Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 23087 |
| ensemblid | ENSG00000104228.13 |
| hgncid | 16285 |
| symbol | TRIM35 |
| name | tripartite motif containing 35 |
| refseq_nuc | NM_171982.5 |
| refseq_prot | NP_741983.2 |
| ensembl_nuc | ENST00000305364.9 |
| ensembl_prot | ENSP00000301924.4 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 27284886 |
| end | 27311272 |
| strand | - |
| ver | v1.2 |
| region | chr8:27284886-27311272 |
| region5000 | chr8:27279886-27316272 |
| regionname0 | TRIM35_chr8_27284886_27311272 |
| regionname5000 | TRIM35_chr8_27279886_27316272 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 493 | 407 | 94 | 83 | 172 | 12 | 44 | 128 | TRIM35_chr8_27279886_27316272 | TRIM35 | MERSP others(488): Show |
chr8 | 27279886 | 27316272 |
| a0002 | 0/0 | 493 | 2 | 0 | 0 | 0 | 2 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | MERSP others(488): Show |
chr8 | 27279886 | 27316272 |
| a0003 | 0/0 | 493 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | MERSP others(488): Show |
chr8 | 27279886 | 27316272 |
| a0004 | 0/0 | 493 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TRIM35_chr8_27279886_27316272 | TRIM35 | MERSP others(488): Show |
chr8 | 27279886 | 27316272 |
| a0005 | 0/0 | 493 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TRIM35_chr8_27279886_27316272 | TRIM35 | MERSP others(488): Show |
chr8 | 27279886 | 27316272 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1479 | 356 | 70 | 79 | 149 | 12 | 44 | TRIM35_chr8_27279886_27316272 | TRIM35 | ATGGA others(1474): Show |
chr8 | 27279886 | 27316272 | ||
| a0001c0002 | 0/0 | 1479 | 21 | 0 | 0 | 21 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | ATGGA others(1474): Show |
chr8 | 27279886 | 27316272 | ||
| a0001c0003 | 0/0 | 1479 | 11 | 11 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | ATGGA others(1474): Show |
chr8 | 27279886 | 27316272 | ||
| a0001c0004 | 0/0 | 1479 | 7 | 6 | 1 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | ATGGA others(1474): Show |
chr8 | 27279886 | 27316272 | ||
| a0001c0005 | 0/0 | 1479 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | ATGGA others(1474): Show |
chr8 | 27279886 | 27316272 | ||
| a0001c0006 | 0/0 | 1479 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | ATGGA others(1474): Show |
chr8 | 27279886 | 27316272 | ||
| a0001c0007 | 0/0 | 1479 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | ATGGA others(1474): Show |
chr8 | 27279886 | 27316272 | ||
| a0001c0009 | 0/0 | 1479 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | ATGGA others(1474): Show |
chr8 | 27279886 | 27316272 | ||
| a0001c0012 | 0/0 | 1479 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | ATGGA others(1474): Show |
chr8 | 27279886 | 27316272 | ||
| a0001c0014 | 0/0 | 1479 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | ATGGA others(1474): Show |
chr8 | 27279886 | 27316272 | ||
| a0001c0015 | 0/0 | 1479 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | ATGGA others(1474): Show |
chr8 | 27279886 | 27316272 | ||
| a0002c0008 | 0/0 | 1479 | 2 | 0 | 0 | 0 | 2 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | ATGGA others(1474): Show |
chr8 | 27279886 | 27316272 | ||
| a0003c0011 | 0/0 | 1479 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | ATGGA others(1474): Show |
chr8 | 27279886 | 27316272 | ||
| a0004c0013 | 0/0 | 1479 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | ATGGA others(1474): Show |
chr8 | 27279886 | 27316272 | ||
| a0005c0010 | 0/0 | 1479 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | ATGGA others(1474): Show |
chr8 | 27279886 | 27316272 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4184 | 130 | 16 | 22 | 72 | 4 | 16 | TRIM35_chr8_27279886_27316272 | TRIM35 | GCAAA others(4179): Show |
chr8 | 27279886 | 27316272 |
| a0001c0001t0002 | 0/1 | 4182 | 76 | 6 | 31 | 20 | 5 | 13 | TRIM35_chr8_27279886_27316272 | TRIM35 | GCAAA others(4177): Show |
chr8 | 27279886 | 27316272 |
| a0001c0001t0003 | 0/0 | 4183 | 35 | 7 | 13 | 9 | 2 | 4 | TRIM35_chr8_27279886_27316272 | TRIM35 | GCAAA others(4178): Show |
chr8 | 27279886 | 27316272 |
| a0001c0001t0004 | 0/0 | 4184 | 32 | 1 | 4 | 21 | 1 | 5 | TRIM35_chr8_27279886_27316272 | TRIM35 | GCAAA others(4179): Show |
chr8 | 27279886 | 27316272 |
| a0001c0001t0005 | 0/0 | 4182 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | GCAAA others(4177): Show |
chr8 | 27279886 | 27316272 |
| a0001c0001t0006 | 1/0 | 4183 | 11 | 3 | 0 | 7 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | GCAAA others(4178): Show |
chr8 | 27279886 | 27316272 |
| a0001c0001t0007 | 0/0 | 4185 | 11 | 2 | 2 | 5 | 0 | 2 | TRIM35_chr8_27279886_27316272 | TRIM35 | GCAAA others(4180): Show |
chr8 | 27279886 | 27316272 |
| a0001c0001t0008 | 0/0 | 4183 | 9 | 8 | 1 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | GCAAA others(4178): Show |
chr8 | 27279886 | 27316272 |
| a0001c0001t0010 | 0/0 | 4185 | 4 | 0 | 1 | 3 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | GCAAA others(4180): Show |
chr8 | 27279886 | 27316272 |
| a0001c0001t0011 | 0/0 | 4182 | 4 | 0 | 0 | 4 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | GCAAA others(4177): Show |
chr8 | 27279886 | 27316272 |
| a0001c0001t0012 | 0/0 | 4184 | 4 | 4 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | GCAAA others(4179): Show |
chr8 | 27279886 | 27316272 |
| a0001c0001t0013 | 0/0 | 4182 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | GCAAA others(4177): Show |
chr8 | 27279886 | 27316272 |
| a0001c0001t0014 | 0/0 | 4182 | 2 | 1 | 1 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | GCAAA others(4177): Show |
chr8 | 27279886 | 27316272 |
| a0001c0001t0015 | 0/0 | 4182 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | GCAAA others(4177): Show |
chr8 | 27279886 | 27316272 |
| a0001c0001t0016 | 0/0 | 4182 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | GCAAA others(4177): Show |
chr8 | 27279886 | 27316272 |
| a0001c0001t0017 | 0/0 | 4184 | 2 | 1 | 0 | 0 | 0 | 1 | TRIM35_chr8_27279886_27316272 | TRIM35 | GCAAA others(4179): Show |
chr8 | 27279886 | 27316272 |
| a0001c0001t0018 | 0/0 | 4184 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | GCAAA others(4179): Show |
chr8 | 27279886 | 27316272 |
| a0001c0001t0019 | 0/0 | 4183 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | GCAAA others(4178): Show |
chr8 | 27279886 | 27316272 |
| a0001c0001t0021 | 0/0 | 4182 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | GCAAA others(4177): Show |
chr8 | 27279886 | 27316272 |
| a0001c0001t0022 | 0/0 | 4183 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | GCAAA others(4178): Show |
chr8 | 27279886 | 27316272 |
| a0001c0001t0023 | 0/0 | 4183 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | GCAAA others(4178): Show |
chr8 | 27279886 | 27316272 |
| a0001c0001t0024 | 0/0 | 4183 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | GCAAA others(4178): Show |
chr8 | 27279886 | 27316272 |
| a0001c0001t0025 | 0/0 | 4184 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | GCAAA others(4179): Show |
chr8 | 27279886 | 27316272 |
| a0001c0001t0026 | 0/0 | 4184 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM35_chr8_27279886_27316272 | TRIM35 | GCAAA others(4179): Show |
chr8 | 27279886 | 27316272 |
| a0001c0001t0027 | 0/0 | 4184 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | GCAAA others(4179): Show |
chr8 | 27279886 | 27316272 |
| a0001c0001t0028 | 0/0 | 4182 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | GCAAA others(4177): Show |
chr8 | 27279886 | 27316272 |
| a0001c0001t0029 | 0/0 | 4183 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | GCAAA others(4178): Show |
chr8 | 27279886 | 27316272 |
| a0001c0001t0030 | 0/0 | 4181 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | GCAAA others(4176): Show |
chr8 | 27279886 | 27316272 |
| a0001c0001t0031 | 0/0 | 4182 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | GCAAA others(4177): Show |
chr8 | 27279886 | 27316272 |
| a0001c0001t0032 | 0/0 | 4183 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | GCAAA others(4178): Show |
chr8 | 27279886 | 27316272 |
| a0001c0001t0033 | 0/0 | 4181 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | GCAAA others(4176): Show |
chr8 | 27279886 | 27316272 |
| a0001c0001t0034 | 0/0 | 4182 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM35_chr8_27279886_27316272 | TRIM35 | GCAAA others(4177): Show |
chr8 | 27279886 | 27316272 |
| a0001c0001t0035 | 0/0 | 4184 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | GCAAA others(4179): Show |
chr8 | 27279886 | 27316272 |
| a0001c0001t0036 | 0/0 | 4182 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | GCAAA others(4177): Show |
chr8 | 27279886 | 27316272 |
| a0001c0001t0037 | 0/0 | 4181 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | GCAAA others(4176): Show |
chr8 | 27279886 | 27316272 |
| a0001c0001t0038 | 0/0 | 4182 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM35_chr8_27279886_27316272 | TRIM35 | GCAAA others(4177): Show |
chr8 | 27279886 | 27316272 |
| a0001c0001t0039 | 0/0 | 4183 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | GCAAA others(4178): Show |
chr8 | 27279886 | 27316272 |
| a0001c0001t0040 | 0/0 | 4184 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | GCAAA others(4179): Show |
chr8 | 27279886 | 27316272 |
| a0001c0001t0041 | 0/0 | 4185 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | GCAAA others(4180): Show |
chr8 | 27279886 | 27316272 |
| a0001c0001t0042 | 0/0 | 4184 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | GCAAA others(4179): Show |
chr8 | 27279886 | 27316272 |
| a0001c0001t0043 | 0/0 | 4182 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | GCAAA others(4177): Show |
chr8 | 27279886 | 27316272 |
| a0001c0001t0045 | 0/0 | 4184 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | GCAAA others(4179): Show |
chr8 | 27279886 | 27316272 |
| a0001c0001t0046 | 0/0 | 4184 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | GCAAA others(4179): Show |
chr8 | 27279886 | 27316272 |
| a0001c0001t0047 | 0/0 | 4184 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | GCAAA others(4179): Show |
chr8 | 27279886 | 27316272 |
| a0001c0002t0005 | 0/0 | 4182 | 18 | 0 | 0 | 18 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | GCAAA others(4177): Show |
chr8 | 27279886 | 27316272 |
| a0001c0002t0006 | 0/0 | 4183 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | GCAAA others(4178): Show |
chr8 | 27279886 | 27316272 |
| a0001c0003t0001 | 0/0 | 4184 | 4 | 4 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | GCAAA others(4179): Show |
chr8 | 27279886 | 27316272 |
| a0001c0003t0006 | 0/0 | 4183 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | GCAAA others(4178): Show |
chr8 | 27279886 | 27316272 |
| a0001c0003t0007 | 0/0 | 4185 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | GCAAA others(4180): Show |
chr8 | 27279886 | 27316272 |
| a0001c0003t0015 | 0/0 | 4182 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | GCAAA others(4177): Show |
chr8 | 27279886 | 27316272 |
| a0001c0003t0020 | 0/0 | 4184 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | GCAAA others(4179): Show |
chr8 | 27279886 | 27316272 |
| a0001c0003t0044 | 0/0 | 4184 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | GCAAA others(4179): Show |
chr8 | 27279886 | 27316272 |
| a0001c0004t0009 | 0/0 | 4181 | 7 | 6 | 1 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | GCAAA others(4176): Show |
chr8 | 27279886 | 27316272 |
| a0001c0005t0001 | 0/0 | 4184 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | GCAAA others(4179): Show |
chr8 | 27279886 | 27316272 |
| a0001c0006t0001 | 0/0 | 4184 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | GCAAA others(4179): Show |
chr8 | 27279886 | 27316272 |
| a0001c0007t0001 | 0/0 | 4184 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | GCAAA others(4179): Show |
chr8 | 27279886 | 27316272 |
| a0001c0009t0003 | 0/0 | 4183 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | GCAAA others(4178): Show |
chr8 | 27279886 | 27316272 |
| a0001c0012t0006 | 0/0 | 4183 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | GCAAA others(4178): Show |
chr8 | 27279886 | 27316272 |
| a0001c0014t0001 | 0/0 | 4184 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | GCAAA others(4179): Show |
chr8 | 27279886 | 27316272 |
| a0001c0015t0001 | 0/0 | 4184 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | GCAAA others(4179): Show |
chr8 | 27279886 | 27316272 |
| a0002c0008t0002 | 0/0 | 4182 | 2 | 0 | 0 | 0 | 2 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | GCAAA others(4177): Show |
chr8 | 27279886 | 27316272 |
| a0003c0011t0001 | 0/0 | 4184 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | GCAAA others(4179): Show |
chr8 | 27279886 | 27316272 |
| a0004c0013t0001 | 0/0 | 4184 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | GCAAA others(4179): Show |
chr8 | 27279886 | 27316272 |
| a0005c0010t0007 | 0/0 | 4185 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | GCAAA others(4180): Show |
chr8 | 27279886 | 27316272 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 44 | 0 | 3 | 39 | 0 | 2 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0001g0005 | 0/0 | 9 | 9 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0001g0006 | 0/0 | 9 | 0 | 1 | 6 | 2 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0001g0008 | 0/0 | 7 | 0 | 0 | 6 | 0 | 1 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0001g0011 | 0/0 | 5 | 0 | 4 | 1 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0002g0002 | 0/0 | 27 | 0 | 14 | 5 | 2 | 6 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0002g0010 | 0/1 | 6 | 1 | 3 | 1 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0002g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0002g0022 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0002g0024 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0002g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0002g0042 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0003g0004 | 0/0 | 10 | 1 | 5 | 3 | 1 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0003g0015 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0003g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0003g0036 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0003g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0003g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0003g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0003g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0003g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0004g0003 | 0/0 | 17 | 1 | 0 | 15 | 0 | 1 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0004g0009 | 0/0 | 6 | 0 | 2 | 0 | 0 | 4 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0004g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0004g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0004g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0004g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0004g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0004g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0004g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0004g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0004g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0005g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0006g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0006g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0006g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0006g0122 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0006g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0006g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0006g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0006g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0007g0012 | 0/0 | 5 | 0 | 1 | 3 | 0 | 1 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0007g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0007g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0007g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0007g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0007g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0007g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0008g0014 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0008g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0008g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0008g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0008g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0008g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0010g0028 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0010g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0010g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0011g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0011g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0012g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0012g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0012g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0012g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0013g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0014g0038 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0015g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0016g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0016g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0017g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0017g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0018g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0019g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0021g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0022g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0023g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0024g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0025g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0026g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0027g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0028g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0029g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0030g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0031g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0032g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0033g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0034g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0035g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0036g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0037g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0038g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0039g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0040g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0041g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0042g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0043g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0045g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0046g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0001t0047g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0002t0005g0007 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0002t0005g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0002t0005g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0002t0005g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0002t0005g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0002t0005g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0002t0006g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0002t0006g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0002t0006g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0003t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0003t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0003t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0003t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0003t0006g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0003t0006g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0003t0007g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0003t0007g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0003t0015g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0003t0020g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0003t0044g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0004t0009g0017 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0004t0009g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0004t0009g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0004t0009g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0005t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0005t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0006t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0006t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0006t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0007t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0009t0003g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0012t0006g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0014t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0001c0015t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0002c0008t0002g0041 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0003c0011t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0004c0013t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| a0005c0010t0007g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0147 | EUR | GBR | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG00099 | hp2 | a0001 | c0001 | t0004 | g0089 | EUR | GBR | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0189 | EUR | GBR | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | GBR | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0002 | EUR | FIN | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG00280 | hp2 | a0001 | c0001 | t0003 | g0004 | EUR | FIN | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0162 | EUR | FIN | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | FIN | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG00408 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | CHS | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG00423 | hp2 | a0001 | c0001 | t0004 | g0098 | EAS | CHS | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0187 | EAS | CHS | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG00544 | hp2 | a0001 | c0001 | t0011 | g0200 | EAS | CHS | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG00558 | hp1 | a0001 | c0001 | t0024 | g0097 | EAS | CHS | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG00558 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | CHS | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG00597 | hp2 | a0001 | c0001 | t0011 | g0023 | EAS | CHS | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG00609 | hp1 | a0001 | c0001 | t0011 | g0023 | EAS | CHS | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG00609 | hp2 | a0001 | c0001 | t0006 | g0020 | EAS | CHS | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | CHS | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG00639 | hp2 | a0001 | c0004 | t0009 | g0017 | AMR | PUR | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG00673 | hp1 | a0001 | c0001 | t0035 | g0136 | EAS | CHS | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG00673 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | CHS | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG00733 | hp1 | a0001 | c0001 | t0040 | g0083 | AMR | PUR | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG00733 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG00738 | hp1 | a0001 | c0001 | t0007 | g0121 | AMR | PUR | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG00738 | hp2 | a0001 | c0001 | t0014 | g0038 | AMR | PUR | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG00741 | hp2 | a0001 | c0001 | t0004 | g0088 | AMR | PUR | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG01069 | hp1 | a0001 | c0001 | t0004 | g0009 | AMR | PUR | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0204 | AMR | PUR | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0024 | AMR | PUR | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0170 | AMR | PUR | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG01071 | hp1 | a0001 | c0001 | t0004 | g0009 | AMR | PUR | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0171 | AMR | PUR | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG01074 | hp1 | a0001 | c0001 | t0004 | g0087 | AMR | PUR | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0202 | AMR | PUR | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG01099 | hp1 | a0001 | c0009 | t0003 | g0176 | AMR | PUR | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0167 | AMR | PUR | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0036 | AMR | PUR | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0042 | AMR | PUR | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0015 | AMR | PUR | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0015 | AMR | PUR | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG01175 | hp2 | a0001 | c0001 | t0010 | g0028 | AMR | PUR | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG01192 | hp2 | a0001 | c0001 | t0041 | g0082 | AMR | PUR | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG01243 | hp1 | a0001 | c0001 | t0008 | g0014 | AMR | PUR | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0024 | AMR | PUR | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0015 | AMR | CLM | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0022 | AMR | CLM | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG01256 | hp1 | a0001 | c0001 | t0031 | g0201 | AMR | CLM | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG01256 | hp2 | a0001 | c0007 | t0001 | g0032 | AMR | CLM | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | CLM | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | CLM | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG01258 | hp2 | a0001 | c0007 | t0001 | g0032 | AMR | CLM | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | CLM | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG01261 | hp2 | a0001 | c0001 | t0003 | g0078 | AMR | CLM | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | CLM | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | CLM | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0215 | AMR | CLM | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG01361 | hp1 | a0001 | c0001 | t0003 | g0216 | AMR | CLM | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | CLM | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG01433 | hp1 | a0003 | c0011 | t0001 | g0146 | AMR | CLM | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0022 | AMR | CLM | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0022 | AMR | CLM | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG01515 | hp2 | a0001 | c0001 | t0003 | g0015 | EUR | IBS | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0062 | EUR | IBS | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG01516 | hp2 | a0002 | c0008 | t0002 | g0041 | EUR | IBS | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG01884 | hp1 | a0001 | c0001 | t0004 | g0003 | AFR | ACB | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG01891 | hp1 | a0001 | c0004 | t0009 | g0017 | AFR | ACB | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG01928 | hp1 | a0001 | c0001 | t0007 | g0012 | AMR | PEL | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0218 | AMR | PEL | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PEL | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PEL | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0192 | AMR | PEL | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | PEL | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG01978 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | PEL | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG01981 | hp1 | a0001 | c0001 | t0021 | g0193 | AMR | PEL | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0198 | AMR | PEL | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | PEL | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG02015 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | KHV | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | KHV | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG02055 | hp1 | a0001 | c0001 | t0007 | g0112 | AFR | ACB | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG02055 | hp2 | a0001 | c0001 | t0008 | g0014 | AFR | ACB | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG02056 | hp1 | a0001 | c0001 | t0004 | g0086 | EAS | KHV | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG02056 | hp2 | a0001 | c0002 | t0005 | g0072 | EAS | KHV | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | KHV | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG02071 | hp2 | a0001 | c0001 | t0006 | g0128 | EAS | KHV | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG02074 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | KHV | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG02074 | hp2 | a0001 | c0001 | t0006 | g0139 | EAS | KHV | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG02080 | hp1 | a0001 | c0001 | t0004 | g0106 | EAS | KHV | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | KHV | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG02129 | hp2 | a0001 | c0001 | t0003 | g0166 | EAS | KHV | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | KHV | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG02145 | hp1 | a0001 | c0012 | t0006 | g0126 | AFR | ACB | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | ACB | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG02165 | hp2 | a0001 | c0001 | t0010 | g0091 | EAS | CDX | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG02257 | hp2 | a0001 | c0001 | t0008 | g0093 | AFR | ACB | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG02258 | hp1 | a0001 | c0001 | t0013 | g0019 | AFR | ACB | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0035 | AFR | ACB | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0197 | AMR | PEL | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0039 | AFR | ACB | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG02280 | hp2 | a0001 | c0001 | t0008 | g0014 | AFR | ACB | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PEL | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | ACB | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG02523 | hp1 | a0001 | c0001 | t0003 | g0061 | EAS | KHV | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG02572 | hp1 | a0001 | c0001 | t0005 | g0219 | AFR | GWD | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG02572 | hp2 | a0001 | c0003 | t0007 | g0052 | AFR | GWD | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0152 | SAS | PJL | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG02615 | hp1 | a0001 | c0001 | t0042 | g0066 | AFR | GWD | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG02615 | hp2 | a0001 | c0001 | t0012 | g0068 | AFR | GWD | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG02622 | hp1 | a0001 | c0001 | t0029 | g0070 | AFR | GWD | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG02622 | hp2 | a0001 | c0001 | t0008 | g0095 | AFR | GWD | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG02630 | hp1 | a0001 | c0004 | t0009 | g0017 | AFR | GWD | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG02630 | hp2 | a0001 | c0005 | t0001 | g0025 | AFR | GWD | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG02647 | hp1 | a0001 | c0003 | t0006 | g0055 | AFR | GWD | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | GWD | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG02683 | hp1 | a0001 | c0001 | t0003 | g0164 | SAS | PJL | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG02717 | hp1 | a0001 | c0001 | t0008 | g0096 | AFR | GWD | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG02717 | hp2 | a0001 | c0001 | t0015 | g0063 | AFR | GWD | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG02723 | hp1 | a0001 | c0004 | t0009 | g0220 | AFR | GWD | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG02723 | hp2 | a0001 | c0001 | t0006 | g0027 | AFR | GWD | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0191 | SAS | PJL | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG02809 | hp1 | a0001 | c0001 | t0028 | g0069 | AFR | GWD | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG02809 | hp2 | a0001 | c0006 | t0001 | g0058 | AFR | GWD | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG02818 | hp1 | a0001 | c0003 | t0006 | g0050 | AFR | GWD | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG02818 | hp2 | a0001 | c0001 | t0016 | g0065 | AFR | GWD | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG02895 | hp1 | a0001 | c0003 | t0001 | g0048 | AFR | GWD | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0173 | AFR | GWD | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG02896 | hp1 | a0001 | c0001 | t0032 | g0168 | AFR | GWD | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG02896 | hp2 | a0001 | c0005 | t0001 | g0025 | AFR | GWD | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG02897 | hp1 | a0001 | c0005 | t0001 | g0047 | AFR | GWD | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG02897 | hp2 | a0001 | c0001 | t0033 | g0172 | AFR | GWD | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG02922 | hp1 | a0001 | c0001 | t0016 | g0064 | AFR | ESN | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG02922 | hp2 | a0001 | c0006 | t0001 | g0054 | AFR | ESN | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG02965 | hp1 | a0001 | c0003 | t0001 | g0057 | AFR | ESN | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0039 | AFR | ESN | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG02970 | hp1 | a0001 | c0001 | t0006 | g0027 | AFR | ESN | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | ESN | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG02976 | hp1 | a0001 | c0001 | t0008 | g0104 | AFR | ESN | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG03041 | hp1 | a0001 | c0003 | t0001 | g0051 | AFR | GWD | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG03041 | hp2 | a0001 | c0001 | t0006 | g0116 | AFR | GWD | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG03098 | hp1 | a0001 | c0004 | t0009 | g0221 | AFR | MSL | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG03098 | hp2 | a0001 | c0001 | t0014 | g0038 | AFR | MSL | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0090 | AFR | ESN | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG03130 | hp2 | a0001 | c0004 | t0009 | g0017 | AFR | ESN | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0185 | AFR | ESN | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG03195 | hp2 | a0001 | c0001 | t0012 | g0080 | AFR | ESN | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG03209 | hp1 | a0001 | c0003 | t0015 | g0045 | AFR | MSL | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG03209 | hp2 | a0001 | c0001 | t0039 | g0067 | AFR | MSL | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG03225 | hp2 | a0001 | c0003 | t0001 | g0046 | AFR | MSL | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0042 | SAS | PJL | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG03239 | hp2 | a0001 | c0001 | t0004 | g0003 | SAS | PJL | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG03453 | hp1 | a0001 | c0003 | t0007 | g0049 | AFR | MSL | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | MSL | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0037 | AFR | MSL | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG03486 | hp2 | a0001 | c0001 | t0045 | g0113 | AFR | MSL | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG03490 | hp2 | a0001 | c0001 | t0004 | g0009 | SAS | PJL | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG03492 | hp2 | a0001 | c0001 | t0004 | g0009 | SAS | PJL | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG03516 | hp1 | a0001 | c0001 | t0025 | g0105 | AFR | ESN | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG03516 | hp2 | a0001 | c0001 | t0007 | g0115 | AFR | ESN | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0004 | AFR | GWD | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG03579 | hp1 | a0001 | c0001 | t0008 | g0014 | AFR | MSL | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0210 | SAS | PJL | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG03654 | hp2 | a0001 | c0001 | t0034 | g0195 | SAS | PJL | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG03669 | hp1 | a0001 | c0001 | t0003 | g0182 | SAS | PJL | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG03688 | hp1 | a0001 | c0001 | t0038 | g0211 | SAS | STU | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0203 | SAS | STU | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG03704 | hp1 | a0001 | c0001 | t0004 | g0009 | SAS | PJL | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0158 | SAS | PJL | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0024 | SAS | PJL | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0196 | SAS | BEB | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | BEB | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0212 | SAS | BEB | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG03834 | hp2 | a0001 | c0001 | t0004 | g0009 | SAS | BEB | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | BEB | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG03942 | hp1 | a0001 | c0001 | t0007 | g0156 | SAS | BEB | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0125 | SAS | BEB | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG04115 | hp1 | a0001 | c0001 | t0017 | g0183 | SAS | STU | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG04115 | hp2 | a0001 | c0001 | t0007 | g0012 | SAS | STU | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0208 | SAS | BEB | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | BEB | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | STU | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG04204 | hp1 | a0001 | c0001 | t0026 | g0138 | SAS | STU | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | STU | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0184 | SAS | STU | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | STU | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | YRI | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA18522 | hp2 | a0001 | c0001 | t0037 | g0169 | AFR | YRI | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA18612 | hp1 | a0001 | c0001 | t0006 | g0020 | EAS | CHB | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA18612 | hp2 | a0001 | c0002 | t0005 | g0013 | EAS | CHB | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA18747 | hp1 | a0001 | c0015 | t0001 | g0224 | EAS | CHB | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA18747 | hp2 | a0001 | c0001 | t0019 | g0044 | EAS | CHB | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA18906 | hp1 | a0001 | c0001 | t0023 | g0094 | AFR | YRI | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0035 | AFR | YRI | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA18940 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA18940 | hp2 | a0001 | c0001 | t0004 | g0103 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA18941 | hp1 | a0001 | c0002 | t0005 | g0018 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA18941 | hp2 | a0001 | c0001 | t0006 | g0141 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA18943 | hp1 | a0001 | c0002 | t0005 | g0026 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA18944 | hp2 | a0001 | c0002 | t0005 | g0026 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA18949 | hp1 | a0001 | c0002 | t0005 | g0007 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA18949 | hp2 | a0001 | c0001 | t0018 | g0043 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA18951 | hp1 | a0001 | c0014 | t0001 | g0223 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA18952 | hp2 | a0001 | c0002 | t0005 | g0013 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA18954 | hp2 | a0001 | c0001 | t0006 | g0174 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA18957 | hp1 | a0001 | c0001 | t0030 | g0194 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA18959 | hp2 | a0001 | c0002 | t0005 | g0007 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA18960 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA18963 | hp1 | a0001 | c0001 | t0003 | g0180 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA18963 | hp2 | a0001 | c0001 | t0007 | g0012 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA18965 | hp2 | a0001 | c0002 | t0005 | g0163 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA18966 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA18967 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA18968 | hp1 | a0001 | c0002 | t0005 | g0018 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA18969 | hp2 | a0001 | c0002 | t0005 | g0013 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA18976 | hp1 | a0001 | c0001 | t0047 | g0102 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA18976 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA18977 | hp1 | a0001 | c0002 | t0005 | g0013 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA18979 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA18980 | hp1 | a0001 | c0002 | t0005 | g0007 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA18985 | hp1 | a0001 | c0001 | t0007 | g0012 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA18988 | hp1 | a0001 | c0002 | t0005 | g0007 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA18990 | hp1 | a0001 | c0002 | t0005 | g0018 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA18990 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA18993 | hp1 | a0001 | c0001 | t0007 | g0012 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA18993 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA18994 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA18994 | hp2 | a0001 | c0002 | t0006 | g0073 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA18999 | hp1 | a0001 | c0001 | t0003 | g0177 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA19000 | hp1 | a0001 | c0001 | t0011 | g0023 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA19001 | hp1 | a0004 | c0013 | t0001 | g0132 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA19001 | hp2 | a0001 | c0001 | t0004 | g0130 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA19002 | hp2 | a0001 | c0001 | t0006 | g0020 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA19003 | hp1 | a0001 | c0001 | t0027 | g0135 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA19003 | hp2 | a0001 | c0002 | t0006 | g0074 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA19005 | hp1 | a0001 | c0001 | t0010 | g0099 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA19006 | hp1 | a0001 | c0002 | t0006 | g0075 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA19007 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA19009 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA19012 | hp2 | a0001 | c0002 | t0005 | g0007 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA19030 | hp1 | a0001 | c0001 | t0046 | g0077 | AFR | LWK | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA19030 | hp2 | a0001 | c0004 | t0009 | g0222 | AFR | LWK | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA19043 | hp1 | a0001 | c0001 | t0012 | g0081 | AFR | LWK | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | LWK | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA19057 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA19063 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA19066 | hp2 | a0001 | c0001 | t0018 | g0043 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA19068 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA19072 | hp1 | a0001 | c0001 | t0004 | g0100 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA19072 | hp2 | a0001 | c0001 | t0007 | g0143 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA19077 | hp1 | a0005 | c0010 | t0007 | g0134 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA19077 | hp2 | a0001 | c0002 | t0005 | g0007 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA19079 | hp2 | a0001 | c0001 | t0010 | g0028 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA19083 | hp1 | a0001 | c0001 | t0003 | g0153 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA19084 | hp1 | a0001 | c0001 | t0007 | g0131 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA19086 | hp2 | a0001 | c0002 | t0005 | g0007 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA19091 | hp1 | a0001 | c0001 | t0003 | g0178 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA19240 | hp1 | a0001 | c0001 | t0013 | g0019 | AFR | YRI | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0079 | AFR | YRI | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ASW | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA20129 | hp2 | a0001 | c0001 | t0008 | g0092 | AFR | ASW | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0207 | EUR | TSI | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA20752 | hp2 | a0002 | c0008 | t0002 | g0041 | EUR | TSI | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0036 | SAS | GIH | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | GIH | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG02109 | hp1 | a0001 | c0001 | t0017 | g0179 | AFR | ACB | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG02109 | hp2 | a0001 | c0001 | t0012 | g0071 | AFR | ACB | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG02486 | hp1 | a0001 | c0006 | t0001 | g0053 | AFR | ACB | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG02486 | hp2 | a0001 | c0001 | t0013 | g0019 | AFR | ACB | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0165 | AFR | ACB | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0037 | AFR | ACB | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | MSL | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG03471 | hp2 | a0001 | c0003 | t0020 | g0059 | AFR | MSL | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG06807 | hp1 | a0001 | c0001 | t0043 | g0085 | AFR | USA | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| HG06807 | hp2 | a0001 | c0003 | t0044 | g0056 | AFR | USA | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA20300 | hp1 | a0001 | c0001 | t0022 | g0084 | AFR | USA | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| NA20300 | hp2 | a0001 | c0001 | t0036 | g0206 | AFR | USA | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0010 | REF | REF | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0006 | g0122 | REF | REF | TRIM35_chr8_27279886_27316272 | TRIM35 | chr8 | 27279886 | 27316272 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:27287573 | C | A | 1 | a0004 | 1 | NA19001.hp1 | missense_variant | MODERATE | c.1459G>T | p.Val487Phe | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 6/6 | 1496/4183 | 1459/1482 | 487/493 | chr8 | 27287573 | |||
| chr8:27288101 | C | T | 1 | a0003 | 1 | HG01433.hp1 | missense_variant | MODERATE | c.931G>A | p.Ala311Thr | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 6/6 | 968/4183 | 931/1482 | 311/493 | chr8 | 27288101 | |||
| chr8:27288105 | G | T | 1 | a0005 | 1 | NA19077.hp1 | missense_variant | MODERATE | c.927C>A | p.Asn309Lys | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 6/6 | 964/4183 | 927/1482 | 309/493 | chr8 | 27288105 | |||
| chr8:27294115 | T | A | 1 | a0002 | 2 | HG01516.hp2 NA20752.hp2 |
missense_variant | MODERATE | c.727A>T | p.Met243Leu | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 3/6 | 764/4183 | 727/1482 | 243/493 | chr8 | 27294115 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:27287616 | G | A | 1 | a0001c0002 | 21 | HG02056.hp2 NA18612.hp2 NA18941.hp1 others(18): Show |
synonymous_variant | LOW | c.1416C>T | p.Ala472Ala | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 6/6 | 1453/4183 | 1416/1482 | 472/493 | chr8 | 27287616 | |||
| chr8:27287745 | A | G | 1 | a0001c0002 | 21 | HG02056.hp2 NA18612.hp2 NA18941.hp1 others(18): Show |
synonymous_variant | LOW | c.1287T>C | p.Arg429Arg | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 6/6 | 1324/4183 | 1287/1482 | 429/493 | chr8 | 27287745 | |||
| chr8:27287895 | C | T | 1 | a0001c0012 | 1 | HG02145.hp1 | synonymous_variant | LOW | c.1137G>A | p.Ser379Ser | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 6/6 | 1174/4183 | 1137/1482 | 379/493 | chr8 | 27287895 | |||
| chr8:27289175 | T | A | 1 | a0001c0007 | 2 | HG01256.hp2 HG01258.hp2 |
synonymous_variant | LOW | c.891A>T | p.Ala297Ala | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 5/6 | 928/4183 | 891/1482 | 297/493 | chr8 | 27289175 | |||
| chr8:27294149 | C | T | 1 | a0001c0005 | 3 | HG02630.hp2 HG02896.hp2 HG02897.hp1 |
synonymous_variant | LOW | c.693G>A | p.Thr231Thr | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 3/6 | 730/4183 | 693/1482 | 231/493 | chr8 | 27294149 | |||
| chr8:27294212 | G | A | 1 | a0001c0006 | 3 | HG02486.hp1 HG02809.hp2 HG02922.hp2 |
synonymous_variant | LOW | c.630C>T | p.Ala210Ala | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 3/6 | 667/4183 | 630/1482 | 210/493 | chr8 | 27294212 | |||
| chr8:27294212 | G | T | 1 | a0001c0009 | 1 | HG01099.hp1 | synonymous_variant | LOW | c.630C>A | p.Ala210Ala | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 3/6 | 667/4183 | 630/1482 | 210/493 | chr8 | 27294212 | |||
| chr8:27310873 | G | A | 1 | a0001c0004 | 7 | HG00639.hp2 HG01891.hp1 HG02630.hp1 others(4): Show |
synonymous_variant | LOW | c.363C>T | p.Cys121Cys | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/6 | 400/4183 | 363/1482 | 121/493 | chr8 | 27310873 | |||
| chr8:27310897 | G | C | 1 | a0001c0014 | 1 | NA18951.hp1 | synonymous_variant | LOW | c.339C>G | p.Leu113Leu | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/6 | 376/4183 | 339/1482 | 113/493 | chr8 | 27310897 | |||
| chr8:27311137 | A | G | 3 | a0001c0003 a0001c0005 a0001c0006 |
17 | HG02486.hp1 HG02572.hp2 HG02630.hp2 others(14): Show |
synonymous_variant | LOW | c.99T>C | p.Thr33Thr | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/6 | 136/4183 | 99/1482 | 33/493 | chr8 | 27311137 | |||
| chr8:27311176 | G | C | 1 | a0001c0015 | 1 | NA18747.hp1 | synonymous_variant | LOW | c.60C>G | p.Leu20Leu | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/6 | 97/4183 | 60/1482 | 20/493 | chr8 | 27311176 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:27284943 | C | T | 3 | a0001c0001t0015 a0001c0001t0016 a0001c0003t0015 |
4 | HG02717.hp2 HG02818.hp2 HG02922.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2607G>A | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 6/6 | 2607 | chr8 | 27284943 | ||||||
| chr8:27285067 | T | C | 1 | a0001c0001t0042 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2483A>G | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 6/6 | 2483 | chr8 | 27285067 | ||||||
| chr8:27285130 | G | A | 4 | a0001c0001t0004 a0001c0001t0010 a0001c0001t0024 others(1): Show |
38 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*2420C>T | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 6/6 | 2420 | chr8 | 27285130 | ||||||
| chr8:27285190 | G | T | 1 | a0001c0001t0034 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2360C>A | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 6/6 | 2360 | chr8 | 27285190 | ||||||
| chr8:27285204 | T | C | 1 | a0001c0001t0016 | 2 | HG02818.hp2 HG02922.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2346A>G | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 6/6 | 2346 | chr8 | 27285204 | ||||||
| chr8:27285471 | C | T | 1 | a0001c0001t0040 | 1 | HG00733.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2079G>A | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 6/6 | 2079 | chr8 | 27285471 | ||||||
| chr8:27285504 | T | A | 1 | a0001c0001t0035 | 1 | HG00673.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2046A>T | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 6/6 | 2046 | chr8 | 27285504 | ||||||
| chr8:27285657 | T | A | 15 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0011 others(12): Show |
128 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(125): Show |
3_prime_UTR_variant | MODIFIER | c.*1893A>T | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 6/6 | 1893 | chr8 | 27285657 | ||||||
| chr8:27285666 | T | TA | 24 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0012 others(21): Show |
197 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(194): Show |
3_prime_UTR_variant | MODIFIER | c.*1883dupT | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 6/6 | 1883 | chr8 | 27285666 | ||||||
| chr8:27285666 | T | TAA | 5 | a0001c0001t0007 a0001c0001t0010 a0001c0001t0041 others(2): Show |
19 | HG00738.hp1 HG01175.hp2 HG01192.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*1882_*1883dupTT | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 6/6 | 1883 | chr8 | 27285666 | ||||||
| chr8:27285666 | TA | T | 17 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0011 others(14): Show |
116 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(113): Show |
3_prime_UTR_variant | MODIFIER | c.*1883delT | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 6/6 | 1883 | chr8 | 27285666 | ||||||
| chr8:27285666 | TAA | T | 4 | a0001c0001t0030 a0001c0001t0033 a0001c0001t0037 others(1): Show |
10 | HG00639.hp2 HG01891.hp1 HG02630.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1882_*1883delTT | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 6/6 | 1882 | chr8 | 27285666 | ||||||
| chr8:27285684 | A | C | 1 | a0001c0001t0032 | 1 | HG02896.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1866T>G | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 6/6 | 1866 | chr8 | 27285684 | ||||||
| chr8:27285728 | A | T | 2 | a0001c0001t0011 a0001c0001t0030 |
5 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1822T>A | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 6/6 | 1822 | chr8 | 27285728 | ||||||
| chr8:27285773 | T | A | 1 | a0001c0001t0036 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1777A>T | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 6/6 | 1777 | chr8 | 27285773 | ||||||
| chr8:27285805 | C | A | 1 | a0001c0001t0013 | 3 | HG02258.hp1 HG02486.hp2 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1745G>T | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 6/6 | 1745 | chr8 | 27285805 | ||||||
| chr8:27285921 | C | T | 1 | a0001c0001t0031 | 1 | HG01256.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1629G>A | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 6/6 | 1629 | chr8 | 27285921 | ||||||
| chr8:27286028 | G | A | 1 | a0001c0001t0037 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1522C>T | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 6/6 | 1522 | chr8 | 27286028 | ||||||
| chr8:27286220 | C | T | 2 | a0001c0001t0011 a0001c0001t0030 |
5 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1330G>A | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 6/6 | 1330 | chr8 | 27286220 | ||||||
| chr8:27286393 | G | A | 1 | a0001c0001t0038 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1157C>T | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 6/6 | 1157 | chr8 | 27286393 | ||||||
| chr8:27286569 | G | A | 6 | a0001c0001t0012 a0001c0001t0028 a0001c0001t0029 others(3): Show |
9 | HG00733.hp1 HG01192.hp2 HG02109.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*981C>T | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 6/6 | 981 | chr8 | 27286569 | ||||||
| chr8:27286571 | A | C | 2 | a0001c0001t0028 a0001c0001t0029 |
2 | HG02622.hp1 HG02809.hp1 |
3_prime_UTR_variant | MODIFIER | c.*979T>G | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 6/6 | 979 | chr8 | 27286571 | ||||||
| chr8:27286851 | G | A | 1 | a0001c0001t0042 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*699C>T | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 6/6 | 699 | chr8 | 27286851 | ||||||
| chr8:27286882 | G | A | 2 | a0001c0001t0008 a0001c0001t0025 |
10 | HG01243.hp1 HG02055.hp2 HG02257.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*668C>T | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 6/6 | 668 | chr8 | 27286882 | ||||||
| chr8:27286901 | C | A | 1 | a0001c0001t0043 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*649G>T | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 6/6 | 649 | chr8 | 27286901 | ||||||
| chr8:27287066 | G | A | 1 | a0001c0003t0044 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*484C>T | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 6/6 | 484 | chr8 | 27287066 | ||||||
| chr8:27287127 | C | T | 1 | a0001c0001t0027 | 1 | NA19003.hp1 | 3_prime_UTR_variant | MODIFIER | c.*423G>A | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 6/6 | 423 | chr8 | 27287127 | ||||||
| chr8:27287130 | A | G | 1 | a0001c0001t0022 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*420T>C | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 6/6 | 420 | chr8 | 27287130 | ||||||
| chr8:27287142 | C | T | 1 | a0001c0001t0026 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*408G>A | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 6/6 | 408 | chr8 | 27287142 | ||||||
| chr8:27287215 | C | G | 10 | a0001c0001t0004 a0001c0001t0008 a0001c0001t0010 others(7): Show |
55 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*335G>C | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 6/6 | 335 | chr8 | 27287215 | ||||||
| chr8:27287312 | C | T | 1 | a0001c0001t0021 | 1 | HG01981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*238G>A | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 6/6 | 238 | chr8 | 27287312 | ||||||
| chr8:27287417 | G | C | 1 | a0001c0001t0045 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*133C>G | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 6/6 | 133 | chr8 | 27287417 | ||||||
| chr8:27287495 | G | A | 1 | a0001c0001t0046 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*55C>T | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 6/6 | 55 | chr8 | 27287495 | ||||||
| chr8:27287530 | C | G | 1 | a0001c0001t0047 | 1 | NA18976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*20G>C | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 6/6 | 20 | chr8 | 27287530 | ||||||
| chr8:27287530 | C | T | 1 | a0001c0003t0020 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*20G>A | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 6/6 | 20 | chr8 | 27287530 | ||||||
| chr8:27287531 | G | C | 1 | a0001c0001t0047 | 1 | NA18976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*19C>G | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 6/6 | 19 | chr8 | 27287531 | ||||||
| chr8:27311241 | G | C | 1 | a0001c0001t0018 | 2 | NA18949.hp2 NA19066.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-6C>G | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/6 | chr8 | 27311241 | |||||||
| chr8:27311261 | C | T | 1 | a0001c0001t0019 | 1 | NA18747.hp2 | 5_prime_UTR_variant | MODIFIER | c.-26G>A | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/6 | 26 | chr8 | 27311261 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:27288315 | C | G | 1 | a0001c0001t0043g0085 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.905-188G>C | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 5/5 | chr8 | 27288315 | |||||||
| chr8:27288328 | C | T | 4 | a0001c0001t0012g0080 a0001c0001t0012g0081 a0001c0001t0040g0083 others(1): Show |
4 | HG00733.hp1 HG01192.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.905-201G>A | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 5/5 | chr8 | 27288328 | |||||||
| chr8:27288388 | G | A | 1 | a0001c0003t0001g0046 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.905-261C>T | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 5/5 | chr8 | 27288388 | |||||||
| chr8:27288544 | C | T | 1 | a0001c0003t0015g0045 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.905-417G>A | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 5/5 | chr8 | 27288544 | |||||||
| chr8:27288728 | C | T | 1 | a0001c0001t0002g0209 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.904+434G>A | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 5/5 | chr8 | 27288728 | |||||||
| chr8:27288752 | C | T | 5 | a0001c0001t0012g0068 a0001c0001t0012g0071 a0001c0001t0028g0069 others(2): Show |
5 | HG02109.hp2 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.904+410G>A | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 5/5 | chr8 | 27288752 | |||||||
| chr8:27288753 | G | A | 2 | a0001c0001t0006g0128 a0001c0001t0019g0044 |
2 | HG02071.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.904+409C>T | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 5/5 | chr8 | 27288753 | |||||||
| chr8:27288786 | G | A | 2 | a0001c0001t0002g0170 a0001c0001t0003g0171 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.904+376C>T | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 5/5 | chr8 | 27288786 | |||||||
| chr8:27288828 | T | C | 4 | a0001c0001t0012g0080 a0001c0001t0012g0081 a0001c0001t0040g0083 others(1): Show |
4 | HG00733.hp1 HG01192.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.904+334A>G | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 5/5 | chr8 | 27288828 | |||||||
| chr8:27288829 | A | G | 142 | a0001c0001t0002g0002 a0001c0001t0002g0010 a0001c0001t0002g0016 others(139): Show |
244 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.904+333T>C | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 5/5 | chr8 | 27288829 | |||||||
| chr8:27288935 | C | A | 1 | a0001c0001t0008g0096 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.904+227G>T | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 5/5 | chr8 | 27288935 | |||||||
| chr8:27289078 | C | T | 1 | a0001c0001t0002g0022 | 3 | HG01255.hp2 HG01433.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.904+84G>A | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 5/5 | chr8 | 27289078 | |||||||
| chr8:27289848 | T | G | 1 | a0001c0001t0003g0079 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.785+308A>C | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 4/5 | chr8 | 27289848 | |||||||
| chr8:27290055 | C | T | 12 | a0001c0003t0001g0046 a0001c0003t0001g0048 a0001c0003t0001g0051 others(9): Show |
13 | HG02572.hp2 HG02630.hp2 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.785+101G>A | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 4/5 | chr8 | 27290055 | |||||||
| chr8:27290199 | A | C | 88 | a0001c0001t0002g0002 a0001c0001t0002g0010 a0001c0001t0002g0016 others(85): Show |
147 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.763-21T>G | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 3/5 | chr8 | 27290199 | |||||||
| chr8:27290374 | G | A | 1 | a0001c0001t0023g0094 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.763-196C>T | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 3/5 | chr8 | 27290374 | |||||||
| chr8:27290422 | G | A | 86 | a0001c0001t0002g0002 a0001c0001t0002g0010 a0001c0001t0002g0016 others(83): Show |
144 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.763-244C>T | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 3/5 | chr8 | 27290422 | |||||||
| chr8:27290461 | G | A | 1 | a0001c0001t0016g0065 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.763-283C>T | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 3/5 | chr8 | 27290461 | |||||||
| chr8:27290790 | A | G | 9 | a0001c0002t0005g0007 a0001c0002t0005g0013 a0001c0002t0005g0018 others(6): Show |
21 | HG02056.hp2 NA18612.hp2 NA18941.hp1 others(18): Show |
intron_variant | MODIFIER | c.763-612T>C | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 3/5 | chr8 | 27290790 | |||||||
| chr8:27291007 | G | A | 2 | a0001c0001t0001g0029 a0001c0001t0007g0121 |
3 | HG00738.hp1 HG01346.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.763-829C>T | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 3/5 | chr8 | 27291007 | |||||||
| chr8:27291016 | T | C | 1 | a0001c0001t0002g0207 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.763-838A>G | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 3/5 | chr8 | 27291016 | |||||||
| chr8:27291058 | C | CA | 9 | a0001c0001t0001g0033 a0001c0001t0001g0114 a0001c0001t0001g0140 others(6): Show |
10 | HG00741.hp1 HG01109.hp2 HG02970.hp2 others(7): Show |
intron_variant | MODIFIER | c.763-881dupT | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 3/5 | chr8 | 27291058 | |||||||
| chr8:27291058 | CA | C | 59 | a0001c0001t0001g0031 a0001c0001t0001g0076 a0001c0001t0001g0111 others(56): Show |
101 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.763-881delT | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 3/5 | chr8 | 27291058 | |||||||
| chr8:27291165 | T | TA | 4 | a0001c0003t0001g0051 a0001c0003t0001g0057 a0001c0003t0006g0050 others(1): Show |
4 | HG02572.hp2 HG02818.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.763-988dupT | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 3/5 | chr8 | 27291165 | |||||||
| chr8:27291249 | G | C | 145 | a0001c0001t0001g0076 a0001c0001t0002g0002 a0001c0001t0002g0010 others(142): Show |
247 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.763-1071C>G | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 3/5 | chr8 | 27291249 | |||||||
| chr8:27291298 | T | C | 9 | a0001c0001t0012g0068 a0001c0001t0012g0071 a0001c0001t0028g0069 others(6): Show |
12 | HG00639.hp2 HG01891.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.763-1120A>G | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 3/5 | chr8 | 27291298 | |||||||
| chr8:27291453 | G | A | 9 | a0001c0002t0005g0007 a0001c0002t0005g0013 a0001c0002t0005g0018 others(6): Show |
21 | HG02056.hp2 NA18612.hp2 NA18941.hp1 others(18): Show |
intron_variant | MODIFIER | c.763-1275C>T | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 3/5 | chr8 | 27291453 | |||||||
| chr8:27291707 | T | C | 1 | a0001c0001t0001g0129 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.763-1529A>G | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 3/5 | chr8 | 27291707 | |||||||
| chr8:27291780 | GAGAGCCC others(22): Show |
G | 1 | a0001c0002t0006g0075 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.763-1631_763-1603d others(31): Show |
TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 3/5 | chr8 | 27291780 | |||||||
| chr8:27291811 | G | C | 1 | a0001c0001t0002g0197 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.763-1633C>G | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 3/5 | chr8 | 27291811 | |||||||
| chr8:27292053 | G | A | 4 | a0001c0004t0009g0017 a0001c0004t0009g0220 a0001c0004t0009g0221 others(1): Show |
7 | HG00639.hp2 HG01891.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.763-1875C>T | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 3/5 | chr8 | 27292053 | |||||||
| chr8:27292064 | T | C | 4 | a0001c0001t0003g0036 a0001c0001t0003g0167 a0001c0001t0040g0083 others(1): Show |
5 | HG00733.hp1 HG01106.hp1 HG01109.hp1 others(2): Show |
intron_variant | MODIFIER | c.763-1886A>G | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 3/5 | chr8 | 27292064 | |||||||
| chr8:27292111 | G | A | 1 | a0001c0001t0002g0185 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.763-1933C>T | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 3/5 | chr8 | 27292111 | |||||||
| chr8:27292184 | T | C | 1 | a0001c0001t0002g0198 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.762+1896A>G | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 3/5 | chr8 | 27292184 | |||||||
| chr8:27292336 | G | T | 16 | a0001c0001t0004g0003 a0001c0001t0004g0009 a0001c0001t0004g0086 others(13): Show |
38 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.762+1744C>A | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 3/5 | chr8 | 27292336 | |||||||
| chr8:27292476 | G | A | 2 | a0001c0001t0001g0147 a0003c0011t0001g0146 |
2 | HG00099.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.762+1604C>T | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 3/5 | chr8 | 27292476 | |||||||
| chr8:27292492 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.762+1588G>A | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 3/5 | chr8 | 27292492 | |||||||
| chr8:27292570 | G | C | 1 | a0001c0001t0002g0187 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.762+1510C>G | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 3/5 | chr8 | 27292570 | |||||||
| chr8:27292708 | G | A | 2 | a0001c0001t0008g0095 a0001c0001t0008g0096 |
2 | HG02622.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.762+1372C>T | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 3/5 | chr8 | 27292708 | |||||||
| chr8:27292769 | G | A | 2 | a0001c0001t0028g0069 a0001c0001t0029g0070 |
2 | HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.762+1311C>T | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 3/5 | chr8 | 27292769 | |||||||
| chr8:27293003 | C | CT | 7 | a0001c0001t0001g0076 a0001c0001t0012g0080 a0001c0001t0013g0019 others(4): Show |
9 | HG00733.hp1 HG01192.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.762+1076dupA | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 3/5 | chr8 | 27293003 | |||||||
| chr8:27293009 | T | TG | 25 | a0001c0001t0004g0003 a0001c0001t0004g0009 a0001c0001t0004g0086 others(22): Show |
50 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.762+1070_762+1071i others(3): Show |
TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 3/5 | chr8 | 27293009 | |||||||
| chr8:27293283 | G | A | 2 | a0001c0001t0028g0069 a0001c0001t0029g0070 |
2 | HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.762+797C>T | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 3/5 | chr8 | 27293283 | |||||||
| chr8:27293323 | T | C | 1 | a0001c0001t0003g0165 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.762+757A>G | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 3/5 | chr8 | 27293323 | |||||||
| chr8:27293353 | A | G | 1 | a0001c0001t0007g0131 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.762+727T>C | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 3/5 | chr8 | 27293353 | |||||||
| chr8:27293396 | G | C | 79 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(76): Show |
165 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(162): Show |
intron_variant | MODIFIER | c.762+684C>G | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 3/5 | chr8 | 27293396 | |||||||
| chr8:27293461 | T | C | 3 | a0001c0001t0002g0173 a0001c0001t0003g0035 a0001c0001t0033g0172 |
4 | HG02258.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.762+619A>G | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 3/5 | chr8 | 27293461 | |||||||
| chr8:27293463 | G | T | 1 | a0001c0001t0001g0129 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.762+617C>A | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 3/5 | chr8 | 27293463 | |||||||
| chr8:27293649 | G | A | 1 | a0001c0001t0002g0187 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.762+431C>T | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 3/5 | chr8 | 27293649 | |||||||
| chr8:27293731 | G | C | 1 | a0001c0001t0004g0088 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.762+349C>G | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 3/5 | chr8 | 27293731 | |||||||
| chr8:27293923 | T | A | 1 | a0001c0001t0001g0137 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.762+157A>T | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 3/5 | chr8 | 27293923 | |||||||
| chr8:27293932 | A | G | 1 | a0001c0001t0002g0192 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.762+148T>C | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 3/5 | chr8 | 27293932 | |||||||
| chr8:27294430 | A | G | 1 | a0001c0001t0001g0076 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.532-120T>C | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 2/5 | chr8 | 27294430 | |||||||
| chr8:27294449 | A | G | 6 | a0001c0001t0004g0098 a0001c0001t0004g0103 a0001c0001t0004g0106 others(3): Show |
6 | HG00423.hp2 HG00558.hp1 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.532-139T>C | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 2/5 | chr8 | 27294449 | |||||||
| chr8:27294513 | T | G | 1 | a0001c0001t0001g0076 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.532-203A>C | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 2/5 | chr8 | 27294513 | |||||||
| chr8:27294571 | T | C | 14 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0021 others(11): Show |
30 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(27): Show |
intron_variant | MODIFIER | c.532-261A>G | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 2/5 | chr8 | 27294571 | |||||||
| chr8:27294672 | AATG | A | 2 | a0001c0001t0003g0015 a0001c0009t0003g0176 |
5 | HG01099.hp1 HG01168.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.532-365_532-363del others(3): Show |
TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 2/5 | chr8 | 27294672 | |||||||
| chr8:27294822 | GT | G | 116 | a0001c0001t0001g0040 a0001c0001t0001g0076 a0001c0001t0001g0101 others(113): Show |
199 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.532-513delA | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 2/5 | chr8 | 27294822 | |||||||
| chr8:27294824 | T | G | 1 | a0001c0002t0005g0026 | 2 | NA18943.hp1 NA18944.hp2 |
intron_variant | MODIFIER | c.532-514A>C | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 2/5 | chr8 | 27294824 | |||||||
| chr8:27294960 | C | T | 1 | a0001c0003t0001g0046 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.532-650G>A | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 2/5 | chr8 | 27294960 | |||||||
| chr8:27294980 | G | A | 45 | a0001c0001t0001g0040 a0001c0001t0001g0199 a0001c0001t0001g0212 others(42): Show |
84 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.532-670C>T | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 2/5 | chr8 | 27294980 | |||||||
| chr8:27295019 | T | C | 45 | a0001c0001t0001g0040 a0001c0001t0001g0199 a0001c0001t0001g0212 others(42): Show |
84 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.532-709A>G | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 2/5 | chr8 | 27295019 | |||||||
| chr8:27295218 | C | T | 5 | a0001c0001t0012g0080 a0001c0001t0012g0081 a0001c0001t0013g0019 others(2): Show |
7 | HG00733.hp1 HG01192.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.532-908G>A | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 2/5 | chr8 | 27295218 | |||||||
| chr8:27295222 | G | A | 9 | a0001c0002t0005g0007 a0001c0002t0005g0013 a0001c0002t0005g0018 others(6): Show |
21 | HG02056.hp2 NA18612.hp2 NA18941.hp1 others(18): Show |
intron_variant | MODIFIER | c.532-912C>T | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 2/5 | chr8 | 27295222 | |||||||
| chr8:27295345 | A | C | 1 | a0001c0001t0001g0076 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.532-1035T>G | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 2/5 | chr8 | 27295345 | |||||||
| chr8:27295353 | A | G | 17 | a0001c0001t0006g0027 a0001c0001t0046g0077 a0001c0003t0001g0046 others(14): Show |
19 | HG02486.hp1 HG02572.hp2 HG02630.hp2 others(16): Show |
intron_variant | MODIFIER | c.532-1043T>C | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 2/5 | chr8 | 27295353 | |||||||
| chr8:27295527 | T | C | 1 | a0001c0001t0014g0038 | 2 | HG00738.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.532-1217A>G | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 2/5 | chr8 | 27295527 | |||||||
| chr8:27295537 | G | GCCCCCCC others(20): Show |
1 | a0001c0002t0006g0075 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.532-1228_532-1227i others(29): Show |
TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 2/5 | chr8 | 27295537 | |||||||
| chr8:27295662 | T | C | 1 | a0001c0001t0013g0019 | 3 | HG02258.hp1 HG02486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.532-1352A>G | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 2/5 | chr8 | 27295662 | |||||||
| chr8:27295769 | G | C | 1 | a0001c0001t0014g0038 | 2 | HG00738.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.532-1459C>G | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 2/5 | chr8 | 27295769 | |||||||
| chr8:27295778 | T | A | 1 | a0001c0001t0003g0177 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.532-1468A>T | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 2/5 | chr8 | 27295778 | |||||||
| chr8:27295796 | T | C | 1 | a0001c0001t0042g0066 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.532-1486A>G | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 2/5 | chr8 | 27295796 | |||||||
| chr8:27295832 | A | T | 9 | a0001c0001t0012g0068 a0001c0001t0012g0071 a0001c0001t0028g0069 others(6): Show |
12 | HG00639.hp2 HG01891.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.532-1522T>A | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 2/5 | chr8 | 27295832 | |||||||
| chr8:27296109 | A | G | 4 | a0001c0001t0015g0063 a0001c0001t0016g0064 a0001c0001t0016g0065 others(1): Show |
4 | HG02717.hp2 HG02818.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.532-1799T>C | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 2/5 | chr8 | 27296109 | |||||||
| chr8:27296145 | G | A | 5 | a0001c0001t0012g0068 a0001c0001t0012g0071 a0001c0001t0028g0069 others(2): Show |
5 | HG02109.hp2 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.532-1835C>T | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 2/5 | chr8 | 27296145 | |||||||
| chr8:27296154 | C | CT | 40 | a0001c0001t0001g0101 a0001c0001t0001g0127 a0001c0001t0002g0062 others(37): Show |
77 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.532-1845dupA | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 2/5 | chr8 | 27296154 | |||||||
| chr8:27296154 | CT | C | 15 | a0001c0001t0001g0076 a0001c0001t0001g0142 a0001c0001t0001g0158 others(12): Show |
16 | HG00733.hp1 HG01069.hp2 HG01074.hp2 others(13): Show |
intron_variant | MODIFIER | c.532-1845delA | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 2/5 | chr8 | 27296154 | |||||||
| chr8:27296156 | T | C | 1 | a0001c0001t0001g0144 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.532-1846A>G | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 2/5 | chr8 | 27296156 | |||||||
| chr8:27296269 | C | G | 5 | a0001c0001t0012g0068 a0001c0001t0012g0071 a0001c0001t0028g0069 others(2): Show |
5 | HG02109.hp2 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.532-1959G>C | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 2/5 | chr8 | 27296269 | |||||||
| chr8:27296281 | C | A | 1 | a0001c0001t0042g0066 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.532-1971G>T | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 2/5 | chr8 | 27296281 | |||||||
| chr8:27296284 | C | T | 1 | a0001c0001t0042g0066 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.532-1974G>A | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 2/5 | chr8 | 27296284 | |||||||
| chr8:27296421 | C | T | 2 | a0001c0001t0028g0069 a0001c0001t0029g0070 |
2 | HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.531+2043G>A | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 2/5 | chr8 | 27296421 | |||||||
| chr8:27296423 | G | A | 27 | a0001c0001t0001g0101 a0001c0001t0002g0090 a0001c0001t0004g0003 others(24): Show |
52 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.531+2041C>T | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 2/5 | chr8 | 27296423 | |||||||
| chr8:27296481 | G | C | 2 | a0001c0001t0003g0036 a0001c0001t0003g0167 |
3 | HG01106.hp1 HG01109.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.531+1983C>G | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 2/5 | chr8 | 27296481 | |||||||
| chr8:27296650 | T | C | 1 | a0001c0001t0002g0203 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.531+1814A>G | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 2/5 | chr8 | 27296650 | |||||||
| chr8:27296688 | A | C | 9 | a0001c0002t0005g0007 a0001c0002t0005g0013 a0001c0002t0005g0018 others(6): Show |
21 | HG02056.hp2 NA18612.hp2 NA18941.hp1 others(18): Show |
intron_variant | MODIFIER | c.531+1776T>G | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 2/5 | chr8 | 27296688 | |||||||
| chr8:27296791 | T | G | 1 | a0001c0001t0042g0066 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.531+1673A>C | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 2/5 | chr8 | 27296791 | |||||||
| chr8:27296933 | T | C | 1 | a0001c0001t0001g0145 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.531+1531A>G | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 2/5 | chr8 | 27296933 | |||||||
| chr8:27296937 | A | G | 1 | a0001c0001t0001g0076 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.531+1527T>C | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 2/5 | chr8 | 27296937 | |||||||
| chr8:27297035 | T | C | 1 | a0001c0001t0001g0076 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.531+1429A>G | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 2/5 | chr8 | 27297035 | |||||||
| chr8:27297141 | C | A | 1 | a0001c0001t0003g0178 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.531+1323G>T | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 2/5 | chr8 | 27297141 | |||||||
| chr8:27297166 | C | A | 1 | a0001c0001t0042g0066 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.531+1298G>T | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 2/5 | chr8 | 27297166 | |||||||
| chr8:27297169 | A | G | 218 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(215): Show |
404 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(401): Show |
intron_variant | MODIFIER | c.531+1295T>C | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 2/5 | chr8 | 27297169 | |||||||
| chr8:27297228 | A | G | 1 | a0001c0001t0001g0076 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.531+1236T>C | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 2/5 | chr8 | 27297228 | |||||||
| chr8:27297264 | A | G | 1 | a0001c0014t0001g0223 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.531+1200T>C | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 2/5 | chr8 | 27297264 | |||||||
| chr8:27297287 | T | C | 1 | a0001c0001t0017g0179 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.531+1177A>G | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 2/5 | chr8 | 27297287 | |||||||
| chr8:27297506 | A | G | 1 | a0001c0001t0001g0108 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.531+958T>C | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 2/5 | chr8 | 27297506 | |||||||
| chr8:27297550 | A | G | 17 | a0001c0001t0006g0027 a0001c0001t0046g0077 a0001c0003t0001g0046 others(14): Show |
19 | HG02486.hp1 HG02572.hp2 HG02630.hp2 others(16): Show |
intron_variant | MODIFIER | c.531+914T>C | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 2/5 | chr8 | 27297550 | |||||||
| chr8:27297606 | G | A | 1 | a0001c0001t0001g0148 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.531+858C>T | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 2/5 | chr8 | 27297606 | |||||||
| chr8:27297618 | C | T | 16 | a0001c0001t0006g0027 a0001c0001t0046g0077 a0001c0003t0001g0046 others(13): Show |
18 | HG02486.hp1 HG02572.hp2 HG02630.hp2 others(15): Show |
intron_variant | MODIFIER | c.531+846G>A | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 2/5 | chr8 | 27297618 | |||||||
| chr8:27297649 | T | C | 1 | a0001c0001t0001g0076 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.531+815A>G | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 2/5 | chr8 | 27297649 | |||||||
| chr8:27297816 | G | A | 1 | a0001c0001t0003g0180 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.531+648C>T | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 2/5 | chr8 | 27297816 | |||||||
| chr8:27297889 | C | T | 1 | a0001c0012t0006g0126 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.531+575G>A | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 2/5 | chr8 | 27297889 | |||||||
| chr8:27297996 | G | A | 1 | a0001c0001t0005g0219 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.531+468C>T | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 2/5 | chr8 | 27297996 | |||||||
| chr8:27298091 | T | C | 1 | a0001c0001t0001g0149 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.531+373A>G | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 2/5 | chr8 | 27298091 | |||||||
| chr8:27298121 | G | T | 1 | a0001c0001t0001g0110 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.531+343C>A | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 2/5 | chr8 | 27298121 | |||||||
| chr8:27298168 | T | C | 5 | a0001c0001t0012g0080 a0001c0001t0012g0081 a0001c0001t0013g0019 others(2): Show |
7 | HG00733.hp1 HG01192.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.531+296A>G | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 2/5 | chr8 | 27298168 | |||||||
| chr8:27298176 | A | G | 1 | a0001c0001t0003g0165 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.531+288T>C | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 2/5 | chr8 | 27298176 | |||||||
| chr8:27298181 | T | C | 1 | a0001c0001t0003g0165 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.531+283A>G | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 2/5 | chr8 | 27298181 | |||||||
| chr8:27298239 | C | G | 1 | a0001c0001t0001g0125 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.531+225G>C | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 2/5 | chr8 | 27298239 | |||||||
| chr8:27298253 | G | A | 1 | a0001c0001t0017g0183 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.531+211C>T | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 2/5 | chr8 | 27298253 | |||||||
| chr8:27298323 | G | A | 5 | a0001c0001t0012g0080 a0001c0001t0012g0081 a0001c0001t0013g0019 others(2): Show |
7 | HG00733.hp1 HG01192.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.531+141C>T | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 2/5 | chr8 | 27298323 | |||||||
| chr8:27298354 | C | G | 1 | a0001c0001t0001g0124 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.531+110G>C | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 2/5 | chr8 | 27298354 | |||||||
| chr8:27298435 | C | A | 2 | a0001c0001t0002g0024 a0001c0001t0002g0204 |
4 | HG01069.hp2 HG01070.hp1 HG01243.hp2 others(1): Show |
intron_variant | MODIFIER | c.531+29G>T | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 2/5 | chr8 | 27298435 | |||||||
| chr8:27298675 | C | T | 1 | a0001c0001t0008g0092 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.436-116G>A | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27298675 | |||||||
| chr8:27298792 | C | T | 16 | a0001c0001t0001g0101 a0001c0001t0004g0003 a0001c0001t0004g0009 others(13): Show |
38 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.436-233G>A | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27298792 | |||||||
| chr8:27298985 | T | C | 16 | a0001c0001t0001g0101 a0001c0001t0004g0003 a0001c0001t0004g0009 others(13): Show |
38 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.436-426A>G | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27298985 | |||||||
| chr8:27299036 | C | G | 1 | a0001c0001t0042g0066 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.436-477G>C | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27299036 | |||||||
| chr8:27299135 | C | T | 5 | a0001c0001t0012g0068 a0001c0001t0012g0071 a0001c0001t0028g0069 others(2): Show |
5 | HG02109.hp2 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.436-576G>A | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27299135 | |||||||
| chr8:27299152 | T | A | 1 | a0001c0001t0001g0150 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.436-593A>T | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27299152 | |||||||
| chr8:27299171 | T | C | 5 | a0001c0001t0012g0068 a0001c0001t0012g0071 a0001c0001t0028g0069 others(2): Show |
5 | HG02109.hp2 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.436-612A>G | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27299171 | |||||||
| chr8:27299316 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.436-757C>T | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27299316 | |||||||
| chr8:27299532 | C | T | 1 | a0001c0001t0001g0076 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.436-973G>A | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27299532 | |||||||
| chr8:27299550 | C | G | 1 | a0001c0001t0002g0191 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.436-991G>C | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27299550 | |||||||
| chr8:27299644 | T | C | 10 | a0001c0001t0005g0219 a0001c0001t0012g0068 a0001c0001t0012g0071 others(7): Show |
10 | HG02109.hp2 HG02572.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.436-1085A>G | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27299644 | |||||||
| chr8:27299660 | G | A | 2 | a0001c0001t0028g0069 a0001c0001t0029g0070 |
2 | HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.436-1101C>T | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27299660 | |||||||
| chr8:27299701 | G | A | 1 | a0001c0001t0001g0021 | 3 | HG03490.hp1 HG03704.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.436-1142C>T | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27299701 | |||||||
| chr8:27299701 | G | C | 1 | a0001c0001t0047g0102 | 1 | NA18976.hp1 | intron_variant | MODIFIER | c.436-1142C>G | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27299701 | |||||||
| chr8:27299790 | C | T | 51 | a0001c0001t0001g0040 a0001c0001t0001g0199 a0001c0001t0001g0212 others(48): Show |
92 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.436-1231G>A | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27299790 | |||||||
| chr8:27299906 | C | T | 1 | a0001c0001t0002g0213 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.436-1347G>A | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27299906 | |||||||
| chr8:27299998 | C | T | 1 | a0001c0001t0001g0076 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.436-1439G>A | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27299998 | |||||||
| chr8:27300020 | G | A | 5 | a0001c0001t0012g0068 a0001c0001t0012g0071 a0001c0001t0028g0069 others(2): Show |
5 | HG02109.hp2 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.436-1461C>T | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27300020 | |||||||
| chr8:27300025 | C | G | 1 | a0001c0001t0001g0076 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.436-1466G>C | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27300025 | |||||||
| chr8:27300073 | A | G | 4 | a0001c0002t0005g0013 a0001c0002t0005g0026 a0001c0002t0005g0072 others(1): Show |
8 | HG02056.hp2 NA18612.hp2 NA18943.hp1 others(5): Show |
intron_variant | MODIFIER | c.436-1514T>C | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27300073 | |||||||
| chr8:27300222 | C | T | 1 | a0001c0001t0001g0076 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.436-1663G>A | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27300222 | |||||||
| chr8:27300223 | C | T | 1 | a0001c0002t0005g0072 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.436-1664G>A | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27300223 | |||||||
| chr8:27300330 | G | A | 17 | a0001c0001t0006g0027 a0001c0001t0046g0077 a0001c0003t0001g0046 others(14): Show |
19 | HG02486.hp1 HG02572.hp2 HG02630.hp2 others(16): Show |
intron_variant | MODIFIER | c.436-1771C>T | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27300330 | |||||||
| chr8:27300428 | A | G | 1 | a0001c0001t0002g0207 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.436-1869T>C | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27300428 | |||||||
| chr8:27300617 | CT | C | 14 | a0001c0001t0005g0219 a0001c0001t0012g0068 a0001c0001t0012g0071 others(11): Show |
17 | HG00639.hp2 HG01891.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.436-2059delA | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27300617 | |||||||
| chr8:27300653 | T | C | 1 | a0001c0001t0002g0205 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.436-2094A>G | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27300653 | |||||||
| chr8:27300948 | C | T | 1 | a0001c0001t0014g0038 | 2 | HG00738.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.436-2389G>A | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27300948 | |||||||
| chr8:27301006 | T | A | 62 | a0001c0001t0001g0040 a0001c0001t0001g0199 a0001c0001t0001g0212 others(59): Show |
103 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.436-2447A>T | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27301006 | |||||||
| chr8:27301122 | A | G | 1 | a0001c0001t0003g0167 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.436-2563T>C | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27301122 | |||||||
| chr8:27301176 | C | G | 27 | a0001c0001t0001g0101 a0001c0001t0002g0090 a0001c0001t0004g0003 others(24): Show |
52 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.436-2617G>C | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27301176 | |||||||
| chr8:27301238 | C | A | 1 | a0001c0001t0036g0206 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.436-2679G>T | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27301238 | |||||||
| chr8:27301271 | C | T | 1 | a0001c0001t0001g0076 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.436-2712G>A | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27301271 | |||||||
| chr8:27301325 | T | A | 1 | a0001c0001t0002g0187 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.436-2766A>T | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27301325 | |||||||
| chr8:27301349 | G | A | 1 | a0001c0001t0002g0207 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.436-2790C>T | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27301349 | |||||||
| chr8:27301456 | A | G | 1 | a0001c0014t0001g0223 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.436-2897T>C | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27301456 | |||||||
| chr8:27301533 | C | T | 4 | a0001c0001t0015g0063 a0001c0001t0016g0064 a0001c0001t0016g0065 others(1): Show |
4 | HG02717.hp2 HG02818.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.436-2974G>A | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27301533 | |||||||
| chr8:27301586 | T | G | 2 | a0001c0001t0006g0027 a0001c0001t0046g0077 |
3 | HG02723.hp2 HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.436-3027A>C | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27301586 | |||||||
| chr8:27301757 | G | A | 1 | a0001c0001t0001g0076 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.436-3198C>T | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27301757 | |||||||
| chr8:27301942 | C | T | 121 | a0001c0001t0001g0040 a0001c0001t0001g0076 a0001c0001t0001g0101 others(118): Show |
205 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.436-3383G>A | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27301942 | |||||||
| chr8:27301958 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.436-3399G>A | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27301958 | |||||||
| chr8:27302118 | C | T | 17 | a0001c0001t0006g0027 a0001c0001t0046g0077 a0001c0003t0001g0046 others(14): Show |
19 | HG02486.hp1 HG02572.hp2 HG02630.hp2 others(16): Show |
intron_variant | MODIFIER | c.436-3559G>A | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27302118 | |||||||
| chr8:27302257 | T | C | 1 | a0001c0001t0001g0076 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.436-3698A>G | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27302257 | |||||||
| chr8:27302319 | G | A | 86 | a0001c0001t0001g0040 a0001c0001t0001g0199 a0001c0001t0001g0212 others(83): Show |
143 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.436-3760C>T | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27302319 | |||||||
| chr8:27302336 | A | G | 2 | a0001c0001t0001g0155 a0001c0001t0007g0156 |
2 | HG02698.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.436-3777T>C | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27302336 | |||||||
| chr8:27302394 | T | C | 1 | a0001c0001t0001g0076 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.436-3835A>G | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27302394 | |||||||
| chr8:27302478 | T | C | 1 | a0001c0001t0001g0076 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.436-3919A>G | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27302478 | |||||||
| chr8:27302623 | G | T | 1 | a0001c0001t0008g0014 | 4 | HG01243.hp1 HG02055.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.436-4064C>A | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27302623 | |||||||
| chr8:27302894 | T | A | 1 | a0001c0001t0004g0089 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.436-4335A>T | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27302894 | |||||||
| chr8:27302994 | C | T | 9 | a0001c0002t0005g0007 a0001c0002t0005g0013 a0001c0002t0005g0018 others(6): Show |
21 | HG02056.hp2 NA18612.hp2 NA18941.hp1 others(18): Show |
intron_variant | MODIFIER | c.436-4435G>A | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27302994 | |||||||
| chr8:27303035 | T | C | 1 | a0001c0001t0001g0181 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.436-4476A>G | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27303035 | |||||||
| chr8:27303079 | A | G | 1 | a0001c0001t0001g0076 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.436-4520T>C | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27303079 | |||||||
| chr8:27303085 | T | C | 44 | a0001c0001t0001g0040 a0001c0001t0001g0199 a0001c0001t0001g0212 others(41): Show |
83 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.436-4526A>G | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27303085 | |||||||
| chr8:27303147 | A | C | 27 | a0001c0001t0001g0101 a0001c0001t0002g0090 a0001c0001t0004g0003 others(24): Show |
52 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.436-4588T>G | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27303147 | |||||||
| chr8:27303282 | T | C | 1 | a0001c0001t0002g0208 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.436-4723A>G | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27303282 | |||||||
| chr8:27303328 | T | C | 1 | a0001c0001t0042g0066 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.436-4769A>G | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27303328 | |||||||
| chr8:27303453 | A | G | 44 | a0001c0001t0001g0040 a0001c0001t0001g0199 a0001c0001t0001g0212 others(41): Show |
83 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.436-4894T>C | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27303453 | |||||||
| chr8:27303459 | T | C | 1 | a0001c0001t0002g0209 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.436-4900A>G | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27303459 | |||||||
| chr8:27303509 | T | C | 3 | a0001c0001t0001g0107 a0001c0001t0001g0151 a0001c0001t0001g0158 |
3 | HG03710.hp1 HG04228.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.436-4950A>G | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27303509 | |||||||
| chr8:27303560 | T | C | 1 | a0001c0001t0002g0188 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.436-5001A>G | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27303560 | |||||||
| chr8:27303716 | A | G | 87 | a0001c0001t0001g0040 a0001c0001t0001g0076 a0001c0001t0001g0199 others(84): Show |
144 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.436-5157T>C | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27303716 | |||||||
| chr8:27303725 | T | C | 221 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(218): Show |
407 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(404): Show |
intron_variant | MODIFIER | c.436-5166A>G | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27303725 | |||||||
| chr8:27303763 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.436-5204C>T | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27303763 | |||||||
| chr8:27304016 | C | T | 2 | a0001c0001t0001g0155 a0001c0001t0007g0156 |
2 | HG02698.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.436-5457G>A | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27304016 | |||||||
| chr8:27304093 | A | T | 3 | a0001c0001t0001g0029 a0001c0001t0001g0120 a0001c0001t0007g0121 |
4 | HG00738.hp1 HG01346.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.436-5534T>A | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27304093 | |||||||
| chr8:27304161 | G | A | 44 | a0001c0001t0001g0040 a0001c0001t0001g0199 a0001c0001t0001g0212 others(41): Show |
83 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.436-5602C>T | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27304161 | |||||||
| chr8:27304276 | A | C | 1 | a0001c0001t0010g0091 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.436-5717T>G | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27304276 | |||||||
| chr8:27304321 | C | T | 3 | a0001c0001t0001g0212 a0001c0001t0002g0210 a0001c0001t0038g0211 |
3 | HG03654.hp1 HG03688.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.436-5762G>A | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27304321 | |||||||
| chr8:27304365 | T | C | 1 | a0001c0001t0003g0037 | 2 | HG02559.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.436-5806A>G | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27304365 | |||||||
| chr8:27304437 | C | G | 1 | a0001c0001t0002g0190 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.436-5878G>C | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27304437 | |||||||
| chr8:27304497 | A | G | 9 | a0001c0002t0005g0007 a0001c0002t0005g0013 a0001c0002t0005g0018 others(6): Show |
21 | HG02056.hp2 NA18612.hp2 NA18941.hp1 others(18): Show |
intron_variant | MODIFIER | c.436-5938T>C | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27304497 | |||||||
| chr8:27304517 | G | A | 3 | a0001c0001t0001g0212 a0001c0001t0002g0210 a0001c0001t0038g0211 |
3 | HG03654.hp1 HG03688.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.436-5958C>T | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27304517 | |||||||
| chr8:27304728 | A | C | 1 | a0001c0003t0015g0045 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.435+6073T>G | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27304728 | |||||||
| chr8:27304781 | T | G | 1 | a0001c0001t0004g0103 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.435+6020A>C | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27304781 | |||||||
| chr8:27304809 | T | C | 1 | a0001c0001t0001g0076 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.435+5992A>G | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27304809 | |||||||
| chr8:27304867 | C | T | 1 | a0001c0001t0001g0076 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.435+5934G>A | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27304867 | |||||||
| chr8:27304919 | G | A | 2 | a0001c0001t0002g0154 a0001c0001t0003g0153 |
2 | NA18991.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.435+5882C>T | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27304919 | |||||||
| chr8:27304920 | A | G | 1 | a0001c0001t0002g0090 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.435+5881T>C | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27304920 | |||||||
| chr8:27304970 | C | T | 1 | a0001c0001t0014g0038 | 2 | HG00738.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.435+5831G>A | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27304970 | |||||||
| chr8:27304985 | C | T | 1 | a0001c0001t0002g0213 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.435+5816G>A | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27304985 | |||||||
| chr8:27305069 | G | T | 1 | a0001c0001t0002g0189 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.435+5732C>A | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27305069 | |||||||
| chr8:27305244 | T | A | 2 | a0001c0001t0008g0104 a0001c0001t0025g0105 |
2 | HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.435+5557A>T | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27305244 | |||||||
| chr8:27305476 | C | T | 1 | a0001c0001t0001g0119 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.435+5325G>A | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27305476 | |||||||
| chr8:27305501 | C | T | 19 | a0001c0001t0006g0027 a0001c0001t0042g0066 a0001c0001t0046g0077 others(16): Show |
21 | HG02486.hp1 HG02572.hp2 HG02615.hp1 others(18): Show |
intron_variant | MODIFIER | c.435+5300G>A | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27305501 | |||||||
| chr8:27305606 | T | C | 121 | a0001c0001t0001g0040 a0001c0001t0001g0076 a0001c0001t0001g0101 others(118): Show |
205 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.435+5195A>G | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27305606 | |||||||
| chr8:27305927 | C | T | 6 | a0001c0001t0003g0078 a0001c0001t0003g0079 a0001c0001t0012g0080 others(3): Show |
6 | HG00733.hp1 HG01192.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.435+4874G>A | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27305927 | |||||||
| chr8:27305938 | G | A | 2 | a0001c0001t0001g0155 a0001c0001t0007g0156 |
2 | HG02698.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.435+4863C>T | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27305938 | |||||||
| chr8:27305998 | G | A | 44 | a0001c0001t0001g0040 a0001c0001t0001g0199 a0001c0001t0001g0212 others(41): Show |
83 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.435+4803C>T | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27305998 | |||||||
| chr8:27306058 | G | A | 1 | a0001c0001t0041g0082 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.435+4743C>T | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27306058 | |||||||
| chr8:27306179 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.435+4622G>A | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27306179 | |||||||
| chr8:27306183 | C | T | 19 | a0001c0001t0001g0117 a0001c0001t0006g0027 a0001c0001t0046g0077 others(16): Show |
21 | HG02486.hp1 HG02572.hp2 HG02630.hp2 others(18): Show |
intron_variant | MODIFIER | c.435+4618G>A | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27306183 | |||||||
| chr8:27306213 | T | C | 1 | a0001c0001t0001g0157 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.435+4588A>G | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27306213 | |||||||
| chr8:27306268 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.435+4533C>T | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27306268 | |||||||
| chr8:27306329 | C | CT | 74 | a0001c0001t0001g0005 a0001c0001t0001g0034 a0001c0001t0001g0040 others(71): Show |
124 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.435+4471dupA | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27306329 | |||||||
| chr8:27306329 | C | T | 1 | a0001c0001t0001g0076 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.435+4472G>A | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27306329 | |||||||
| chr8:27306388 | C | T | 5 | a0001c0001t0002g0016 a0001c0001t0002g0186 a0001c0001t0002g0187 others(2): Show |
8 | HG00438.hp2 HG02135.hp1 NA18956.hp2 others(5): Show |
intron_variant | MODIFIER | c.435+4413G>A | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27306388 | |||||||
| chr8:27306546 | G | A | 2 | a0001c0001t0002g0215 a0001c0001t0003g0216 |
2 | HG01358.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.435+4255C>T | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27306546 | |||||||
| chr8:27306629 | T | C | 42 | a0001c0001t0001g0040 a0001c0001t0001g0199 a0001c0001t0001g0212 others(39): Show |
80 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(77): Show |
intron_variant | MODIFIER | c.435+4172A>G | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27306629 | |||||||
| chr8:27306700 | A | G | 1 | a0001c0001t0001g0109 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.435+4101T>C | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27306700 | |||||||
| chr8:27306731 | G | A | 1 | a0001c0001t0012g0071 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.435+4070C>T | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27306731 | |||||||
| chr8:27306794 | G | A | 8 | a0001c0001t0002g0217 a0001c0001t0003g0078 a0001c0001t0003g0079 others(5): Show |
10 | HG00733.hp1 HG01192.hp2 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.435+4007C>T | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27306794 | |||||||
| chr8:27306847 | C | T | 1 | a0001c0001t0014g0038 | 2 | HG00738.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.435+3954G>A | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27306847 | |||||||
| chr8:27306932 | G | A | 87 | a0001c0001t0001g0040 a0001c0001t0001g0076 a0001c0001t0001g0199 others(84): Show |
144 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.435+3869C>T | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27306932 | |||||||
| chr8:27307089 | T | G | 1 | a0001c0001t0004g0106 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.435+3712A>C | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27307089 | |||||||
| chr8:27307097 | G | A | 1 | a0001c0001t0001g0159 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.435+3704C>T | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27307097 | |||||||
| chr8:27307147 | C | T | 1 | a0001c0001t0001g0076 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.435+3654G>A | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27307147 | |||||||
| chr8:27307251 | G | A | 1 | a0001c0001t0001g0160 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.435+3550C>T | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27307251 | |||||||
| chr8:27307275 | T | C | 1 | a0001c0001t0001g0076 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.435+3526A>G | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27307275 | |||||||
| chr8:27307357 | C | T | 4 | a0001c0001t0004g0009 a0001c0001t0004g0087 a0001c0001t0004g0088 others(1): Show |
9 | HG00099.hp2 HG00741.hp2 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.435+3444G>A | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27307357 | |||||||
| chr8:27307423 | C | G | 1 | a0001c0002t0005g0013 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.435+3378G>C | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27307423 | |||||||
| chr8:27307573 | C | T | 1 | a0001c0001t0004g0086 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.435+3228G>A | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27307573 | |||||||
| chr8:27307604 | C | T | 9 | a0001c0002t0005g0007 a0001c0002t0005g0013 a0001c0002t0005g0018 others(6): Show |
21 | HG02056.hp2 NA18612.hp2 NA18941.hp1 others(18): Show |
intron_variant | MODIFIER | c.435+3197G>A | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27307604 | |||||||
| chr8:27307745 | A | G | 1 | a0001c0001t0001g0076 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.435+3056T>C | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27307745 | |||||||
| chr8:27307823 | T | C | 19 | a0001c0001t0005g0219 a0001c0001t0012g0068 a0001c0001t0012g0071 others(16): Show |
31 | HG02056.hp2 HG02109.hp2 HG02572.hp1 others(28): Show |
intron_variant | MODIFIER | c.435+2978A>G | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27307823 | |||||||
| chr8:27307969 | T | C | 12 | a0001c0003t0001g0048 a0001c0003t0001g0051 a0001c0003t0001g0057 others(9): Show |
12 | HG02486.hp1 HG02572.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.435+2832A>G | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27307969 | |||||||
| chr8:27308044 | A | T | 1 | a0001c0001t0003g0165 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.435+2757T>A | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27308044 | |||||||
| chr8:27308053 | G | A | 2 | a0001c0001t0028g0069 a0001c0001t0029g0070 |
2 | HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.435+2748C>T | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27308053 | |||||||
| chr8:27308102 | A | G | 1 | a0001c0001t0043g0085 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.435+2699T>C | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27308102 | |||||||
| chr8:27308173 | T | C | 18 | a0001c0001t0006g0027 a0001c0001t0046g0077 a0001c0003t0001g0046 others(15): Show |
20 | HG02486.hp1 HG02572.hp2 HG02630.hp2 others(17): Show |
intron_variant | MODIFIER | c.435+2628A>G | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27308173 | |||||||
| chr8:27308191 | TAA | T | 18 | a0001c0001t0006g0027 a0001c0001t0046g0077 a0001c0003t0001g0046 others(15): Show |
20 | HG02486.hp1 HG02572.hp2 HG02630.hp2 others(17): Show |
intron_variant | MODIFIER | c.435+2608_435+2609d others(4): Show |
TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27308191 | |||||||
| chr8:27308476 | C | A | 1 | a0001c0001t0001g0034 | 2 | HG02257.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.435+2325G>T | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27308476 | |||||||
| chr8:27308485 | T | C | 20 | a0001c0001t0001g0076 a0001c0001t0006g0027 a0001c0001t0042g0066 others(17): Show |
22 | HG02486.hp1 HG02572.hp2 HG02615.hp1 others(19): Show |
intron_variant | MODIFIER | c.435+2316A>G | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27308485 | |||||||
| chr8:27308555 | C | G | 1 | a0001c0001t0002g0039 | 2 | HG02280.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.435+2246G>C | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27308555 | |||||||
| chr8:27308627 | G | A | 1 | a0001c0001t0001g0161 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.435+2174C>T | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27308627 | |||||||
| chr8:27308728 | C | G | 2 | a0001c0001t0001g0011 a0001c0001t0001g0108 |
6 | HG00735.hp2 HG01952.hp1 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.435+2073G>C | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27308728 | |||||||
| chr8:27308869 | C | T | 1 | a0001c0001t0002g0184 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.435+1932G>A | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27308869 | |||||||
| chr8:27308881 | T | C | 2 | a0001c0001t0003g0182 a0001c0001t0017g0183 |
2 | HG03669.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.435+1920A>G | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27308881 | |||||||
| chr8:27309228 | C | G | 1 | a0001c0001t0001g0076 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.435+1573G>C | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27309228 | |||||||
| chr8:27309475 | C | T | 1 | a0001c0001t0001g0076 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.435+1326G>A | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27309475 | |||||||
| chr8:27309476 | G | A | 2 | a0001c0001t0040g0083 a0001c0003t0020g0059 |
2 | HG00733.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.435+1325C>T | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27309476 | |||||||
| chr8:27309477 | G | C | 1 | a0001c0001t0002g0218 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.435+1324C>G | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27309477 | |||||||
| chr8:27309620 | T | C | 1 | a0001c0001t0001g0162 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.435+1181A>G | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27309620 | |||||||
| chr8:27309625 | G | GCTCTGAC others(53): Show |
1 | a0001c0001t0001g0107 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.435+1116_435+1175d others(62): Show |
TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27309625 | |||||||
| chr8:27309768 | AG | A | 5 | a0001c0001t0012g0068 a0001c0001t0012g0071 a0001c0001t0028g0069 others(2): Show |
5 | HG02109.hp2 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.435+1032delC | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27309768 | |||||||
| chr8:27309827 | T | TA | 40 | a0001c0001t0001g0101 a0001c0001t0002g0090 a0001c0001t0004g0003 others(37): Show |
80 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.435+973dupT | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27309827 | |||||||
| chr8:27309889 | G | C | 9 | a0001c0002t0005g0007 a0001c0002t0005g0013 a0001c0002t0005g0018 others(6): Show |
21 | HG02056.hp2 NA18612.hp2 NA18941.hp1 others(18): Show |
intron_variant | MODIFIER | c.435+912C>G | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27309889 | |||||||
| chr8:27309907 | G | A | 30 | a0001c0001t0001g0076 a0001c0001t0001g0101 a0001c0001t0002g0090 others(27): Show |
56 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.435+894C>T | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27309907 | |||||||
| chr8:27309973 | T | C | 30 | a0001c0001t0001g0076 a0001c0001t0001g0101 a0001c0001t0002g0090 others(27): Show |
56 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.435+828A>G | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27309973 | |||||||
| chr8:27309982 | CA | C | 78 | a0001c0001t0001g0040 a0001c0001t0001g0101 a0001c0001t0001g0199 others(75): Show |
144 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.435+818delT | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27309982 | |||||||
| chr8:27309982 | CAA | C | 43 | a0001c0001t0001g0076 a0001c0001t0005g0219 a0001c0001t0006g0027 others(40): Show |
61 | HG00639.hp2 HG00738.hp2 HG01891.hp1 others(58): Show |
intron_variant | MODIFIER | c.435+817_435+818del others(2): Show |
TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27309982 | |||||||
| chr8:27310364 | G | C | 1 | a0001c0002t0005g0163 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.435+437C>G | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27310364 | |||||||
| chr8:27310425 | T | C | 29 | a0001c0001t0001g0008 a0001c0001t0001g0175 a0001c0001t0001g0181 others(26): Show |
54 | HG00280.hp2 HG00408.hp1 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.435+376A>G | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27310425 | |||||||
| chr8:27310511 | G | T | 1 | a0001c0001t0002g0062 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.435+290C>A | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27310511 | |||||||
| chr8:27310513 | G | A | 45 | a0001c0001t0001g0040 a0001c0001t0001g0199 a0001c0001t0001g0212 others(42): Show |
85 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.435+288C>T | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27310513 | |||||||
| chr8:27310515 | G | T | 1 | a0001c0001t0003g0061 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.435+286C>A | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27310515 | |||||||
| chr8:27310530 | T | C | 1 | a0001c0001t0005g0219 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.435+271A>G | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27310530 | |||||||
| chr8:27310634 | A | C | 1 | a0001c0001t0001g0060 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.435+167T>G | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27310634 | |||||||
| chr8:27310638 | A | C | 1 | a0001c0001t0001g0060 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.435+163T>G | TRIM35 | ENSG00000104228.13 | transcript | ENST00000305364.9 | protein_coding | 1/5 | chr8 | 27310638 |