Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 57159 |
| ensemblid | ENSG00000138100.14 |
| hgncid | 16008 |
| symbol | TRIM54 |
| name | tripartite motif containing 54 |
| refseq_nuc | NM_187841.3 |
| refseq_prot | NP_912730.2 |
| ensembl_nuc | ENST00000380075.7 |
| ensembl_prot | ENSP00000369415.3 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 27282429 |
| end | 27307435 |
| strand | + |
| ver | v1.2 |
| region | chr2:27282429-27307435 |
| region5000 | chr2:27277429-27312435 |
| regionname0 | TRIM54_chr2_27282429_27307435 |
| regionname5000 | TRIM54_chr2_27277429_27312435 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 358 | 274 | 86 | 60 | 86 | 14 | 26 | 62 | TRIM54_chr2_27277429_27312435 | TRIM54 | MNFTV others(353): Show |
chr2 | 27277429 | 27312435 |
| a0002 | 0/0 | 358 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | MNFTV others(353): Show |
chr2 | 27277429 | 27312435 |
| a0003 | 0/0 | 358 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | MNFTV others(353): Show |
chr2 | 27277429 | 27312435 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1074 | 267 | 81 | 58 | 86 | 14 | 26 | TRIM54_chr2_27277429_27312435 | TRIM54 | ATGAA others(1069): Show |
chr2 | 27277429 | 27312435 | ||
| a0001c0002 | 0/0 | 1074 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | ATGAA others(1069): Show |
chr2 | 27277429 | 27312435 | ||
| a0001c0003 | 0/0 | 1074 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | ATGAA others(1069): Show |
chr2 | 27277429 | 27312435 | ||
| a0001c0006 | 0/0 | 1074 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | ATGAA others(1069): Show |
chr2 | 27277429 | 27312435 | ||
| a0001c0007 | 0/0 | 1074 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | ATGAA others(1069): Show |
chr2 | 27277429 | 27312435 | ||
| a0002c0004 | 0/0 | 1074 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM54_chr2_27277429_27312435 | TRIM54 | ATGAA others(1069): Show |
chr2 | 27277429 | 27312435 | ||
| a0003c0005 | 0/0 | 1074 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM54_chr2_27277429_27312435 | TRIM54 | ATGAA others(1069): Show |
chr2 | 27277429 | 27312435 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1930 | 259 | 76 | 56 | 85 | 14 | 26 | TRIM54_chr2_27277429_27312435 | TRIM54 | AAACA others(1925): Show |
chr2 | 27277429 | 27312435 |
| a0001c0001t0002 | 0/0 | 1930 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | AAACA others(1925): Show |
chr2 | 27277429 | 27312435 |
| a0001c0001t0003 | 0/0 | 1930 | 2 | 1 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | AAACA others(1925): Show |
chr2 | 27277429 | 27312435 |
| a0001c0001t0004 | 0/0 | 1930 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | AAACA others(1925): Show |
chr2 | 27277429 | 27312435 |
| a0001c0001t0006 | 0/0 | 1930 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | AAACA others(1925): Show |
chr2 | 27277429 | 27312435 |
| a0001c0001t0007 | 0/0 | 1930 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | AAACA others(1925): Show |
chr2 | 27277429 | 27312435 |
| a0001c0002t0001 | 0/0 | 1930 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | AAACA others(1925): Show |
chr2 | 27277429 | 27312435 |
| a0001c0003t0001 | 0/0 | 1930 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | AAACA others(1925): Show |
chr2 | 27277429 | 27312435 |
| a0001c0006t0001 | 0/0 | 1930 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | AAACA others(1925): Show |
chr2 | 27277429 | 27312435 |
| a0001c0007t0005 | 0/0 | 1930 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | AAACA others(1925): Show |
chr2 | 27277429 | 27312435 |
| a0002c0004t0001 | 0/0 | 1930 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM54_chr2_27277429_27312435 | TRIM54 | AAACA others(1925): Show |
chr2 | 27277429 | 27312435 |
| a0003c0005t0001 | 0/0 | 1930 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM54_chr2_27277429_27312435 | TRIM54 | AAACA others(1925): Show |
chr2 | 27277429 | 27312435 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 8 | 0 | 2 | 4 | 0 | 2 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0002 | 0/0 | 8 | 0 | 2 | 4 | 1 | 1 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0003 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0004 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0005 | 0/0 | 5 | 0 | 4 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0006 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0007 | 1/0 | 4 | 0 | 1 | 2 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0011 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0013 | 0/0 | 3 | 1 | 0 | 0 | 2 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0206 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0002g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0003g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0003g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0004g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0006g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0001t0007g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0002t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0002t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0002t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0003t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0006t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0001c0007t0005g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0002c0004t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| a0003c0005t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0011 | EUR | GBR | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0013 | EUR | GBR | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0133 | EUR | FIN | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0089 | EUR | FIN | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0114 | EUR | FIN | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0120 | EUR | FIN | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | CHS | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | CHS | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | CHS | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | CHS | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | CHS | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0140 | AMR | PUR | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG01109 | hp2 | a0001 | c0001 | t0004 | g0067 | AMR | PUR | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | CLM | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG01256 | hp2 | a0001 | c0003 | t0001 | g0024 | AMR | CLM | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG01257 | hp1 | a0001 | c0003 | t0001 | g0024 | AMR | CLM | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | CLM | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | CLM | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | CLM | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | CLM | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | CLM | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | CLM | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | CLM | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | CLM | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | CLM | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | CLM | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0107 | EUR | IBS | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0176 | EUR | IBS | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0032 | EUR | IBS | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0080 | EUR | IBS | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | ACB | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | ACB | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | ACB | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | ACB | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PEL | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | PEL | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PEL | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | PEL | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PEL | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PEL | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | KHV | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | KHV | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | KHV | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | KHV | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | KHV | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | KHV | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | KHV | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | CDX | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | ACB | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | ACB | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | ACB | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0149 | AFR | ACB | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | GWD | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG02602 | hp1 | a0002 | c0004 | t0001 | g0117 | SAS | PJL | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG02622 | hp2 | a0001 | c0002 | t0001 | g0033 | AFR | GWD | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | GWD | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | GWD | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG02698 | hp1 | a0003 | c0005 | t0001 | g0001 | SAS | PJL | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0205 | SAS | PJL | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0069 | SAS | PJL | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | GWD | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | ESN | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | ESN | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | ESN | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | ESN | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | ESN | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG03041 | hp2 | a0001 | c0007 | t0005 | g0152 | AFR | GWD | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | MSL | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG03098 | hp2 | a0001 | c0006 | t0001 | g0054 | AFR | MSL | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | ESN | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | ESN | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ESN | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | ESN | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | ESN | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | ESN | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | MSL | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0027 | AFR | MSL | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | MSL | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | MSL | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG03453 | hp2 | a0001 | c0002 | t0001 | g0035 | AFR | MSL | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0150 | AFR | MSL | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | MSL | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0169 | SAS | PJL | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | ESN | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ESN | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0201 | SAS | STU | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0187 | SAS | BEB | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0178 | SAS | STU | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | STU | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | STU | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0177 | SAS | STU | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | YRI | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | YRI | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | CHB | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | CHB | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | YRI | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0027 | AFR | YRI | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| NA18988 | hp1 | a0001 | c0001 | t0007 | g0182 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | LWK | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | LWK | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | YRI | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | YRI | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | ASW | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ASW | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0121 | EUR | TSI | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0013 | EUR | TSI | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0113 | EUR | TSI | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | CLM | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | CLM | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | ACB | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | ACB | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | ACB | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG02559 | hp1 | a0001 | c0002 | t0001 | g0034 | AFR | ACB | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | ACB | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | MSL | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | USA | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | USA | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| NA20300 | hp1 | a0001 | c0001 | t0006 | g0148 | AFR | USA | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | USA | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | LWK | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | LWK | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0206 | REF | REF | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0007 | REF | REF | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:27299361 | G | A | 1 | a0003 | 1 | HG02698.hp1 | missense_variant | MODERATE | c.458G>A | p.Gly153Asp | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/9 | 761/1930 | 458/1077 | 153/358 | chr2 | 27299361 | |||
| chr2:27305007 | G | T | 1 | a0002 | 1 | HG02602.hp1 | missense_variant | MODERATE | c.562G>T | p.Val188Leu | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 4/9 | 865/1930 | 562/1077 | 188/358 | chr2 | 27305007 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:27282812 | C | T | 1 | a0001c0007 | 1 | HG03041.hp2 | synonymous_variant | LOW | c.81C>T | p.Pro27Pro | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/9 | 384/1930 | 81/1077 | 27/358 | chr2 | 27282812 | |||
| chr2:27282869 | G | A | 1 | a0002c0004 | 1 | HG02602.hp1 | synonymous_variant | LOW | c.138G>A | p.Leu46Leu | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/9 | 441/1930 | 138/1077 | 46/358 | chr2 | 27282869 | |||
| chr2:27282890 | C | T | 1 | a0001c0003 | 2 | HG01256.hp2 HG01257.hp1 |
synonymous_variant | LOW | c.159C>T | p.Asp53Asp | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/9 | 462/1930 | 159/1077 | 53/358 | chr2 | 27282890 | |||
| chr2:27304982 | G | A | 1 | a0001c0002 | 3 | HG02559.hp1 HG02622.hp2 HG03453.hp2 |
synonymous_variant | LOW | c.537G>A | p.Ala179Ala | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 4/9 | 840/1930 | 537/1077 | 179/358 | chr2 | 27304982 | |||
| chr2:27305727 | T | C | 1 | a0001c0006 | 1 | HG03098.hp2 | synonymous_variant | LOW | c.753T>C | p.Arg251Arg | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 5/9 | 1056/1930 | 753/1077 | 251/358 | chr2 | 27305727 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:27282533 | G | A | 1 | a0001c0001t0004 | 1 | HG01109.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-199G>A | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/9 | chr2 | 27282533 | |||||||
| chr2:27282578 | C | A | 1 | a0001c0001t0003 | 2 | HG01074.hp1 HG03486.hp1 |
5_prime_UTR_variant | MODIFIER | c.-154C>A | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/9 | 154 | chr2 | 27282578 | ||||||
| chr2:27306918 | C | T | 1 | a0001c0001t0002 | 3 | HG02451.hp1 HG03209.hp2 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*33C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 9/9 | 377 | chr2 | 27306918 | ||||||
| chr2:27307002 | T | C | 1 | a0001c0007t0005 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*117T>C | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 9/9 | 461 | chr2 | 27307002 | ||||||
| chr2:27307066 | C | T | 1 | a0001c0001t0004 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*181C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 9/9 | 525 | chr2 | 27307066 | ||||||
| chr2:27307159 | C | T | 1 | a0001c0001t0007 | 1 | NA18988.hp1 | 3_prime_UTR_variant | MODIFIER | c.*274C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 9/9 | 618 | chr2 | 27307159 | ||||||
| chr2:27307298 | C | G | 1 | a0001c0001t0006 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*413C>G | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 9/9 | 757 | chr2 | 27307298 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:27282914 | C | T | 62 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0014 others(59): Show |
76 | HG00597.hp2 HG00735.hp1 HG00738.hp1 others(73): Show |
intron_variant | MODIFIER | c.168+15C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27282914 | |||||||
| chr2:27283122 | C | T | 2 | a0001c0001t0001g0028 a0001c0001t0001g0154 |
3 | NA18906.hp1 NA19043.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.168+223C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27283122 | |||||||
| chr2:27283304 | AAAAC | A | 4 | a0001c0001t0001g0036 a0001c0002t0001g0033 a0001c0002t0001g0034 others(1): Show |
4 | HG02559.hp1 HG02622.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.168+417_168+420del others(4): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27283304 | ||||||
| chr2:27283349 | G | A | 1 | a0001c0001t0001g0037 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.168+450G>A | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27283349 | |||||||
| chr2:27283543 | T | C | 10 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(7): Show |
10 | HG01891.hp1 HG01891.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.168+644T>C | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27283543 | |||||||
| chr2:27283681 | C | CT | 6 | a0001c0001t0001g0151 a0001c0001t0001g0153 a0001c0001t0001g0208 others(3): Show |
6 | HG01934.hp2 HG02897.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.168+795dupT | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27283681 | ||||||
| chr2:27283681 | CT | C | 7 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(4): Show |
7 | HG02074.hp1 HG02486.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.168+795delT | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27283681 | ||||||
| chr2:27283763 | G | GGCACACA others(15): Show |
1 | a0001c0001t0001g0205 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.168+872_168+873ins others(22): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27283763 | ||||||
| chr2:27283764 | G | GCACACAC others(21): Show |
1 | a0001c0001t0001g0204 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.168+872_168+873ins others(28): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27283764 | ||||||
| chr2:27283764 | G | GCACACAC others(21): Show |
1 | a0001c0001t0001g0207 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.168+872_168+873ins others(28): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27283764 | ||||||
| chr2:27283764 | GCA | G | 3 | a0001c0001t0001g0036 a0001c0001t0002g0149 a0001c0001t0003g0150 |
3 | HG02451.hp1 HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.168+879_168+880del others(2): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27283764 | ||||||
| chr2:27283764 | GCACACAC others(19): Show |
G | 3 | a0001c0001t0001g0028 a0001c0001t0001g0041 a0001c0001t0001g0154 |
4 | HG06807.hp1 NA18906.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.168+881_168+906del others(26): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27283764 | ||||||
| chr2:27283766 | A | ACACACGC others(9): Show |
1 | a0001c0001t0001g0014 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.168+872_168+873ins others(16): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27283766 | ||||||
| chr2:27283766 | A | ACACACGC others(13): Show |
2 | a0001c0001t0001g0180 a0001c0001t0001g0198 |
2 | NA18966.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.168+872_168+873ins others(20): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27283766 | ||||||
| chr2:27283766 | A | ACACACGC others(15): Show |
1 | a0001c0001t0001g0168 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.168+872_168+873ins others(22): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27283766 | ||||||
| chr2:27283766 | ACACACAC others(11): Show |
A | 1 | a0001c0002t0001g0034 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.168+881_168+898del others(18): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27283766 | ||||||
| chr2:27283768 | A | ACACGCAC others(9): Show |
1 | a0001c0001t0001g0191 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.168+872_168+873ins others(16): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27283768 | ||||||
| chr2:27283768 | A | ACACGCAC others(11): Show |
3 | a0001c0001t0001g0014 a0001c0001t0001g0193 a0001c0001t0001g0202 |
3 | HG00597.hp2 HG00738.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.168+872_168+873ins others(18): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27283768 | ||||||
| chr2:27283768 | A | ACACGCAC others(13): Show |
2 | a0001c0001t0001g0029 a0001c0001t0001g0178 |
2 | HG04199.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.168+872_168+873ins others(20): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27283768 | ||||||
| chr2:27283768 | A | ACGCACGC others(11): Show |
1 | a0001c0001t0001g0166 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.168+870_168+871ins others(18): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27283768 | ||||||
| chr2:27283768 | A | ACGCACGC others(13): Show |
1 | a0001c0001t0001g0200 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.168+870_168+871ins others(20): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27283768 | ||||||
| chr2:27283770 | A | ACGCACGC others(5): Show |
1 | a0001c0001t0001g0005 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.168+872_168+873ins others(12): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27283770 | ||||||
| chr2:27283770 | A | ACGCACGC others(7): Show |
3 | a0001c0001t0001g0005 a0001c0001t0001g0175 a0001c0001t0001g0196 |
5 | HG01074.hp2 HG01255.hp1 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.168+872_168+873ins others(14): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27283770 | ||||||
| chr2:27283770 | A | ACGCACGC others(9): Show |
7 | a0001c0001t0001g0004 a0001c0001t0001g0032 a0001c0001t0001g0184 others(4): Show |
7 | HG02015.hp1 HG02015.hp2 NA18939.hp1 others(4): Show |
intron_variant | MODIFIER | c.168+872_168+873ins others(16): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27283770 | ||||||
| chr2:27283770 | A | ACGCACGC others(11): Show |
3 | a0001c0001t0001g0029 a0001c0001t0001g0170 a0001c0001t0001g0174 |
3 | HG01257.hp2 HG01258.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.168+872_168+873ins others(18): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27283770 | ||||||
| chr2:27283770 | A | G | 3 | a0001c0001t0001g0166 a0001c0001t0001g0171 a0001c0001t0001g0200 |
3 | HG01496.hp2 HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.168+871A>G | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27283770 | |||||||
| chr2:27283770 | ACACACAC others(7): Show |
A | 5 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(2): Show |
5 | HG00733.hp1 HG01167.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.168+881_168+894del others(14): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27283770 | ||||||
| chr2:27283772 | A | G | 38 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0014 others(35): Show |
43 | HG00735.hp1 HG00741.hp1 HG01123.hp2 others(40): Show |
intron_variant | MODIFIER | c.168+873A>G | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27283772 | |||||||
| chr2:27283774 | A | G | 2 | a0001c0001t0001g0171 a0001c0001t0001g0194 |
2 | HG00735.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.168+875A>G | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27283774 | |||||||
| chr2:27283776 | A | G | 42 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0014 others(39): Show |
47 | HG00735.hp1 HG00741.hp1 HG01074.hp1 others(44): Show |
intron_variant | MODIFIER | c.168+877A>G | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27283776 | |||||||
| chr2:27283778 | A | ACG | 3 | a0001c0001t0001g0040 a0001c0001t0001g0065 a0001c0001t0001g0076 |
3 | NA18747.hp1 NA18966.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.168+885_168+886dup others(2): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27283778 | ||||||
| chr2:27283778 | A | ACGCGCGC others(3): Show |
1 | a0001c0001t0001g0145 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.168+886_168+887ins others(10): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27283778 | ||||||
| chr2:27283778 | A | G | 42 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0014 others(39): Show |
47 | HG00735.hp1 HG00741.hp1 HG01074.hp1 others(44): Show |
intron_variant | MODIFIER | c.168+879A>G | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27283778 | |||||||
| chr2:27283778 | ACG | A | 10 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0018 others(7): Show |
17 | HG00639.hp2 HG00738.hp2 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.168+885_168+886del others(2): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27283778 | ||||||
| chr2:27283780 | G | A | 28 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0014 others(25): Show |
33 | HG00597.hp2 HG00738.hp1 HG01074.hp1 others(30): Show |
intron_variant | MODIFIER | c.168+881G>A | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27283780 | |||||||
| chr2:27283782 | G | A | 30 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0014 others(27): Show |
35 | HG00597.hp2 HG00738.hp1 HG01074.hp1 others(32): Show |
intron_variant | MODIFIER | c.168+883G>A | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27283782 | |||||||
| chr2:27283782 | G | GCA | 7 | a0001c0001t0001g0017 a0001c0001t0001g0053 a0001c0001t0001g0055 others(4): Show |
8 | HG01243.hp1 HG01884.hp2 HG02735.hp2 others(5): Show |
intron_variant | MODIFIER | c.168+884_168+885ins others(2): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27283782 | ||||||
| chr2:27283782 | GCGCA | G | 5 | a0001c0001t0001g0009 a0001c0001t0001g0042 a0001c0001t0001g0043 others(2): Show |
5 | HG01109.hp2 HG01346.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.168+885_168+888del others(4): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27283782 | ||||||
| chr2:27283784 | G | A | 50 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(47): Show |
59 | HG00597.hp2 HG00738.hp1 HG01074.hp1 others(56): Show |
intron_variant | MODIFIER | c.168+885G>A | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27283784 | |||||||
| chr2:27283784 | G | GCA | 30 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(27): Show |
38 | HG00140.hp1 HG00558.hp1 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.168+921_168+922dup others(2): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27283784 | ||||||
| chr2:27283784 | G | GCACA | 20 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(17): Show |
24 | HG00609.hp1 HG00733.hp2 HG01192.hp1 others(21): Show |
intron_variant | MODIFIER | c.168+919_168+922dup others(4): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27283784 | ||||||
| chr2:27283784 | G | GCACACA | 22 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(19): Show |
24 | HG00558.hp2 HG00735.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.168+917_168+922dup others(6): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27283784 | ||||||
| chr2:27283784 | G | GCACACAC others(1): Show |
6 | a0001c0001t0001g0002 a0001c0001t0001g0074 a0001c0001t0001g0159 others(3): Show |
6 | HG01192.hp2 HG01515.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.168+915_168+922dup others(8): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27283784 | ||||||
| chr2:27283784 | G | GCACACAC others(3): Show |
6 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0025 others(3): Show |
6 | HG01361.hp2 HG02165.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.168+913_168+922dup others(10): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27283784 | ||||||
| chr2:27283784 | G | GCACACAC others(5): Show |
1 | a0001c0001t0001g0199 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.168+911_168+922dup others(12): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27283784 | ||||||
| chr2:27283784 | G | GCGCACA | 4 | a0001c0001t0001g0068 a0001c0001t0001g0114 a0001c0001t0001g0208 others(1): Show |
4 | HG00323.hp1 HG02647.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.168+886_168+887ins others(6): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27283784 | ||||||
| chr2:27283784 | G | GCGCACAC others(1): Show |
3 | a0001c0001t0001g0004 a0001c0001t0001g0032 a0001c0001t0001g0181 |
3 | HG00741.hp1 HG01516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.168+886_168+887ins others(8): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27283784 | ||||||
| chr2:27283784 | G | GCGCACAC others(3): Show |
6 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0030 others(3): Show |
6 | HG02129.hp1 HG02976.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.168+886_168+887ins others(10): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27283784 | ||||||
| chr2:27283784 | G | GCGCACAC others(5): Show |
3 | a0001c0001t0001g0004 a0001c0001t0001g0031 a0001c0001t0001g0210 |
3 | HG01934.hp2 HG02630.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.168+886_168+887ins others(12): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27283784 | ||||||
| chr2:27283784 | G | GCGCACAC others(7): Show |
9 | a0001c0001t0001g0004 a0001c0001t0001g0030 a0001c0001t0001g0158 others(6): Show |
9 | HG01123.hp2 HG01891.hp1 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.168+886_168+887ins others(14): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27283784 | ||||||
| chr2:27283784 | G | GCGCGCAC others(3): Show |
1 | a0001c0001t0001g0183 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.168+886_168+887ins others(10): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27283784 | ||||||
| chr2:27283784 | G | GCGCGCAC others(7): Show |
3 | a0001c0001t0001g0156 a0001c0001t0001g0173 a0001c0001t0001g0188 |
3 | HG02486.hp2 HG02886.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.168+886_168+887ins others(14): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27283784 | ||||||
| chr2:27283784 | G | GCGCGCAC others(9): Show |
3 | a0001c0001t0001g0169 a0001c0001t0001g0179 a0001c0001t0001g0189 |
3 | HG01243.hp2 HG01346.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.168+886_168+887ins others(16): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27283784 | ||||||
| chr2:27283784 | G | GCGCGCGC others(5): Show |
1 | a0001c0001t0001g0171 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.168+886_168+887ins others(12): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27283784 | ||||||
| chr2:27283784 | GCA | G | 8 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0097 others(5): Show |
8 | HG00609.hp2 HG00735.hp2 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.168+921_168+922del others(2): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27283784 | ||||||
| chr2:27283784 | GCACACAC others(3): Show |
G | 1 | a0001c0001t0001g0038 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.168+913_168+922del others(10): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27283784 | ||||||
| chr2:27283786 | A | G | 2 | a0001c0001t0001g0165 a0001c0001t0001g0187 |
2 | HG01934.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.168+887A>G | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27283786 | |||||||
| chr2:27283788 | A | G | 2 | a0001c0001t0001g0097 a0001c0001t0001g0187 |
2 | HG03831.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.168+889A>G | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27283788 | |||||||
| chr2:27283790 | A | G | 1 | a0001c0001t0001g0187 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.168+891A>G | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27283790 | |||||||
| chr2:27283800 | A | G | 1 | a0001c0001t0006g0148 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.168+901A>G | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27283800 | |||||||
| chr2:27283821 | C | CACACACA others(8): Show |
1 | a0001c0001t0001g0165 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.168+922_168+923ins others(15): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27283821 | |||||||
| chr2:27283964 | C | T | 2 | a0001c0001t0001g0013 a0001c0001t0001g0153 |
4 | HG00140.hp2 HG03195.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.168+1065C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27283964 | |||||||
| chr2:27283993 | C | T | 2 | a0001c0001t0002g0027 a0001c0001t0002g0149 |
3 | HG02451.hp1 HG03209.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.168+1094C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27283993 | |||||||
| chr2:27284112 | G | A | 3 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0043 |
7 | HG00738.hp2 HG02559.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.168+1213G>A | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27284112 | |||||||
| chr2:27284117 | A | T | 1 | a0001c0001t0001g0203 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.168+1218A>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27284117 | |||||||
| chr2:27284290 | A | C | 1 | a0001c0007t0005g0152 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.168+1391A>C | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27284290 | |||||||
| chr2:27284387 | C | T | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | NA19010.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.168+1488C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27284387 | |||||||
| chr2:27284577 | C | T | 1 | a0001c0001t0001g0202 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.168+1678C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27284577 | |||||||
| chr2:27284704 | G | T | 1 | a0001c0001t0001g0145 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.168+1805G>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27284704 | |||||||
| chr2:27285280 | A | G | 1 | a0001c0001t0001g0201 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.168+2381A>G | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27285280 | |||||||
| chr2:27285372 | C | T | 16 | a0001c0001t0001g0028 a0001c0001t0001g0036 a0001c0001t0001g0041 others(13): Show |
18 | HG00733.hp1 HG01074.hp1 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.168+2473C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27285372 | |||||||
| chr2:27285588 | T | C | 1 | a0001c0001t0001g0044 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.168+2689T>C | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27285588 | |||||||
| chr2:27285682 | C | T | 1 | a0001c0007t0005g0152 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.168+2783C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27285682 | |||||||
| chr2:27285683 | G | A | 17 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0045 others(14): Show |
22 | HG00639.hp2 HG01167.hp2 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.168+2784G>A | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27285683 | |||||||
| chr2:27285815 | T | C | 16 | a0001c0001t0001g0028 a0001c0001t0001g0036 a0001c0001t0001g0041 others(13): Show |
18 | HG00733.hp1 HG01074.hp1 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.168+2916T>C | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27285815 | |||||||
| chr2:27285842 | C | T | 62 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0014 others(59): Show |
76 | HG00597.hp2 HG00735.hp1 HG00738.hp1 others(73): Show |
intron_variant | MODIFIER | c.168+2943C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27285842 | |||||||
| chr2:27286115 | T | C | 6 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0060 others(3): Show |
8 | HG00438.hp2 HG00558.hp1 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.168+3216T>C | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27286115 | |||||||
| chr2:27286164 | T | C | 115 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(112): Show |
145 | HG00597.hp2 HG00639.hp2 HG00733.hp1 others(142): Show |
intron_variant | MODIFIER | c.168+3265T>C | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27286164 | |||||||
| chr2:27286165 | AT | A | 5 | a0001c0001t0001g0020 a0001c0001t0001g0036 a0001c0001t0001g0075 others(2): Show |
6 | HG01074.hp1 HG03453.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.168+3279delT | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27286165 | ||||||
| chr2:27286190 | A | T | 16 | a0001c0001t0001g0028 a0001c0001t0001g0036 a0001c0001t0001g0041 others(13): Show |
18 | HG00733.hp1 HG01074.hp1 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.168+3291A>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27286190 | |||||||
| chr2:27286720 | T | C | 1 | a0001c0007t0005g0152 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.168+3821T>C | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27286720 | |||||||
| chr2:27287026 | G | A | 9 | a0001c0001t0001g0006 a0001c0001t0001g0045 a0001c0001t0001g0046 others(6): Show |
12 | HG00639.hp2 HG01167.hp2 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.168+4127G>A | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27287026 | |||||||
| chr2:27287286 | C | T | 2 | a0001c0001t0001g0019 a0001c0001t0001g0074 |
3 | HG02257.hp2 HG02818.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.168+4387C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27287286 | |||||||
| chr2:27287444 | G | A | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | NA19010.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.168+4545G>A | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27287444 | |||||||
| chr2:27287512 | G | T | 1 | a0001c0001t0001g0139 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.168+4613G>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27287512 | |||||||
| chr2:27287527 | A | AT | 20 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0026 others(17): Show |
27 | HG00639.hp2 HG01167.hp2 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.168+4638dupT | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27287527 | ||||||
| chr2:27287649 | G | A | 1 | a0001c0001t0001g0076 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.168+4750G>A | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27287649 | |||||||
| chr2:27287729 | A | G | 1 | a0001c0001t0001g0200 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.168+4830A>G | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27287729 | |||||||
| chr2:27287765 | G | A | 1 | a0001c0001t0001g0166 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.168+4866G>A | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27287765 | |||||||
| chr2:27287941 | C | T | 1 | a0001c0001t0006g0148 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.168+5042C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27287941 | |||||||
| chr2:27287959 | C | G | 5 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(2): Show |
5 | HG01891.hp1 HG02486.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.168+5060C>G | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27287959 | |||||||
| chr2:27287980 | A | G | 1 | a0001c0001t0001g0158 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.168+5081A>G | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27287980 | |||||||
| chr2:27288170 | T | A | 2 | a0001c0001t0001g0077 a0001c0001t0001g0078 |
2 | NA18984.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.168+5271T>A | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27288170 | |||||||
| chr2:27288304 | C | T | 2 | a0001c0001t0001g0020 a0001c0001t0001g0075 |
3 | NA18963.hp2 NA19057.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.168+5405C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27288304 | |||||||
| chr2:27289232 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.168+6333G>A | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27289232 | |||||||
| chr2:27289239 | A | G | 1 | a0001c0001t0001g0151 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.168+6340A>G | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27289239 | |||||||
| chr2:27289563 | C | T | 1 | a0001c0001t0001g0205 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.168+6664C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27289563 | |||||||
| chr2:27289785 | A | C | 1 | a0001c0001t0001g0138 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.168+6886A>C | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27289785 | |||||||
| chr2:27289860 | C | CT | 34 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0025 others(31): Show |
42 | HG00280.hp1 HG00733.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.168+6990dupT | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27289860 | ||||||
| chr2:27289860 | CT | C | 15 | a0001c0001t0001g0017 a0001c0001t0001g0028 a0001c0001t0001g0041 others(12): Show |
17 | HG00639.hp1 HG00733.hp1 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.168+6990delT | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27289860 | ||||||
| chr2:27289860 | CTTTTTTT others(5): Show |
C | 7 | a0001c0001t0001g0036 a0001c0001t0001g0141 a0001c0001t0003g0140 others(4): Show |
7 | HG01074.hp1 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.168+6979_168+6990d others(14): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27289860 | ||||||
| chr2:27289862 | T | C | 1 | a0001c0001t0001g0064 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.168+6963T>C | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27289862 | |||||||
| chr2:27289915 | A | G | 9 | a0001c0001t0001g0005 a0001c0001t0001g0189 a0001c0001t0001g0190 others(6): Show |
13 | HG00597.hp2 HG01074.hp2 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.168+7016A>G | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27289915 | |||||||
| chr2:27290010 | T | G | 62 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0014 others(59): Show |
76 | HG00597.hp2 HG00735.hp1 HG00738.hp1 others(73): Show |
intron_variant | MODIFIER | c.168+7111T>G | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27290010 | |||||||
| chr2:27290199 | A | T | 14 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 others(11): Show |
14 | HG00438.hp2 HG01074.hp1 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.168+7300A>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27290199 | |||||||
| chr2:27290200 | T | A | 6 | a0001c0001t0001g0009 a0001c0001t0001g0053 a0001c0001t0001g0055 others(3): Show |
8 | HG01243.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.168+7301T>A | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27290200 | |||||||
| chr2:27290539 | G | A | 2 | a0001c0001t0001g0155 a0001c0001t0001g0158 |
2 | HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.168+7640G>A | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27290539 | |||||||
| chr2:27290550 | G | T | 17 | a0001c0001t0001g0028 a0001c0001t0001g0036 a0001c0001t0001g0041 others(14): Show |
19 | HG00733.hp1 HG01074.hp1 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.168+7651G>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27290550 | |||||||
| chr2:27290810 | C | T | 1 | a0001c0003t0001g0024 | 2 | HG01256.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.169-7757C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27290810 | |||||||
| chr2:27290938 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.169-7629C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27290938 | |||||||
| chr2:27291056 | A | G | 1 | a0001c0001t0001g0188 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.169-7511A>G | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27291056 | |||||||
| chr2:27291074 | C | T | 1 | a0001c0001t0001g0037 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.169-7493C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27291074 | |||||||
| chr2:27291248 | A | G | 79 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0014 others(76): Show |
95 | HG00597.hp2 HG00733.hp1 HG00735.hp1 others(92): Show |
intron_variant | MODIFIER | c.169-7319A>G | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27291248 | |||||||
| chr2:27291362 | A | AAAAC | 2 | a0001c0001t0001g0019 a0001c0001t0001g0074 |
3 | HG02257.hp2 HG02818.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.169-7193_169-7190d others(6): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27291362 | ||||||
| chr2:27291448 | GTT | G | 17 | a0001c0001t0001g0028 a0001c0001t0001g0036 a0001c0001t0001g0041 others(14): Show |
19 | HG00733.hp1 HG01074.hp1 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.169-7114_169-7113d others(4): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27291448 | ||||||
| chr2:27291471 | C | G | 7 | a0001c0001t0001g0036 a0001c0001t0001g0141 a0001c0001t0003g0140 others(4): Show |
7 | HG01074.hp1 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.169-7096C>G | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27291471 | |||||||
| chr2:27291572 | AAC | A | 5 | a0001c0001t0001g0018 a0001c0001t0001g0064 a0001c0001t0001g0066 others(2): Show |
6 | HG02257.hp1 HG02258.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.169-6991_169-6990d others(4): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27291572 | ||||||
| chr2:27291589 | T | G | 1 | a0001c0001t0004g0067 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.169-6978T>G | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27291589 | |||||||
| chr2:27291773 | A | G | 11 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0016 others(8): Show |
17 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(14): Show |
intron_variant | MODIFIER | c.169-6794A>G | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27291773 | |||||||
| chr2:27291886 | C | T | 2 | a0001c0001t0001g0187 a0001c0001t0004g0067 |
2 | HG01109.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.169-6681C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27291886 | |||||||
| chr2:27291895 | C | T | 2 | a0001c0001t0001g0123 a0001c0001t0001g0124 |
2 | NA18981.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.169-6672C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27291895 | |||||||
| chr2:27291904 | G | C | 1 | a0001c0001t0001g0036 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.169-6663G>C | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27291904 | |||||||
| chr2:27291970 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.169-6597C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27291970 | |||||||
| chr2:27292237 | A | G | 62 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0014 others(59): Show |
76 | HG00597.hp2 HG00735.hp1 HG00738.hp1 others(73): Show |
intron_variant | MODIFIER | c.169-6330A>G | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27292237 | |||||||
| chr2:27292262 | A | T | 1 | a0001c0001t0001g0122 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.169-6305A>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27292262 | |||||||
| chr2:27292292 | T | C | 17 | a0001c0001t0001g0028 a0001c0001t0001g0036 a0001c0001t0001g0041 others(14): Show |
19 | HG00733.hp1 HG01074.hp1 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.169-6275T>C | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27292292 | |||||||
| chr2:27292444 | C | T | 10 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0018 others(7): Show |
14 | HG01884.hp1 HG01981.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.169-6123C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27292444 | |||||||
| chr2:27292491 | G | A | 2 | a0001c0001t0001g0080 a0001c0001t0001g0085 |
2 | HG01516.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.169-6076G>A | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27292491 | |||||||
| chr2:27292538 | A | T | 1 | a0001c0001t0001g0023 | 2 | HG00558.hp2 NA18939.hp2 |
intron_variant | MODIFIER | c.169-6029A>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27292538 | |||||||
| chr2:27292659 | C | T | 112 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(109): Show |
142 | HG00597.hp2 HG00639.hp2 HG00733.hp1 others(139): Show |
intron_variant | MODIFIER | c.169-5908C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27292659 | |||||||
| chr2:27292724 | C | T | 5 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(2): Show |
5 | HG00639.hp2 HG01167.hp2 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.169-5843C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27292724 | |||||||
| chr2:27292869 | C | G | 1 | a0001c0007t0005g0152 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.169-5698C>G | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27292869 | |||||||
| chr2:27292980 | C | T | 1 | a0001c0001t0001g0028 | 2 | NA19043.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.169-5587C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27292980 | |||||||
| chr2:27293396 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.169-5171G>A | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27293396 | |||||||
| chr2:27293422 | C | T | 2 | a0001c0001t0001g0121 a0001c0001t0001g0136 |
2 | HG01175.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.169-5145C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27293422 | |||||||
| chr2:27293477 | G | A | 1 | a0001c0001t0001g0052 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.169-5090G>A | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27293477 | |||||||
| chr2:27293888 | T | C | 1 | a0001c0001t0001g0145 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.169-4679T>C | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27293888 | |||||||
| chr2:27293892 | A | G | 1 | a0001c0001t0001g0120 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.169-4675A>G | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27293892 | |||||||
| chr2:27294062 | A | G | 1 | a0001c0001t0001g0158 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.169-4505A>G | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27294062 | |||||||
| chr2:27294163 | C | CT | 3 | a0001c0001t0001g0119 a0001c0001t0001g0146 a0001c0001t0001g0147 |
3 | NA18982.hp1 NA19010.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.169-4403dupT | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27294163 | ||||||
| chr2:27294309 | C | T | 1 | a0001c0001t0001g0162 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.169-4258C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27294309 | |||||||
| chr2:27294579 | G | C | 1 | a0001c0001t0001g0063 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.169-3988G>C | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27294579 | |||||||
| chr2:27294592 | G | C | 3 | a0001c0001t0001g0028 a0001c0001t0001g0041 a0001c0001t0001g0154 |
4 | HG06807.hp1 NA18906.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.169-3975G>C | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27294592 | |||||||
| chr2:27294634 | G | T | 3 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0043 |
7 | HG00738.hp2 HG02559.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.169-3933G>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27294634 | |||||||
| chr2:27294815 | A | G | 100 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(97): Show |
125 | HG00597.hp2 HG00639.hp2 HG00733.hp1 others(122): Show |
intron_variant | MODIFIER | c.169-3752A>G | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27294815 | |||||||
| chr2:27294869 | G | A | 1 | a0001c0001t0001g0159 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.169-3698G>A | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27294869 | |||||||
| chr2:27294889 | CA | C | 180 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(177): Show |
239 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.169-3657delA | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27294889 | ||||||
| chr2:27295122 | A | G | 17 | a0001c0001t0001g0028 a0001c0001t0001g0036 a0001c0001t0001g0041 others(14): Show |
19 | HG00733.hp1 HG01074.hp1 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.169-3445A>G | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27295122 | |||||||
| chr2:27295127 | G | A | 1 | a0001c0007t0005g0152 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.169-3440G>A | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27295127 | |||||||
| chr2:27295132 | C | A | 1 | a0001c0001t0001g0089 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.169-3435C>A | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27295132 | |||||||
| chr2:27295453 | G | C | 2 | a0001c0001t0001g0121 a0001c0001t0001g0136 |
2 | HG01175.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.169-3114G>C | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27295453 | |||||||
| chr2:27295523 | G | A | 1 | a0001c0001t0001g0168 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.169-3044G>A | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27295523 | |||||||
| chr2:27295596 | G | A | 7 | a0001c0001t0001g0028 a0001c0001t0001g0041 a0001c0001t0001g0142 others(4): Show |
8 | HG00733.hp1 HG01167.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.169-2971G>A | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27295596 | |||||||
| chr2:27295641 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.169-2926C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27295641 | |||||||
| chr2:27296007 | G | T | 3 | a0001c0001t0001g0167 a0001c0001t0001g0186 a0001c0001t0001g0198 |
3 | NA18955.hp2 NA18982.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.169-2560G>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27296007 | |||||||
| chr2:27296236 | G | A | 2 | a0001c0001t0002g0027 a0001c0001t0002g0149 |
3 | HG02451.hp1 HG03209.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.169-2331G>A | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27296236 | |||||||
| chr2:27296264 | A | G | 1 | a0002c0004t0001g0117 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.169-2303A>G | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27296264 | |||||||
| chr2:27296285 | G | T | 112 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(109): Show |
142 | HG00597.hp2 HG00639.hp2 HG00733.hp1 others(139): Show |
intron_variant | MODIFIER | c.169-2282G>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27296285 | |||||||
| chr2:27296386 | G | A | 112 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(109): Show |
142 | HG00597.hp2 HG00639.hp2 HG00733.hp1 others(139): Show |
intron_variant | MODIFIER | c.169-2181G>A | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27296386 | |||||||
| chr2:27296522 | G | A | 2 | a0001c0001t0001g0065 a0001c0001t0001g0068 |
2 | HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.169-2045G>A | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27296522 | |||||||
| chr2:27296588 | C | T | 3 | a0001c0001t0001g0145 a0001c0001t0002g0027 a0001c0001t0002g0149 |
4 | HG02451.hp1 HG02922.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.169-1979C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27296588 | |||||||
| chr2:27296631 | G | A | 7 | a0001c0001t0001g0036 a0001c0001t0001g0141 a0001c0001t0003g0140 others(4): Show |
7 | HG01074.hp1 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.169-1936G>A | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27296631 | |||||||
| chr2:27296722 | C | T | 2 | a0001c0001t0001g0089 a0001c0001t0001g0116 |
2 | HG00280.hp2 HG01069.hp2 |
intron_variant | MODIFIER | c.169-1845C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27296722 | |||||||
| chr2:27297052 | C | A | 1 | a0001c0001t0001g0090 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.169-1515C>A | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27297052 | |||||||
| chr2:27297282 | A | G | 1 | a0001c0001t0001g0061 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.169-1285A>G | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27297282 | |||||||
| chr2:27297388 | C | A | 3 | a0001c0002t0001g0033 a0001c0002t0001g0034 a0001c0002t0001g0035 |
3 | HG02559.hp1 HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.169-1179C>A | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27297388 | |||||||
| chr2:27297834 | A | G | 3 | a0001c0001t0001g0028 a0001c0001t0001g0041 a0001c0001t0001g0154 |
4 | HG06807.hp1 NA18906.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.169-733A>G | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27297834 | |||||||
| chr2:27297881 | T | G | 1 | a0001c0002t0001g0033 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.169-686T>G | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27297881 | |||||||
| chr2:27297980 | C | CA | 47 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0018 others(44): Show |
55 | HG00639.hp2 HG00733.hp1 HG01074.hp1 others(52): Show |
intron_variant | MODIFIER | c.169-566dupA | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27297980 | ||||||
| chr2:27297980 | C | CAA | 8 | a0001c0001t0001g0052 a0001c0001t0001g0055 a0001c0001t0001g0059 others(5): Show |
8 | HG01257.hp2 HG01884.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.169-567_169-566dup others(2): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27297980 | ||||||
| chr2:27297980 | C | CAAA | 44 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0014 others(41): Show |
57 | HG00597.hp2 HG00738.hp1 HG00741.hp1 others(54): Show |
intron_variant | MODIFIER | c.169-568_169-566dup others(3): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27297980 | ||||||
| chr2:27297980 | C | CAAAA | 6 | a0001c0001t0001g0030 a0001c0001t0001g0171 a0001c0001t0001g0172 others(3): Show |
7 | HG00735.hp1 HG01243.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.169-569_169-566dup others(4): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27297980 | ||||||
| chr2:27298002 | G | A | 3 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0001g0174 |
3 | HG01257.hp2 HG01258.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.169-565G>A | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27298002 | |||||||
| chr2:27298125 | A | G | 1 | a0001c0001t0001g0185 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.169-442A>G | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27298125 | |||||||
| chr2:27298239 | C | G | 2 | a0001c0001t0001g0170 a0001c0001t0001g0174 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.169-328C>G | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27298239 | |||||||
| chr2:27298294 | A | T | 1 | a0001c0001t0001g0089 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.169-273A>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27298294 | |||||||
| chr2:27298299 | A | G | 2 | a0001c0001t0001g0170 a0001c0001t0001g0174 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.169-268A>G | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27298299 | |||||||
| chr2:27298361 | G | A | 2 | a0001c0001t0001g0080 a0001c0001t0001g0085 |
2 | HG01516.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.169-206G>A | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27298361 | |||||||
| chr2:27298395 | A | G | 1 | a0001c0001t0001g0145 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.169-172A>G | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27298395 | |||||||
| chr2:27298960 | G | T | 1 | a0001c0002t0001g0035 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.341+221G>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 2/8 | chr2 | 27298960 | |||||||
| chr2:27299166 | G | A | 1 | a0001c0001t0001g0142 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.342-79G>A | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 2/8 | chr2 | 27299166 | |||||||
| chr2:27299195 | T | A | 1 | a0001c0001t0001g0175 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.342-50T>A | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 2/8 | chr2 | 27299195 | |||||||
| chr2:27299675 | C | CCTAT | 87 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(84): Show |
113 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(110): Show |
intron_variant | MODIFIER | c.513+297_513+300dup others(4): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 27299675 | ||||||
| chr2:27299675 | C | CCTATCTA others(1): Show |
27 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0018 others(24): Show |
35 | HG00323.hp1 HG00597.hp2 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.513+293_513+300dup others(8): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 27299675 | ||||||
| chr2:27299675 | C | CCTATCTA others(5): Show |
2 | a0001c0001t0001g0115 a0001c0001t0001g0184 |
2 | HG02109.hp1 NA18939.hp1 |
intron_variant | MODIFIER | c.513+289_513+300dup others(12): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 27299675 | ||||||
| chr2:27299675 | CCTAT | C | 12 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0042 others(9): Show |
17 | HG00738.hp2 HG01243.hp1 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.513+297_513+300del others(4): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 27299675 | ||||||
| chr2:27299675 | CCTATCTA others(5): Show |
C | 1 | a0001c0001t0001g0094 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.513+289_513+300del others(12): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 27299675 | ||||||
| chr2:27299884 | G | C | 1 | a0001c0001t0001g0175 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.513+468G>C | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27299884 | |||||||
| chr2:27299884 | G | GT | 17 | a0001c0001t0001g0028 a0001c0001t0001g0036 a0001c0001t0001g0041 others(14): Show |
19 | HG00733.hp1 HG01074.hp1 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.513+477dupT | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 27299884 | ||||||
| chr2:27299884 | G | T | 1 | a0001c0001t0001g0178 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.513+468G>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27299884 | |||||||
| chr2:27300221 | G | A | 4 | a0001c0001t0001g0011 a0001c0001t0001g0093 a0001c0001t0001g0107 others(1): Show |
6 | HG00140.hp1 HG01433.hp2 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.513+805G>A | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27300221 | |||||||
| chr2:27300373 | A | C | 1 | a0001c0001t0004g0067 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.513+957A>C | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27300373 | |||||||
| chr2:27300406 | C | G | 17 | a0001c0001t0001g0028 a0001c0001t0001g0036 a0001c0001t0001g0041 others(14): Show |
19 | HG00733.hp1 HG01074.hp1 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.513+990C>G | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27300406 | |||||||
| chr2:27300451 | C | T | 4 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0162 others(1): Show |
4 | HG01891.hp2 HG02109.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.513+1035C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27300451 | |||||||
| chr2:27300550 | C | CTACTAAT others(24): Show |
62 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0014 others(59): Show |
76 | HG00597.hp2 HG00735.hp1 HG00738.hp1 others(73): Show |
intron_variant | MODIFIER | c.513+1155_513+1156i others(33): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 27300550 | ||||||
| chr2:27300550 | CTACTAAT others(24): Show |
C | 2 | a0001c0001t0001g0112 a0001c0001t0001g0134 |
2 | HG01358.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.513+1177_513+1207d others(33): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 27300550 | ||||||
| chr2:27300568 | A | ATTATTAG others(21): Show |
3 | a0001c0001t0001g0041 a0001c0001t0001g0142 a0001c0007t0005g0152 |
3 | HG03041.hp2 HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.513+1155_513+1156i others(30): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 27300568 | ||||||
| chr2:27300568 | A | ATTATTAG others(49): Show |
5 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0145 others(2): Show |
6 | HG00733.hp1 HG01167.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.513+1155_513+1156i others(58): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 27300568 | ||||||
| chr2:27300572 | G | T | 53 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0009 others(50): Show |
69 | HG00639.hp2 HG00733.hp1 HG00738.hp2 others(66): Show |
intron_variant | MODIFIER | c.513+1156G>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27300572 | |||||||
| chr2:27300616 | T | C | 1 | a0001c0001t0007g0182 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.513+1200T>C | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27300616 | |||||||
| chr2:27300814 | C | T | 1 | a0001c0001t0001g0106 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.513+1398C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27300814 | |||||||
| chr2:27301135 | C | CT | 20 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0018 others(17): Show |
24 | HG01074.hp1 HG01884.hp1 HG01981.hp1 others(21): Show |
intron_variant | MODIFIER | c.513+1741dupT | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 27301135 | ||||||
| chr2:27301135 | CT | C | 8 | a0001c0001t0001g0049 a0001c0001t0001g0055 a0001c0001t0001g0075 others(5): Show |
8 | HG01169.hp2 HG01515.hp2 HG01516.hp2 others(5): Show |
intron_variant | MODIFIER | c.513+1741delT | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 27301135 | ||||||
| chr2:27301225 | C | T | 1 | a0001c0001t0001g0056 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.513+1809C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27301225 | |||||||
| chr2:27301288 | C | T | 4 | a0001c0001t0001g0018 a0001c0001t0001g0066 a0001c0001t0001g0071 others(1): Show |
5 | HG02257.hp1 HG02258.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.513+1872C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27301288 | |||||||
| chr2:27301617 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.513+2201C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27301617 | |||||||
| chr2:27301618 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.513+2202G>A | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27301618 | |||||||
| chr2:27301642 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.513+2226C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27301642 | |||||||
| chr2:27301648 | C | T | 1 | a0001c0001t0001g0085 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.513+2232C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27301648 | |||||||
| chr2:27301660 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.513+2244C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27301660 | |||||||
| chr2:27302108 | T | C | 1 | a0001c0001t0001g0125 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.513+2692T>C | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27302108 | |||||||
| chr2:27302176 | C | T | 17 | a0001c0001t0001g0028 a0001c0001t0001g0036 a0001c0001t0001g0041 others(14): Show |
19 | HG00733.hp1 HG01074.hp1 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.513+2760C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27302176 | |||||||
| chr2:27302246 | C | T | 14 | a0001c0001t0001g0028 a0001c0001t0001g0036 a0001c0001t0001g0041 others(11): Show |
15 | HG00733.hp1 HG01074.hp1 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.514-2713C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27302246 | |||||||
| chr2:27302312 | G | A | 9 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0064 others(6): Show |
11 | HG01884.hp1 HG01981.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.514-2647G>A | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27302312 | |||||||
| chr2:27302395 | A | G | 101 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(98): Show |
129 | HG00597.hp2 HG00639.hp2 HG00735.hp1 others(126): Show |
intron_variant | MODIFIER | c.514-2564A>G | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27302395 | |||||||
| chr2:27302415 | C | T | 1 | a0001c0001t0001g0142 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.514-2544C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27302415 | |||||||
| chr2:27302482 | G | A | 92 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(89): Show |
116 | HG00597.hp2 HG00639.hp2 HG00735.hp1 others(113): Show |
intron_variant | MODIFIER | c.514-2477G>A | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27302482 | |||||||
| chr2:27302566 | C | T | 1 | a0001c0001t0001g0176 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.514-2393C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27302566 | |||||||
| chr2:27302722 | C | T | 1 | a0001c0001t0001g0132 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.514-2237C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27302722 | |||||||
| chr2:27302756 | A | C | 1 | a0001c0001t0002g0149 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.514-2203A>C | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27302756 | |||||||
| chr2:27302793 | A | G | 71 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0014 others(68): Show |
85 | HG00597.hp2 HG00735.hp1 HG00738.hp1 others(82): Show |
intron_variant | MODIFIER | c.514-2166A>G | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27302793 | |||||||
| chr2:27302915 | G | C | 4 | a0001c0001t0001g0142 a0001c0001t0001g0145 a0001c0001t0002g0027 others(1): Show |
5 | HG02451.hp1 HG02922.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.514-2044G>C | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27302915 | |||||||
| chr2:27303175 | A | C | 1 | a0001c0001t0001g0036 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.514-1784A>C | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27303175 | |||||||
| chr2:27303411 | C | T | 1 | a0001c0001t0001g0110 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.514-1548C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27303411 | |||||||
| chr2:27303547 | C | T | 3 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0052 |
3 | HG00639.hp2 HG02615.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.514-1412C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27303547 | |||||||
| chr2:27303548 | T | TA | 7 | a0001c0001t0001g0071 a0001c0001t0001g0141 a0001c0001t0003g0140 others(4): Show |
7 | HG01074.hp1 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.514-1397dupA | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 27303548 | ||||||
| chr2:27303606 | G | A | 1 | a0001c0001t0001g0204 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.514-1353G>A | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27303606 | |||||||
| chr2:27303760 | A | G | 1 | a0001c0001t0001g0020 | 2 | NA18963.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.514-1199A>G | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27303760 | |||||||
| chr2:27303780 | C | CA | 3 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 |
3 | HG00733.hp1 HG01167.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.514-1173dupA | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 27303780 | ||||||
| chr2:27303813 | C | G | 59 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0014 others(56): Show |
73 | HG00597.hp2 HG00735.hp1 HG00738.hp1 others(70): Show |
intron_variant | MODIFIER | c.514-1146C>G | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27303813 | |||||||
| chr2:27303870 | T | TA | 3 | a0001c0001t0001g0145 a0001c0001t0002g0027 a0001c0001t0002g0149 |
4 | HG02451.hp1 HG02922.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.514-1082dupA | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 27303870 | ||||||
| chr2:27303922 | C | T | 2 | a0001c0001t0001g0030 a0001c0001t0001g0181 |
3 | HG03139.hp1 HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.514-1037C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27303922 | |||||||
| chr2:27304053 | A | T | 1 | a0001c0001t0001g0022 | 2 | HG03017.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.514-906A>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27304053 | |||||||
| chr2:27304213 | AATAT | A | 3 | a0001c0001t0001g0028 a0001c0001t0001g0041 a0001c0001t0001g0154 |
4 | HG06807.hp1 NA18906.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.514-736_514-733del others(4): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 27304213 | ||||||
| chr2:27304221 | TATATAGA others(3): Show |
T | 1 | a0001c0001t0001g0171 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.514-734_514-725del others(10): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 27304221 | ||||||
| chr2:27304223 | T | TATAG | 11 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0064 others(8): Show |
12 | HG00639.hp1 HG01069.hp1 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.514-712_514-709dup others(4): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 27304223 | ||||||
| chr2:27304223 | T | TATAGATA others(1): Show |
4 | a0001c0001t0001g0018 a0001c0001t0001g0066 a0001c0001t0001g0071 others(1): Show |
5 | HG02257.hp1 HG02258.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.514-716_514-709dup others(8): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 27304223 | ||||||
| chr2:27304223 | TATAG | T | 17 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0022 others(14): Show |
21 | HG00733.hp1 HG01074.hp1 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.514-712_514-709del others(4): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 27304223 | ||||||
| chr2:27304223 | TATAGATA others(1): Show |
T | 59 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0014 others(56): Show |
73 | HG00597.hp2 HG00735.hp1 HG00738.hp1 others(70): Show |
intron_variant | MODIFIER | c.514-716_514-709del others(8): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 27304223 | ||||||
| chr2:27304261 | GATAT | G | 6 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0165 others(3): Show |
8 | HG01934.hp1 HG02630.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.514-684_514-681del others(4): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 27304261 | ||||||
| chr2:27304271 | T | G | 5 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0143 others(2): Show |
5 | HG00733.hp1 HG01109.hp2 HG01167.hp1 others(2): Show |
intron_variant | MODIFIER | c.514-688T>G | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27304271 | |||||||
| chr2:27304275 | T | G | 106 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(103): Show |
131 | HG00597.hp2 HG00639.hp2 HG00733.hp1 others(128): Show |
intron_variant | MODIFIER | c.514-684T>G | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27304275 | |||||||
| chr2:27304285 | T | C | 3 | a0001c0001t0001g0018 a0001c0001t0001g0071 a0001c0001t0001g0073 |
4 | HG02257.hp1 HG02258.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.514-674T>C | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27304285 | |||||||
| chr2:27304378 | T | A | 73 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0014 others(70): Show |
89 | HG00597.hp2 HG00733.hp1 HG00735.hp1 others(86): Show |
intron_variant | MODIFIER | c.514-581T>A | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27304378 | |||||||
| chr2:27304386 | A | ACCAGCCT others(743): Show |
1 | a0001c0001t0001g0210 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.514-563_514-562ins others(750): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 27304386 | ||||||
| chr2:27304386 | A | ACCAGCCT others(744): Show |
1 | a0001c0001t0001g0097 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.514-563_514-562ins others(751): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 27304386 | ||||||
| chr2:27304386 | A | ACCAGCCT others(743): Show |
2 | a0001c0001t0001g0143 a0001c0001t0001g0144 |
2 | HG00733.hp1 HG01167.hp1 |
intron_variant | MODIFIER | c.514-563_514-562ins others(750): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 27304386 | ||||||
| chr2:27304386 | A | ACCAGCCT others(743): Show |
1 | a0001c0001t0001g0095 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.514-563_514-562ins others(750): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 27304386 | ||||||
| chr2:27304386 | A | ACCAGCCT others(743): Show |
1 | a0001c0001t0001g0126 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.514-563_514-562ins others(750): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 27304386 | ||||||
| chr2:27304386 | A | ACCAGCCT others(743): Show |
1 | a0001c0001t0001g0047 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.514-563_514-562ins others(750): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 27304386 | ||||||
| chr2:27304386 | A | ACCAGCCT others(743): Show |
1 | a0001c0001t0001g0159 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.514-563_514-562ins others(750): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 27304386 | ||||||
| chr2:27304386 | A | ACCAGCCT others(743): Show |
2 | a0001c0001t0001g0019 a0001c0001t0001g0074 |
3 | HG02257.hp2 HG02818.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.514-563_514-562ins others(750): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 27304386 | ||||||
| chr2:27304386 | A | ACCAGCCT others(742): Show |
4 | a0001c0001t0001g0087 a0001c0001t0001g0103 a0001c0001t0001g0108 others(1): Show |
4 | HG01069.hp1 HG03669.hp2 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.514-563_514-562ins others(749): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 27304386 | ||||||
| chr2:27304386 | A | ACCAGCCT others(743): Show |
1 | a0001c0001t0001g0145 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.514-563_514-562ins others(750): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 27304386 | ||||||
| chr2:27304386 | A | ACCAGCCT others(743): Show |
1 | a0001c0001t0001g0062 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.514-563_514-562ins others(750): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 27304386 | ||||||
| chr2:27304386 | A | ACCAGCCT others(744): Show |
1 | a0001c0001t0001g0058 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.514-563_514-562ins others(751): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 27304386 | ||||||
| chr2:27304386 | A | ACCAGCCT others(743): Show |
1 | a0001c0001t0001g0104 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.514-563_514-562ins others(750): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 27304386 | ||||||
| chr2:27304413 | C | T | 1 | a0001c0001t0001g0142 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.514-546C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27304413 | |||||||
| chr2:27304424 | A | T | 8 | a0001c0001t0001g0084 a0001c0001t0001g0102 a0001c0001t0001g0120 others(5): Show |
8 | HG00323.hp2 HG00733.hp2 HG01123.hp1 others(5): Show |
intron_variant | MODIFIER | c.514-535A>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27304424 | |||||||
| chr2:27304430 | A | T | 1 | a0001c0001t0001g0097 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.514-529A>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27304430 | |||||||
| chr2:27304453 | G | A | 118 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(115): Show |
149 | HG00597.hp2 HG00639.hp2 HG00733.hp1 others(146): Show |
intron_variant | MODIFIER | c.514-506G>A | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27304453 | |||||||
| chr2:27304465 | T | C | 8 | a0001c0001t0001g0039 a0001c0001t0001g0089 a0001c0001t0001g0092 others(5): Show |
8 | HG00280.hp2 HG01069.hp2 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.514-494T>C | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27304465 | |||||||
| chr2:27304518 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.514-441C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27304518 | |||||||
| chr2:27304666 | A | T | 1 | a0001c0001t0001g0078 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.514-293A>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27304666 | |||||||
| chr2:27304802 | G | A | 2 | a0001c0001t0001g0101 a0001c0001t0001g0111 |
2 | HG02080.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.514-157G>A | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27304802 | |||||||
| chr2:27304884 | G | A | 1 | a0001c0001t0001g0081 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.514-75G>A | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27304884 | |||||||
| chr2:27304890 | C | T | 15 | a0001c0001t0001g0028 a0001c0001t0001g0041 a0001c0001t0001g0141 others(12): Show |
17 | HG00733.hp1 HG01074.hp1 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.514-69C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27304890 | |||||||
| chr2:27304901 | G | A | 15 | a0001c0001t0001g0028 a0001c0001t0001g0041 a0001c0001t0001g0141 others(12): Show |
17 | HG00733.hp1 HG01074.hp1 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.514-58G>A | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27304901 | |||||||
| chr2:27305101 | C | G | 13 | a0001c0001t0001g0006 a0001c0001t0001g0045 a0001c0001t0001g0046 others(10): Show |
16 | HG00639.hp2 HG01167.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.609+47C>G | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 4/8 | chr2 | 27305101 | |||||||
| chr2:27305824 | T | C | 115 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(112): Show |
145 | HG00597.hp2 HG00639.hp2 HG00733.hp1 others(142): Show |
splice_region_variant&intron_variant | LOW | c.843+7T>C | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 5/8 | chr2 | 27305824 | |||||||
| chr2:27306037 | G | A | 1 | a0001c0001t0001g0192 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.844-43G>A | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 5/8 | chr2 | 27306037 | |||||||
| chr2:27306398 | C | T | 2 | a0001c0001t0001g0104 a0001c0001t0001g0105 |
2 | HG01071.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.992-58C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 7/8 | chr2 | 27306398 | |||||||
| chr2:27306571 | G | T | 1 | a0001c0001t0001g0068 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.*1+29G>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 8/8 | chr2 | 27306571 | |||||||
| chr2:27306575 | G | C | 1 | a0001c0001t0001g0015 | 2 | NA19070.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.*1+33G>C | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 8/8 | chr2 | 27306575 |