 | a0001 | c0002 | t0007 | g0077 | AMR | PUR | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG01167 | hp2 | a0002 | c0004 | t0001 | g0221 | AMR | PUR | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG01168 | hp1 | a0002 | c0004 | t0001 | g0200 | AMR | PUR | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0329 | AMR | PUR | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG01169 | hp1 | a0001 | c0002 | t0007 | g0078 | AMR | PUR | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0330 | AMR | PUR | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0323 | AMR | PUR | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG01175 | hp2 | a0001 | c0002 | t0005 | g0079 | AMR | PUR | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG01243 | hp2 | a0001 | c0003 | t0013 | g0315 | AMR | PUR | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0300 | AMR | CLM | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG01255 | hp2 | a0001 | c0003 | t0011 | g0051 | AMR | CLM | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG01256 | hp1 | a0001 | c0003 | t0003 | g0117 | AMR | CLM | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG01256 | hp2 | a0001 | c0007 | t0001 | g0161 | AMR | CLM | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0324 | AMR | CLM | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG01257 | hp2 | a0001 | c0002 | t0008 | g0093 | AMR | CLM | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG01258 | hp1 | a0001 | c0003 | t0003 | g0110 | AMR | CLM | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0322 | AMR | CLM | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG01261 | hp1 | a0001 | c0001 | t0004 | g0365 | AMR | CLM | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG01261 | hp2 | a0001 | c0002 | t0007 | g0012 | AMR | CLM | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0016 | AMR | CLM | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG01358 | hp1 | a0001 | c0003 | t0003 | g0125 | AMR | CLM | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0299 | AMR | CLM | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0295 | AMR | CLM | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0248 | AMR | CLM | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG01496 | hp1 | a0001 | c0007 | t0001 | g0164 | AMR | CLM | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG01496 | hp2 | a0001 | c0003 | t0003 | g0102 | AMR | CLM | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0319 | EUR | IBS | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG01516 | hp2 | a0001 | c0002 | t0007 | g0012 | EUR | IBS | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG01517 | hp1 | a0001 | c0002 | t0007 | g0075 | EUR | IBS | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG01517 | hp2 | a0001 | c0001 | t0004 | g0343 | EUR | IBS | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG01884 | hp1 | a0001 | c0002 | t0008 | g0096 | AFR | ACB | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG01884 | hp2 | a0001 | c0002 | t0005 | g0002 | AFR | ACB | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG01891 | hp1 | a0001 | c0002 | t0005 | g0002 | AFR | ACB | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG01891 | hp2 | a0001 | c0002 | t0018 | g0066 | AFR | ACB | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG01928 | hp1 | a0002 | c0004 | t0001 | g0235 | AMR | PEL | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG01928 | hp2 | a0001 | c0003 | t0003 | g0130 | AMR | PEL | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG01934 | hp1 | a0001 | c0002 | t0007 | g0020 | AMR | PEL | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG01934 | hp2 | a0001 | c0003 | t0003 | g0127 | AMR | PEL | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG01943 | hp1 | a0002 | c0004 | t0001 | g0195 | AMR | PEL | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG01943 | hp2 | a0001 | c0003 | t0003 | g0024 | AMR | PEL | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | PEL | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG01952 | hp2 | a0001 | c0003 | t0003 | g0137 | AMR | PEL | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG01975 | hp1 | a0001 | c0003 | t0009 | g0144 | AMR | PEL | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG01975 | hp2 | a0001 | c0003 | t0003 | g0139 | AMR | PEL | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PEL | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG01978 | hp2 | a0001 | c0003 | t0003 | g0024 | AMR | PEL | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PEL | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0238 | AMR | PEL | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG02004 | hp1 | a0001 | c0003 | t0003 | g0098 | AMR | PEL | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG02004 | hp2 | a0001 | c0003 | t0003 | g0129 | AMR | PEL | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG02015 | hp1 | a0001 | c0005 | t0001 | g0302 | EAS | KHV | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0325 | EAS | KHV | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0239 | EAS | KHV | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0251 | EAS | KHV | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG02040 | hp1 | a0001 | c0003 | t0003 | g0150 | EAS | KHV | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG02040 | hp2 | a0001 | c0002 | t0006 | g0019 | EAS | KHV | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0272 | AFR | ACB | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG02055 | hp2 | a0001 | c0002 | t0005 | g0152 | AFR | ACB | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | KHV | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG02056 | hp2 | a0001 | c0005 | t0001 | g0017 | EAS | KHV | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0275 | EAS | KHV | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0227 | EAS | KHV | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0278 | EAS | KHV | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG02074 | hp2 | a0003 | c0006 | t0005 | g0050 | EAS | KHV | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG02080 | hp1 | a0001 | c0001 | t0004 | g0018 | EAS | KHV | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG02080 | hp2 | a0001 | c0005 | t0001 | g0311 | EAS | KHV | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG02083 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | KHV | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG02083 | hp2 | a0001 | c0003 | t0003 | g0022 | EAS | KHV | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG02129 | hp1 | a0001 | c0005 | t0001 | g0017 | EAS | KHV | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0252 | EAS | KHV | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG02135 | hp1 | a0001 | c0010 | t0024 | g0345 | EAS | KHV | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0276 | EAS | KHV | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG02145 | hp1 | a0001 | c0003 | t0011 | g0052 | AFR | ACB | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG02145 | hp2 | a0001 | c0002 | t0008 | g0086 | AFR | ACB | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0298 | AMR | PEL | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG02148 | hp2 | a0001 | c0003 | t0003 | g0132 | AMR | PEL | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG02155 | hp1 | a0001 | c0003 | t0003 | g0140 | EAS | CDX | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0215 | EAS | CDX | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG02165 | hp1 | a0001 | c0001 | t0003 | g0105 | EAS | CDX | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | CDX | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG02257 | hp1 | a0001 | c0002 | t0017 | g0088 | AFR | ACB | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0271 | AFR | ACB | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0361 | AFR | ACB | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG02258 | hp2 | a0001 | c0002 | t0008 | g0084 | AFR | ACB | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG02273 | hp1 | a0001 | c0003 | t0003 | g0128 | AMR | PEL | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG02273 | hp2 | a0002 | c0004 | t0001 | g0196 | AMR | PEL | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG02280 | hp1 | a0001 | c0002 | t0005 | g0005 | AFR | ACB | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG02280 | hp2 | a0001 | c0005 | t0001 | g0308 | AFR | ACB | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG02293 | hp1 | a0002 | c0004 | t0001 | g0201 | AMR | PEL | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PEL | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0260 | AMR | PEL | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG02300 | hp2 | a0001 | c0003 | t0003 | g0121 | AMR | PEL | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG02451 | hp1 | a0001 | c0005 | t0001 | g0037 | AFR | ACB | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG02451 | hp2 | a0001 | c0002 | t0020 | g0119 | AFR | ACB | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG02523 | hp1 | a0001 | c0002 | t0006 | g0019 | EAS | KHV | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG02523 | hp2 | a0001 | c0001 | t0022 | g0281 | EAS | KHV | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0364 | AFR | GWD | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG02572 | hp2 | a0001 | c0002 | t0005 | g0011 | AFR | GWD | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG02602 | hp1 | a0001 | c0003 | t0021 | g0143 | SAS | PJL | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG02602 | hp2 | a0001 | c0003 | t0003 | g0100 | SAS | PJL | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG02615 | hp1 | a0001 | c0005 | t0001 | g0037 | AFR | GWD | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG02615 | hp2 | a0001 | c0002 | t0005 | g0002 | AFR | GWD | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | GWD | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG02622 | hp2 | a0001 | c0002 | t0005 | g0068 | AFR | GWD | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG02630 | hp1 | a0001 | c0002 | t0019 | g0095 | AFR | GWD | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | GWD | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG02647 | hp1 | a0001 | c0002 | t0008 | g0080 | AFR | GWD | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG02647 | hp2 | a0001 | c0005 | t0001 | g0309 | AFR | GWD | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0259 | SAS | PJL | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG02683 | hp2 | a0001 | c0003 | t0003 | g0099 | SAS | PJL | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0362 | SAS | PJL | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0264 | SAS | PJL | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG02717 | hp1 | a0001 | c0003 | t0011 | g0149 | AFR | GWD | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG02717 | hp2 | a0001 | c0002 | t0008 | g0087 | AFR | GWD | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG02723 | hp1 | a0001 | c0002 | t0008 | g0085 | AFR | GWD | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG02735 | hp1 | a0003 | c0006 | t0005 | g0048 | SAS | PJL | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG02735 | hp2 | a0001 | c0005 | t0001 | g0310 | SAS | PJL | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG02738 | hp1 | a0001 | c0001 | t0012 | g0094 | SAS | PJL | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG02738 | hp2 | a0001 | c0002 | t0008 | g0092 | SAS | PJL | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0247 | AFR | GWD | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG02818 | hp1 | a0001 | c0005 | t0001 | g0312 | AFR | GWD | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG02818 | hp2 | a0001 | c0002 | t0007 | g0008 | AFR | GWD | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0246 | AFR | GWD | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG02886 | hp2 | a0001 | c0009 | t0001 | g0192 | AFR | GWD | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG02895 | hp1 | a0001 | c0005 | t0001 | g0314 | AFR | GWD | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG02895 | hp2 | a0001 | c0002 | t0005 | g0151 | AFR | GWD | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG02896 | hp1 | a0001 | c0005 | t0001 | g0301 | AFR | GWD | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0294 | AFR | GWD | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG02922 | hp1 | a0001 | c0003 | t0003 | g0133 | AFR | ESN | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG02922 | hp2 | a0001 | c0002 | t0005 | g0005 | AFR | ESN | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG02965 | hp1 | a0001 | c0002 | t0007 | g0012 | AFR | ESN | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG02965 | hp2 | a0001 | c0002 | t0005 | g0005 | AFR | ESN | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | ESN | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG02970 | hp2 | a0001 | c0002 | t0005 | g0005 | AFR | ESN | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0273 | AFR | ESN | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG02976 | hp2 | a0001 | c0001 | t0004 | g0306 | AFR | ESN | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0214 | SAS | PJL | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG03017 | hp2 | a0003 | c0006 | t0005 | g0044 | SAS | PJL | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG03041 | hp1 | a0001 | c0002 | t0007 | g0073 | AFR | GWD | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0291 | AFR | GWD | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG03098 | hp1 | a0001 | c0003 | t0013 | g0316 | AFR | MSL | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG03098 | hp2 | a0001 | c0002 | t0005 | g0002 | AFR | MSL | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG03130 | hp1 | a0001 | c0002 | t0005 | g0011 | AFR | ESN | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG03130 | hp2 | a0001 | c0002 | t0007 | g0074 | AFR | ESN | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG03139 | hp1 | a0001 | c0002 | t0007 | g0008 | AFR | ESN | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0363 | AFR | ESN | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | ESN | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG03195 | hp2 | a0001 | c0002 | t0007 | g0021 | AFR | ESN | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG03209 | hp1 | a0001 | c0003 | t0011 | g0053 | AFR | MSL | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0297 | AFR | MSL | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG03225 | hp1 | a0001 | c0002 | t0008 | g0083 | AFR | MSL | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0286 | AFR | MSL | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG03239 | hp1 | a0001 | c0001 | t0004 | g0344 | SAS | PJL | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0230 | SAS | PJL | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0284 | AFR | MSL | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG03453 | hp2 | a0001 | c0008 | t0016 | g0081 | AFR | MSL | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG03486 | hp1 | a0001 | c0002 | t0007 | g0021 | AFR | MSL | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | MSL | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG03490 | hp1 | a0001 | c0003 | t0009 | g0146 | SAS | PJL | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG03490 | hp2 | a0001 | c0001 | t0004 | g0336 | SAS | PJL | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG03492 | hp1 | a0001 | c0001 | t0004 | g0018 | SAS | PJL | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG03492 | hp2 | a0001 | c0003 | t0009 | g0026 | SAS | PJL | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG03516 | hp1 | a0001 | c0001 | t0014 | g0267 | AFR | ESN | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG03516 | hp2 | a0001 | c0002 | t0005 | g0154 | AFR | ESN | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG03540 | hp1 | a0001 | c0003 | t0025 | g0355 | AFR | GWD | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0287 | AFR | GWD | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG03579 | hp1 | a0001 | c0005 | t0001 | g0313 | AFR | MSL | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0293 | AFR | MSL | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG03654 | hp1 | a0003 | c0006 | t0005 | g0046 | SAS | PJL | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG03654 | hp2 | a0001 | c0001 | t0012 | g0090 | SAS | PJL | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG03669 | hp1 | a0001 | c0003 | t0009 | g0142 | SAS | PJL | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG03669 | hp2 | a0002 | c0004 | t0001 | g0199 | SAS | PJL | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG03688 | hp1 | a0001 | c0003 | t0009 | g0026 | SAS | STU | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0006 | SAS | STU | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG03704 | hp1 | a0001 | c0001 | t0004 | g0285 | SAS | PJL | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG03704 | hp2 | a0003 | c0006 | t0005 | g0049 | SAS | PJL | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG03710 | hp1 | a0001 | c0001 | t0004 | g0018 | SAS | PJL | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG03710 | hp2 | a0001 | c0003 | t0003 | g0118 | SAS | PJL | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG03831 | hp1 | a0001 | c0002 | t0005 | g0069 | SAS | BEB | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | BEB | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG03834 | hp1 | a0001 | c0002 | t0005 | g0027 | SAS | BEB | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG03834 | hp2 | a0001 | c0001 | t0004 | g0001 | SAS | BEB | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | BEB | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0206 | SAS | BEB | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0223 | SAS | BEB | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG03942 | hp2 | a0001 | c0003 | t0009 | g0141 | SAS | BEB | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0263 | SAS | STU | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0258 | SAS | STU | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG04184 | hp1 | a0001 | c0002 | t0005 | g0076 | SAS | BEB | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG04184 | hp2 | a0001 | c0001 | t0004 | g0041 | SAS | BEB | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0320 | SAS | STU | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG04199 | hp2 | a0001 | c0005 | t0001 | g0304 | SAS | STU | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0168 | SAS | STU | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG04204 | hp2 | a0001 | c0001 | t0004 | g0041 | SAS | STU | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG04228 | hp1 | a0001 | c0001 | t0004 | g0001 | SAS | STU | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG04228 | hp2 | a0003 | c0006 | t0005 | g0047 | SAS | STU | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA18522 | hp1 | a0001 | c0002 | t0008 | g0091 | AFR | YRI | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | YRI | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA18612 | hp1 | a0002 | c0004 | t0001 | g0198 | EAS | CHB | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA18612 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | CHB | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA18747 | hp1 | a0002 | c0004 | t0001 | g0194 | EAS | CHB | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA18747 | hp2 | a0001 | c0001 | t0004 | g0351 | EAS | CHB | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | YRI | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA18906 | hp2 | a0001 | c0001 | t0014 | g0269 | AFR | YRI | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA18939 | hp1 | a0001 | c0002 | t0006 | g0064 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA18943 | hp1 | a0001 | c0001 | t0004 | g0358 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0274 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA18946 | hp1 | a0001 | c0003 | t0003 | g0107 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA18946 | hp2 | a0004 | c0011 | t0002 | g0277 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA18948 | hp2 | a0001 | c0002 | t0005 | g0027 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA18949 | hp1 | a0001 | c0002 | t0006 | g0058 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA18952 | hp2 | a0001 | c0001 | t0004 | g0359 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA18953 | hp1 | a0001 | c0001 | t0004 | g0349 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA18953 | hp2 | a0001 | c0003 | t0003 | g0124 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA18956 | hp1 | a0001 | c0003 | t0003 | g0108 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA18956 | hp2 | a0002 | c0004 | t0001 | g0242 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA18959 | hp1 | a0001 | c0002 | t0006 | g0065 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA18960 | hp1 | a0001 | c0001 | t0004 | g0350 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA18964 | hp1 | a0001 | c0001 | t0004 | g0043 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA18964 | hp2 | a0001 | c0002 | t0015 | g0063 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA18965 | hp1 | a0001 | c0002 | t0006 | g0062 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA18966 | hp1 | a0001 | c0001 | t0004 | g0042 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0280 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA18967 | hp1 | a0001 | c0003 | t0003 | g0103 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA18968 | hp1 | a0001 | c0002 | t0006 | g0055 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA18969 | hp1 | a0001 | c0003 | t0003 | g0111 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA18970 | hp1 | a0001 | c0003 | t0003 | g0136 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA18970 | hp2 | a0001 | c0002 | t0006 | g0056 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA18972 | hp2 | a0001 | c0003 | t0003 | g0157 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0255 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA18974 | hp1 | a0002 | c0004 | t0001 | g0236 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA18974 | hp2 | a0001 | c0002 | t0006 | g0009 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA18975 | hp1 | a0001 | c0003 | t0003 | g0131 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA18975 | hp2 | a0001 | c0001 | t0004 | g0360 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA18979 | hp2 | a0001 | c0003 | t0003 | g0116 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA18980 | hp1 | a0001 | c0003 | t0003 | g0106 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA18982 | hp1 | a0001 | c0002 | t0006 | g0070 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA18983 | hp2 | a0001 | c0001 | t0004 | g0160 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0334 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA18986 | hp1 | a0001 | c0003 | t0003 | g0138 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA18987 | hp1 | a0001 | c0002 | t0006 | g0009 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA18987 | hp2 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA18989 | hp1 | a0002 | c0004 | t0001 | g0218 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA18990 | hp1 | a0001 | c0003 | t0003 | g0025 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA18993 | hp1 | a0002 | c0004 | t0001 | g0197 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA18998 | hp1 | a0001 | c0002 | t0006 | g0158 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA18999 | hp2 | a0001 | c0001 | t0004 | g0341 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA19000 | hp1 | a0001 | c0003 | t0002 | g0317 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA19000 | hp2 | a0001 | c0003 | t0003 | g0023 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0333 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA19001 | hp2 | a0001 | c0001 | t0004 | g0357 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA19002 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA19002 | hp2 | a0001 | c0003 | t0003 | g0023 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA19003 | hp1 | a0001 | c0001 | t0004 | g0347 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA19003 | hp2 | a0002 | c0004 | t0001 | g0219 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0279 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA19004 | hp2 | a0001 | c0001 | t0004 | g0040 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA19005 | hp1 | a0001 | c0005 | t0001 | g0017 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA19005 | hp2 | a0001 | c0003 | t0003 | g0109 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA19009 | hp1 | a0001 | c0001 | t0004 | g0340 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA19011 | hp1 | a0001 | c0003 | t0003 | g0135 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA19030 | hp1 | a0001 | c0002 | t0007 | g0008 | AFR | LWK | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA19030 | hp2 | a0001 | c0002 | t0008 | g0097 | AFR | LWK | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA19054 | hp2 | a0001 | c0001 | t0004 | g0042 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA19055 | hp2 | a0002 | c0004 | t0001 | g0166 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA19056 | hp1 | a0002 | c0004 | t0001 | g0220 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA19057 | hp1 | a0002 | c0004 | t0001 | g0217 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA19058 | hp1 | a0001 | c0001 | t0004 | g0040 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA19059 | hp1 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA19059 | hp2 | a0002 | c0004 | t0001 | g0202 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA19062 | hp1 | a0001 | c0002 | t0006 | g0061 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA19063 | hp2 | a0001 | c0003 | t0003 | g0126 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA19065 | hp1 | a0002 | c0004 | t0001 | g0234 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA19068 | hp1 | a0001 | c0002 | t0006 | g0067 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA19068 | hp2 | a0001 | c0003 | t0003 | g0113 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA19070 | hp1 | a0001 | c0001 | t0004 | g0043 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA19072 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA19072 | hp2 | a0001 | c0005 | t0001 | g0305 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA19080 | hp1 | a0001 | c0003 | t0003 | g0120 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA19080 | hp2 | a0001 | c0005 | t0001 | g0303 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA19082 | hp1 | a0001 | c0001 | t0004 | g0338 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA19082 | hp2 | a0001 | c0002 | t0006 | g0010 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA19083 | hp2 | a0001 | c0002 | t0006 | g0010 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA19084 | hp1 | a0002 | c0004 | t0001 | g0282 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA19086 | hp1 | a0001 | c0002 | t0006 | g0060 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA19086 | hp2 | a0001 | c0003 | t0003 | g0155 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA19087 | hp2 | a0001 | c0002 | t0006 | g0057 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA19088 | hp2 | a0001 | c0002 | t0006 | g0009 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA19089 | hp1 | a0001 | c0002 | t0006 | g0059 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA19090 | hp1 | a0002 | c0004 | t0023 | g0162 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA19091 | hp2 | a0001 | c0002 | t0006 | g0010 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA19240 | hp1 | a0001 | c0002 | t0005 | g0156 | AFR | YRI | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA19240 | hp2 | a0001 | c0002 | t0005 | g0002 | AFR | YRI | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA20129 | hp1 | a0001 | c0002 | t0010 | g0004 | AFR | ASW | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ASW | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA20752 | hp1 | a0005 | c0012 | t0004 | g0346 | EUR | TSI | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA20752 | hp2 | a0001 | c0001 | t0004 | g0318 | EUR | TSI | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0188 | EUR | TSI | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0159 | EUR | TSI | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA20905 | hp1 | a0003 | c0006 | t0005 | g0045 | SAS | GIH | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA20905 | hp2 | a0001 | c0002 | t0008 | g0089 | SAS | GIH | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG01123 | hp1 | a0001 | c0001 | t0004 | g0342 | AMR | CLM | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG01123 | hp2 | a0001 | c0003 | t0003 | g0114 | AMR | CLM | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG02109 | hp1 | a0001 | c0005 | t0001 | g0307 | AFR | ACB | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0289 | AFR | ACB | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG02486 | hp1 | a0001 | c0002 | t0005 | g0002 | AFR | ACB | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG02559 | hp1 | a0001 | c0003 | t0011 | g0148 | AFR | ACB | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG02559 | hp2 | a0001 | c0001 | t0004 | g0001 | AFR | ACB | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG03471 | hp1 | a0001 | c0002 | t0005 | g0153 | AFR | MSL | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0290 | AFR | MSL | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0288 | AFR | USA | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| HG06807 | hp2 | a0001 | c0002 | t0010 | g0004 | AFR | USA | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA20300 | hp1 | a0001 | c0003 | t0003 | g0115 | AFR | USA | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA20300 | hp2 | a0001 | c0002 | t0007 | g0054 | AFR | USA | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0283 | AFR | LWK | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | LWK | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0004 | g0352 | REF | REF | TRIM26_chr6_30179455_30218406 | TRIM26 | chr6 | 30179455 | 30218406 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:30196690 | C | A | 1 | a0002 | 22 | HG00673.hp1 HG01167.hp2 HG01168.hp1 others(19): Show |
missense_variant | MODERATE | c.591G>T | p.Gln197His | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/10 | 1068/3518 | 591/1620 | 197/539 | chr6 | 30196690 | |||
| chr6:30198698 | C | T | 1 | a0003 | 7 | HG02074.hp2 HG02735.hp1 HG03017.hp2 others(4): Show |
missense_variant | MODERATE | c.406G>A | p.Val136Ile | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 4/10 | 883/3518 | 406/1620 | 136/539 | chr6 | 30198698 | |||
| chr6:30198838 | G | A | 1 | a0004 | 1 | NA18946.hp2 | missense_variant | MODERATE | c.266C>T | p.Pro89Leu | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 4/10 | 743/3518 | 266/1620 | 89/539 | chr6 | 30198838 | |||
| chr6:30198847 | C | A | 1 | a0005 | 1 | NA20752.hp1 | missense_variant | MODERATE | c.257G>T | p.Gly86Val | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 4/10 | 734/3518 | 257/1620 | 86/539 | chr6 | 30198847 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:30186272 | G | A | 1 | a0001c0007 | 3 | HG00639.hp1 HG01256.hp2 HG01496.hp1 |
synonymous_variant | LOW | c.1224C>T | p.Asp408Asp | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 10/10 | 1701/3518 | 1224/1620 | 408/539 | chr6 | 30186272 | |||
| chr6:30186422 | T | C | 2 | a0001c0002 a0001c0003 |
156 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(153): Show |
synonymous_variant | LOW | c.1074A>G | p.Leu358Leu | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 10/10 | 1551/3518 | 1074/1620 | 358/539 | chr6 | 30186422 | |||
| chr6:30189192 | C | T | 1 | a0001c0009 | 1 | HG02886.hp2 | synonymous_variant | LOW | c.912G>A | p.Leu304Leu | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 9/10 | 1389/3518 | 912/1620 | 304/539 | chr6 | 30189192 | |||
| chr6:30196720 | G | A | 1 | a0001c0005 | 18 | HG02015.hp1 HG02056.hp2 HG02080.hp2 others(15): Show |
synonymous_variant | LOW | c.561C>T | p.Tyr187Tyr | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/10 | 1038/3518 | 561/1620 | 187/539 | chr6 | 30196720 | |||
| chr6:30198441 | G | A | 1 | a0001c0010 | 1 | HG02135.hp1 | synonymous_variant | LOW | c.522C>T | p.Ile174Ile | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 5/10 | 999/3518 | 522/1620 | 174/539 | chr6 | 30198441 | |||
| chr6:30198489 | C | T | 3 | a0001c0002 a0001c0008 a0003c0006 |
94 | HG00099.hp2 HG00738.hp2 HG00741.hp2 others(91): Show |
synonymous_variant | LOW | c.474G>A | p.Arg158Arg | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 5/10 | 951/3518 | 474/1620 | 158/539 | chr6 | 30198489 | |||
| chr6:30198855 | C | T | 1 | a0003c0006 | 7 | HG02074.hp2 HG02735.hp1 HG03017.hp2 others(4): Show |
synonymous_variant | LOW | c.249G>A | p.Val83Val | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 4/10 | 726/3518 | 249/1620 | 83/539 | chr6 | 30198855 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:30184486 | T | C | 1 | a0001c0001t0022 | 1 | HG02523.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1390A>G | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 10/10 | 1390 | chr6 | 30184486 | ||||||
| chr6:30184590 | A | G | 2 | a0001c0001t0003 a0001c0003t0003 |
53 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*1286T>C | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 10/10 | 1286 | chr6 | 30184590 | ||||||
| chr6:30184651 | G | A | 1 | a0001c0003t0013 | 2 | HG01243.hp2 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1225C>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 10/10 | 1225 | chr6 | 30184651 | ||||||
| chr6:30184659 | T | A | 1 | a0001c0002t0018 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1217A>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 10/10 | 1217 | chr6 | 30184659 | ||||||
| chr6:30184690 | G | T | 2 | a0001c0002t0010 a0001c0008t0016 |
7 | HG00099.hp2 HG00738.hp2 HG01069.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1186C>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 10/10 | 1186 | chr6 | 30184690 | ||||||
| chr6:30185005 | G | C | 1 | a0001c0002t0017 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*871C>G | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 10/10 | 871 | chr6 | 30185005 | ||||||
| chr6:30185012 | C | T | 5 | a0001c0001t0003 a0001c0003t0003 a0001c0003t0009 others(2): Show |
67 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*864G>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 10/10 | 864 | chr6 | 30185012 | ||||||
| chr6:30185026 | G | A | 1 | a0001c0003t0021 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*850C>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 10/10 | 850 | chr6 | 30185026 | ||||||
| chr6:30185184 | T | C | 2 | a0001c0003t0009 a0001c0003t0021 |
9 | HG00738.hp1 HG01109.hp2 HG01975.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*692A>G | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 10/10 | 692 | chr6 | 30185184 | ||||||
| chr6:30185221 | AG | A | 2 | a0001c0003t0009 a0001c0003t0021 |
9 | HG00738.hp1 HG01109.hp2 HG01975.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*654delC | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 10/10 | 654 | chr6 | 30185221 | ||||||
| chr6:30185276 | C | A | 1 | a0001c0001t0014 | 2 | HG03516.hp1 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*600G>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 10/10 | 600 | chr6 | 30185276 | ||||||
| chr6:30185280 | G | A | 1 | a0001c0010t0024 | 1 | HG02135.hp1 | 3_prime_UTR_variant | MODIFIER | c.*596C>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 10/10 | 596 | chr6 | 30185280 | ||||||
| chr6:30185321 | C | G | 1 | a0002c0004t0023 | 1 | NA19090.hp1 | 3_prime_UTR_variant | MODIFIER | c.*555G>C | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 10/10 | 555 | chr6 | 30185321 | ||||||
| chr6:30185586 | G | A | 1 | a0001c0002t0010 | 6 | HG00099.hp2 HG00738.hp2 HG01069.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*290C>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 10/10 | 290 | chr6 | 30185586 | ||||||
| chr6:30185600 | G | A | 1 | a0001c0002t0015 | 1 | NA18964.hp2 | 3_prime_UTR_variant | MODIFIER | c.*276C>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 10/10 | 276 | chr6 | 30185600 | ||||||
| chr6:30185732 | C | T | 1 | a0001c0003t0025 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*144G>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 10/10 | 144 | chr6 | 30185732 | ||||||
| chr6:30199109 | C | T | 6 | a0001c0002t0008 a0001c0002t0010 a0001c0002t0017 others(3): Show |
22 | HG00099.hp2 HG00738.hp2 HG01069.hp2 others(19): Show |
5_prime_UTR_variant | MODIFIER | c.-6G>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 4/10 | 6 | chr6 | 30199109 | ||||||
| chr6:30199142 | G | A | 1 | a0001c0002t0019 | 1 | HG02630.hp1 | 5_prime_UTR_variant | MODIFIER | c.-39C>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 4/10 | 39 | chr6 | 30199142 | ||||||
| chr6:30199158 | G | A | 4 | a0001c0001t0004 a0001c0001t0012 a0001c0010t0024 others(1): Show |
49 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(46): Show |
5_prime_UTR_variant | MODIFIER | c.-55C>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 4/10 | 55 | chr6 | 30199158 | ||||||
| chr6:30199168 | A | G | 1 | a0001c0002t0007 | 17 | HG01074.hp1 HG01099.hp1 HG01167.hp1 others(14): Show |
5_prime_UTR_variant | MODIFIER | c.-65T>C | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 4/10 | 65 | chr6 | 30199168 | ||||||
| chr6:30199244 | A | G | 2 | a0001c0002t0006 a0001c0002t0015 |
22 | HG02040.hp2 HG02523.hp1 NA18939.hp1 others(19): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-141T>C | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 4/10 | chr6 | 30199244 | |||||||
| chr6:30201052 | C | T | 4 | a0001c0001t0002 a0001c0001t0022 a0001c0003t0002 others(1): Show |
84 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(81): Show |
5_prime_UTR_variant | MODIFIER | c.-179G>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 3/10 | 1949 | chr6 | 30201052 | ||||||
| chr6:30204661 | C | A | 1 | a0001c0003t0025 | 1 | HG03540.hp1 | 5_prime_UTR_variant | MODIFIER | c.-271G>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 2/10 | 5558 | chr6 | 30204661 | ||||||
| chr6:30204736 | A | C | 12 | a0001c0001t0012 a0001c0002t0005 a0001c0002t0006 others(9): Show |
95 | HG00099.hp2 HG00738.hp2 HG00741.hp2 others(92): Show |
5_prime_UTR_variant | MODIFIER | c.-346T>G | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 2/10 | 5633 | chr6 | 30204736 | ||||||
| chr6:30213340 | A | G | 18 | a0001c0001t0003 a0001c0001t0012 a0001c0002t0005 others(15): Show |
163 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(160): Show |
5_prime_UTR_variant | MODIFIER | c.-411T>C | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/10 | 14237 | chr6 | 30213340 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:30186570 | A | AG | 14 | a0001c0001t0002g0034 a0001c0001t0002g0163 a0001c0001t0002g0204 others(11): Show |
15 | HG00408.hp2 HG00597.hp2 HG02027.hp1 others(12): Show |
intron_variant | MODIFIER | c.938-13dupC | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 9/9 | chr6 | 30186570 | |||||||
| chr6:30186573 | G | GA | 41 | a0001c0001t0001g0032 a0001c0001t0001g0038 a0001c0001t0001g0169 others(38): Show |
44 | HG00423.hp2 HG00544.hp1 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.938-16dupT | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 9/9 | chr6 | 30186573 | |||||||
| chr6:30186573 | G | GAA | 47 | a0001c0001t0003g0105 a0001c0002t0005g0005 a0001c0002t0005g0027 others(44): Show |
59 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.938-17_938-16dupTT | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 9/9 | chr6 | 30186573 | |||||||
| chr6:30186573 | G | GAAA | 59 | a0001c0002t0005g0002 a0001c0002t0005g0011 a0001c0002t0005g0068 others(56): Show |
74 | HG00438.hp2 HG00558.hp1 HG00673.hp2 others(71): Show |
intron_variant | MODIFIER | c.938-18_938-16dupTT others(1): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 9/9 | chr6 | 30186573 | |||||||
| chr6:30186573 | GA | G | 17 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(14): Show |
20 | HG00621.hp2 HG00735.hp2 HG01978.hp1 others(17): Show |
intron_variant | MODIFIER | c.938-16delT | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 9/9 | chr6 | 30186573 | |||||||
| chr6:30186574 | A | G | 55 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0014 others(52): Show |
69 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(66): Show |
intron_variant | MODIFIER | c.938-16T>C | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 9/9 | chr6 | 30186574 | |||||||
| chr6:30186897 | G | A | 1 | a0001c0003t0003g0116 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.938-339C>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 9/9 | chr6 | 30186897 | |||||||
| chr6:30186940 | C | T | 1 | a0002c0004t0001g0196 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.938-382G>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 9/9 | chr6 | 30186940 | |||||||
| chr6:30187133 | C | T | 69 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0014 others(66): Show |
84 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.938-575G>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 9/9 | chr6 | 30187133 | |||||||
| chr6:30187151 | G | A | 343 | a0001c0001t0001g0013 a0001c0001t0001g0028 a0001c0001t0001g0029 others(340): Show |
412 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(409): Show |
intron_variant | MODIFIER | c.938-593C>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 9/9 | chr6 | 30187151 | |||||||
| chr6:30187268 | A | C | 343 | a0001c0001t0001g0013 a0001c0001t0001g0028 a0001c0001t0001g0029 others(340): Show |
412 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(409): Show |
intron_variant | MODIFIER | c.938-710T>G | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 9/9 | chr6 | 30187268 | |||||||
| chr6:30187276 | A | T | 12 | a0001c0001t0001g0036 a0001c0001t0001g0243 a0001c0001t0001g0244 others(9): Show |
13 | HG00639.hp1 HG01109.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.938-718T>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 9/9 | chr6 | 30187276 | |||||||
| chr6:30187323 | G | A | 3 | a0001c0001t0002g0254 a0001c0001t0002g0255 a0001c0001t0002g0261 |
3 | NA18973.hp1 NA18995.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.938-765C>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 9/9 | chr6 | 30187323 | |||||||
| chr6:30187331 | C | T | 129 | a0001c0001t0003g0105 a0001c0002t0005g0002 a0001c0002t0005g0005 others(126): Show |
160 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.938-773G>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 9/9 | chr6 | 30187331 | |||||||
| chr6:30187354 | A | G | 131 | a0001c0001t0003g0105 a0001c0002t0005g0002 a0001c0002t0005g0005 others(128): Show |
162 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.938-796T>C | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 9/9 | chr6 | 30187354 | |||||||
| chr6:30187362 | G | A | 3 | a0001c0001t0002g0204 a0001c0001t0002g0213 a0001c0001t0002g0239 |
3 | HG00408.hp2 HG00597.hp2 HG02027.hp1 |
intron_variant | MODIFIER | c.938-804C>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 9/9 | chr6 | 30187362 | |||||||
| chr6:30187369 | C | G | 22 | a0001c0001t0001g0013 a0001c0001t0001g0028 a0001c0001t0001g0029 others(19): Show |
28 | HG00621.hp2 HG00735.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.938-811G>C | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 9/9 | chr6 | 30187369 | |||||||
| chr6:30187372 | G | C | 10 | a0001c0002t0008g0080 a0001c0002t0008g0083 a0001c0002t0008g0084 others(7): Show |
14 | HG00099.hp2 HG00738.hp2 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.938-814C>G | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 9/9 | chr6 | 30187372 | |||||||
| chr6:30187406 | C | T | 1 | a0001c0001t0004g0365 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.938-848G>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 9/9 | chr6 | 30187406 | |||||||
| chr6:30187441 | A | AAAGCTCT others(5): Show |
1 | a0001c0002t0006g0056 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.938-895_938-884dup others(12): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 9/9 | chr6 | 30187441 | |||||||
| chr6:30187533 | C | T | 1 | a0001c0003t0025g0355 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.938-975G>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 9/9 | chr6 | 30187533 | |||||||
| chr6:30187535 | A | T | 1 | a0002c0004t0001g0202 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.938-977T>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 9/9 | chr6 | 30187535 | |||||||
| chr6:30187536 | C | T | 131 | a0001c0001t0003g0105 a0001c0002t0005g0002 a0001c0002t0005g0005 others(128): Show |
162 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.938-978G>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 9/9 | chr6 | 30187536 | |||||||
| chr6:30187723 | T | C | 1 | a0001c0001t0002g0015 | 3 | HG00323.hp1 HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.938-1165A>G | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 9/9 | chr6 | 30187723 | |||||||
| chr6:30187747 | A | T | 9 | a0001c0001t0001g0036 a0001c0001t0001g0243 a0001c0001t0001g0244 others(6): Show |
10 | HG01109.hp1 HG01243.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.938-1189T>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 9/9 | chr6 | 30187747 | |||||||
| chr6:30187775 | G | A | 1 | a0001c0002t0005g0071 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.938-1217C>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 9/9 | chr6 | 30187775 | |||||||
| chr6:30187849 | C | T | 1 | a0001c0002t0008g0097 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.938-1291G>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 9/9 | chr6 | 30187849 | |||||||
| chr6:30187917 | C | CA | 22 | a0001c0001t0001g0170 a0001c0001t0001g0295 a0001c0001t0001g0323 others(19): Show |
22 | HG00280.hp2 HG00423.hp2 HG00639.hp1 others(19): Show |
intron_variant | MODIFIER | c.937+1249dupT | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 9/9 | chr6 | 30187917 | |||||||
| chr6:30187917 | CA | C | 26 | a0001c0001t0001g0013 a0001c0001t0001g0028 a0001c0001t0001g0029 others(23): Show |
32 | HG00558.hp2 HG00621.hp2 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.937+1249delT | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 9/9 | chr6 | 30187917 | |||||||
| chr6:30187917 | CAAAAAAA others(1): Show |
C | 6 | a0001c0001t0001g0246 a0001c0001t0001g0247 a0001c0001t0001g0248 others(3): Show |
6 | HG01361.hp2 HG02055.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.937+1242_937+1249d others(10): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 9/9 | chr6 | 30187917 | |||||||
| chr6:30187945 | C | T | 1 | a0001c0001t0002g0276 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.937+1222G>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 9/9 | chr6 | 30187945 | |||||||
| chr6:30187946 | G | A | 2 | a0001c0001t0001g0283 a0002c0004t0001g0219 |
2 | NA19003.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.937+1221C>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 9/9 | chr6 | 30187946 | |||||||
| chr6:30187990 | C | T | 17 | a0001c0002t0008g0080 a0001c0002t0008g0083 a0001c0002t0008g0084 others(14): Show |
21 | HG00099.hp2 HG00738.hp2 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.937+1177G>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 9/9 | chr6 | 30187990 | |||||||
| chr6:30188016 | G | A | 7 | a0001c0001t0001g0032 a0001c0001t0001g0189 a0001c0001t0001g0190 others(4): Show |
8 | HG02630.hp2 HG02723.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.937+1151C>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 9/9 | chr6 | 30188016 | |||||||
| chr6:30188087 | C | T | 51 | a0001c0001t0002g0006 a0001c0001t0002g0014 a0001c0001t0002g0015 others(48): Show |
63 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(60): Show |
intron_variant | MODIFIER | c.937+1080G>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 9/9 | chr6 | 30188087 | |||||||
| chr6:30188088 | G | A | 1 | a0001c0003t0003g0115 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.937+1079C>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 9/9 | chr6 | 30188088 | |||||||
| chr6:30188151 | C | T | 12 | a0001c0001t0001g0036 a0001c0001t0001g0243 a0001c0001t0001g0244 others(9): Show |
13 | HG00639.hp1 HG01109.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.937+1016G>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 9/9 | chr6 | 30188151 | |||||||
| chr6:30188213 | G | A | 7 | a0003c0006t0005g0044 a0003c0006t0005g0045 a0003c0006t0005g0046 others(4): Show |
7 | HG02074.hp2 HG02735.hp1 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.937+954C>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 9/9 | chr6 | 30188213 | |||||||
| chr6:30188215 | C | A | 124 | a0001c0001t0003g0105 a0001c0002t0005g0002 a0001c0002t0005g0005 others(121): Show |
155 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.937+952G>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 9/9 | chr6 | 30188215 | |||||||
| chr6:30188217 | C | CA | 15 | a0001c0001t0001g0003 a0001c0001t0001g0038 a0001c0001t0001g0187 others(12): Show |
21 | HG01070.hp1 HG01071.hp2 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.937+949dupT | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 9/9 | chr6 | 30188217 | |||||||
| chr6:30188217 | C | CAA | 16 | a0001c0001t0001g0013 a0001c0001t0001g0028 a0001c0001t0001g0029 others(13): Show |
22 | HG00621.hp2 HG00639.hp2 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.937+948_937+949dup others(2): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 9/9 | chr6 | 30188217 | |||||||
| chr6:30188217 | C | CAAA | 7 | a0001c0001t0001g0030 a0001c0001t0001g0168 a0001c0001t0001g0169 others(4): Show |
8 | HG00735.hp2 HG02056.hp1 HG04204.hp1 others(5): Show |
intron_variant | MODIFIER | c.937+947_937+949dup others(3): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 9/9 | chr6 | 30188217 | |||||||
| chr6:30188217 | C | CAAAAAA | 22 | a0001c0001t0001g0036 a0001c0001t0001g0243 a0001c0001t0001g0244 others(19): Show |
23 | HG00639.hp1 HG01167.hp2 HG01168.hp1 others(20): Show |
intron_variant | MODIFIER | c.937+944_937+949dup others(6): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 9/9 | chr6 | 30188217 | |||||||
| chr6:30188217 | C | CAAAAAAA | 43 | a0001c0001t0001g0159 a0001c0001t0001g0245 a0001c0001t0001g0268 others(40): Show |
54 | HG00140.hp1 HG00544.hp1 HG00673.hp1 others(51): Show |
intron_variant | MODIFIER | c.937+943_937+949dup others(7): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 9/9 | chr6 | 30188217 | |||||||
| chr6:30188217 | C | CAAAAAAA others(1): Show |
55 | a0001c0001t0001g0286 a0001c0001t0001g0287 a0001c0001t0001g0289 others(52): Show |
69 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.937+942_937+949dup others(8): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 9/9 | chr6 | 30188217 | |||||||
| chr6:30188217 | C | CAAAAAAA others(2): Show |
33 | a0001c0001t0001g0288 a0001c0001t0002g0016 a0001c0001t0002g0033 others(30): Show |
36 | HG00099.hp1 HG00597.hp2 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.937+941_937+949dup others(9): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 9/9 | chr6 | 30188217 | |||||||
| chr6:30188217 | C | CAAAAAAA others(3): Show |
13 | a0001c0001t0002g0015 a0001c0001t0002g0203 a0001c0001t0002g0223 others(10): Show |
15 | HG00323.hp1 HG00423.hp2 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.937+940_937+949dup others(10): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 9/9 | chr6 | 30188217 | |||||||
| chr6:30188217 | C | CAAAAAAA others(4): Show |
3 | a0001c0001t0001g0271 a0001c0001t0001g0300 a0001c0001t0002g0206 |
3 | HG01255.hp1 HG02257.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.937+939_937+949dup others(11): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 9/9 | chr6 | 30188217 | |||||||
| chr6:30188217 | C | CAAAAAAA others(5): Show |
5 | a0001c0001t0001g0247 a0001c0001t0001g0248 a0001c0001t0001g0272 others(2): Show |
5 | HG00438.hp1 HG01361.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.937+938_937+949dup others(12): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 9/9 | chr6 | 30188217 | |||||||
| chr6:30188217 | CAA | C | 7 | a0003c0006t0005g0044 a0003c0006t0005g0045 a0003c0006t0005g0046 others(4): Show |
7 | HG02074.hp2 HG02735.hp1 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.937+948_937+949del others(2): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 9/9 | chr6 | 30188217 | |||||||
| chr6:30188217 | CAAAAAAA | C | 62 | a0001c0001t0003g0105 a0001c0002t0006g0056 a0001c0003t0003g0022 others(59): Show |
67 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.937+943_937+949del others(7): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 9/9 | chr6 | 30188217 | |||||||
| chr6:30188217 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0246 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.937+940_937+949del others(10): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 9/9 | chr6 | 30188217 | |||||||
| chr6:30188238 | A | AAAAAG | 31 | a0001c0002t0005g0002 a0001c0002t0005g0005 a0001c0002t0005g0068 others(28): Show |
50 | HG01074.hp1 HG01099.hp1 HG01167.hp1 others(47): Show |
intron_variant | MODIFIER | c.937+924_937+928dup others(5): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 9/9 | chr6 | 30188238 | |||||||
| chr6:30188238 | A | AAAAG | 23 | a0001c0002t0005g0011 a0001c0002t0005g0071 a0001c0002t0005g0079 others(20): Show |
29 | HG00099.hp2 HG00738.hp2 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.937+928_937+929ins others(4): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 9/9 | chr6 | 30188238 | |||||||
| chr6:30188238 | A | G | 73 | a0001c0001t0003g0105 a0001c0002t0005g0027 a0001c0002t0006g0056 others(70): Show |
79 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.937+929T>C | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 9/9 | chr6 | 30188238 | |||||||
| chr6:30188243 | G | A | 2 | a0001c0001t0002g0251 a0001c0001t0002g0252 |
2 | HG02027.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.937+924C>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 9/9 | chr6 | 30188243 | |||||||
| chr6:30188322 | C | T | 1 | a0003c0006t0005g0049 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.937+845G>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 9/9 | chr6 | 30188322 | |||||||
| chr6:30188323 | T | C | 7 | a0001c0001t0001g0032 a0001c0001t0001g0189 a0001c0001t0001g0190 others(4): Show |
8 | HG02630.hp2 HG02723.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.937+844A>G | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 9/9 | chr6 | 30188323 | |||||||
| chr6:30188460 | T | C | 1 | a0001c0002t0017g0088 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.937+707A>G | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 9/9 | chr6 | 30188460 | |||||||
| chr6:30188477 | C | T | 20 | a0001c0001t0001g0159 a0001c0001t0001g0286 a0001c0001t0001g0287 others(17): Show |
20 | HG00733.hp2 HG01081.hp1 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.937+690G>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 9/9 | chr6 | 30188477 | |||||||
| chr6:30188528 | G | T | 1 | a0001c0002t0019g0095 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.937+639C>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 9/9 | chr6 | 30188528 | |||||||
| chr6:30188559 | G | A | 1 | a0001c0002t0019g0095 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.937+608C>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 9/9 | chr6 | 30188559 | |||||||
| chr6:30188665 | A | T | 1 | a0001c0001t0001g0248 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.937+502T>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 9/9 | chr6 | 30188665 | |||||||
| chr6:30188696 | C | T | 22 | a0002c0004t0001g0166 a0002c0004t0001g0194 a0002c0004t0001g0195 others(19): Show |
22 | HG00673.hp1 HG01167.hp2 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.937+471G>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 9/9 | chr6 | 30188696 | |||||||
| chr6:30188719 | T | A | 107 | a0001c0001t0003g0105 a0001c0002t0005g0002 a0001c0002t0005g0005 others(104): Show |
134 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.937+448A>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 9/9 | chr6 | 30188719 | |||||||
| chr6:30188925 | G | T | 1 | a0001c0002t0008g0097 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.937+242C>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 9/9 | chr6 | 30188925 | |||||||
| chr6:30189025 | G | A | 23 | a0001c0001t0001g0013 a0001c0001t0001g0028 a0001c0001t0001g0029 others(20): Show |
29 | HG00621.hp2 HG00735.hp2 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.937+142C>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 9/9 | chr6 | 30189025 | |||||||
| chr6:30189326 | A | C | 1 | a0001c0003t0025g0355 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.904+92T>G | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 8/9 | chr6 | 30189326 | |||||||
| chr6:30189377 | C | T | 7 | a0003c0006t0005g0044 a0003c0006t0005g0045 a0003c0006t0005g0046 others(4): Show |
7 | HG02074.hp2 HG02735.hp1 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.904+41G>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 8/9 | chr6 | 30189377 | |||||||
| chr6:30189822 | C | CT | 131 | a0001c0001t0003g0105 a0001c0002t0005g0002 a0001c0002t0005g0005 others(128): Show |
162 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.788+190_788+191ins others(1): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 7/9 | chr6 | 30189822 | |||||||
| chr6:30189877 | G | A | 131 | a0001c0001t0003g0105 a0001c0002t0005g0002 a0001c0002t0005g0005 others(128): Show |
162 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.788+136C>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 7/9 | chr6 | 30189877 | |||||||
| chr6:30189977 | G | C | 1 | a0001c0002t0008g0092 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.788+36C>G | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 7/9 | chr6 | 30189977 | |||||||
| chr6:30190108 | T | C | 1 | a0001c0003t0003g0155 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.766-73A>G | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30190108 | |||||||
| chr6:30190350 | G | A | 17 | a0001c0002t0008g0080 a0001c0002t0008g0083 a0001c0002t0008g0084 others(14): Show |
21 | HG00099.hp2 HG00738.hp2 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.766-315C>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30190350 | |||||||
| chr6:30190376 | G | A | 1 | a0001c0003t0025g0355 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.766-341C>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30190376 | |||||||
| chr6:30190605 | A | G | 7 | a0003c0006t0005g0044 a0003c0006t0005g0045 a0003c0006t0005g0046 others(4): Show |
7 | HG02074.hp2 HG02735.hp1 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.766-570T>C | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30190605 | |||||||
| chr6:30191163 | C | T | 2 | a0001c0003t0003g0124 a0001c0003t0003g0155 |
2 | NA18953.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.766-1128G>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30191163 | |||||||
| chr6:30191262 | C | G | 129 | a0001c0001t0003g0105 a0001c0002t0005g0002 a0001c0002t0005g0005 others(126): Show |
160 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.766-1227G>C | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30191262 | |||||||
| chr6:30191273 | T | C | 1 | a0001c0003t0003g0155 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.766-1238A>G | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30191273 | |||||||
| chr6:30191404 | TA | T | 79 | a0001c0001t0001g0186 a0001c0001t0001g0246 a0001c0001t0001g0247 others(76): Show |
104 | HG00099.hp2 HG00738.hp1 HG00738.hp2 others(101): Show |
intron_variant | MODIFIER | c.766-1370delT | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30191404 | |||||||
| chr6:30191404 | TAA | T | 61 | a0001c0001t0003g0105 a0001c0002t0005g0011 a0001c0002t0005g0068 others(58): Show |
67 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.766-1371_766-1370d others(4): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30191404 | |||||||
| chr6:30191422 | A | G | 11 | a0001c0002t0007g0008 a0001c0002t0007g0012 a0001c0002t0007g0020 others(8): Show |
17 | HG01074.hp1 HG01099.hp1 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.766-1387T>C | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30191422 | |||||||
| chr6:30191462 | A | G | 1 | a0002c0004t0023g0162 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.766-1427T>C | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30191462 | |||||||
| chr6:30191489 | T | C | 3 | a0001c0007t0001g0161 a0001c0007t0001g0164 a0001c0007t0001g0165 |
3 | HG00639.hp1 HG01256.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.766-1454A>G | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30191489 | |||||||
| chr6:30191520 | T | C | 13 | a0001c0002t0005g0069 a0001c0002t0005g0076 a0001c0002t0007g0008 others(10): Show |
19 | HG01074.hp1 HG01099.hp1 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.766-1485A>G | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30191520 | |||||||
| chr6:30191523 | T | TA | 48 | a0001c0001t0003g0105 a0001c0003t0003g0022 a0001c0003t0003g0023 others(45): Show |
52 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.766-1489dupT | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30191523 | |||||||
| chr6:30191573 | C | T | 3 | a0001c0001t0001g0329 a0001c0001t0001g0330 a0001c0002t0008g0085 |
3 | HG01168.hp2 HG01169.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.766-1538G>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30191573 | |||||||
| chr6:30192077 | A | C | 129 | a0001c0001t0003g0105 a0001c0002t0005g0002 a0001c0002t0005g0005 others(126): Show |
160 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.766-2042T>G | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30192077 | |||||||
| chr6:30192254 | G | A | 6 | a0001c0002t0005g0011 a0001c0002t0005g0068 a0001c0002t0005g0071 others(3): Show |
8 | HG00741.hp2 HG01106.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.766-2219C>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30192254 | |||||||
| chr6:30192278 | G | C | 279 | a0001c0001t0001g0032 a0001c0001t0001g0159 a0001c0001t0001g0189 others(276): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.766-2243C>G | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30192278 | |||||||
| chr6:30192294 | A | C | 1 | a0001c0003t0003g0101 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.766-2259T>G | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30192294 | |||||||
| chr6:30192437 | T | C | 6 | a0001c0001t0001g0032 a0001c0001t0001g0189 a0001c0001t0001g0190 others(3): Show |
7 | HG02630.hp2 HG02723.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.766-2402A>G | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30192437 | |||||||
| chr6:30192511 | G | A | 1 | a0001c0001t0004g0365 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.766-2476C>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30192511 | |||||||
| chr6:30193024 | A | G | 3 | a0001c0001t0001g0361 a0001c0001t0001g0363 a0001c0001t0001g0364 |
3 | HG02258.hp1 HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.766-2989T>C | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30193024 | |||||||
| chr6:30193062 | G | GTA | 3 | a0003c0006t0005g0044 a0003c0006t0005g0047 a0003c0006t0005g0050 |
3 | HG02074.hp2 HG03017.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.766-3029_766-3028d others(4): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30193062 | |||||||
| chr6:30193062 | G | GTATA | 4 | a0003c0006t0005g0045 a0003c0006t0005g0046 a0003c0006t0005g0048 others(1): Show |
4 | HG02735.hp1 HG03654.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.766-3031_766-3028d others(6): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30193062 | |||||||
| chr6:30193062 | GTA | G | 285 | a0001c0001t0001g0032 a0001c0001t0001g0036 a0001c0001t0001g0159 others(282): Show |
348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.766-3029_766-3028d others(4): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30193062 | |||||||
| chr6:30193081 | TATATACA others(19): Show |
T | 1 | a0001c0008t0016g0081 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.766-3072_766-3047d others(28): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30193081 | |||||||
| chr6:30193100 | C | A | 129 | a0001c0001t0003g0105 a0001c0002t0005g0002 a0001c0002t0005g0005 others(126): Show |
160 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.766-3065G>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30193100 | |||||||
| chr6:30193114 | A | G | 1 | a0001c0008t0016g0081 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.766-3079T>C | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30193114 | |||||||
| chr6:30193120 | A | G | 129 | a0001c0001t0003g0105 a0001c0002t0005g0002 a0001c0002t0005g0005 others(126): Show |
160 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.766-3085T>C | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30193120 | |||||||
| chr6:30193125 | TATATAC | T | 49 | a0001c0002t0005g0002 a0001c0002t0005g0005 a0001c0002t0005g0011 others(46): Show |
71 | HG00741.hp2 HG01074.hp1 HG01099.hp1 others(68): Show |
intron_variant | MODIFIER | c.766-3096_766-3091d others(8): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30193125 | |||||||
| chr6:30193127 | TATAC | T | 12 | a0001c0003t0003g0024 a0001c0003t0003g0109 a0001c0003t0003g0115 others(9): Show |
13 | HG00609.hp2 HG01943.hp2 HG01975.hp2 others(10): Show |
intron_variant | MODIFIER | c.766-3096_766-3093d others(6): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30193127 | |||||||
| chr6:30193129 | T | C | 25 | a0001c0001t0004g0040 a0001c0001t0004g0042 a0001c0001t0004g0043 others(22): Show |
28 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(25): Show |
intron_variant | MODIFIER | c.766-3094A>G | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30193129 | |||||||
| chr6:30193129 | TAC | T | 32 | a0001c0001t0003g0105 a0001c0003t0003g0022 a0001c0003t0003g0023 others(29): Show |
35 | HG00140.hp2 HG00438.hp2 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.766-3096_766-3095d others(4): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30193129 | |||||||
| chr6:30193130 | ACATATAT others(3): Show |
A | 17 | a0001c0002t0008g0080 a0001c0002t0008g0083 a0001c0002t0008g0084 others(14): Show |
21 | HG00099.hp2 HG00738.hp2 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.766-3105_766-3096d others(12): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30193130 | |||||||
| chr6:30193130 | ACATATAT others(5): Show |
A | 2 | a0001c0002t0008g0093 a0001c0008t0016g0081 |
2 | HG01257.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.766-3107_766-3096d others(14): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30193130 | |||||||
| chr6:30193131 | C | T | 18 | a0001c0003t0003g0099 a0001c0003t0003g0100 a0001c0003t0003g0101 others(15): Show |
19 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(16): Show |
intron_variant | MODIFIER | c.766-3096G>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30193131 | |||||||
| chr6:30193132 | A | G | 19 | a0001c0003t0003g0099 a0001c0003t0003g0100 a0001c0003t0003g0101 others(16): Show |
20 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(17): Show |
intron_variant | MODIFIER | c.766-3097T>C | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30193132 | |||||||
| chr6:30193134 | A | G | 52 | a0001c0001t0003g0105 a0001c0003t0003g0022 a0001c0003t0003g0023 others(49): Show |
56 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.766-3099T>C | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30193134 | |||||||
| chr6:30193136 | A | G | 125 | a0001c0001t0001g0159 a0001c0001t0001g0246 a0001c0001t0001g0247 others(122): Show |
133 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.766-3101T>C | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30193136 | |||||||
| chr6:30193136 | ATG | A | 54 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0014 others(51): Show |
68 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(65): Show |
intron_variant | MODIFIER | c.766-3103_766-3102d others(4): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30193136 | |||||||
| chr6:30193142 | G | A | 16 | a0001c0002t0008g0080 a0001c0002t0008g0083 a0001c0002t0008g0084 others(13): Show |
20 | HG00099.hp2 HG00738.hp2 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.766-3107C>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30193142 | |||||||
| chr6:30193144 | G | A | 1 | a0001c0002t0008g0093 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.766-3109C>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30193144 | |||||||
| chr6:30193150 | G | A | 1 | a0001c0003t0011g0149 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.766-3115C>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30193150 | |||||||
| chr6:30193152 | G | A | 12 | a0001c0003t0003g0099 a0001c0003t0003g0100 a0001c0003t0003g0101 others(9): Show |
12 | HG00323.hp2 HG00558.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.766-3117C>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30193152 | |||||||
| chr6:30193152 | G | GTATATAT others(3): Show |
2 | a0001c0001t0001g0287 a0001c0001t0001g0288 |
2 | HG03540.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.766-3118_766-3117i others(12): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30193152 | |||||||
| chr6:30193152 | G | GTATATAT others(5): Show |
1 | a0001c0001t0001g0290 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.766-3118_766-3117i others(14): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30193152 | |||||||
| chr6:30193152 | G | GTATATAT others(7): Show |
1 | a0001c0001t0001g0289 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.766-3118_766-3117i others(16): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30193152 | |||||||
| chr6:30193154 | G | A | 58 | a0001c0001t0001g0159 a0001c0001t0001g0286 a0001c0001t0001g0287 others(55): Show |
61 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.766-3119C>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30193154 | |||||||
| chr6:30193156 | G | A | 78 | a0001c0001t0001g0159 a0001c0001t0001g0286 a0001c0001t0001g0287 others(75): Show |
83 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.766-3121C>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30193156 | |||||||
| chr6:30193158 | G | A | 147 | a0001c0001t0001g0159 a0001c0001t0001g0286 a0001c0001t0001g0287 others(144): Show |
175 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.766-3123C>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30193158 | |||||||
| chr6:30193158 | G | GTA | 8 | a0002c0004t0001g0166 a0002c0004t0001g0198 a0002c0004t0001g0202 others(5): Show |
8 | NA18612.hp1 NA18956.hp2 NA18989.hp1 others(5): Show |
intron_variant | MODIFIER | c.766-3124_766-3123i others(4): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30193158 | |||||||
| chr6:30193158 | G | GTATATA | 10 | a0001c0001t0004g0042 a0001c0001t0004g0043 a0001c0001t0004g0340 others(7): Show |
12 | HG01517.hp2 HG02135.hp1 HG03239.hp1 others(9): Show |
intron_variant | MODIFIER | c.766-3124_766-3123i others(8): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30193158 | |||||||
| chr6:30193158 | G | GTATATAT others(11): Show |
2 | a0001c0001t0004g0306 a0001c0001t0004g0365 |
2 | HG01261.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.766-3124_766-3123i others(20): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30193158 | |||||||
| chr6:30193160 | G | A | 244 | a0001c0001t0001g0036 a0001c0001t0001g0159 a0001c0001t0001g0243 others(241): Show |
298 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.766-3125C>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30193160 | |||||||
| chr6:30193160 | G | GTA | 11 | a0001c0003t0025g0355 a0002c0004t0001g0194 a0002c0004t0001g0195 others(8): Show |
11 | HG00673.hp1 HG01167.hp2 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.766-3126_766-3125i others(4): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30193160 | |||||||
| chr6:30193162 | G | A | 278 | a0001c0001t0001g0036 a0001c0001t0001g0159 a0001c0001t0001g0189 others(275): Show |
333 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(330): Show |
intron_variant | MODIFIER | c.766-3127C>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30193162 | |||||||
| chr6:30193162 | G | GTGTA | 3 | a0001c0001t0001g0248 a0001c0001t0001g0329 a0001c0001t0001g0330 |
3 | HG01168.hp2 HG01169.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.766-3128_766-3127i others(6): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30193162 | |||||||
| chr6:30193164 | A | G | 1 | a0001c0001t0001g0190 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.766-3129T>C | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30193164 | |||||||
| chr6:30193178 | A | T | 16 | a0001c0002t0005g0079 a0001c0002t0006g0009 a0001c0002t0006g0010 others(13): Show |
21 | HG01175.hp2 HG02040.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.766-3143T>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30193178 | |||||||
| chr6:30193180 | A | T | 48 | a0001c0002t0005g0002 a0001c0002t0005g0011 a0001c0002t0005g0027 others(45): Show |
62 | HG00741.hp2 HG01074.hp1 HG01099.hp1 others(59): Show |
intron_variant | MODIFIER | c.766-3145T>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30193180 | |||||||
| chr6:30193181 | TA | T | 3 | a0001c0001t0002g0206 a0001c0001t0002g0252 a0001c0001t0002g0258 |
3 | HG02129.hp2 HG03927.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.766-3147delT | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30193181 | |||||||
| chr6:30193182 | A | ATATATAT others(29): Show |
1 | a0001c0005t0001g0304 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.766-3148_766-3147i others(38): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30193182 | |||||||
| chr6:30193182 | A | ATATATAT others(25): Show |
1 | a0001c0005t0001g0309 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.766-3148_766-3147i others(34): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30193182 | |||||||
| chr6:30193182 | A | ATATATAT others(21): Show |
1 | a0001c0005t0001g0313 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.766-3148_766-3147i others(30): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30193182 | |||||||
| chr6:30193182 | A | ATATATAT others(21): Show |
1 | a0001c0005t0001g0310 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.766-3148_766-3147i others(30): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30193182 | |||||||
| chr6:30193182 | A | ATATATAT others(19): Show |
2 | a0001c0005t0001g0303 a0001c0005t0001g0308 |
2 | HG02280.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.766-3148_766-3147i others(28): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30193182 | |||||||
| chr6:30193182 | A | ATATATAT others(17): Show |
2 | a0001c0005t0001g0037 a0001c0005t0001g0307 |
3 | HG02109.hp1 HG02451.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.766-3148_766-3147i others(26): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30193182 | |||||||
| chr6:30193182 | A | ATATATAT others(19): Show |
3 | a0001c0001t0001g0190 a0001c0005t0001g0017 a0001c0005t0001g0311 |
4 | HG02080.hp2 HG02129.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.766-3148_766-3147i others(28): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30193182 | |||||||
| chr6:30193182 | A | ATATATAT others(14): Show |
2 | a0001c0005t0001g0301 a0001c0009t0001g0192 |
2 | HG02886.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.766-3148_766-3147i others(23): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30193182 | |||||||
| chr6:30193182 | A | ATATATAT others(17): Show |
2 | a0001c0005t0001g0302 a0001c0005t0001g0305 |
2 | HG02015.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.766-3148_766-3147i others(26): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30193182 | |||||||
| chr6:30193182 | A | ATATATAT others(19): Show |
1 | a0001c0005t0001g0017 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.766-3148_766-3147i others(28): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30193182 | |||||||
| chr6:30193182 | A | ATATATAT others(13): Show |
3 | a0001c0001t0001g0189 a0001c0005t0001g0312 a0001c0005t0001g0314 |
3 | HG02630.hp2 HG02818.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.766-3148_766-3147i others(22): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30193182 | |||||||
| chr6:30193182 | A | ATATATAT others(19): Show |
1 | a0001c0001t0001g0032 | 2 | HG02723.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.766-3148_766-3147i others(28): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30193182 | |||||||
| chr6:30193182 | A | ATATATAT others(9): Show |
1 | a0001c0001t0001g0191 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.766-3148_766-3147i others(18): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30193182 | |||||||
| chr6:30193182 | A | ATATATAT others(3): Show |
1 | a0001c0001t0004g0360 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.766-3148_766-3147i others(12): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30193182 | |||||||
| chr6:30193182 | A | ATATTT | 6 | a0001c0001t0004g0001 a0001c0001t0004g0018 a0001c0001t0004g0041 others(3): Show |
13 | HG00140.hp1 HG01074.hp2 HG02080.hp1 others(10): Show |
intron_variant | MODIFIER | c.766-3148_766-3147i others(7): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30193182 | |||||||
| chr6:30193182 | A | ATT | 12 | a0001c0001t0001g0003 a0001c0001t0001g0038 a0001c0001t0001g0039 others(9): Show |
18 | HG01071.hp2 HG01516.hp1 HG02015.hp2 others(15): Show |
intron_variant | MODIFIER | c.766-3149_766-3148d others(4): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30193182 | |||||||
| chr6:30193182 | A | T | 87 | a0001c0001t0001g0187 a0001c0001t0001g0246 a0001c0001t0001g0248 others(84): Show |
116 | HG00099.hp2 HG00438.hp1 HG00738.hp2 others(113): Show |
intron_variant | MODIFIER | c.766-3147T>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30193182 | |||||||
| chr6:30193182 | AT | A | 7 | a0001c0001t0002g0188 a0001c0001t0002g0209 a0001c0001t0002g0263 others(4): Show |
7 | HG00639.hp1 HG01256.hp2 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.766-3148delA | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30193182 | |||||||
| chr6:30193183 | T | TA | 25 | a0001c0001t0001g0013 a0001c0001t0001g0028 a0001c0001t0001g0029 others(22): Show |
31 | HG00735.hp2 HG01106.hp1 HG01346.hp2 others(28): Show |
intron_variant | MODIFIER | c.766-3149_766-3148i others(3): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30193183 | |||||||
| chr6:30193183 | T | TATA | 10 | a0001c0001t0001g0167 a0001c0001t0001g0268 a0001c0001t0001g0284 others(7): Show |
10 | HG00621.hp2 HG00733.hp2 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.766-3149_766-3148i others(5): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30193183 | |||||||
| chr6:30193183 | T | TATATA | 8 | a0001c0001t0001g0036 a0001c0001t0001g0243 a0001c0001t0001g0244 others(5): Show |
9 | HG00099.hp1 HG01243.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.766-3149_766-3148i others(7): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30193183 | |||||||
| chr6:30193183 | T | TATATATA | 5 | a0001c0001t0001g0286 a0001c0001t0001g0293 a0001c0001t0001g0294 others(2): Show |
5 | HG01123.hp1 HG02896.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.766-3149_766-3148i others(9): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30193183 | |||||||
| chr6:30193183 | T | TATATATA others(2): Show |
3 | a0001c0001t0001g0299 a0001c0001t0001g0361 a0001c0001t0001g0364 |
3 | HG01358.hp2 HG02258.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.766-3149_766-3148i others(11): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30193183 | |||||||
| chr6:30193183 | T | TATATATA others(4): Show |
1 | a0001c0001t0001g0362 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.766-3149_766-3148i others(13): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30193183 | |||||||
| chr6:30193183 | T | TATATATA others(10): Show |
1 | a0001c0001t0001g0363 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.766-3149_766-3148i others(19): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30193183 | |||||||
| chr6:30193184 | T | A | 33 | a0001c0001t0001g0180 a0001c0001t0001g0273 a0001c0001t0001g0287 others(30): Show |
33 | HG00609.hp1 HG00673.hp1 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.766-3149A>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30193184 | |||||||
| chr6:30193185 | T | A | 35 | a0001c0001t0001g0036 a0001c0001t0001g0159 a0001c0001t0001g0175 others(32): Show |
36 | HG00639.hp1 HG00733.hp2 HG01109.hp1 others(33): Show |
intron_variant | MODIFIER | c.766-3150A>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30193185 | |||||||
| chr6:30193186 | T | A | 23 | a0001c0001t0001g0167 a0001c0001t0001g0287 a0001c0001t0001g0288 others(20): Show |
23 | HG00621.hp2 HG01081.hp1 HG01167.hp2 others(20): Show |
intron_variant | MODIFIER | c.766-3151A>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30193186 | |||||||
| chr6:30193187 | T | A | 8 | a0001c0001t0001g0286 a0001c0001t0001g0291 a0001c0001t0001g0293 others(5): Show |
8 | HG00639.hp1 HG02258.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.766-3152A>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30193187 | |||||||
| chr6:30193188 | T | A | 9 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0001t0001g0289 others(6): Show |
9 | HG01081.hp1 HG01167.hp2 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.766-3153A>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30193188 | |||||||
| chr6:30193189 | T | A | 2 | a0001c0001t0001g0291 a0001c0007t0001g0165 |
2 | HG00639.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.766-3154A>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30193189 | |||||||
| chr6:30193190 | T | A | 4 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0001t0001g0289 others(1): Show |
4 | HG02109.hp2 HG03471.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.766-3155A>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30193190 | |||||||
| chr6:30193193 | T | C | 17 | a0001c0002t0006g0065 a0001c0002t0008g0085 a0001c0002t0008g0086 others(14): Show |
21 | HG00099.hp2 HG00738.hp2 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.766-3158A>G | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30193193 | |||||||
| chr6:30193193 | T | TC | 34 | a0001c0002t0005g0011 a0001c0002t0005g0068 a0001c0002t0005g0069 others(31): Show |
47 | HG00741.hp2 HG01074.hp1 HG01099.hp1 others(44): Show |
intron_variant | MODIFIER | c.766-3159_766-3158i others(3): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30193193 | |||||||
| chr6:30193193 | T | TTC | 9 | a0001c0002t0005g0002 a0001c0002t0005g0005 a0001c0002t0005g0027 others(6): Show |
18 | HG01884.hp2 HG01891.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.766-3159_766-3158i others(4): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30193193 | |||||||
| chr6:30193193 | T | TTTC | 13 | a0001c0002t0006g0059 a0001c0002t0018g0066 a0001c0003t0009g0026 others(10): Show |
14 | HG00738.hp1 HG01891.hp2 HG02735.hp1 others(11): Show |
intron_variant | MODIFIER | c.766-3159_766-3158i others(5): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30193193 | |||||||
| chr6:30193193 | T | TTTTTC | 7 | a0001c0003t0003g0099 a0001c0003t0003g0100 a0001c0003t0003g0130 others(4): Show |
7 | HG01109.hp2 HG01928.hp2 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.766-3159_766-3158i others(7): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30193193 | |||||||
| chr6:30193193 | T | TTTTTTC | 7 | a0001c0003t0003g0115 a0001c0003t0003g0116 a0001c0003t0003g0127 others(4): Show |
7 | HG01934.hp2 HG01952.hp2 HG02004.hp2 others(4): Show |
intron_variant | MODIFIER | c.766-3159_766-3158i others(8): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30193193 | |||||||
| chr6:30193193 | T | TTTTTTTC | 31 | a0001c0001t0003g0105 a0001c0003t0003g0022 a0001c0003t0003g0023 others(28): Show |
34 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.766-3159_766-3158i others(9): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30193193 | |||||||
| chr6:30193193 | T | TTTTTTTT others(1): Show |
5 | a0001c0003t0003g0024 a0001c0003t0003g0104 a0001c0003t0003g0121 others(2): Show |
6 | HG00558.hp1 HG01255.hp2 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.766-3159_766-3158i others(10): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30193193 | |||||||
| chr6:30193339 | G | A | 1 | a0001c0002t0008g0092 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.765+3177C>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30193339 | |||||||
| chr6:30193428 | T | C | 130 | a0001c0001t0003g0105 a0001c0002t0005g0002 a0001c0002t0005g0005 others(127): Show |
161 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.765+3088A>G | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30193428 | |||||||
| chr6:30193451 | A | G | 2 | a0001c0001t0002g0263 a0001c0001t0002g0264 |
2 | HG02698.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.765+3065T>C | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30193451 | |||||||
| chr6:30193693 | A | G | 15 | a0001c0005t0001g0017 a0001c0005t0001g0037 a0001c0005t0001g0301 others(12): Show |
18 | HG02015.hp1 HG02056.hp2 HG02080.hp2 others(15): Show |
intron_variant | MODIFIER | c.765+2823T>C | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30193693 | |||||||
| chr6:30193732 | C | T | 123 | a0001c0001t0003g0105 a0001c0002t0005g0002 a0001c0002t0005g0005 others(120): Show |
154 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.765+2784G>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30193732 | |||||||
| chr6:30193759 | G | A | 2 | a0001c0002t0010g0004 a0001c0002t0010g0082 |
6 | HG00099.hp2 HG00738.hp2 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.765+2757C>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30193759 | |||||||
| chr6:30193911 | T | A | 1 | a0001c0003t0003g0133 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.765+2605A>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30193911 | |||||||
| chr6:30193929 | T | C | 1 | a0001c0001t0001g0293 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.765+2587A>G | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30193929 | |||||||
| chr6:30193936 | T | C | 2 | a0001c0003t0011g0052 a0001c0003t0011g0053 |
2 | HG02145.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.765+2580A>G | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30193936 | |||||||
| chr6:30193997 | A | G | 3 | a0001c0001t0001g0187 a0001c0001t0001g0329 a0001c0001t0001g0330 |
3 | HG01168.hp2 HG01169.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.765+2519T>C | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30193997 | |||||||
| chr6:30194061 | T | C | 1 | a0001c0001t0004g0348 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.765+2455A>G | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30194061 | |||||||
| chr6:30194151 | G | A | 1 | a0001c0003t0009g0141 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.765+2365C>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30194151 | |||||||
| chr6:30194392 | G | C | 1 | a0001c0001t0001g0300 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.765+2124C>G | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30194392 | |||||||
| chr6:30194403 | T | C | 1 | a0001c0001t0001g0300 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.765+2113A>G | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30194403 | |||||||
| chr6:30194458 | G | C | 1 | a0001c0005t0001g0303 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.765+2058C>G | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30194458 | |||||||
| chr6:30194468 | T | G | 7 | a0001c0001t0001g0246 a0001c0001t0001g0247 a0001c0001t0001g0248 others(4): Show |
7 | HG01361.hp2 HG02055.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.765+2048A>C | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30194468 | |||||||
| chr6:30194628 | G | A | 2 | a0001c0002t0008g0091 a0001c0002t0008g0092 |
2 | HG02738.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.765+1888C>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30194628 | |||||||
| chr6:30194681 | C | G | 62 | a0001c0001t0003g0105 a0001c0003t0003g0022 a0001c0003t0003g0023 others(59): Show |
67 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.765+1835G>C | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30194681 | |||||||
| chr6:30194727 | C | T | 1 | a0001c0005t0001g0037 | 2 | HG02451.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.765+1789G>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30194727 | |||||||
| chr6:30194728 | G | A | 18 | a0001c0002t0008g0080 a0001c0002t0008g0083 a0001c0002t0008g0084 others(15): Show |
22 | HG00099.hp2 HG00738.hp2 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.765+1788C>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30194728 | |||||||
| chr6:30194840 | G | T | 1 | a0001c0003t0025g0355 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.765+1676C>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30194840 | |||||||
| chr6:30194883 | G | A | 3 | a0001c0005t0001g0304 a0001c0005t0001g0310 a0001c0005t0001g0311 |
3 | HG02080.hp2 HG02735.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.765+1633C>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30194883 | |||||||
| chr6:30195032 | A | G | 49 | a0001c0001t0003g0105 a0001c0003t0003g0022 a0001c0003t0003g0023 others(46): Show |
53 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(50): Show |
intron_variant | MODIFIER | c.765+1484T>C | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30195032 | |||||||
| chr6:30195177 | A | G | 1 | a0001c0005t0001g0308 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.765+1339T>C | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30195177 | |||||||
| chr6:30195262 | G | A | 1 | a0001c0001t0002g0261 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.765+1254C>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30195262 | |||||||
| chr6:30195318 | T | C | 7 | a0003c0006t0005g0044 a0003c0006t0005g0045 a0003c0006t0005g0046 others(4): Show |
7 | HG02074.hp2 HG02735.hp1 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.765+1198A>G | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30195318 | |||||||
| chr6:30195548 | C | T | 7 | a0003c0006t0005g0044 a0003c0006t0005g0045 a0003c0006t0005g0046 others(4): Show |
7 | HG02074.hp2 HG02735.hp1 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.765+968G>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30195548 | |||||||
| chr6:30195582 | G | A | 1 | a0001c0001t0002g0193 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.765+934C>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30195582 | |||||||
| chr6:30195663 | T | C | 1 | a0002c0004t0001g0202 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.765+853A>G | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30195663 | |||||||
| chr6:30195871 | G | T | 2 | a0001c0001t0012g0090 a0001c0001t0012g0094 |
2 | HG02738.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.765+645C>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30195871 | |||||||
| chr6:30195974 | T | A | 7 | a0003c0006t0005g0044 a0003c0006t0005g0045 a0003c0006t0005g0046 others(4): Show |
7 | HG02074.hp2 HG02735.hp1 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.765+542A>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30195974 | |||||||
| chr6:30195980 | G | A | 7 | a0003c0006t0005g0044 a0003c0006t0005g0045 a0003c0006t0005g0046 others(4): Show |
7 | HG02074.hp2 HG02735.hp1 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.765+536C>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30195980 | |||||||
| chr6:30196178 | G | A | 61 | a0001c0002t0005g0002 a0001c0002t0005g0005 a0001c0002t0005g0011 others(58): Show |
87 | HG00099.hp2 HG00738.hp2 HG00741.hp2 others(84): Show |
intron_variant | MODIFIER | c.765+338C>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30196178 | |||||||
| chr6:30196219 | G | A | 1 | a0001c0003t0025g0355 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.765+297C>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | 30196219 | |||||||
| chr6:30196881 | A | T | 6 | a0001c0001t0001g0286 a0001c0001t0001g0287 a0001c0001t0001g0288 others(3): Show |
6 | HG02109.hp2 HG03041.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.535-135T>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 5/9 | chr6 | 30196881 | |||||||
| chr6:30196931 | T | C | 1 | a0001c0001t0001g0176 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.535-185A>G | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 5/9 | chr6 | 30196931 | |||||||
| chr6:30197085 | C | T | 22 | a0002c0004t0001g0166 a0002c0004t0001g0194 a0002c0004t0001g0195 others(19): Show |
22 | HG00673.hp1 HG01167.hp2 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.535-339G>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 5/9 | chr6 | 30197085 | |||||||
| chr6:30197121 | G | C | 9 | a0001c0001t0001g0003 a0001c0001t0001g0038 a0001c0001t0001g0039 others(6): Show |
16 | NA18945.hp1 NA18955.hp1 NA18963.hp2 others(13): Show |
intron_variant | MODIFIER | c.535-375C>G | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 5/9 | chr6 | 30197121 | |||||||
| chr6:30197125 | G | A | 1 | a0001c0001t0002g0264 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.535-379C>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 5/9 | chr6 | 30197125 | |||||||
| chr6:30197491 | C | T | 1 | a0001c0009t0001g0192 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.535-745G>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 5/9 | chr6 | 30197491 | |||||||
| chr6:30197496 | C | T | 61 | a0001c0002t0005g0002 a0001c0002t0005g0005 a0001c0002t0005g0011 others(58): Show |
87 | HG00099.hp2 HG00738.hp2 HG00741.hp2 others(84): Show |
intron_variant | MODIFIER | c.535-750G>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 5/9 | chr6 | 30197496 | |||||||
| chr6:30197539 | T | A | 48 | a0001c0001t0003g0105 a0001c0003t0003g0022 a0001c0003t0003g0023 others(45): Show |
52 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.535-793A>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 5/9 | chr6 | 30197539 | |||||||
| chr6:30197706 | T | A | 1 | a0001c0001t0001g0032 | 2 | HG02723.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.534+723A>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 5/9 | chr6 | 30197706 | |||||||
| chr6:30197749 | A | G | 7 | a0003c0006t0005g0044 a0003c0006t0005g0045 a0003c0006t0005g0046 others(4): Show |
7 | HG02074.hp2 HG02735.hp1 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.534+680T>C | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 5/9 | chr6 | 30197749 | |||||||
| chr6:30197836 | C | T | 1 | a0002c0004t0001g0202 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.534+593G>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 5/9 | chr6 | 30197836 | |||||||
| chr6:30197837 | T | C | 1 | a0002c0004t0001g0202 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.534+592A>G | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 5/9 | chr6 | 30197837 | |||||||
| chr6:30197885 | G | A | 18 | a0001c0002t0008g0080 a0001c0002t0008g0083 a0001c0002t0008g0084 others(15): Show |
22 | HG00099.hp2 HG00738.hp2 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.534+544C>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 5/9 | chr6 | 30197885 | |||||||
| chr6:30197936 | G | A | 1 | a0001c0001t0001g0170 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.534+493C>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 5/9 | chr6 | 30197936 | |||||||
| chr6:30198000 | C | T | 1 | a0001c0002t0008g0087 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.534+429G>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 5/9 | chr6 | 30198000 | |||||||
| chr6:30198007 | C | T | 1 | a0001c0001t0002g0240 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.534+422G>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 5/9 | chr6 | 30198007 | |||||||
| chr6:30198009 | C | T | 1 | a0001c0001t0002g0240 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.534+420G>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 5/9 | chr6 | 30198009 | |||||||
| chr6:30198114 | T | G | 1 | a0001c0001t0004g0350 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.534+315A>C | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 5/9 | chr6 | 30198114 | |||||||
| chr6:30198185 | G | C | 1 | a0001c0010t0024g0345 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.534+244C>G | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 5/9 | chr6 | 30198185 | |||||||
| chr6:30198191 | G | A | 1 | a0001c0002t0019g0095 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.534+238C>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 5/9 | chr6 | 30198191 | |||||||
| chr6:30198273 | T | C | 1 | a0001c0001t0002g0233 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.534+156A>G | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 5/9 | chr6 | 30198273 | |||||||
| chr6:30198319 | C | T | 1 | a0002c0004t0001g0194 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.534+110G>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 5/9 | chr6 | 30198319 | |||||||
| chr6:30199289 | G | A | 3 | a0001c0003t0011g0051 a0001c0003t0011g0052 a0001c0003t0011g0053 |
3 | HG01255.hp2 HG02145.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-161-25C>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 3/9 | chr6 | 30199289 | |||||||
| chr6:30199517 | C | T | 308 | a0001c0001t0001g0032 a0001c0001t0001g0036 a0001c0001t0001g0159 others(305): Show |
371 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(368): Show |
intron_variant | MODIFIER | c.-161-253G>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 3/9 | chr6 | 30199517 | |||||||
| chr6:30199627 | G | GT | 17 | a0001c0001t0001g0187 a0001c0001t0001g0292 a0001c0001t0001g0329 others(14): Show |
17 | HG00597.hp1 HG01081.hp1 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.-161-364dupA | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 3/9 | chr6 | 30199627 | |||||||
| chr6:30199638 | TTG | T | 24 | a0001c0002t0008g0080 a0001c0002t0008g0083 a0001c0002t0008g0084 others(21): Show |
28 | HG00099.hp2 HG00738.hp2 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.-161-376_-161-375d others(4): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 3/9 | chr6 | 30199638 | |||||||
| chr6:30199640 | G | T | 4 | a0001c0002t0005g0076 a0001c0002t0005g0152 a0001c0002t0006g0055 others(1): Show |
4 | HG02055.hp2 HG04184.hp1 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.-161-376C>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 3/9 | chr6 | 30199640 | |||||||
| chr6:30199641 | G | T | 1 | a0001c0001t0002g0333 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-161-377C>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 3/9 | chr6 | 30199641 | |||||||
| chr6:30199641 | GT | G | 38 | a0001c0002t0005g0002 a0001c0002t0005g0005 a0001c0002t0005g0011 others(35): Show |
60 | HG00741.hp2 HG01074.hp1 HG01099.hp1 others(57): Show |
intron_variant | MODIFIER | c.-161-378delA | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 3/9 | chr6 | 30199641 | |||||||
| chr6:30199642 | T | G | 28 | a0001c0002t0005g0076 a0001c0002t0005g0152 a0001c0002t0006g0055 others(25): Show |
32 | HG00099.hp2 HG00738.hp2 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.-161-378A>C | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 3/9 | chr6 | 30199642 | |||||||
| chr6:30199699 | T | C | 47 | a0001c0001t0003g0105 a0001c0003t0003g0022 a0001c0003t0003g0023 others(44): Show |
51 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(48): Show |
intron_variant | MODIFIER | c.-161-435A>G | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 3/9 | chr6 | 30199699 | |||||||
| chr6:30199724 | C | A | 1 | a0001c0002t0008g0083 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-161-460G>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 3/9 | chr6 | 30199724 | |||||||
| chr6:30199782 | A | G | 1 | a0001c0001t0001g0300 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-161-518T>C | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 3/9 | chr6 | 30199782 | |||||||
| chr6:30199786 | A | G | 1 | a0001c0001t0001g0300 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-161-522T>C | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 3/9 | chr6 | 30199786 | |||||||
| chr6:30199797 | T | C | 1 | a0003c0006t0005g0047 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-161-533A>G | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 3/9 | chr6 | 30199797 | |||||||
| chr6:30199826 | C | T | 4 | a0001c0002t0008g0089 a0001c0002t0008g0093 a0001c0002t0008g0096 others(1): Show |
4 | HG01257.hp2 HG01884.hp1 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.-161-562G>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 3/9 | chr6 | 30199826 | |||||||
| chr6:30199851 | T | C | 7 | a0003c0006t0005g0044 a0003c0006t0005g0045 a0003c0006t0005g0046 others(4): Show |
7 | HG02074.hp2 HG02735.hp1 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.-161-587A>G | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 3/9 | chr6 | 30199851 | |||||||
| chr6:30199857 | T | C | 1 | a0001c0001t0002g0262 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-161-593A>G | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 3/9 | chr6 | 30199857 | |||||||
| chr6:30200008 | A | C | 20 | a0001c0001t0001g0159 a0001c0001t0001g0286 a0001c0001t0001g0287 others(17): Show |
20 | HG00733.hp2 HG01081.hp1 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.-161-744T>G | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 3/9 | chr6 | 30200008 | |||||||
| chr6:30200058 | C | T | 59 | a0001c0002t0005g0002 a0001c0002t0005g0005 a0001c0002t0005g0011 others(56): Show |
85 | HG00099.hp2 HG00738.hp2 HG00741.hp2 others(82): Show |
intron_variant | MODIFIER | c.-161-794G>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 3/9 | chr6 | 30200058 | |||||||
| chr6:30200060 | G | A | 1 | a0001c0001t0002g0223 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-161-796C>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 3/9 | chr6 | 30200060 | |||||||
| chr6:30200096 | C | A | 1 | a0001c0002t0008g0084 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-161-832G>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 3/9 | chr6 | 30200096 | |||||||
| chr6:30200124 | T | A | 43 | a0001c0002t0005g0002 a0001c0002t0005g0005 a0001c0002t0005g0011 others(40): Show |
65 | HG00741.hp2 HG01074.hp1 HG01099.hp1 others(62): Show |
intron_variant | MODIFIER | c.-161-860A>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 3/9 | chr6 | 30200124 | |||||||
| chr6:30200130 | A | G | 6 | a0001c0002t0005g0011 a0001c0002t0005g0068 a0001c0002t0005g0071 others(3): Show |
8 | HG00741.hp2 HG01106.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.-161-866T>C | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 3/9 | chr6 | 30200130 | |||||||
| chr6:30200130 | A | T | 1 | a0001c0003t0025g0355 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-161-866T>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 3/9 | chr6 | 30200130 | |||||||
| chr6:30200330 | C | A | 2 | a0001c0001t0002g0263 a0001c0001t0002g0264 |
2 | HG02698.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.-162+705G>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 3/9 | chr6 | 30200330 | |||||||
| chr6:30200419 | C | T | 5 | a0001c0001t0001g0032 a0001c0001t0001g0189 a0001c0001t0001g0190 others(2): Show |
6 | HG02630.hp2 HG02723.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-162+616G>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 3/9 | chr6 | 30200419 | |||||||
| chr6:30200425 | T | C | 43 | a0001c0002t0005g0002 a0001c0002t0005g0005 a0001c0002t0005g0011 others(40): Show |
65 | HG00741.hp2 HG01074.hp1 HG01099.hp1 others(62): Show |
intron_variant | MODIFIER | c.-162+610A>G | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 3/9 | chr6 | 30200425 | |||||||
| chr6:30200478 | C | T | 9 | a0001c0001t0001g0003 a0001c0001t0001g0038 a0001c0001t0001g0039 others(6): Show |
16 | NA18945.hp1 NA18955.hp1 NA18963.hp2 others(13): Show |
intron_variant | MODIFIER | c.-162+557G>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 3/9 | chr6 | 30200478 | |||||||
| chr6:30200524 | A | G | 3 | a0001c0007t0001g0161 a0001c0007t0001g0164 a0001c0007t0001g0165 |
3 | HG00639.hp1 HG01256.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.-162+511T>C | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 3/9 | chr6 | 30200524 | |||||||
| chr6:30200533 | G | A | 1 | a0001c0002t0005g0079 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-162+502C>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 3/9 | chr6 | 30200533 | |||||||
| chr6:30200542 | G | T | 24 | a0001c0002t0008g0080 a0001c0002t0008g0083 a0001c0002t0008g0084 others(21): Show |
28 | HG00099.hp2 HG00738.hp2 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.-162+493C>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 3/9 | chr6 | 30200542 | |||||||
| chr6:30200719 | C | T | 43 | a0001c0002t0005g0002 a0001c0002t0005g0005 a0001c0002t0005g0011 others(40): Show |
65 | HG00741.hp2 HG01074.hp1 HG01099.hp1 others(62): Show |
intron_variant | MODIFIER | c.-162+316G>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 3/9 | chr6 | 30200719 | |||||||
| chr6:30201195 | A | C | 22 | a0002c0004t0001g0166 a0002c0004t0001g0194 a0002c0004t0001g0195 others(19): Show |
22 | HG00673.hp1 HG01167.hp2 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.-265-57T>G | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 2/9 | chr6 | 30201195 | |||||||
| chr6:30201315 | A | G | 19 | a0001c0001t0012g0090 a0001c0001t0012g0094 a0001c0002t0008g0080 others(16): Show |
23 | HG00099.hp2 HG00738.hp2 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.-265-177T>C | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 2/9 | chr6 | 30201315 | |||||||
| chr6:30201362 | T | C | 6 | a0001c0001t0012g0090 a0001c0001t0012g0094 a0001c0002t0008g0089 others(3): Show |
6 | HG01257.hp2 HG01884.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.-265-224A>G | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 2/9 | chr6 | 30201362 | |||||||
| chr6:30201449 | G | A | 4 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0001t0001g0289 others(1): Show |
4 | HG02109.hp2 HG03471.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.-265-311C>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 2/9 | chr6 | 30201449 | |||||||
| chr6:30201483 | G | A | 1 | a0001c0003t0025g0355 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-265-345C>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 2/9 | chr6 | 30201483 | |||||||
| chr6:30201550 | A | G | 62 | a0001c0001t0012g0090 a0001c0001t0012g0094 a0001c0002t0005g0002 others(59): Show |
88 | HG00099.hp2 HG00738.hp2 HG00741.hp2 others(85): Show |
intron_variant | MODIFIER | c.-265-412T>C | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 2/9 | chr6 | 30201550 | |||||||
| chr6:30201574 | G | C | 7 | a0003c0006t0005g0044 a0003c0006t0005g0045 a0003c0006t0005g0046 others(4): Show |
7 | HG02074.hp2 HG02735.hp1 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.-265-436C>G | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 2/9 | chr6 | 30201574 | |||||||
| chr6:30201574 | G | T | 1 | a0001c0002t0008g0087 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-265-436C>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 2/9 | chr6 | 30201574 | |||||||
| chr6:30201698 | T | C | 69 | a0001c0001t0012g0090 a0001c0001t0012g0094 a0001c0002t0005g0002 others(66): Show |
95 | HG00099.hp2 HG00738.hp2 HG00741.hp2 others(92): Show |
intron_variant | MODIFIER | c.-265-560A>G | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 2/9 | chr6 | 30201698 | |||||||
| chr6:30201773 | G | A | 2 | a0001c0002t0005g0069 a0001c0002t0005g0076 |
2 | HG03831.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.-265-635C>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 2/9 | chr6 | 30201773 | |||||||
| chr6:30201796 | C | T | 69 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0014 others(66): Show |
84 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.-265-658G>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 2/9 | chr6 | 30201796 | |||||||
| chr6:30201847 | C | CA | 27 | a0001c0001t0001g0013 a0001c0001t0001g0028 a0001c0001t0001g0029 others(24): Show |
33 | HG00735.hp2 HG01106.hp1 HG01257.hp2 others(30): Show |
intron_variant | MODIFIER | c.-265-710dupT | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 2/9 | chr6 | 30201847 | |||||||
| chr6:30201893 | C | T | 15 | a0001c0005t0001g0017 a0001c0005t0001g0037 a0001c0005t0001g0301 others(12): Show |
18 | HG02015.hp1 HG02056.hp2 HG02080.hp2 others(15): Show |
intron_variant | MODIFIER | c.-265-755G>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 2/9 | chr6 | 30201893 | |||||||
| chr6:30201941 | T | C | 1 | a0001c0001t0001g0290 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-265-803A>G | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 2/9 | chr6 | 30201941 | |||||||
| chr6:30201959 | G | A | 7 | a0003c0006t0005g0044 a0003c0006t0005g0045 a0003c0006t0005g0046 others(4): Show |
7 | HG02074.hp2 HG02735.hp1 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.-265-821C>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 2/9 | chr6 | 30201959 | |||||||
| chr6:30202155 | GA | G | 69 | a0001c0001t0012g0090 a0001c0001t0012g0094 a0001c0002t0005g0002 others(66): Show |
95 | HG00099.hp2 HG00738.hp2 HG00741.hp2 others(92): Show |
intron_variant | MODIFIER | c.-265-1018delT | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 2/9 | chr6 | 30202155 | |||||||
| chr6:30202237 | C | T | 7 | a0003c0006t0005g0044 a0003c0006t0005g0045 a0003c0006t0005g0046 others(4): Show |
7 | HG02074.hp2 HG02735.hp1 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.-265-1099G>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 2/9 | chr6 | 30202237 | |||||||
| chr6:30202280 | C | G | 71 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0014 others(68): Show |
86 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.-265-1142G>C | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 2/9 | chr6 | 30202280 | |||||||
| chr6:30202289 | T | A | 7 | a0003c0006t0005g0044 a0003c0006t0005g0045 a0003c0006t0005g0046 others(4): Show |
7 | HG02074.hp2 HG02735.hp1 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.-265-1151A>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 2/9 | chr6 | 30202289 | |||||||
| chr6:30202374 | CGACTGCC others(27): Show |
C | 1 | a0002c0004t0001g0202 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.-265-1270_-265-123 others(38): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 2/9 | chr6 | 30202374 | |||||||
| chr6:30202375 | G | A | 9 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0171 others(6): Show |
11 | HG02056.hp1 NA18939.hp2 NA18968.hp2 others(8): Show |
intron_variant | MODIFIER | c.-265-1237C>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 2/9 | chr6 | 30202375 | |||||||
| chr6:30202463 | C | T | 4 | a0001c0001t0003g0105 a0001c0003t0003g0022 a0001c0003t0003g0023 others(1): Show |
6 | HG00621.hp1 HG02083.hp2 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.-265-1325G>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 2/9 | chr6 | 30202463 | |||||||
| chr6:30202474 | A | G | 1 | a0001c0003t0025g0355 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-265-1336T>C | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 2/9 | chr6 | 30202474 | |||||||
| chr6:30202493 | A | T | 1 | a0001c0001t0001g0032 | 2 | HG02723.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-265-1355T>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 2/9 | chr6 | 30202493 | |||||||
| chr6:30202503 | A | G | 69 | a0001c0001t0012g0090 a0001c0001t0012g0094 a0001c0002t0005g0002 others(66): Show |
95 | HG00099.hp2 HG00738.hp2 HG00741.hp2 others(92): Show |
intron_variant | MODIFIER | c.-265-1365T>C | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 2/9 | chr6 | 30202503 | |||||||
| chr6:30202510 | A | G | 12 | a0001c0002t0008g0080 a0001c0002t0008g0083 a0001c0002t0008g0084 others(9): Show |
16 | HG00099.hp2 HG00738.hp2 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.-265-1372T>C | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 2/9 | chr6 | 30202510 | |||||||
| chr6:30202642 | A | G | 1 | a0001c0002t0017g0088 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-265-1504T>C | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 2/9 | chr6 | 30202642 | |||||||
| chr6:30202733 | T | C | 69 | a0001c0001t0012g0090 a0001c0001t0012g0094 a0001c0002t0005g0002 others(66): Show |
95 | HG00099.hp2 HG00738.hp2 HG00741.hp2 others(92): Show |
intron_variant | MODIFIER | c.-265-1595A>G | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 2/9 | chr6 | 30202733 | |||||||
| chr6:30202748 | C | T | 69 | a0001c0001t0012g0090 a0001c0001t0012g0094 a0001c0002t0005g0002 others(66): Show |
95 | HG00099.hp2 HG00738.hp2 HG00741.hp2 others(92): Show |
intron_variant | MODIFIER | c.-265-1610G>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 2/9 | chr6 | 30202748 | |||||||
| chr6:30202827 | T | G | 3 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0183 |
3 | HG01952.hp1 HG01978.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.-265-1689A>C | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 2/9 | chr6 | 30202827 | |||||||
| chr6:30202851 | T | TA | 62 | a0001c0001t0002g0228 a0001c0001t0002g0233 a0001c0001t0012g0090 others(59): Show |
88 | HG00099.hp2 HG00738.hp2 HG00741.hp2 others(85): Show |
intron_variant | MODIFIER | c.-265-1714dupT | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 2/9 | chr6 | 30202851 | |||||||
| chr6:30202866 | G | A | 2 | a0001c0003t0013g0315 a0001c0003t0013g0316 |
2 | HG01243.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-265-1728C>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 2/9 | chr6 | 30202866 | |||||||
| chr6:30202922 | C | T | 3 | a0001c0007t0001g0161 a0001c0007t0001g0164 a0001c0007t0001g0165 |
3 | HG00639.hp1 HG01256.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.-266+1734G>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 2/9 | chr6 | 30202922 | |||||||
| chr6:30203046 | C | CT | 10 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0173 others(7): Show |
10 | HG02165.hp1 HG03540.hp1 NA18946.hp1 others(7): Show |
intron_variant | MODIFIER | c.-266+1609dupA | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 2/9 | chr6 | 30203046 | |||||||
| chr6:30203046 | CT | C | 81 | a0001c0001t0001g0187 a0001c0001t0001g0291 a0001c0001t0002g0006 others(78): Show |
97 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.-266+1609delA | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 2/9 | chr6 | 30203046 | |||||||
| chr6:30203046 | CTT | C | 48 | a0001c0001t0002g0163 a0001c0001t0002g0229 a0001c0001t0002g0265 others(45): Show |
69 | HG00099.hp2 HG00738.hp2 HG00741.hp2 others(66): Show |
intron_variant | MODIFIER | c.-266+1608_-266+160 others(6): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 2/9 | chr6 | 30203046 | |||||||
| chr6:30203046 | CTTT | C | 24 | a0001c0002t0006g0009 a0001c0002t0006g0010 a0001c0002t0006g0019 others(21): Show |
29 | HG02040.hp2 HG02074.hp2 HG02523.hp1 others(26): Show |
intron_variant | MODIFIER | c.-266+1607_-266+160 others(7): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 2/9 | chr6 | 30203046 | |||||||
| chr6:30203052 | T | C | 45 | a0001c0001t0012g0090 a0001c0001t0012g0094 a0001c0002t0005g0002 others(42): Show |
66 | HG00099.hp2 HG00738.hp2 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.-266+1604A>G | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 2/9 | chr6 | 30203052 | |||||||
| chr6:30203053 | T | C | 24 | a0001c0002t0006g0009 a0001c0002t0006g0010 a0001c0002t0006g0019 others(21): Show |
29 | HG02040.hp2 HG02074.hp2 HG02523.hp1 others(26): Show |
intron_variant | MODIFIER | c.-266+1603A>G | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 2/9 | chr6 | 30203053 | |||||||
| chr6:30203129 | G | T | 69 | a0001c0001t0012g0090 a0001c0001t0012g0094 a0001c0002t0005g0002 others(66): Show |
95 | HG00099.hp2 HG00738.hp2 HG00741.hp2 others(92): Show |
intron_variant | MODIFIER | c.-266+1527C>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 2/9 | chr6 | 30203129 | |||||||
| chr6:30203169 | G | A | 7 | a0003c0006t0005g0044 a0003c0006t0005g0045 a0003c0006t0005g0046 others(4): Show |
7 | HG02074.hp2 HG02735.hp1 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.-266+1487C>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 2/9 | chr6 | 30203169 | |||||||
| chr6:30203193 | A | G | 69 | a0001c0001t0012g0090 a0001c0001t0012g0094 a0001c0002t0005g0002 others(66): Show |
95 | HG00099.hp2 HG00738.hp2 HG00741.hp2 others(92): Show |
intron_variant | MODIFIER | c.-266+1463T>C | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 2/9 | chr6 | 30203193 | |||||||
| chr6:30203434 | G | A | 6 | a0001c0001t0012g0090 a0001c0001t0012g0094 a0001c0002t0008g0089 others(3): Show |
6 | HG01257.hp2 HG01884.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.-266+1222C>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 2/9 | chr6 | 30203434 | |||||||
| chr6:30203501 | C | T | 7 | a0003c0006t0005g0044 a0003c0006t0005g0045 a0003c0006t0005g0046 others(4): Show |
7 | HG02074.hp2 HG02735.hp1 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.-266+1155G>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 2/9 | chr6 | 30203501 | |||||||
| chr6:30203507 | C | T | 19 | a0001c0001t0012g0090 a0001c0001t0012g0094 a0001c0002t0008g0080 others(16): Show |
23 | HG00099.hp2 HG00738.hp2 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.-266+1149G>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 2/9 | chr6 | 30203507 | |||||||
| chr6:30203520 | A | G | 2 | a0001c0002t0006g0064 a0001c0002t0006g0065 |
2 | NA18939.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.-266+1136T>C | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 2/9 | chr6 | 30203520 | |||||||
| chr6:30203523 | C | G | 43 | a0001c0002t0005g0002 a0001c0002t0005g0005 a0001c0002t0005g0011 others(40): Show |
65 | HG00741.hp2 HG01074.hp1 HG01099.hp1 others(62): Show |
intron_variant | MODIFIER | c.-266+1133G>C | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 2/9 | chr6 | 30203523 | |||||||
| chr6:30203572 | C | T | 1 | a0001c0001t0002g0230 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-266+1084G>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 2/9 | chr6 | 30203572 | |||||||
| chr6:30203592 | G | T | 69 | a0001c0001t0012g0090 a0001c0001t0012g0094 a0001c0002t0005g0002 others(66): Show |
95 | HG00099.hp2 HG00738.hp2 HG00741.hp2 others(92): Show |
intron_variant | MODIFIER | c.-266+1064C>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 2/9 | chr6 | 30203592 | |||||||
| chr6:30203625 | C | T | 7 | a0001c0001t0001g0246 a0001c0001t0001g0247 a0001c0001t0001g0248 others(4): Show |
7 | HG01361.hp2 HG02055.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.-266+1031G>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 2/9 | chr6 | 30203625 | |||||||
| chr6:30203631 | G | A | 1 | a0001c0002t0019g0095 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-266+1025C>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 2/9 | chr6 | 30203631 | |||||||
| chr6:30203640 | C | T | 69 | a0001c0001t0012g0090 a0001c0001t0012g0094 a0001c0002t0005g0002 others(66): Show |
95 | HG00099.hp2 HG00738.hp2 HG00741.hp2 others(92): Show |
intron_variant | MODIFIER | c.-266+1016G>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 2/9 | chr6 | 30203640 | |||||||
| chr6:30203708 | C | T | 1 | a0001c0003t0003g0104 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-266+948G>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 2/9 | chr6 | 30203708 | |||||||
| chr6:30203709 | G | A | 1 | a0001c0001t0002g0213 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-266+947C>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 2/9 | chr6 | 30203709 | |||||||
| chr6:30203769 | T | C | 1 | a0001c0002t0008g0097 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-266+887A>G | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 2/9 | chr6 | 30203769 | |||||||
| chr6:30203798 | C | CT | 88 | a0001c0001t0001g0159 a0001c0001t0001g0171 a0001c0001t0001g0292 others(85): Show |
93 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.-266+857dupA | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 2/9 | chr6 | 30203798 | |||||||
| chr6:30203798 | C | CTT | 49 | a0001c0001t0001g0286 a0001c0001t0001g0287 a0001c0001t0001g0288 others(46): Show |
71 | HG00741.hp2 HG01074.hp1 HG01106.hp2 others(68): Show |
intron_variant | MODIFIER | c.-266+856_-266+857d others(4): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 2/9 | chr6 | 30203798 | |||||||
| chr6:30203838 | G | A | 1 | a0001c0001t0001g0300 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-266+818C>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 2/9 | chr6 | 30203838 | |||||||
| chr6:30204023 | C | T | 1 | a0001c0001t0001g0243 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-266+633G>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 2/9 | chr6 | 30204023 | |||||||
| chr6:30204050 | T | C | 70 | a0001c0001t0002g0230 a0001c0001t0012g0090 a0001c0001t0012g0094 others(67): Show |
96 | HG00099.hp2 HG00738.hp2 HG00741.hp2 others(93): Show |
intron_variant | MODIFIER | c.-266+606A>G | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 2/9 | chr6 | 30204050 | |||||||
| chr6:30204104 | C | T | 313 | a0001c0001t0001g0032 a0001c0001t0001g0036 a0001c0001t0001g0159 others(310): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.-266+552G>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 2/9 | chr6 | 30204104 | |||||||
| chr6:30204145 | T | C | 35 | a0001c0001t0004g0001 a0001c0001t0004g0018 a0001c0001t0004g0040 others(32): Show |
47 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(44): Show |
intron_variant | MODIFIER | c.-266+511A>G | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 2/9 | chr6 | 30204145 | |||||||
| chr6:30204358 | T | C | 8 | a0001c0003t0009g0026 a0001c0003t0009g0141 a0001c0003t0009g0142 others(5): Show |
9 | HG00738.hp1 HG01109.hp2 HG01975.hp1 others(6): Show |
intron_variant | MODIFIER | c.-266+298A>G | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 2/9 | chr6 | 30204358 | |||||||
| chr6:30204456 | G | A | 43 | a0001c0002t0005g0002 a0001c0002t0005g0005 a0001c0002t0005g0011 others(40): Show |
65 | HG00741.hp2 HG01074.hp1 HG01099.hp1 others(62): Show |
intron_variant | MODIFIER | c.-266+200C>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 2/9 | chr6 | 30204456 | |||||||
| chr6:30204488 | T | C | 2 | a0001c0002t0008g0085 a0001c0002t0008g0086 |
2 | HG02145.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.-266+168A>G | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 2/9 | chr6 | 30204488 | |||||||
| chr6:30204594 | T | A | 11 | a0001c0001t0002g0007 a0001c0001t0002g0163 a0001c0001t0002g0193 others(8): Show |
14 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(11): Show |
intron_variant | MODIFIER | c.-266+62A>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 2/9 | chr6 | 30204594 | |||||||
| chr6:30204608 | A | C | 50 | a0001c0001t0004g0001 a0001c0001t0004g0018 a0001c0001t0004g0040 others(47): Show |
65 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.-266+48T>G | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 2/9 | chr6 | 30204608 | |||||||
| chr6:30204615 | A | G | 9 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0171 others(6): Show |
11 | HG02056.hp1 NA18939.hp2 NA18968.hp2 others(8): Show |
intron_variant | MODIFIER | c.-266+41T>C | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 2/9 | chr6 | 30204615 | |||||||
| chr6:30204794 | CA | C | 69 | a0001c0001t0012g0090 a0001c0002t0005g0002 a0001c0002t0005g0005 others(66): Show |
95 | HG00099.hp2 HG00738.hp2 HG00741.hp2 others(92): Show |
intron_variant | MODIFIER | c.-375-30delT | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30204794 | |||||||
| chr6:30204874 | A | G | 1 | a0001c0001t0004g0336 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-375-109T>C | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30204874 | |||||||
| chr6:30205173 | G | A | 71 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0014 others(68): Show |
86 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.-375-408C>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30205173 | |||||||
| chr6:30205262 | A | G | 1 | a0001c0001t0001g0320 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-375-497T>C | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30205262 | |||||||
| chr6:30205553 | G | A | 69 | a0001c0001t0012g0090 a0001c0001t0012g0094 a0001c0002t0005g0002 others(66): Show |
95 | HG00099.hp2 HG00738.hp2 HG00741.hp2 others(92): Show |
intron_variant | MODIFIER | c.-375-788C>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30205553 | |||||||
| chr6:30205565 | C | T | 4 | a0001c0001t0002g0163 a0001c0001t0002g0249 a0001c0001t0002g0274 others(1): Show |
4 | HG02071.hp1 NA18943.hp2 NA18987.hp2 others(1): Show |
intron_variant | MODIFIER | c.-375-800G>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30205565 | |||||||
| chr6:30205697 | C | T | 1 | a0001c0001t0001g0325 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-375-932G>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30205697 | |||||||
| chr6:30205761 | G | A | 3 | a0001c0002t0010g0004 a0001c0002t0010g0082 a0001c0008t0016g0081 |
7 | HG00099.hp2 HG00738.hp2 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.-375-996C>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30205761 | |||||||
| chr6:30205767 | G | A | 63 | a0001c0001t0003g0105 a0001c0002t0020g0119 a0001c0003t0003g0022 others(60): Show |
68 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.-375-1002C>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30205767 | |||||||
| chr6:30205768 | G | A | 63 | a0001c0001t0003g0105 a0001c0002t0020g0119 a0001c0003t0003g0022 others(60): Show |
68 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.-375-1003C>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30205768 | |||||||
| chr6:30205898 | T | C | 1 | a0001c0001t0002g0231 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.-375-1133A>G | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30205898 | |||||||
| chr6:30206185 | G | A | 7 | a0003c0006t0005g0044 a0003c0006t0005g0045 a0003c0006t0005g0046 others(4): Show |
7 | HG02074.hp2 HG02735.hp1 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.-375-1420C>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30206185 | |||||||
| chr6:30206354 | C | T | 69 | a0001c0001t0012g0090 a0001c0001t0012g0094 a0001c0002t0005g0002 others(66): Show |
95 | HG00099.hp2 HG00738.hp2 HG00741.hp2 others(92): Show |
intron_variant | MODIFIER | c.-375-1589G>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30206354 | |||||||
| chr6:30206355 | G | A | 70 | a0001c0001t0001g0237 a0001c0001t0002g0006 a0001c0001t0002g0007 others(67): Show |
85 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.-375-1590C>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30206355 | |||||||
| chr6:30206651 | A | T | 19 | a0001c0001t0012g0090 a0001c0001t0012g0094 a0001c0002t0008g0080 others(16): Show |
23 | HG00099.hp2 HG00738.hp2 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.-375-1886T>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30206651 | |||||||
| chr6:30206700 | C | T | 2 | a0001c0002t0008g0085 a0001c0002t0008g0086 |
2 | HG02145.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.-375-1935G>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30206700 | |||||||
| chr6:30206813 | C | T | 25 | a0001c0001t0004g0040 a0001c0001t0004g0042 a0001c0001t0004g0043 others(22): Show |
28 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(25): Show |
intron_variant | MODIFIER | c.-375-2048G>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30206813 | |||||||
| chr6:30206856 | C | A | 69 | a0001c0001t0012g0090 a0001c0001t0012g0094 a0001c0002t0005g0002 others(66): Show |
95 | HG00099.hp2 HG00738.hp2 HG00741.hp2 others(92): Show |
intron_variant | MODIFIER | c.-375-2091G>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30206856 | |||||||
| chr6:30206865 | C | T | 1 | a0001c0003t0003g0133 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-375-2100G>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30206865 | |||||||
| chr6:30206874 | C | T | 1 | a0001c0002t0020g0119 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-375-2109G>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30206874 | |||||||
| chr6:30207135 | G | C | 2 | a0001c0003t0013g0315 a0001c0003t0013g0316 |
2 | HG01243.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-375-2370C>G | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30207135 | |||||||
| chr6:30207265 | T | C | 4 | a0001c0001t0001g0361 a0001c0001t0001g0362 a0001c0001t0001g0363 others(1): Show |
4 | HG02258.hp1 HG02572.hp1 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.-375-2500A>G | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30207265 | |||||||
| chr6:30207359 | C | T | 2 | a0001c0003t0013g0315 a0001c0003t0013g0316 |
2 | HG01243.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-375-2594G>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30207359 | |||||||
| chr6:30207541 | C | T | 43 | a0001c0002t0005g0002 a0001c0002t0005g0005 a0001c0002t0005g0011 others(40): Show |
65 | HG00741.hp2 HG01074.hp1 HG01099.hp1 others(62): Show |
intron_variant | MODIFIER | c.-375-2776G>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30207541 | |||||||
| chr6:30207551 | G | A | 1 | a0001c0003t0003g0132 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-375-2786C>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30207551 | |||||||
| chr6:30207795 | C | T | 2 | a0001c0003t0011g0148 a0001c0003t0011g0149 |
2 | HG02559.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-375-3030G>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30207795 | |||||||
| chr6:30207945 | C | T | 1 | a0001c0003t0003g0118 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-375-3180G>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30207945 | |||||||
| chr6:30207946 | C | T | 1 | a0001c0003t0009g0141 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-375-3181G>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30207946 | |||||||
| chr6:30208070 | A | C | 132 | a0001c0001t0003g0105 a0001c0001t0012g0090 a0001c0001t0012g0094 others(129): Show |
163 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.-375-3305T>G | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30208070 | |||||||
| chr6:30208292 | G | C | 1 | a0001c0003t0011g0053 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-375-3527C>G | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30208292 | |||||||
| chr6:30208300 | G | A | 1 | a0001c0003t0025g0355 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-375-3535C>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30208300 | |||||||
| chr6:30208345 | C | T | 12 | a0001c0001t0001g0036 a0001c0001t0001g0243 a0001c0001t0001g0244 others(9): Show |
13 | HG00639.hp1 HG01109.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.-375-3580G>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30208345 | |||||||
| chr6:30208367 | C | T | 1 | a0001c0001t0001g0170 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-375-3602G>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30208367 | |||||||
| chr6:30208458 | C | T | 1 | a0001c0001t0001g0294 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-375-3693G>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30208458 | |||||||
| chr6:30208515 | C | CT | 20 | a0001c0001t0001g0036 a0001c0001t0001g0243 a0001c0001t0001g0244 others(17): Show |
21 | HG01109.hp1 HG01243.hp1 HG02074.hp2 others(18): Show |
intron_variant | MODIFIER | c.-375-3751dupA | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30208515 | |||||||
| chr6:30208515 | CT | C | 40 | a0001c0001t0001g0159 a0001c0001t0001g0283 a0001c0001t0001g0294 others(37): Show |
44 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.-375-3751delA | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30208515 | |||||||
| chr6:30208515 | CTT | C | 102 | a0001c0001t0003g0105 a0001c0001t0012g0090 a0001c0001t0012g0094 others(99): Show |
128 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.-375-3752_-375-375 others(6): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30208515 | |||||||
| chr6:30208534 | C | G | 132 | a0001c0001t0003g0105 a0001c0001t0012g0090 a0001c0001t0012g0094 others(129): Show |
163 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.-375-3769G>C | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30208534 | |||||||
| chr6:30208581 | A | G | 22 | a0002c0004t0001g0166 a0002c0004t0001g0194 a0002c0004t0001g0195 others(19): Show |
22 | HG00673.hp1 HG01167.hp2 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.-375-3816T>C | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30208581 | |||||||
| chr6:30208818 | T | C | 1 | a0001c0003t0003g0098 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-375-4053A>G | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30208818 | |||||||
| chr6:30208904 | A | ATC | 25 | a0001c0002t0005g0002 a0001c0002t0005g0005 a0001c0002t0005g0027 others(22): Show |
35 | HG00609.hp2 HG00738.hp1 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.-375-4140_-375-413 others(6): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30208904 | |||||||
| chr6:30208904 | A | ATCTG | 34 | a0001c0002t0006g0055 a0001c0002t0006g0056 a0001c0002t0006g0064 others(31): Show |
40 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(37): Show |
intron_variant | MODIFIER | c.-375-4140_-375-413 others(8): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30208904 | |||||||
| chr6:30208904 | A | ATCTGTG | 37 | a0001c0001t0003g0105 a0001c0002t0005g0151 a0001c0002t0006g0009 others(34): Show |
44 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.-375-4140_-375-413 others(10): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30208904 | |||||||
| chr6:30208904 | A | ATCTGTGT others(1): Show |
3 | a0001c0003t0003g0102 a0003c0006t0005g0044 a0003c0006t0005g0045 |
3 | HG01496.hp2 HG03017.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.-375-4140_-375-413 others(12): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30208904 | |||||||
| chr6:30208904 | A | ATG | 13 | a0001c0001t0001g0237 a0001c0001t0001g0319 a0001c0001t0002g0238 others(10): Show |
13 | HG00597.hp1 HG01516.hp1 HG01928.hp1 others(10): Show |
intron_variant | MODIFIER | c.-375-4141_-375-414 others(6): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30208904 | |||||||
| chr6:30208904 | A | ATGTG | 34 | a0001c0001t0001g0167 a0001c0001t0001g0185 a0001c0001t0002g0006 others(31): Show |
43 | HG00621.hp2 HG00639.hp2 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.-375-4143_-375-414 others(8): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30208904 | |||||||
| chr6:30208904 | A | ATGTGTG | 26 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0033 others(23): Show |
31 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(28): Show |
intron_variant | MODIFIER | c.-375-4145_-375-414 others(10): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30208904 | |||||||
| chr6:30208904 | ATG | A | 85 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0029 others(82): Show |
108 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.-375-4141_-375-414 others(6): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30208904 | |||||||
| chr6:30208904 | ATGTG | A | 9 | a0001c0001t0001g0283 a0001c0001t0004g0349 a0001c0001t0004g0350 others(6): Show |
9 | HG01167.hp1 HG01169.hp1 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.-375-4143_-375-414 others(8): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30208904 | |||||||
| chr6:30208904 | ATGTGTG | A | 10 | a0001c0001t0001g0284 a0001c0001t0001g0331 a0001c0001t0001g0332 others(7): Show |
19 | HG00140.hp1 HG00558.hp2 HG01070.hp1 others(16): Show |
intron_variant | MODIFIER | c.-375-4145_-375-414 others(10): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30208904 | |||||||
| chr6:30208904 | ATGTGTGT others(3): Show |
A | 1 | a0003c0006t0005g0050 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-375-4149_-375-414 others(14): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30208904 | |||||||
| chr6:30208904 | ATGTGTGT others(9): Show |
A | 20 | a0001c0001t0001g0159 a0001c0001t0001g0286 a0001c0001t0001g0287 others(17): Show |
20 | HG00733.hp2 HG01081.hp1 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.-375-4155_-375-414 others(20): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30208904 | |||||||
| chr6:30208906 | G | C | 17 | a0001c0001t0012g0090 a0001c0001t0012g0094 a0001c0002t0005g0011 others(14): Show |
20 | HG00741.hp2 HG01074.hp1 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.-375-4141C>G | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30208906 | |||||||
| chr6:30208908 | G | C | 12 | a0001c0002t0005g0076 a0001c0002t0007g0008 a0001c0002t0007g0012 others(9): Show |
17 | HG01261.hp2 HG01516.hp2 HG01517.hp1 others(14): Show |
intron_variant | MODIFIER | c.-375-4143C>G | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30208908 | |||||||
| chr6:30208910 | G | C | 3 | a0001c0002t0005g0079 a0001c0002t0007g0077 a0001c0002t0007g0078 |
3 | HG01167.hp1 HG01169.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.-375-4145C>G | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30208910 | |||||||
| chr6:30208916 | G | A | 1 | a0001c0001t0001g0184 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-375-4151C>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30208916 | |||||||
| chr6:30208916 | G | C | 1 | a0003c0006t0005g0050 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-375-4151C>G | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30208916 | |||||||
| chr6:30209055 | T | C | 1 | a0001c0001t0001g0300 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-376+4250A>G | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30209055 | |||||||
| chr6:30209147 | T | G | 16 | a0001c0001t0004g0306 a0001c0005t0001g0017 a0001c0005t0001g0037 others(13): Show |
19 | HG02015.hp1 HG02056.hp2 HG02080.hp2 others(16): Show |
intron_variant | MODIFIER | c.-376+4158A>C | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30209147 | |||||||
| chr6:30209458 | G | A | 2 | a0001c0003t0013g0315 a0001c0003t0013g0316 |
2 | HG01243.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-376+3847C>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30209458 | |||||||
| chr6:30209829 | G | A | 8 | a0001c0003t0009g0026 a0001c0003t0009g0141 a0001c0003t0009g0142 others(5): Show |
9 | HG00738.hp1 HG01109.hp2 HG01975.hp1 others(6): Show |
intron_variant | MODIFIER | c.-376+3476C>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30209829 | |||||||
| chr6:30209848 | TAAATAA | T | 5 | a0001c0001t0001g0032 a0001c0001t0001g0189 a0001c0001t0001g0190 others(2): Show |
6 | HG02630.hp2 HG02723.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-376+3451_-376+345 others(10): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30209848 | |||||||
| chr6:30209935 | G | A | 2 | a0001c0003t0011g0148 a0001c0003t0011g0149 |
2 | HG02559.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-376+3370C>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30209935 | |||||||
| chr6:30209944 | C | T | 1 | a0001c0001t0002g0193 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-376+3361G>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30209944 | |||||||
| chr6:30209963 | T | C | 1 | a0001c0003t0002g0317 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-376+3342A>G | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30209963 | |||||||
| chr6:30209984 | A | T | 3 | a0001c0002t0006g0055 a0001c0002t0006g0056 a0001c0002t0006g0158 |
3 | NA18968.hp1 NA18970.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.-376+3321T>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30209984 | |||||||
| chr6:30210083 | T | C | 132 | a0001c0001t0003g0105 a0001c0001t0012g0090 a0001c0001t0012g0094 others(129): Show |
163 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.-376+3222A>G | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30210083 | |||||||
| chr6:30210140 | G | C | 125 | a0001c0001t0003g0105 a0001c0001t0012g0090 a0001c0001t0012g0094 others(122): Show |
156 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.-376+3165C>G | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30210140 | |||||||
| chr6:30210161 | C | T | 1 | a0001c0003t0025g0355 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-376+3144G>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30210161 | |||||||
| chr6:30210162 | G | A | 19 | a0001c0001t0012g0090 a0001c0001t0012g0094 a0001c0002t0008g0080 others(16): Show |
23 | HG00099.hp2 HG00738.hp2 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.-376+3143C>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30210162 | |||||||
| chr6:30210169 | C | T | 3 | a0001c0003t0003g0099 a0001c0003t0003g0100 a0001c0003t0003g0101 |
3 | HG00323.hp2 HG02602.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.-376+3136G>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30210169 | |||||||
| chr6:30210192 | G | A | 1 | a0001c0003t0025g0355 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-376+3113C>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30210192 | |||||||
| chr6:30210209 | CA | C | 131 | a0001c0001t0003g0105 a0001c0001t0012g0090 a0001c0001t0012g0094 others(128): Show |
162 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.-376+3095delT | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30210209 | |||||||
| chr6:30210293 | C | T | 1 | a0001c0002t0008g0097 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-376+3012G>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30210293 | |||||||
| chr6:30210510 | C | T | 132 | a0001c0001t0003g0105 a0001c0001t0012g0090 a0001c0001t0012g0094 others(129): Show |
163 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.-376+2795G>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30210510 | |||||||
| chr6:30210651 | T | C | 1 | a0001c0002t0008g0097 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-376+2654A>G | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30210651 | |||||||
| chr6:30210673 | TAA | T | 5 | a0001c0001t0001g0032 a0001c0001t0001g0189 a0001c0001t0001g0190 others(2): Show |
6 | HG02630.hp2 HG02723.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-376+2630_-376+263 others(6): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30210673 | |||||||
| chr6:30210723 | G | T | 2 | a0001c0002t0007g0008 a0001c0002t0007g0054 |
4 | HG02818.hp2 HG03139.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.-376+2582C>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30210723 | |||||||
| chr6:30210724 | A | AATAACT | 132 | a0001c0001t0003g0105 a0001c0001t0012g0090 a0001c0001t0012g0094 others(129): Show |
163 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.-376+2580_-376+258 others(10): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30210724 | |||||||
| chr6:30211023 | A | G | 1 | a0001c0001t0002g0188 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-376+2282T>C | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30211023 | |||||||
| chr6:30211249 | A | C | 132 | a0001c0001t0003g0105 a0001c0001t0012g0090 a0001c0001t0012g0094 others(129): Show |
163 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.-376+2056T>G | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30211249 | |||||||
| chr6:30211375 | T | C | 132 | a0001c0001t0003g0105 a0001c0001t0012g0090 a0001c0001t0012g0094 others(129): Show |
163 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.-376+1930A>G | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30211375 | |||||||
| chr6:30211387 | T | C | 321 | a0001c0001t0001g0032 a0001c0001t0001g0036 a0001c0001t0001g0159 others(318): Show |
384 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(381): Show |
intron_variant | MODIFIER | c.-376+1918A>G | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30211387 | |||||||
| chr6:30211399 | A | T | 1 | a0001c0001t0004g0318 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-376+1906T>A | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30211399 | |||||||
| chr6:30211411 | G | C | 7 | a0001c0002t0005g0002 a0001c0002t0005g0005 a0001c0002t0005g0027 others(4): Show |
16 | HG01884.hp2 HG01891.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.-376+1894C>G | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30211411 | |||||||
| chr6:30211447 | A | C | 1 | a0001c0003t0003g0098 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-376+1858T>G | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30211447 | |||||||
| chr6:30211491 | T | C | 23 | a0001c0001t0001g0013 a0001c0001t0001g0028 a0001c0001t0001g0029 others(20): Show |
29 | HG00621.hp2 HG00735.hp2 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.-376+1814A>G | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30211491 | |||||||
| chr6:30211645 | G | A | 63 | a0001c0001t0003g0105 a0001c0002t0020g0119 a0001c0003t0003g0022 others(60): Show |
68 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.-376+1660C>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30211645 | |||||||
| chr6:30211856 | G | GA | 132 | a0001c0001t0003g0105 a0001c0001t0012g0090 a0001c0001t0012g0094 others(129): Show |
163 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.-376+1448_-376+144 others(5): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30211856 | |||||||
| chr6:30212194 | GA | G | 3 | a0001c0003t0011g0051 a0001c0003t0011g0052 a0001c0003t0011g0053 |
3 | HG01255.hp2 HG02145.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-376+1110delT | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30212194 | |||||||
| chr6:30212228 | T | G | 1 | a0001c0001t0004g0356 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-376+1077A>C | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30212228 | |||||||
| chr6:30212415 | T | C | 7 | a0001c0001t0004g0042 a0001c0001t0004g0043 a0001c0001t0004g0160 others(4): Show |
9 | NA18943.hp1 NA18952.hp2 NA18964.hp1 others(6): Show |
intron_variant | MODIFIER | c.-376+890A>G | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30212415 | |||||||
| chr6:30212469 | T | C | 132 | a0001c0001t0003g0105 a0001c0001t0012g0090 a0001c0001t0012g0094 others(129): Show |
163 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.-376+836A>G | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30212469 | |||||||
| chr6:30212499 | T | C | 7 | a0003c0006t0005g0044 a0003c0006t0005g0045 a0003c0006t0005g0046 others(4): Show |
7 | HG02074.hp2 HG02735.hp1 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.-376+806A>G | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30212499 | |||||||
| chr6:30212503 | T | C | 7 | a0001c0002t0005g0002 a0001c0002t0005g0005 a0001c0002t0005g0027 others(4): Show |
16 | HG01884.hp2 HG01891.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.-376+802A>G | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30212503 | |||||||
| chr6:30212516 | T | C | 1 | a0001c0003t0003g0155 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-376+789A>G | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30212516 | |||||||
| chr6:30212723 | A | C | 7 | a0003c0006t0005g0044 a0003c0006t0005g0045 a0003c0006t0005g0046 others(4): Show |
7 | HG02074.hp2 HG02735.hp1 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.-376+582T>G | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30212723 | |||||||
| chr6:30212730 | G | A | 1 | a0001c0002t0005g0156 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-376+575C>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30212730 | |||||||
| chr6:30212915 | CA | C | 150 | a0001c0001t0001g0032 a0001c0001t0001g0036 a0001c0001t0001g0159 others(147): Show |
170 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.-376+389delT | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30212915 | |||||||
| chr6:30212915 | CAA | C | 29 | a0001c0001t0001g0013 a0001c0001t0001g0028 a0001c0001t0001g0029 others(26): Show |
35 | HG00621.hp2 HG00639.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.-376+388_-376+389d others(4): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30212915 | |||||||
| chr6:30212915 | CAAA | C | 132 | a0001c0001t0003g0105 a0001c0001t0012g0090 a0001c0001t0012g0094 others(129): Show |
163 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.-376+387_-376+389d others(5): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30212915 | |||||||
| chr6:30212932 | A | G | 133 | a0001c0001t0003g0105 a0001c0001t0004g0160 a0001c0001t0012g0090 others(130): Show |
164 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.-376+373T>C | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30212932 | |||||||
| chr6:30213114 | T | C | 4 | a0001c0001t0001g0361 a0001c0001t0001g0362 a0001c0001t0001g0363 others(1): Show |
4 | HG02258.hp1 HG02572.hp1 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.-376+191A>G | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30213114 | |||||||
| chr6:30213250 | G | A | 1 | a0001c0001t0004g0365 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-376+55C>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30213250 | |||||||
| chr6:30213262 | G | A | 1 | a0001c0002t0006g0158 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-376+43C>T | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30213262 | |||||||
| chr6:30213299 | A | G | 1 | a0001c0001t0001g0159 | 1 | NA20805.hp2 | splice_region_variant&intron_variant | LOW | c.-376+6T>C | TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | 30213299 |