Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 85363 |
| ensemblid | ENSG00000132256.20 |
| hgncid | 16276 |
| symbol | TRIM5 |
| name | tripartite motif containing 5 |
| refseq_nuc | NM_033034.3 |
| refseq_prot | NP_149023.2 |
| ensembl_nuc | ENST00000380034.8 |
| ensembl_prot | ENSP00000369373.3 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 5663195 |
| end | 5685074 |
| strand | - |
| ver | v1.2 |
| region | chr11:5663195-5685074 |
| region5000 | chr11:5658195-5690074 |
| regionname0 | TRIM5_chr11_5663195_5685074 |
| regionname5000 | TRIM5_chr11_5658195_5690074 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 493 | 158 | 55 | 23 | 61 | 4 | 14 | 44 | TRIM5_chr11_5658195_5690074 | TRIM5 | MASGI others(488): Show |
chr11 | 5658195 | 5690074 |
| a0002 | 0/0 | 493 | 130 | 24 | 14 | 80 | 4 | 8 | 56 | TRIM5_chr11_5658195_5690074 | TRIM5 | MASGI others(488): Show |
chr11 | 5658195 | 5690074 |
| a0003 | 0/1 | 493 | 59 | 2 | 14 | 39 | 0 | 3 | 37 | TRIM5_chr11_5658195_5690074 | TRIM5 | MASGI others(488): Show |
chr11 | 5658195 | 5690074 |
| a0004 | 0/0 | 493 | 52 | 9 | 18 | 15 | 4 | 6 | 12 | TRIM5_chr11_5658195_5690074 | TRIM5 | MASGI others(488): Show |
chr11 | 5658195 | 5690074 |
| a0005 | 0/0 | 493 | 29 | 0 | 4 | 15 | 1 | 9 | 15 | TRIM5_chr11_5658195_5690074 | TRIM5 | MASGI others(488): Show |
chr11 | 5658195 | 5690074 |
| a0006 | 0/0 | 493 | 5 | 0 | 1 | 0 | 2 | 2 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | MASGI others(488): Show |
chr11 | 5658195 | 5690074 |
| a0007 | 0/0 | 493 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | MASGI others(488): Show |
chr11 | 5658195 | 5690074 |
| a0008 | 0/0 | 493 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | MASGI others(488): Show |
chr11 | 5658195 | 5690074 |
| a0009 | 0/0 | 493 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | MASGI others(488): Show |
chr11 | 5658195 | 5690074 |
| a0010 | 0/0 | 493 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | MASGI others(488): Show |
chr11 | 5658195 | 5690074 |
| a0011 | 0/0 | 493 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | MASGI others(488): Show |
chr11 | 5658195 | 5690074 |
| a0012 | 0/0 | 493 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | MASGI others(488): Show |
chr11 | 5658195 | 5690074 |
| a0013 | 0/0 | 493 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | MASGI others(488): Show |
chr11 | 5658195 | 5690074 |
| a0014 | 0/0 | 493 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | MASGI others(488): Show |
chr11 | 5658195 | 5690074 |
| a0015 | 0/0 | 493 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | MASGI others(488): Show |
chr11 | 5658195 | 5690074 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002 | 0/0 | 1479 | 128 | 31 | 20 | 60 | 4 | 13 | TRIM5_chr11_5658195_5690074 | TRIM5 | ATGGC others(1474): Show |
chr11 | 5658195 | 5690074 | ||
| a0001c0006 | 1/0 | 1479 | 19 | 15 | 1 | 1 | 0 | 1 | TRIM5_chr11_5658195_5690074 | TRIM5 | ATGGC others(1474): Show |
chr11 | 5658195 | 5690074 | ||
| a0001c0007 | 0/0 | 1479 | 11 | 9 | 2 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | ATGGC others(1474): Show |
chr11 | 5658195 | 5690074 | ||
| a0002c0001 | 0/0 | 1479 | 129 | 24 | 14 | 79 | 4 | 8 | TRIM5_chr11_5658195_5690074 | TRIM5 | ATGGC others(1474): Show |
chr11 | 5658195 | 5690074 | ||
| a0002c0012 | 0/0 | 1479 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | ATGGC others(1474): Show |
chr11 | 5658195 | 5690074 | ||
| a0003c0003 | 0/1 | 1479 | 57 | 2 | 14 | 37 | 0 | 3 | TRIM5_chr11_5658195_5690074 | TRIM5 | ATGGC others(1474): Show |
chr11 | 5658195 | 5690074 | ||
| a0003c0011 | 0/0 | 1479 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | ATGGC others(1474): Show |
chr11 | 5658195 | 5690074 | ||
| a0004c0004 | 0/0 | 1479 | 52 | 9 | 18 | 15 | 4 | 6 | TRIM5_chr11_5658195_5690074 | TRIM5 | ATGGC others(1474): Show |
chr11 | 5658195 | 5690074 | ||
| a0005c0005 | 0/0 | 1479 | 29 | 0 | 4 | 15 | 1 | 9 | TRIM5_chr11_5658195_5690074 | TRIM5 | ATGGC others(1474): Show |
chr11 | 5658195 | 5690074 | ||
| a0006c0008 | 0/0 | 1479 | 5 | 0 | 1 | 0 | 2 | 2 | TRIM5_chr11_5658195_5690074 | TRIM5 | ATGGC others(1474): Show |
chr11 | 5658195 | 5690074 | ||
| a0007c0009 | 0/0 | 1479 | 4 | 3 | 1 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | ATGGC others(1474): Show |
chr11 | 5658195 | 5690074 | ||
| a0008c0010 | 0/0 | 1479 | 2 | 0 | 1 | 0 | 0 | 1 | TRIM5_chr11_5658195_5690074 | TRIM5 | ATGGC others(1474): Show |
chr11 | 5658195 | 5690074 | ||
| a0009c0013 | 0/0 | 1479 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | ATGGC others(1474): Show |
chr11 | 5658195 | 5690074 | ||
| a0010c0015 | 0/0 | 1479 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | ATGGC others(1474): Show |
chr11 | 5658195 | 5690074 | ||
| a0011c0019 | 0/0 | 1479 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | ATGGC others(1474): Show |
chr11 | 5658195 | 5690074 | ||
| a0012c0016 | 0/0 | 1479 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | ATGGC others(1474): Show |
chr11 | 5658195 | 5690074 | ||
| a0013c0018 | 0/0 | 1479 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM5_chr11_5658195_5690074 | TRIM5 | ATGGC others(1474): Show |
chr11 | 5658195 | 5690074 | ||
| a0014c0017 | 0/0 | 1479 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | ATGGC others(1474): Show |
chr11 | 5658195 | 5690074 | ||
| a0015c0014 | 0/0 | 1479 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | ATGGC others(1474): Show |
chr11 | 5658195 | 5690074 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0001 | 0/0 | 3365 | 74 | 4 | 9 | 50 | 2 | 9 | TRIM5_chr11_5658195_5690074 | TRIM5 | AAGAA others(3360): Show |
chr11 | 5658195 | 5690074 |
| a0001c0002t0006 | 0/0 | 3365 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | AAGAA others(3360): Show |
chr11 | 5658195 | 5690074 |
| a0001c0002t0007 | 0/0 | 3364 | 11 | 7 | 2 | 0 | 0 | 2 | TRIM5_chr11_5658195_5690074 | TRIM5 | AAGAA others(3359): Show |
chr11 | 5658195 | 5690074 |
| a0001c0002t0009 | 0/0 | 3373 | 6 | 0 | 3 | 0 | 1 | 2 | TRIM5_chr11_5658195_5690074 | TRIM5 | AAGAA others(3368): Show |
chr11 | 5658195 | 5690074 |
| a0001c0002t0010 | 0/0 | 3373 | 6 | 6 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | AAGAA others(3368): Show |
chr11 | 5658195 | 5690074 |
| a0001c0002t0011 | 0/0 | 3365 | 6 | 0 | 0 | 6 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | AAGAA others(3360): Show |
chr11 | 5658195 | 5690074 |
| a0001c0002t0012 | 0/0 | 3373 | 5 | 5 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | AAGAA others(3368): Show |
chr11 | 5658195 | 5690074 |
| a0001c0002t0014 | 0/0 | 3365 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | AAGAA others(3360): Show |
chr11 | 5658195 | 5690074 |
| a0001c0002t0015 | 0/0 | 3365 | 4 | 0 | 3 | 0 | 1 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | AAGAA others(3360): Show |
chr11 | 5658195 | 5690074 |
| a0001c0002t0016 | 0/0 | 3366 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | AAGAA others(3361): Show |
chr11 | 5658195 | 5690074 |
| a0001c0002t0017 | 0/0 | 3364 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | AAGAA others(3359): Show |
chr11 | 5658195 | 5690074 |
| a0001c0002t0018 | 0/0 | 3365 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | AAGAA others(3360): Show |
chr11 | 5658195 | 5690074 |
| a0001c0002t0019 | 0/0 | 3364 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | AAGAA others(3359): Show |
chr11 | 5658195 | 5690074 |
| a0001c0002t0028 | 0/0 | 3364 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | AAGAA others(3359): Show |
chr11 | 5658195 | 5690074 |
| a0001c0002t0029 | 0/0 | 3366 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | AAGAA others(3361): Show |
chr11 | 5658195 | 5690074 |
| a0001c0002t0033 | 0/0 | 3364 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | AAGAA others(3359): Show |
chr11 | 5658195 | 5690074 |
| a0001c0002t0040 | 0/0 | 3374 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | AAGAA others(3369): Show |
chr11 | 5658195 | 5690074 |
| a0001c0002t0042 | 0/0 | 3364 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | AAGAA others(3359): Show |
chr11 | 5658195 | 5690074 |
| a0001c0002t0046 | 0/0 | 3365 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | AAGAA others(3360): Show |
chr11 | 5658195 | 5690074 |
| a0001c0002t0047 | 0/0 | 3365 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | AAGAA others(3360): Show |
chr11 | 5658195 | 5690074 |
| a0001c0002t0049 | 0/0 | 3365 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | AAGAA others(3360): Show |
chr11 | 5658195 | 5690074 |
| a0001c0006t0002 | 0/0 | 3365 | 8 | 8 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | AAGAA others(3360): Show |
chr11 | 5658195 | 5690074 |
| a0001c0006t0004 | 0/0 | 3365 | 2 | 0 | 0 | 1 | 0 | 1 | TRIM5_chr11_5658195_5690074 | TRIM5 | AAGAA others(3360): Show |
chr11 | 5658195 | 5690074 |
| a0001c0006t0007 | 1/0 | 3364 | 3 | 2 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | AAGAA others(3359): Show |
chr11 | 5658195 | 5690074 |
| a0001c0006t0016 | 0/0 | 3366 | 3 | 2 | 1 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | AAGAA others(3361): Show |
chr11 | 5658195 | 5690074 |
| a0001c0006t0021 | 0/0 | 3365 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | AAGAA others(3360): Show |
chr11 | 5658195 | 5690074 |
| a0001c0006t0022 | 0/0 | 3366 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | AAGAA others(3361): Show |
chr11 | 5658195 | 5690074 |
| a0001c0006t0035 | 0/0 | 3364 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | AAGAA others(3359): Show |
chr11 | 5658195 | 5690074 |
| a0001c0007t0002 | 0/0 | 3365 | 11 | 9 | 2 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | AAGAA others(3360): Show |
chr11 | 5658195 | 5690074 |
| a0002c0001t0002 | 0/0 | 3365 | 50 | 7 | 9 | 26 | 4 | 4 | TRIM5_chr11_5658195_5690074 | TRIM5 | AAGAA others(3360): Show |
chr11 | 5658195 | 5690074 |
| a0002c0001t0003 | 0/0 | 3365 | 51 | 7 | 3 | 40 | 0 | 1 | TRIM5_chr11_5658195_5690074 | TRIM5 | AAGAA others(3360): Show |
chr11 | 5658195 | 5690074 |
| a0002c0001t0004 | 0/0 | 3365 | 4 | 0 | 0 | 2 | 0 | 2 | TRIM5_chr11_5658195_5690074 | TRIM5 | AAGAA others(3360): Show |
chr11 | 5658195 | 5690074 |
| a0002c0001t0006 | 0/0 | 3365 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | AAGAA others(3360): Show |
chr11 | 5658195 | 5690074 |
| a0002c0001t0014 | 0/0 | 3365 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | AAGAA others(3360): Show |
chr11 | 5658195 | 5690074 |
| a0002c0001t0020 | 0/0 | 3365 | 3 | 2 | 1 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | AAGAA others(3360): Show |
chr11 | 5658195 | 5690074 |
| a0002c0001t0022 | 0/0 | 3366 | 2 | 0 | 0 | 1 | 0 | 1 | TRIM5_chr11_5658195_5690074 | TRIM5 | AAGAA others(3361): Show |
chr11 | 5658195 | 5690074 |
| a0002c0001t0023 | 0/0 | 3364 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | AAGAA others(3359): Show |
chr11 | 5658195 | 5690074 |
| a0002c0001t0026 | 0/0 | 3365 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | AAGAA others(3360): Show |
chr11 | 5658195 | 5690074 |
| a0002c0001t0027 | 0/0 | 3364 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | AAGAA others(3359): Show |
chr11 | 5658195 | 5690074 |
| a0002c0001t0032 | 0/0 | 3365 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | AAGAA others(3360): Show |
chr11 | 5658195 | 5690074 |
| a0002c0001t0034 | 0/0 | 3365 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | AAGAA others(3360): Show |
chr11 | 5658195 | 5690074 |
| a0002c0001t0038 | 0/0 | 3365 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | AAGAA others(3360): Show |
chr11 | 5658195 | 5690074 |
| a0002c0001t0041 | 0/0 | 3365 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | AAGAA others(3360): Show |
chr11 | 5658195 | 5690074 |
| a0002c0001t0045 | 0/0 | 3365 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | AAGAA others(3360): Show |
chr11 | 5658195 | 5690074 |
| a0002c0001t0050 | 0/0 | 3365 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | AAGAA others(3360): Show |
chr11 | 5658195 | 5690074 |
| a0002c0001t0053 | 0/0 | 3365 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | AAGAA others(3360): Show |
chr11 | 5658195 | 5690074 |
| a0002c0012t0002 | 0/0 | 3365 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | AAGAA others(3360): Show |
chr11 | 5658195 | 5690074 |
| a0003c0003t0001 | 0/1 | 3365 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | AAGAA others(3360): Show |
chr11 | 5658195 | 5690074 |
| a0003c0003t0002 | 0/0 | 3365 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | AAGAA others(3360): Show |
chr11 | 5658195 | 5690074 |
| a0003c0003t0005 | 0/0 | 3365 | 21 | 0 | 6 | 15 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | AAGAA others(3360): Show |
chr11 | 5658195 | 5690074 |
| a0003c0003t0006 | 0/0 | 3365 | 16 | 0 | 6 | 9 | 0 | 1 | TRIM5_chr11_5658195_5690074 | TRIM5 | AAGAA others(3360): Show |
chr11 | 5658195 | 5690074 |
| a0003c0003t0008 | 0/0 | 3365 | 10 | 0 | 0 | 10 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | AAGAA others(3360): Show |
chr11 | 5658195 | 5690074 |
| a0003c0003t0024 | 0/0 | 3365 | 3 | 2 | 1 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | AAGAA others(3360): Show |
chr11 | 5658195 | 5690074 |
| a0003c0003t0025 | 0/0 | 3365 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM5_chr11_5658195_5690074 | TRIM5 | AAGAA others(3360): Show |
chr11 | 5658195 | 5690074 |
| a0003c0003t0043 | 0/0 | 3365 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM5_chr11_5658195_5690074 | TRIM5 | AAGAA others(3360): Show |
chr11 | 5658195 | 5690074 |
| a0003c0003t0044 | 0/0 | 3365 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | AAGAA others(3360): Show |
chr11 | 5658195 | 5690074 |
| a0003c0003t0052 | 0/0 | 3366 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | AAGAA others(3361): Show |
chr11 | 5658195 | 5690074 |
| a0003c0011t0001 | 0/0 | 3365 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | AAGAA others(3360): Show |
chr11 | 5658195 | 5690074 |
| a0003c0011t0048 | 0/0 | 3366 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | AAGAA others(3361): Show |
chr11 | 5658195 | 5690074 |
| a0004c0004t0002 | 0/0 | 3365 | 4 | 2 | 0 | 2 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | AAGAA others(3360): Show |
chr11 | 5658195 | 5690074 |
| a0004c0004t0004 | 0/0 | 3365 | 31 | 2 | 14 | 7 | 4 | 4 | TRIM5_chr11_5658195_5690074 | TRIM5 | AAGAA others(3360): Show |
chr11 | 5658195 | 5690074 |
| a0004c0004t0013 | 0/0 | 3365 | 5 | 0 | 0 | 3 | 0 | 2 | TRIM5_chr11_5658195_5690074 | TRIM5 | AAGAA others(3360): Show |
chr11 | 5658195 | 5690074 |
| a0004c0004t0017 | 0/0 | 3364 | 3 | 2 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | AAGAA others(3359): Show |
chr11 | 5658195 | 5690074 |
| a0004c0004t0018 | 0/0 | 3365 | 3 | 0 | 3 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | AAGAA others(3360): Show |
chr11 | 5658195 | 5690074 |
| a0004c0004t0021 | 0/0 | 3365 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | AAGAA others(3360): Show |
chr11 | 5658195 | 5690074 |
| a0004c0004t0036 | 0/0 | 3365 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | AAGAA others(3360): Show |
chr11 | 5658195 | 5690074 |
| a0004c0004t0037 | 0/0 | 3365 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | AAGAA others(3360): Show |
chr11 | 5658195 | 5690074 |
| a0004c0004t0039 | 0/0 | 3366 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | AAGAA others(3361): Show |
chr11 | 5658195 | 5690074 |
| a0004c0004t0051 | 0/0 | 3365 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | AAGAA others(3360): Show |
chr11 | 5658195 | 5690074 |
| a0005c0005t0001 | 0/0 | 3365 | 18 | 0 | 4 | 9 | 1 | 4 | TRIM5_chr11_5658195_5690074 | TRIM5 | AAGAA others(3360): Show |
chr11 | 5658195 | 5690074 |
| a0005c0005t0002 | 0/0 | 3365 | 6 | 0 | 0 | 5 | 0 | 1 | TRIM5_chr11_5658195_5690074 | TRIM5 | AAGAA others(3360): Show |
chr11 | 5658195 | 5690074 |
| a0005c0005t0019 | 0/0 | 3364 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | AAGAA others(3359): Show |
chr11 | 5658195 | 5690074 |
| a0005c0005t0025 | 0/0 | 3365 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM5_chr11_5658195_5690074 | TRIM5 | AAGAA others(3360): Show |
chr11 | 5658195 | 5690074 |
| a0005c0005t0030 | 0/0 | 3364 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM5_chr11_5658195_5690074 | TRIM5 | AAGAA others(3359): Show |
chr11 | 5658195 | 5690074 |
| a0006c0008t0001 | 0/0 | 3365 | 5 | 0 | 1 | 0 | 2 | 2 | TRIM5_chr11_5658195_5690074 | TRIM5 | AAGAA others(3360): Show |
chr11 | 5658195 | 5690074 |
| a0007c0009t0019 | 0/0 | 3364 | 2 | 1 | 1 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | AAGAA others(3359): Show |
chr11 | 5658195 | 5690074 |
| a0007c0009t0031 | 0/0 | 3373 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | AAGAA others(3368): Show |
chr11 | 5658195 | 5690074 |
| a0008c0010t0002 | 0/0 | 3365 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | AAGAA others(3360): Show |
chr11 | 5658195 | 5690074 |
| a0008c0010t0004 | 0/0 | 3365 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM5_chr11_5658195_5690074 | TRIM5 | AAGAA others(3360): Show |
chr11 | 5658195 | 5690074 |
| a0009c0013t0004 | 0/0 | 3365 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | AAGAA others(3360): Show |
chr11 | 5658195 | 5690074 |
| a0010c0015t0004 | 0/0 | 3365 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | AAGAA others(3360): Show |
chr11 | 5658195 | 5690074 |
| a0011c0019t0001 | 0/0 | 3365 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | AAGAA others(3360): Show |
chr11 | 5658195 | 5690074 |
| a0012c0016t0002 | 0/0 | 3365 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | AAGAA others(3360): Show |
chr11 | 5658195 | 5690074 |
| a0013c0018t0001 | 0/0 | 3365 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM5_chr11_5658195_5690074 | TRIM5 | AAGAA others(3360): Show |
chr11 | 5658195 | 5690074 |
| a0014c0017t0009 | 0/0 | 3373 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | AAGAA others(3368): Show |
chr11 | 5658195 | 5690074 |
| a0015c0014t0001 | 0/0 | 3365 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | AAGAA others(3360): Show |
chr11 | 5658195 | 5690074 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0001g0001 | 0/0 | 24 | 0 | 5 | 13 | 2 | 4 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0002t0001g0008 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0002t0001g0010 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0002t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0002t0001g0029 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0002t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0002t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0002t0001g0033 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0002t0001g0034 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0002t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0002t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0002t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0002t0006g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0002t0007g0020 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0002t0007g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0002t0007g0048 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0002t0007g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0002t0007g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0002t0007g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0002t0007g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0002t0009g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0002t0009g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0002t0009g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0002t0009g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0002t0009g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0002t0010g0009 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0002t0010g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0002t0011g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0002t0011g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0002t0011g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0002t0012g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0002t0012g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0002t0012g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0002t0012g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0002t0012g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0002t0014g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0002t0015g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0002t0015g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0002t0015g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0002t0016g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0002t0017g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0002t0018g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0002t0019g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0002t0028g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0002t0029g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0002t0029g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0002t0033g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0002t0040g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0002t0042g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0002t0046g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0002t0047g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0002t0049g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0006t0002g0056 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0006t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0006t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0006t0002g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0006t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0006t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0006t0002g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0006t0004g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0006t0004g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0006t0007g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0006t0007g0225 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0006t0007g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0006t0016g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0006t0016g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0006t0016g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0006t0021g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0006t0022g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0006t0035g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0007t0002g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0007t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0007t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0007t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0007t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0007t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0007t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0007t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0001c0007t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0002c0001t0002g0003 | 0/0 | 17 | 0 | 6 | 11 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0002c0001t0002g0011 | 0/0 | 5 | 0 | 0 | 0 | 2 | 3 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0002c0001t0002g0024 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0002c0001t0002g0038 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0002c0001t0002g0041 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0002c0001t0002g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0002c0001t0002g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0002c0001t0002g0053 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0002c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0002c0001t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0002c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0002c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0002c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0002c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0002c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0002c0001t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0002c0001t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0002c0001t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0002c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0002c0001t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0002c0001t0002g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0002c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0002c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0002c0001t0003g0002 | 0/0 | 17 | 0 | 2 | 15 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0002c0001t0003g0012 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0002c0001t0003g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0002c0001t0003g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0002c0001t0003g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0002c0001t0003g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0002c0001t0003g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0002c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0002c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0002c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0002c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0002c0001t0003g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0002c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0002c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0002c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0002c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0002c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0002c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0002c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0002c0001t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0002c0001t0003g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0002c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0002c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0002c0001t0003g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0002c0001t0004g0052 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0002c0001t0004g0054 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0002c0001t0006g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0002c0001t0006g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0002c0001t0014g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0002c0001t0020g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0002c0001t0020g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0002c0001t0022g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0002c0001t0022g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0002c0001t0023g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0002c0001t0023g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0002c0001t0023g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0002c0001t0026g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0002c0001t0026g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0002c0001t0027g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0002c0001t0027g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0002c0001t0032g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0002c0001t0034g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0002c0001t0038g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0002c0001t0041g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0002c0001t0045g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0002c0001t0050g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0002c0001t0053g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0002c0012t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0003c0003t0001g0142 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0003c0003t0002g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0003c0003t0005g0005 | 0/0 | 8 | 0 | 2 | 6 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0003c0003t0005g0057 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0003c0003t0005g0058 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0003c0003t0005g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0003c0003t0005g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0003c0003t0005g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0003c0003t0005g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0003c0003t0005g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0003c0003t0005g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0003c0003t0005g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0003c0003t0005g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0003c0003t0005g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0003c0003t0006g0007 | 0/0 | 7 | 0 | 4 | 3 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0003c0003t0006g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0003c0003t0006g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0003c0003t0006g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0003c0003t0006g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0003c0003t0006g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0003c0003t0006g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0003c0003t0006g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0003c0003t0006g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0003c0003t0008g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0003c0003t0008g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0003c0003t0008g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0003c0003t0008g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0003c0003t0008g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0003c0003t0024g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0003c0003t0024g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0003c0003t0024g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0003c0003t0025g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0003c0003t0043g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0003c0003t0044g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0003c0003t0052g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0003c0011t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0003c0011t0048g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0004c0004t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0004c0004t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0004c0004t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0004c0004t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0004c0004t0004g0004 | 0/0 | 13 | 1 | 9 | 0 | 1 | 2 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0004c0004t0004g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0004c0004t0004g0043 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0004c0004t0004g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0004c0004t0004g0045 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0004c0004t0004g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0004c0004t0004g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0004c0004t0004g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0004c0004t0004g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0004c0004t0004g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0004c0004t0004g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0004c0004t0004g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0004c0004t0004g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0004c0004t0004g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0004c0004t0004g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0004c0004t0013g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0004c0004t0013g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0004c0004t0013g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0004c0004t0013g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0004c0004t0013g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0004c0004t0017g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0004c0004t0017g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0004c0004t0017g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0004c0004t0018g0023 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0004c0004t0021g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0004c0004t0021g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0004c0004t0036g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0004c0004t0037g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0004c0004t0039g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0004c0004t0051g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0005c0005t0001g0006 | 0/0 | 7 | 0 | 3 | 4 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0005c0005t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0005c0005t0001g0037 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0005c0005t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0005c0005t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0005c0005t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0005c0005t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0005c0005t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0005c0005t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0005c0005t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0005c0005t0002g0015 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0005c0005t0002g0055 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0005c0005t0019g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0005c0005t0025g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0005c0005t0025g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0005c0005t0030g0035 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0006c0008t0001g0040 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0006c0008t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0006c0008t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0006c0008t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0007c0009t0019g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0007c0009t0019g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0007c0009t0031g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0007c0009t0031g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0008c0010t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0008c0010t0004g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0009c0013t0004g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0010c0015t0004g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0011c0019t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0012c0016t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0013c0018t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0014c0017t0009g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| a0015c0014t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0004 | c0004 | t0004 | g0004 | EUR | GBR | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG00099 | hp2 | a0001 | c0002 | t0015 | g0073 | EUR | GBR | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG00140 | hp1 | a0005 | c0005 | t0001 | g0126 | EUR | GBR | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG00140 | hp2 | a0004 | c0004 | t0004 | g0170 | EUR | GBR | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG00323 | hp1 | a0002 | c0001 | t0002 | g0011 | EUR | FIN | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG00323 | hp2 | a0004 | c0004 | t0004 | g0043 | EUR | FIN | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG00408 | hp1 | a0002 | c0001 | t0003 | g0012 | EAS | CHS | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG00408 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG00423 | hp1 | a0002 | c0001 | t0003 | g0012 | EAS | CHS | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG00423 | hp2 | a0002 | c0001 | t0002 | g0003 | EAS | CHS | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG00438 | hp1 | a0002 | c0001 | t0002 | g0003 | EAS | CHS | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG00438 | hp2 | a0002 | c0001 | t0003 | g0002 | EAS | CHS | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG00544 | hp1 | a0001 | c0002 | t0001 | g0008 | EAS | CHS | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG00544 | hp2 | a0003 | c0003 | t0002 | g0046 | EAS | CHS | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG00558 | hp1 | a0002 | c0001 | t0003 | g0012 | EAS | CHS | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG00558 | hp2 | a0002 | c0001 | t0002 | g0003 | EAS | CHS | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG00609 | hp1 | a0001 | c0002 | t0006 | g0116 | EAS | CHS | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG00609 | hp2 | a0002 | c0001 | t0003 | g0219 | EAS | CHS | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG00639 | hp1 | a0004 | c0004 | t0004 | g0162 | AMR | PUR | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG00639 | hp2 | a0001 | c0007 | t0002 | g0155 | AMR | PUR | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG00642 | hp1 | a0001 | c0002 | t0046 | g0115 | AMR | PUR | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG00642 | hp2 | a0004 | c0004 | t0004 | g0004 | AMR | PUR | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG00673 | hp1 | a0001 | c0002 | t0001 | g0031 | EAS | CHS | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG00673 | hp2 | a0003 | c0003 | t0005 | g0058 | EAS | CHS | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG00733 | hp1 | a0002 | c0001 | t0002 | g0038 | AMR | PUR | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG00733 | hp2 | a0003 | c0003 | t0006 | g0007 | AMR | PUR | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG00735 | hp2 | a0002 | c0001 | t0002 | g0003 | AMR | PUR | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG00738 | hp1 | a0003 | c0003 | t0006 | g0007 | AMR | PUR | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG00738 | hp2 | a0001 | c0002 | t0009 | g0257 | AMR | PUR | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG00741 | hp1 | a0001 | c0002 | t0009 | g0256 | AMR | PUR | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG00741 | hp2 | a0009 | c0013 | t0004 | g0160 | AMR | PUR | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG01069 | hp1 | a0004 | c0004 | t0004 | g0004 | AMR | PUR | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG01069 | hp2 | a0001 | c0002 | t0018 | g0209 | AMR | PUR | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG01070 | hp1 | a0001 | c0002 | t0001 | g0101 | AMR | PUR | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG01070 | hp2 | a0004 | c0004 | t0004 | g0004 | AMR | PUR | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG01074 | hp1 | a0003 | c0003 | t0005 | g0005 | AMR | PUR | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG01074 | hp2 | a0010 | c0015 | t0004 | g0192 | AMR | PUR | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG01081 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG01081 | hp2 | a0004 | c0004 | t0004 | g0004 | AMR | PUR | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG01099 | hp1 | a0001 | c0002 | t0015 | g0072 | AMR | PUR | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG01099 | hp2 | a0006 | c0008 | t0001 | g0151 | AMR | PUR | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG01106 | hp1 | a0003 | c0003 | t0006 | g0007 | AMR | PUR | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG01106 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG01109 | hp1 | a0007 | c0009 | t0019 | g0253 | AMR | PUR | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG01109 | hp2 | a0002 | c0001 | t0002 | g0003 | AMR | PUR | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG01167 | hp1 | a0004 | c0004 | t0004 | g0004 | AMR | PUR | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG01167 | hp2 | a0001 | c0002 | t0015 | g0027 | AMR | PUR | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG01168 | hp1 | a0004 | c0004 | t0004 | g0004 | AMR | PUR | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG01168 | hp2 | a0003 | c0003 | t0006 | g0146 | AMR | PUR | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG01169 | hp1 | a0004 | c0004 | t0004 | g0164 | AMR | PUR | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG01169 | hp2 | a0001 | c0002 | t0015 | g0027 | AMR | PUR | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG01192 | hp1 | a0002 | c0001 | t0002 | g0003 | AMR | PUR | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG01192 | hp2 | a0001 | c0002 | t0049 | g0108 | AMR | PUR | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG01243 | hp1 | a0001 | c0007 | t0002 | g0194 | AMR | PUR | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG01243 | hp2 | a0001 | c0002 | t0007 | g0020 | AMR | PUR | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG01255 | hp1 | a0003 | c0003 | t0024 | g0262 | AMR | CLM | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG01255 | hp2 | a0004 | c0004 | t0004 | g0045 | AMR | CLM | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG01256 | hp1 | a0003 | c0003 | t0044 | g0145 | AMR | CLM | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG01256 | hp2 | a0004 | c0004 | t0004 | g0004 | AMR | CLM | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG01257 | hp1 | a0004 | c0004 | t0004 | g0004 | AMR | CLM | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG01257 | hp2 | a0002 | c0001 | t0003 | g0002 | AMR | CLM | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG01261 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG01261 | hp2 | a0004 | c0004 | t0004 | g0045 | AMR | CLM | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG01346 | hp1 | a0003 | c0003 | t0005 | g0005 | AMR | CLM | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG01346 | hp2 | a0001 | c0006 | t0016 | g0158 | AMR | CLM | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG01358 | hp1 | a0002 | c0001 | t0002 | g0003 | AMR | CLM | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG01358 | hp2 | a0001 | c0002 | t0001 | g0099 | AMR | CLM | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG01433 | hp1 | a0001 | c0002 | t0007 | g0048 | AMR | CLM | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG01433 | hp2 | a0004 | c0004 | t0004 | g0176 | AMR | CLM | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG01496 | hp1 | a0001 | c0002 | t0009 | g0255 | AMR | CLM | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG01496 | hp2 | a0003 | c0003 | t0005 | g0274 | AMR | CLM | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG01515 | hp1 | a0006 | c0008 | t0001 | g0040 | EUR | IBS | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG01515 | hp2 | a0002 | c0001 | t0002 | g0041 | EUR | IBS | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG01516 | hp1 | a0001 | c0002 | t0001 | g0001 | EUR | IBS | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG01516 | hp2 | a0002 | c0001 | t0002 | g0011 | EUR | IBS | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG01517 | hp1 | a0002 | c0001 | t0002 | g0041 | EUR | IBS | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG01517 | hp2 | a0006 | c0008 | t0001 | g0040 | EUR | IBS | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG01884 | hp1 | a0001 | c0002 | t0001 | g0103 | AFR | ACB | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG01884 | hp2 | a0001 | c0006 | t0016 | g0254 | AFR | ACB | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG01891 | hp1 | a0002 | c0001 | t0026 | g0064 | AFR | ACB | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG01891 | hp2 | a0002 | c0001 | t0002 | g0050 | AFR | ACB | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG01928 | hp1 | a0008 | c0010 | t0002 | g0208 | AMR | PEL | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG01928 | hp2 | a0003 | c0003 | t0005 | g0272 | AMR | PEL | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG01934 | hp1 | a0004 | c0004 | t0018 | g0023 | AMR | PEL | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG01934 | hp2 | a0004 | c0004 | t0004 | g0004 | AMR | PEL | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG01943 | hp1 | a0002 | c0001 | t0002 | g0003 | AMR | PEL | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG01943 | hp2 | a0002 | c0001 | t0020 | g0060 | AMR | PEL | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG01975 | hp1 | a0003 | c0003 | t0005 | g0271 | AMR | PEL | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG01975 | hp2 | a0002 | c0001 | t0002 | g0234 | AMR | PEL | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG01978 | hp1 | a0002 | c0001 | t0002 | g0227 | AMR | PEL | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG01978 | hp2 | a0004 | c0004 | t0051 | g0266 | AMR | PEL | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG01981 | hp1 | a0005 | c0005 | t0001 | g0006 | AMR | PEL | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG01981 | hp2 | a0005 | c0005 | t0001 | g0131 | AMR | PEL | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG01993 | hp1 | a0003 | c0003 | t0005 | g0273 | AMR | PEL | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG01993 | hp2 | a0002 | c0001 | t0053 | g0268 | AMR | PEL | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02004 | hp1 | a0005 | c0005 | t0001 | g0006 | AMR | PEL | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02004 | hp2 | a0003 | c0003 | t0006 | g0148 | AMR | PEL | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02015 | hp1 | a0002 | c0001 | t0002 | g0003 | EAS | KHV | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02015 | hp2 | a0001 | c0002 | t0001 | g0017 | EAS | KHV | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02027 | hp1 | a0001 | c0002 | t0001 | g0033 | EAS | KHV | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02027 | hp2 | a0002 | c0001 | t0050 | g0267 | EAS | KHV | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02040 | hp1 | a0002 | c0001 | t0002 | g0003 | EAS | KHV | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02040 | hp2 | a0001 | c0002 | t0001 | g0008 | EAS | KHV | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0033 | AFR | ACB | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02055 | hp2 | a0001 | c0006 | t0002 | g0056 | AFR | ACB | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02056 | hp1 | a0001 | c0002 | t0001 | g0017 | EAS | KHV | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02056 | hp2 | a0002 | c0001 | t0003 | g0002 | EAS | KHV | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02071 | hp1 | a0002 | c0001 | t0003 | g0182 | EAS | KHV | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02071 | hp2 | a0004 | c0004 | t0002 | g0091 | EAS | KHV | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02074 | hp1 | a0001 | c0002 | t0001 | g0102 | EAS | KHV | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02074 | hp2 | a0002 | c0001 | t0003 | g0196 | EAS | KHV | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02080 | hp1 | a0002 | c0001 | t0003 | g0183 | EAS | KHV | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02080 | hp2 | a0001 | c0002 | t0001 | g0008 | EAS | KHV | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02083 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02083 | hp2 | a0002 | c0001 | t0003 | g0002 | EAS | KHV | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02129 | hp1 | a0002 | c0001 | t0006 | g0107 | EAS | KHV | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02129 | hp2 | a0001 | c0006 | t0004 | g0226 | EAS | KHV | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02132 | hp1 | a0001 | c0002 | t0001 | g0017 | EAS | KHV | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02132 | hp2 | a0002 | c0001 | t0003 | g0012 | EAS | KHV | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02135 | hp1 | a0001 | c0002 | t0001 | g0100 | EAS | KHV | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02135 | hp2 | a0002 | c0001 | t0002 | g0003 | EAS | KHV | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02145 | hp1 | a0007 | c0009 | t0019 | g0252 | AFR | ACB | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02145 | hp2 | a0001 | c0002 | t0029 | g0135 | AFR | ACB | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02148 | hp1 | a0002 | c0001 | t0002 | g0003 | AMR | PEL | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02148 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02155 | hp1 | a0004 | c0004 | t0004 | g0132 | EAS | CDX | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02155 | hp2 | a0002 | c0001 | t0006 | g0214 | EAS | CDX | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02165 | hp1 | a0002 | c0001 | t0002 | g0003 | EAS | CDX | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02165 | hp2 | a0001 | c0002 | t0001 | g0110 | EAS | CDX | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02257 | hp1 | a0002 | c0001 | t0002 | g0181 | AFR | ACB | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02257 | hp2 | a0002 | c0001 | t0003 | g0159 | AFR | ACB | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02258 | hp1 | a0001 | c0002 | t0007 | g0048 | AFR | ACB | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02258 | hp2 | a0004 | c0004 | t0021 | g0168 | AFR | ACB | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02273 | hp1 | a0005 | c0005 | t0001 | g0006 | AMR | PEL | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02273 | hp2 | a0002 | c0001 | t0003 | g0002 | AMR | PEL | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02280 | hp1 | a0011 | c0019 | t0001 | g0125 | AFR | ACB | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02280 | hp2 | a0001 | c0007 | t0002 | g0153 | AFR | ACB | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02293 | hp1 | a0004 | c0004 | t0018 | g0023 | AMR | PEL | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02293 | hp2 | a0001 | c0002 | t0001 | g0118 | AMR | PEL | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02300 | hp1 | a0004 | c0004 | t0018 | g0023 | AMR | PEL | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02300 | hp2 | a0002 | c0001 | t0003 | g0186 | AMR | PEL | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02451 | hp1 | a0004 | c0004 | t0004 | g0177 | AFR | ACB | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02451 | hp2 | a0003 | c0003 | t0024 | g0263 | AFR | ACB | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02523 | hp1 | a0002 | c0001 | t0003 | g0012 | EAS | KHV | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02523 | hp2 | a0002 | c0001 | t0003 | g0002 | EAS | KHV | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02572 | hp1 | a0004 | c0004 | t0002 | g0134 | AFR | GWD | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02572 | hp2 | a0001 | c0006 | t0007 | g0260 | AFR | GWD | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02602 | hp1 | a0003 | c0003 | t0006 | g0147 | SAS | PJL | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02602 | hp2 | a0001 | c0002 | t0001 | g0119 | SAS | PJL | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02615 | hp1 | a0001 | c0002 | t0010 | g0009 | AFR | GWD | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02615 | hp2 | a0001 | c0002 | t0017 | g0178 | AFR | GWD | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02622 | hp1 | a0002 | c0001 | t0026 | g0063 | AFR | GWD | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02622 | hp2 | a0001 | c0002 | t0010 | g0009 | AFR | GWD | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02630 | hp1 | a0001 | c0006 | t0007 | g0174 | AFR | GWD | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02630 | hp2 | a0001 | c0002 | t0012 | g0062 | AFR | GWD | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02647 | hp1 | a0002 | c0001 | t0034 | g0071 | AFR | GWD | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02647 | hp2 | a0001 | c0002 | t0001 | g0247 | AFR | GWD | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02683 | hp1 | a0004 | c0004 | t0004 | g0004 | SAS | PJL | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02683 | hp2 | a0002 | c0001 | t0002 | g0011 | SAS | PJL | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02698 | hp1 | a0002 | c0001 | t0002 | g0011 | SAS | PJL | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02698 | hp2 | a0004 | c0004 | t0004 | g0043 | SAS | PJL | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02717 | hp1 | a0001 | c0002 | t0040 | g0210 | AFR | GWD | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02717 | hp2 | a0001 | c0002 | t0010 | g0009 | AFR | GWD | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02723 | hp1 | a0001 | c0007 | t0002 | g0154 | AFR | GWD | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02723 | hp2 | a0001 | c0002 | t0010 | g0009 | AFR | GWD | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02735 | hp1 | a0001 | c0002 | t0001 | g0138 | SAS | PJL | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02735 | hp2 | a0004 | c0004 | t0004 | g0004 | SAS | PJL | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02809 | hp1 | a0007 | c0009 | t0031 | g0075 | AFR | GWD | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02809 | hp2 | a0001 | c0006 | t0021 | g0179 | AFR | GWD | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02818 | hp1 | a0001 | c0002 | t0028 | g0042 | AFR | GWD | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02818 | hp2 | a0004 | c0004 | t0002 | g0074 | AFR | GWD | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02886 | hp1 | a0002 | c0001 | t0002 | g0228 | AFR | GWD | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02886 | hp2 | a0002 | c0001 | t0003 | g0018 | AFR | GWD | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02895 | hp1 | a0001 | c0002 | t0010 | g0009 | AFR | GWD | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02895 | hp2 | a0001 | c0002 | t0012 | g0067 | AFR | GWD | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02896 | hp1 | a0001 | c0002 | t0012 | g0066 | AFR | GWD | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02896 | hp2 | a0001 | c0006 | t0016 | g0250 | AFR | GWD | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02897 | hp1 | a0001 | c0002 | t0010 | g0059 | AFR | GWD | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02897 | hp2 | a0001 | c0002 | t0012 | g0065 | AFR | GWD | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02922 | hp1 | a0004 | c0004 | t0021 | g0169 | AFR | ESN | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02922 | hp2 | a0004 | c0004 | t0017 | g0076 | AFR | ESN | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02965 | hp1 | a0002 | c0001 | t0003 | g0206 | AFR | ESN | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02965 | hp2 | a0002 | c0001 | t0014 | g0016 | AFR | ESN | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02970 | hp1 | a0001 | c0007 | t0002 | g0019 | AFR | ESN | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02970 | hp2 | a0001 | c0002 | t0016 | g0241 | AFR | ESN | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02976 | hp1 | a0001 | c0007 | t0002 | g0019 | AFR | ESN | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02976 | hp2 | a0002 | c0001 | t0003 | g0246 | AFR | ESN | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG03017 | hp1 | a0005 | c0005 | t0001 | g0124 | SAS | PJL | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG03017 | hp2 | a0005 | c0005 | t0001 | g0037 | SAS | PJL | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG03041 | hp1 | a0001 | c0007 | t0002 | g0019 | AFR | GWD | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG03041 | hp2 | a0004 | c0004 | t0004 | g0004 | AFR | GWD | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG03098 | hp1 | a0001 | c0002 | t0033 | g0070 | AFR | MSL | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG03098 | hp2 | a0002 | c0001 | t0002 | g0229 | AFR | MSL | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG03130 | hp1 | a0002 | c0001 | t0002 | g0050 | AFR | ESN | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG03130 | hp2 | a0002 | c0001 | t0003 | g0018 | AFR | ESN | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG03139 | hp1 | a0002 | c0001 | t0020 | g0026 | AFR | ESN | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG03139 | hp2 | a0001 | c0002 | t0028 | g0042 | AFR | ESN | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG03209 | hp1 | a0002 | c0001 | t0003 | g0077 | AFR | MSL | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG03209 | hp2 | a0001 | c0006 | t0002 | g0249 | AFR | MSL | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG03239 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG03239 | hp2 | a0002 | c0001 | t0002 | g0011 | SAS | PJL | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG03453 | hp1 | a0002 | c0001 | t0014 | g0016 | AFR | MSL | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG03453 | hp2 | a0002 | c0001 | t0002 | g0038 | AFR | MSL | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG03486 | hp1 | a0012 | c0016 | t0002 | g0222 | AFR | MSL | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG03486 | hp2 | a0001 | c0002 | t0007 | g0187 | AFR | MSL | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG03491 | hp1 | a0001 | c0002 | t0009 | g0032 | SAS | PJL | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG03491 | hp2 | a0005 | c0005 | t0025 | g0122 | SAS | PJL | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG03492 | hp1 | a0003 | c0003 | t0025 | g0128 | SAS | PJL | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG03492 | hp2 | a0001 | c0002 | t0009 | g0032 | SAS | PJL | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG03516 | hp1 | a0002 | c0001 | t0032 | g0061 | AFR | ESN | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG03516 | hp2 | a0001 | c0002 | t0007 | g0215 | AFR | ESN | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG03540 | hp1 | a0001 | c0006 | t0002 | g0261 | AFR | GWD | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG03540 | hp2 | a0007 | c0009 | t0031 | g0251 | AFR | GWD | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG03579 | hp1 | a0001 | c0006 | t0002 | g0245 | AFR | MSL | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG03579 | hp2 | a0001 | c0002 | t0007 | g0020 | AFR | MSL | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG03654 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG03654 | hp2 | a0003 | c0003 | t0043 | g0143 | SAS | PJL | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG03669 | hp1 | a0005 | c0005 | t0001 | g0083 | SAS | PJL | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG03669 | hp2 | a0001 | c0002 | t0007 | g0171 | SAS | PJL | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG03688 | hp1 | a0001 | c0006 | t0004 | g0191 | SAS | STU | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG03688 | hp2 | a0001 | c0002 | t0001 | g0117 | SAS | STU | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG03704 | hp1 | a0005 | c0005 | t0001 | g0084 | SAS | PJL | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG03704 | hp2 | a0001 | c0002 | t0001 | g0097 | SAS | PJL | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG03710 | hp1 | a0006 | c0008 | t0001 | g0150 | SAS | PJL | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG03831 | hp1 | a0005 | c0005 | t0002 | g0015 | SAS | BEB | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG03831 | hp2 | a0013 | c0018 | t0001 | g0085 | SAS | BEB | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG03834 | hp1 | a0005 | c0005 | t0025 | g0123 | SAS | BEB | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG03834 | hp2 | a0001 | c0002 | t0007 | g0172 | SAS | BEB | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG03942 | hp1 | a0005 | c0005 | t0030 | g0035 | SAS | BEB | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG03942 | hp2 | a0008 | c0010 | t0004 | g0216 | SAS | BEB | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG04115 | hp1 | a0004 | c0004 | t0004 | g0161 | SAS | STU | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG04115 | hp2 | a0002 | c0001 | t0004 | g0052 | SAS | STU | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG04184 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | BEB | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG04184 | hp2 | a0005 | c0005 | t0030 | g0035 | SAS | BEB | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG04199 | hp1 | a0002 | c0001 | t0003 | g0218 | SAS | STU | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG04199 | hp2 | a0006 | c0008 | t0001 | g0149 | SAS | STU | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG04204 | hp1 | a0004 | c0004 | t0013 | g0165 | SAS | STU | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG04204 | hp2 | a0002 | c0001 | t0004 | g0052 | SAS | STU | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG04228 | hp1 | a0002 | c0001 | t0022 | g0233 | SAS | STU | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG04228 | hp2 | a0002 | c0001 | t0002 | g0024 | SAS | STU | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18522 | hp1 | a0002 | c0001 | t0014 | g0016 | AFR | YRI | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18522 | hp2 | a0001 | c0006 | t0002 | g0244 | AFR | YRI | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18612 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CHB | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18612 | hp2 | a0004 | c0004 | t0002 | g0223 | EAS | CHB | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18747 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CHB | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18747 | hp2 | a0002 | c0001 | t0003 | g0190 | EAS | CHB | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18906 | hp1 | a0001 | c0006 | t0035 | g0175 | AFR | YRI | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18906 | hp2 | a0001 | c0002 | t0007 | g0047 | AFR | YRI | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18939 | hp1 | a0001 | c0002 | t0001 | g0106 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18939 | hp2 | a0001 | c0002 | t0011 | g0021 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18940 | hp1 | a0005 | c0005 | t0001 | g0036 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18940 | hp2 | a0002 | c0001 | t0002 | g0199 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18942 | hp1 | a0001 | c0002 | t0011 | g0205 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18942 | hp2 | a0002 | c0001 | t0002 | g0086 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18943 | hp1 | a0002 | c0001 | t0003 | g0002 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18943 | hp2 | a0001 | c0002 | t0001 | g0031 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18944 | hp1 | a0003 | c0003 | t0008 | g0013 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18944 | hp2 | a0001 | c0002 | t0011 | g0049 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18945 | hp1 | a0002 | c0001 | t0002 | g0003 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18945 | hp2 | a0002 | c0001 | t0003 | g0022 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18947 | hp1 | a0002 | c0001 | t0002 | g0024 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18947 | hp2 | a0001 | c0002 | t0001 | g0105 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18948 | hp1 | a0002 | c0001 | t0002 | g0053 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18948 | hp2 | a0002 | c0001 | t0023 | g0200 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18949 | hp1 | a0002 | c0001 | t0004 | g0054 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18949 | hp2 | a0001 | c0002 | t0047 | g0109 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18950 | hp1 | a0001 | c0002 | t0011 | g0021 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18950 | hp2 | a0002 | c0001 | t0003 | g0202 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18952 | hp1 | a0002 | c0001 | t0003 | g0002 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18952 | hp2 | a0002 | c0001 | t0003 | g0022 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18953 | hp1 | a0003 | c0003 | t0005 | g0265 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18953 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18954 | hp1 | a0003 | c0003 | t0008 | g0025 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18954 | hp2 | a0005 | c0005 | t0002 | g0055 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18956 | hp1 | a0004 | c0004 | t0004 | g0044 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18956 | hp2 | a0003 | c0003 | t0005 | g0005 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18957 | hp1 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18957 | hp2 | a0002 | c0001 | t0002 | g0003 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18959 | hp1 | a0001 | c0002 | t0001 | g0120 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18959 | hp2 | a0002 | c0001 | t0003 | g0198 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18960 | hp1 | a0001 | c0002 | t0011 | g0021 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18960 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18961 | hp1 | a0005 | c0005 | t0001 | g0006 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18961 | hp2 | a0002 | c0001 | t0045 | g0236 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0030 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18962 | hp2 | a0001 | c0002 | t0001 | g0111 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18964 | hp1 | a0003 | c0003 | t0008 | g0264 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18964 | hp2 | a0002 | c0001 | t0003 | g0002 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18966 | hp1 | a0001 | c0002 | t0001 | g0029 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18966 | hp2 | a0003 | c0003 | t0002 | g0046 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18967 | hp1 | a0003 | c0003 | t0052 | g0270 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18967 | hp2 | a0005 | c0005 | t0001 | g0006 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18968 | hp1 | a0003 | c0003 | t0008 | g0141 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18968 | hp2 | a0002 | c0001 | t0003 | g0022 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18970 | hp1 | a0003 | c0003 | t0008 | g0013 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18971 | hp1 | a0003 | c0003 | t0006 | g0207 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18971 | hp2 | a0001 | c0002 | t0001 | g0130 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18972 | hp1 | a0005 | c0005 | t0001 | g0036 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18972 | hp2 | a0002 | c0001 | t0003 | g0014 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18973 | hp1 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18973 | hp2 | a0002 | c0001 | t0003 | g0014 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18974 | hp1 | a0003 | c0003 | t0005 | g0057 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18974 | hp2 | a0002 | c0001 | t0002 | g0051 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18975 | hp1 | a0003 | c0003 | t0006 | g0039 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18975 | hp2 | a0002 | c0001 | t0003 | g0002 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18977 | hp1 | a0003 | c0011 | t0001 | g0140 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18977 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18978 | hp1 | a0002 | c0001 | t0002 | g0211 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18978 | hp2 | a0001 | c0002 | t0001 | g0098 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18979 | hp1 | a0002 | c0001 | t0003 | g0184 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18979 | hp2 | a0003 | c0003 | t0005 | g0275 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18980 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18980 | hp2 | a0002 | c0001 | t0038 | g0220 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18981 | hp1 | a0002 | c0001 | t0027 | g0087 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18981 | hp2 | a0005 | c0005 | t0001 | g0006 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18982 | hp1 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18982 | hp2 | a0002 | c0001 | t0027 | g0232 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18983 | hp1 | a0005 | c0005 | t0002 | g0015 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18983 | hp2 | a0002 | c0001 | t0003 | g0185 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18984 | hp1 | a0002 | c0001 | t0002 | g0213 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18984 | hp2 | a0005 | c0005 | t0002 | g0055 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18985 | hp1 | a0001 | c0002 | t0011 | g0049 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18985 | hp2 | a0003 | c0003 | t0008 | g0025 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18986 | hp1 | a0002 | c0001 | t0003 | g0002 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18986 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18987 | hp1 | a0002 | c0001 | t0003 | g0204 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18987 | hp2 | a0003 | c0003 | t0008 | g0013 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18988 | hp1 | a0002 | c0001 | t0003 | g0014 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18988 | hp2 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18989 | hp1 | a0001 | c0002 | t0001 | g0094 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18989 | hp2 | a0003 | c0003 | t0005 | g0057 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18990 | hp1 | a0003 | c0003 | t0006 | g0007 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18990 | hp2 | a0002 | c0001 | t0003 | g0002 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18991 | hp1 | a0002 | c0001 | t0004 | g0054 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18991 | hp2 | a0003 | c0003 | t0006 | g0137 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18992 | hp1 | a0001 | c0002 | t0001 | g0088 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18992 | hp2 | a0002 | c0001 | t0002 | g0230 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18993 | hp1 | a0003 | c0003 | t0005 | g0005 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18993 | hp2 | a0002 | c0001 | t0003 | g0002 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18995 | hp1 | a0001 | c0002 | t0001 | g0030 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18995 | hp2 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18997 | hp1 | a0002 | c0001 | t0002 | g0195 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18997 | hp2 | a0005 | c0005 | t0001 | g0129 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18998 | hp1 | a0001 | c0002 | t0001 | g0104 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18998 | hp2 | a0002 | c0001 | t0023 | g0201 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18999 | hp1 | a0005 | c0005 | t0002 | g0015 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18999 | hp2 | a0003 | c0003 | t0005 | g0005 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA19000 | hp1 | a0003 | c0011 | t0048 | g0127 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA19000 | hp2 | a0002 | c0001 | t0003 | g0197 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA19001 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA19001 | hp2 | a0005 | c0005 | t0001 | g0006 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA19002 | hp1 | a0004 | c0004 | t0004 | g0028 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA19002 | hp2 | a0003 | c0003 | t0006 | g0007 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA19003 | hp1 | a0002 | c0012 | t0002 | g0224 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA19003 | hp2 | a0002 | c0001 | t0002 | g0003 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA19005 | hp1 | a0002 | c0001 | t0002 | g0235 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA19005 | hp2 | a0004 | c0004 | t0004 | g0092 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA19006 | hp1 | a0002 | c0001 | t0003 | g0002 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA19006 | hp2 | a0003 | c0003 | t0008 | g0238 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA19007 | hp1 | a0003 | c0003 | t0008 | g0025 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA19007 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA19009 | hp1 | a0002 | c0001 | t0003 | g0014 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA19009 | hp2 | a0001 | c0002 | t0001 | g0133 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA19010 | hp1 | a0003 | c0003 | t0006 | g0039 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA19010 | hp2 | a0002 | c0001 | t0003 | g0189 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA19011 | hp1 | a0004 | c0004 | t0004 | g0028 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA19011 | hp2 | a0002 | c0001 | t0022 | g0221 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA19012 | hp1 | a0002 | c0001 | t0002 | g0053 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA19012 | hp2 | a0003 | c0003 | t0005 | g0269 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA19030 | hp1 | a0002 | c0001 | t0041 | g0136 | AFR | LWK | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA19030 | hp2 | a0001 | c0006 | t0022 | g0243 | AFR | LWK | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA19043 | hp1 | a0001 | c0007 | t0002 | g0139 | AFR | LWK | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA19043 | hp2 | a0001 | c0002 | t0029 | g0173 | AFR | LWK | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA19055 | hp1 | a0002 | c0001 | t0003 | g0002 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA19055 | hp2 | a0005 | c0005 | t0019 | g0078 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA19056 | hp1 | a0003 | c0003 | t0008 | g0013 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA19056 | hp2 | a0001 | c0002 | t0042 | g0112 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA19057 | hp1 | a0001 | c0002 | t0001 | g0114 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA19057 | hp2 | a0003 | c0003 | t0006 | g0237 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA19062 | hp1 | a0003 | c0003 | t0005 | g0277 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA19062 | hp2 | a0001 | c0002 | t0001 | g0089 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA19064 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA19064 | hp2 | a0004 | c0004 | t0013 | g0079 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA19065 | hp1 | a0004 | c0004 | t0013 | g0081 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA19065 | hp2 | a0004 | c0004 | t0017 | g0163 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA19068 | hp1 | a0002 | c0001 | t0023 | g0203 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA19068 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA19070 | hp1 | a0003 | c0003 | t0005 | g0005 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA19070 | hp2 | a0003 | c0003 | t0006 | g0239 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA19074 | hp1 | a0002 | c0001 | t0002 | g0242 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA19074 | hp2 | a0005 | c0005 | t0002 | g0015 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA19075 | hp1 | a0003 | c0003 | t0005 | g0005 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA19075 | hp2 | a0005 | c0005 | t0001 | g0121 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA19076 | hp1 | a0001 | c0002 | t0001 | g0113 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA19076 | hp2 | a0004 | c0004 | t0013 | g0082 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA19077 | hp1 | a0002 | c0001 | t0002 | g0051 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA19077 | hp2 | a0002 | c0001 | t0003 | g0002 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA19078 | hp1 | a0004 | c0004 | t0039 | g0080 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA19078 | hp2 | a0004 | c0004 | t0004 | g0044 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA19080 | hp1 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA19080 | hp2 | a0003 | c0003 | t0005 | g0058 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA19081 | hp1 | a0002 | c0001 | t0002 | g0212 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA19081 | hp2 | a0001 | c0002 | t0001 | g0090 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA19082 | hp1 | a0003 | c0003 | t0005 | g0005 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA19082 | hp2 | a0002 | c0001 | t0003 | g0002 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA19084 | hp1 | a0003 | c0003 | t0005 | g0276 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA19084 | hp2 | a0002 | c0001 | t0002 | g0003 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA19086 | hp1 | a0003 | c0003 | t0006 | g0007 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA19086 | hp2 | a0001 | c0002 | t0019 | g0095 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA19088 | hp1 | a0002 | c0001 | t0002 | g0024 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA19088 | hp2 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA19091 | hp1 | a0002 | c0001 | t0003 | g0188 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA19091 | hp2 | a0004 | c0004 | t0004 | g0093 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA19240 | hp1 | a0001 | c0007 | t0002 | g0152 | AFR | YRI | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA19240 | hp2 | a0001 | c0002 | t0014 | g0069 | AFR | YRI | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA20129 | hp1 | a0004 | c0004 | t0017 | g0240 | AFR | ASW | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA20129 | hp2 | a0001 | c0002 | t0007 | g0020 | AFR | ASW | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA20752 | hp1 | a0004 | c0004 | t0004 | g0180 | EUR | TSI | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA20752 | hp2 | a0001 | c0002 | t0001 | g0001 | EUR | TSI | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA20805 | hp1 | a0015 | c0014 | t0001 | g0096 | EUR | TSI | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA20805 | hp2 | a0001 | c0002 | t0009 | g0258 | EUR | TSI | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA20905 | hp1 | a0001 | c0002 | t0001 | g0034 | SAS | GIH | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA20905 | hp2 | a0004 | c0004 | t0013 | g0217 | SAS | GIH | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG01123 | hp1 | a0001 | c0002 | t0001 | g0034 | AMR | CLM | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG01123 | hp2 | a0003 | c0003 | t0006 | g0007 | AMR | CLM | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02109 | hp1 | a0002 | c0001 | t0020 | g0026 | AFR | ACB | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02109 | hp2 | a0001 | c0006 | t0002 | g0056 | AFR | ACB | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02486 | hp1 | a0002 | c0001 | t0003 | g0018 | AFR | ACB | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02486 | hp2 | a0001 | c0006 | t0002 | g0157 | AFR | ACB | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02559 | hp1 | a0001 | c0007 | t0002 | g0156 | AFR | ACB | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG02559 | hp2 | a0001 | c0002 | t0007 | g0047 | AFR | ACB | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG03471 | hp1 | a0001 | c0007 | t0002 | g0193 | AFR | MSL | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG03471 | hp2 | a0001 | c0006 | t0002 | g0248 | AFR | MSL | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG06807 | hp1 | a0002 | c0001 | t0002 | g0231 | AFR | USA | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| HG06807 | hp2 | a0014 | c0017 | t0009 | g0259 | AFR | USA | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18955 | hp1 | a0004 | c0004 | t0036 | g0167 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA18955 | hp2 | a0005 | c0005 | t0001 | g0037 | EAS | JPT | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA20300 | hp1 | a0001 | c0002 | t0001 | g0029 | AFR | USA | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA20300 | hp2 | a0003 | c0003 | t0024 | g0144 | AFR | USA | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA21309 | hp1 | a0004 | c0004 | t0037 | g0166 | AFR | LWK | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| NA21309 | hp2 | a0001 | c0002 | t0012 | g0068 | AFR | LWK | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| homoSapiens | chm13v2 | a0003 | c0003 | t0001 | g0142 | REF | REF | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| homoSapiens | grch38p0 | a0001 | c0006 | t0007 | g0225 | REF | REF | TRIM5_chr11_5658195_5690074 | TRIM5 | chr11 | 5658195 | 5690074 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:5664855 | G | A | 1 | a0012 | 1 | HG03486.hp1 | missense_variant | MODERATE | c.1436C>T | p.Pro479Leu | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 8/8 | 1704/3364 | 1436/1482 | 479/493 | chr11 | 5664855 | |||
| chr11:5664960 | T | C | 1 | a0014 | 1 | HG06807.hp2 | missense_variant | MODERATE | c.1331A>G | p.Tyr444Cys | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 8/8 | 1599/3364 | 1331/1482 | 444/493 | chr11 | 5664960 | |||
| chr11:5665036 | G | A | 3 | a0006 a0010 a0011 |
7 | HG01074.hp2 HG01099.hp2 HG01515.hp1 others(4): Show |
missense_variant | MODERATE | c.1255C>T | p.His419Tyr | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 8/8 | 1523/3364 | 1255/1482 | 419/493 | chr11 | 5665036 | |||
| chr11:5667710 | C | T | 3 | a0002 a0008 a0012 |
133 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(130): Show |
missense_variant&splice_region_variant | MODERATE | c.746G>A | p.Gly249Asp | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 5/8 | 1014/3364 | 746/1482 | 249/493 | chr11 | 5667710 | |||
| chr11:5679771 | C | T | 3 | a0004 a0008 a0009 |
55 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(52): Show |
missense_variant | MODERATE | c.407G>A | p.Arg136Gln | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 2/8 | 675/3364 | 407/1482 | 136/493 | chr11 | 5679771 | |||
| chr11:5679816 | T | C | 1 | a0013 | 1 | HG03831.hp2 | missense_variant | MODERATE | c.362A>G | p.Gln121Arg | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 2/8 | 630/3364 | 362/1482 | 121/493 | chr11 | 5679816 | |||
| chr11:5679822 | C | T | 1 | a0015 | 1 | NA20805.hp1 | missense_variant | MODERATE | c.356G>A | p.Arg119Gln | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 2/8 | 624/3364 | 356/1482 | 119/493 | chr11 | 5679822 | |||
| chr11:5679844 | C | A | 2 | a0005 a0011 |
30 | HG00140.hp1 HG01981.hp1 HG01981.hp2 others(27): Show |
missense_variant | MODERATE | c.334G>T | p.Val112Phe | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 2/8 | 602/3364 | 334/1482 | 112/493 | chr11 | 5679844 | |||
| chr11:5679849 | C | T | 1 | a0009 | 1 | HG00741.hp2 | missense_variant | MODERATE | c.329G>A | p.Gly110Glu | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 2/8 | 597/3364 | 329/1482 | 110/493 | chr11 | 5679849 | |||
| chr11:5680051 | G | A | 2 | a0003 a0006 |
63 | HG00544.hp2 HG00673.hp2 HG00733.hp2 others(60): Show |
missense_variant | MODERATE | c.127C>T | p.His43Tyr | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 2/8 | 395/3364 | 127/1482 | 43/493 | chr11 | 5680051 | |||
| chr11:5680087 | C | T | 1 | a0007 | 4 | HG01109.hp1 HG02145.hp1 HG02809.hp1 others(1): Show |
missense_variant | MODERATE | c.91G>A | p.Gly31Ser | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 2/8 | 359/3364 | 91/1482 | 31/493 | chr11 | 5680087 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:5678261 | T | C | 1 | a0001c0007 | 11 | HG00639.hp2 HG01243.hp1 HG02280.hp2 others(8): Show |
synonymous_variant | LOW | c.687A>G | p.Arg229Arg | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/8 | 955/3364 | 687/1482 | 229/493 | chr11 | 5678261 | |||
| chr11:5679110 | T | C | 14 | a0001c0002 a0002c0001 a0002c0012 others(11): Show |
353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
synonymous_variant | LOW | c.477A>G | p.Leu159Leu | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 3/8 | 745/3364 | 477/1482 | 159/493 | chr11 | 5679110 | |||
| chr11:5679941 | C | T | 1 | a0002c0012 | 1 | NA19003.hp1 | synonymous_variant | LOW | c.237G>A | p.Lys79Lys | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 2/8 | 505/3364 | 237/1482 | 79/493 | chr11 | 5679941 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:5663227 | G | A | 5 | a0001c0002t0018 a0001c0002t0046 a0003c0003t0043 others(2): Show |
7 | HG00642.hp1 HG01069.hp2 HG01934.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1582C>T | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 8/8 | 1582 | chr11 | 5663227 | ||||||
| chr11:5663294 | T | A | 1 | a0001c0002t0011 | 6 | NA18939.hp2 NA18942.hp1 NA18944.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1515A>T | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 8/8 | 1515 | chr11 | 5663294 | ||||||
| chr11:5663331 | G | A | 1 | a0004c0004t0036 | 1 | NA18955.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1478C>T | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 8/8 | 1478 | chr11 | 5663331 | ||||||
| chr11:5663336 | A | C | 4 | a0003c0003t0008 a0004c0004t0013 a0004c0004t0036 others(1): Show |
17 | HG04204.hp1 NA18944.hp1 NA18954.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1473T>G | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 8/8 | 1473 | chr11 | 5663336 | ||||||
| chr11:5663395 | T | C | 1 | a0003c0003t0044 | 1 | HG01256.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1414A>G | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 8/8 | 1414 | chr11 | 5663395 | ||||||
| chr11:5663437 | G | A | 2 | a0001c0002t0016 a0001c0006t0016 |
4 | HG01346.hp2 HG01884.hp2 HG02896.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1372C>T | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 8/8 | 1372 | chr11 | 5663437 | ||||||
| chr11:5663486 | T | A | 1 | a0002c0001t0045 | 1 | NA18961.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1323A>T | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 8/8 | 1323 | chr11 | 5663486 | ||||||
| chr11:5663506 | T | C | 1 | a0001c0002t0047 | 1 | NA18949.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1303A>G | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 8/8 | 1303 | chr11 | 5663506 | ||||||
| chr11:5663545 | A | G | 80 | a0001c0002t0001 a0001c0002t0006 a0001c0002t0009 others(77): Show |
427 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(424): Show |
3_prime_UTR_variant | MODIFIER | c.*1264T>C | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 8/8 | 1264 | chr11 | 5663545 | ||||||
| chr11:5663657 | A | G | 31 | a0001c0002t0006 a0001c0002t0014 a0001c0006t0002 others(28): Show |
201 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(198): Show |
3_prime_UTR_variant | MODIFIER | c.*1152T>C | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 8/8 | 1152 | chr11 | 5663657 | ||||||
| chr11:5663675 | C | T | 2 | a0001c0002t0016 a0001c0006t0016 |
4 | HG01346.hp2 HG01884.hp2 HG02896.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1134G>A | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 8/8 | 1134 | chr11 | 5663675 | ||||||
| chr11:5663707 | G | A | 3 | a0001c0002t0029 a0004c0004t0037 a0007c0009t0031 |
5 | HG02145.hp2 HG02809.hp1 HG03540.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1102C>T | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 8/8 | 1102 | chr11 | 5663707 | ||||||
| chr11:5663716 | G | A | 1 | a0001c0002t0042 | 1 | NA19056.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1093C>T | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 8/8 | 1093 | chr11 | 5663716 | ||||||
| chr11:5663973 | G | A | 1 | a0001c0002t0028 | 2 | HG02818.hp1 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*836C>T | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 8/8 | 836 | chr11 | 5663973 | ||||||
| chr11:5664030 | C | T | 3 | a0001c0002t0029 a0003c0003t0043 a0007c0009t0031 |
5 | HG02145.hp2 HG02809.hp1 HG03540.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*779G>A | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 8/8 | 779 | chr11 | 5664030 | ||||||
| chr11:5664150 | G | A | 1 | a0002c0001t0038 | 1 | NA18980.hp2 | 3_prime_UTR_variant | MODIFIER | c.*659C>T | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 8/8 | 659 | chr11 | 5664150 | ||||||
| chr11:5664155 | C | T | 3 | a0001c0006t0021 a0003c0003t0024 a0004c0004t0021 |
6 | HG01255.hp1 HG02258.hp2 HG02451.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*654G>A | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 8/8 | 654 | chr11 | 5664155 | ||||||
| chr11:5664201 | C | CA | 57 | a0001c0002t0001 a0001c0002t0006 a0001c0002t0011 others(54): Show |
378 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(375): Show |
3_prime_UTR_variant | MODIFIER | c.*607dupT | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 8/8 | 607 | chr11 | 5664201 | ||||||
| chr11:5664201 | C | CAA | 8 | a0001c0002t0016 a0001c0002t0029 a0001c0006t0016 others(5): Show |
12 | HG01346.hp2 HG01884.hp2 HG02145.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*606_*607dupTT | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 8/8 | 607 | chr11 | 5664201 | ||||||
| chr11:5664201 | C | CAAAAAAA others(2): Show |
5 | a0001c0002t0009 a0001c0002t0010 a0001c0002t0012 others(2): Show |
20 | HG00738.hp2 HG00741.hp1 HG01496.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*599_*607dupTTTTTT others(3): Show |
TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 8/8 | 607 | chr11 | 5664201 | ||||||
| chr11:5664201 | C | CAAAAAAA others(3): Show |
1 | a0001c0002t0040 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*598_*607dupTTTTTT others(4): Show |
TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 8/8 | 607 | chr11 | 5664201 | ||||||
| chr11:5664209 | A | G | 1 | a0001c0006t0035 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*600T>C | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 8/8 | 600 | chr11 | 5664209 | ||||||
| chr11:5664258 | A | G | 1 | a0001c0006t0035 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*551T>C | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 8/8 | 551 | chr11 | 5664258 | ||||||
| chr11:5664389 | C | A | 4 | a0002c0001t0003 a0002c0001t0023 a0002c0001t0032 others(1): Show |
56 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*420G>T | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 8/8 | 420 | chr11 | 5664389 | ||||||
| chr11:5664507 | T | C | 2 | a0003c0003t0025 a0005c0005t0025 |
3 | HG03491.hp2 HG03492.hp1 HG03834.hp1 |
3_prime_UTR_variant | MODIFIER | c.*302A>G | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 8/8 | 302 | chr11 | 5664507 | ||||||
| chr11:5664525 | C | T | 2 | a0001c0002t0016 a0001c0006t0016 |
4 | HG01346.hp2 HG01884.hp2 HG02896.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*284G>A | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 8/8 | 284 | chr11 | 5664525 | ||||||
| chr11:5664569 | T | G | 2 | a0002c0001t0034 a0002c0001t0041 |
2 | HG02647.hp1 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*240A>C | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 8/8 | 240 | chr11 | 5664569 | ||||||
| chr11:5664607 | T | C | 1 | a0002c0001t0026 | 2 | HG01891.hp1 HG02622.hp1 |
3_prime_UTR_variant | MODIFIER | c.*202A>G | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 8/8 | 202 | chr11 | 5664607 | ||||||
| chr11:5664681 | G | A | 1 | a0001c0002t0049 | 1 | HG01192.hp2 | 3_prime_UTR_variant | MODIFIER | c.*128C>T | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 8/8 | 128 | chr11 | 5664681 | ||||||
| chr11:5680179 | G | C | 33 | a0001c0002t0001 a0001c0002t0006 a0001c0002t0009 others(30): Show |
186 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(183): Show |
5_prime_UTR_variant | MODIFIER | c.-2C>G | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 2/8 | 2 | chr11 | 5680179 | ||||||
| chr11:5684988 | A | G | 1 | a0001c0002t0015 | 4 | HG00099.hp2 HG01099.hp1 HG01167.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-182T>C | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/8 | 4811 | chr11 | 5684988 | ||||||
| chr11:5684996 | C | T | 6 | a0001c0002t0012 a0001c0002t0014 a0001c0002t0033 others(3): Show |
13 | HG01891.hp1 HG02622.hp1 HG02630.hp2 others(10): Show |
5_prime_UTR_variant | MODIFIER | c.-190G>A | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/8 | 4819 | chr11 | 5684996 | ||||||
| chr11:5685053 | A | G | 3 | a0001c0002t0010 a0002c0001t0020 a0002c0001t0032 |
10 | HG01943.hp2 HG02109.hp1 HG02615.hp1 others(7): Show |
5_prime_UTR_variant | MODIFIER | c.-247T>C | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/8 | 4876 | chr11 | 5685053 | ||||||
| chr11:5685056 | G | C | 5 | a0002c0001t0050 a0002c0001t0053 a0003c0003t0005 others(2): Show |
25 | HG00673.hp2 HG01074.hp1 HG01346.hp1 others(22): Show |
5_prime_UTR_variant | MODIFIER | c.-250C>G | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/8 | 4879 | chr11 | 5685056 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:5665434 | T | A | 1 | a0004c0004t0004g0093 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.896-39A>T | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 7/7 | chr11 | 5665434 | |||||||
| chr11:5665465 | A | G | 2 | a0002c0001t0034g0071 a0002c0001t0041g0136 |
2 | HG02647.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.896-70T>C | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 7/7 | chr11 | 5665465 | |||||||
| chr11:5665477 | G | A | 5 | a0001c0002t0017g0178 a0004c0004t0017g0076 a0004c0004t0017g0240 others(2): Show |
5 | HG01109.hp1 HG02145.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.896-82C>T | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 7/7 | chr11 | 5665477 | |||||||
| chr11:5665640 | T | A | 4 | a0003c0003t0005g0058 a0003c0003t0005g0275 a0003c0003t0006g0207 others(1): Show |
5 | HG00673.hp2 NA18971.hp1 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.895+16A>T | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 7/7 | chr11 | 5665640 | |||||||
| chr11:5665865 | ATATCTAT others(2): Show |
A | 3 | a0001c0002t0001g0034 a0001c0002t0001g0118 a0001c0002t0001g0119 |
4 | HG01123.hp1 HG02293.hp2 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.868+107_868+115del others(9): Show |
TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 6/7 | chr11 | 5665865 | |||||||
| chr11:5666090 | T | TA | 117 | a0001c0002t0006g0116 a0001c0002t0033g0070 a0001c0002t0047g0109 others(114): Show |
195 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(192): Show |
intron_variant | MODIFIER | c.768-10dupT | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 5/7 | chr11 | 5666090 | |||||||
| chr11:5666101 | A | C | 2 | a0001c0002t0029g0135 a0001c0002t0029g0173 |
2 | HG02145.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.768-20T>G | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 5/7 | chr11 | 5666101 | |||||||
| chr11:5666332 | G | C | 134 | a0001c0002t0006g0116 a0001c0002t0014g0069 a0001c0006t0002g0056 others(131): Show |
218 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(215): Show |
intron_variant | MODIFIER | c.768-251C>G | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 5/7 | chr11 | 5666332 | |||||||
| chr11:5666378 | T | TA | 12 | a0001c0002t0001g0103 a0001c0002t0016g0241 a0001c0006t0016g0158 others(9): Show |
12 | HG00639.hp2 HG01346.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.768-298dupT | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 5/7 | chr11 | 5666378 | |||||||
| chr11:5666378 | TA | T | 25 | a0001c0002t0009g0032 a0001c0002t0009g0255 a0001c0002t0009g0258 others(22): Show |
31 | HG01169.hp1 HG01496.hp1 HG02145.hp2 others(28): Show |
intron_variant | MODIFIER | c.768-298delT | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 5/7 | chr11 | 5666378 | |||||||
| chr11:5666419 | C | T | 1 | a0001c0002t0040g0210 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.768-338G>A | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 5/7 | chr11 | 5666419 | |||||||
| chr11:5666648 | A | T | 2 | a0003c0003t0005g0057 a0003c0003t0006g0237 |
3 | NA18974.hp1 NA18989.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.768-567T>A | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 5/7 | chr11 | 5666648 | |||||||
| chr11:5666737 | C | T | 3 | a0001c0002t0001g0008 a0001c0002t0001g0113 a0001c0002t0042g0112 |
8 | HG00544.hp1 HG02040.hp2 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.768-656G>A | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 5/7 | chr11 | 5666737 | |||||||
| chr11:5666794 | G | C | 162 | a0001c0002t0006g0116 a0001c0002t0007g0020 a0001c0002t0007g0047 others(159): Show |
256 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(253): Show |
intron_variant | MODIFIER | c.768-713C>G | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 5/7 | chr11 | 5666794 | |||||||
| chr11:5666874 | C | T | 2 | a0001c0006t0002g0248 a0001c0006t0002g0249 |
2 | HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.768-793G>A | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 5/7 | chr11 | 5666874 | |||||||
| chr11:5667165 | A | G | 4 | a0005c0005t0001g0006 a0005c0005t0001g0121 a0005c0005t0001g0131 others(1): Show |
10 | HG01981.hp1 HG01981.hp2 HG02004.hp1 others(7): Show |
intron_variant | MODIFIER | c.767+524T>C | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 5/7 | chr11 | 5667165 | |||||||
| chr11:5667331 | C | T | 5 | a0001c0002t0017g0178 a0004c0004t0017g0076 a0004c0004t0017g0240 others(2): Show |
5 | HG01109.hp1 HG02145.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.767+358G>A | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 5/7 | chr11 | 5667331 | |||||||
| chr11:5667340 | GGGA | G | 12 | a0001c0002t0009g0032 a0001c0002t0009g0255 a0001c0002t0009g0258 others(9): Show |
17 | HG01496.hp1 HG02615.hp1 HG02622.hp2 others(14): Show |
intron_variant | MODIFIER | c.767+346_767+348del others(3): Show |
TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 5/7 | chr11 | 5667340 | |||||||
| chr11:5667342 | G | A | 1 | a0001c0002t0028g0042 | 2 | HG02818.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.767+347C>T | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 5/7 | chr11 | 5667342 | |||||||
| chr11:5667378 | T | G | 17 | a0001c0002t0007g0020 a0001c0002t0007g0047 a0001c0002t0007g0048 others(14): Show |
22 | HG01109.hp1 HG01243.hp2 HG01433.hp1 others(19): Show |
intron_variant | MODIFIER | c.767+311A>C | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 5/7 | chr11 | 5667378 | |||||||
| chr11:5667411 | G | A | 10 | a0001c0002t0014g0069 a0001c0007t0002g0019 a0001c0007t0002g0139 others(7): Show |
12 | HG00639.hp2 HG01243.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.767+278C>T | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 5/7 | chr11 | 5667411 | |||||||
| chr11:5667432 | C | T | 1 | a0001c0006t0002g0157 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.767+257G>A | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 5/7 | chr11 | 5667432 | |||||||
| chr11:5667451 | G | A | 2 | a0001c0006t0002g0056 a0001c0006t0002g0261 |
3 | HG02055.hp2 HG02109.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.767+238C>T | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 5/7 | chr11 | 5667451 | |||||||
| chr11:5667453 | C | T | 73 | a0002c0001t0002g0003 a0002c0001t0002g0011 a0002c0001t0002g0024 others(70): Show |
132 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.767+236G>A | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 5/7 | chr11 | 5667453 | |||||||
| chr11:5667473 | A | G | 1 | a0002c0001t0002g0231 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.767+216T>C | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 5/7 | chr11 | 5667473 | |||||||
| chr11:5667576 | G | T | 1 | a0001c0002t0040g0210 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.767+113C>A | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 5/7 | chr11 | 5667576 | |||||||
| chr11:5667718 | A | G | 4 | a0002c0001t0002g0053 a0002c0001t0002g0212 a0002c0001t0002g0235 others(1): Show |
5 | HG02155.hp2 NA18948.hp1 NA19005.hp1 others(2): Show |
splice_region_variant&intron_variant | LOW | c.745-7T>C | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5667718 | |||||||
| chr11:5667914 | G | C | 61 | a0001c0002t0006g0116 a0001c0002t0014g0069 a0001c0006t0002g0056 others(58): Show |
86 | HG00544.hp2 HG00609.hp1 HG00639.hp2 others(83): Show |
intron_variant | MODIFIER | c.745-203C>G | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5667914 | |||||||
| chr11:5667915 | C | G | 12 | a0001c0002t0009g0032 a0001c0002t0009g0255 a0001c0002t0009g0258 others(9): Show |
17 | HG01496.hp1 HG02615.hp1 HG02622.hp2 others(14): Show |
intron_variant | MODIFIER | c.745-204G>C | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5667915 | |||||||
| chr11:5667960 | T | A | 2 | a0001c0002t0029g0135 a0001c0002t0029g0173 |
2 | HG02145.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.745-249A>T | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5667960 | |||||||
| chr11:5668249 | T | C | 1 | a0001c0006t0002g0249 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.745-538A>G | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5668249 | |||||||
| chr11:5668271 | C | T | 33 | a0001c0002t0007g0020 a0001c0002t0007g0047 a0001c0002t0007g0048 others(30): Show |
43 | HG01109.hp1 HG01243.hp2 HG01433.hp1 others(40): Show |
intron_variant | MODIFIER | c.745-560G>A | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5668271 | |||||||
| chr11:5668311 | C | CAT | 32 | a0001c0002t0007g0020 a0001c0002t0007g0047 a0001c0002t0007g0048 others(29): Show |
41 | HG01109.hp1 HG01243.hp2 HG01433.hp1 others(38): Show |
intron_variant | MODIFIER | c.745-602_745-601dup others(2): Show |
TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5668311 | |||||||
| chr11:5668450 | TTTTC | T | 17 | a0001c0002t0007g0020 a0001c0002t0007g0047 a0001c0002t0007g0048 others(14): Show |
22 | HG01109.hp1 HG01243.hp2 HG01433.hp1 others(19): Show |
intron_variant | MODIFIER | c.745-743_745-740del others(4): Show |
TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5668450 | |||||||
| chr11:5668471 | T | G | 1 | a0005c0005t0001g0124 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.745-760A>C | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5668471 | |||||||
| chr11:5668511 | G | A | 74 | a0002c0001t0002g0003 a0002c0001t0002g0011 a0002c0001t0002g0024 others(71): Show |
133 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.745-800C>T | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5668511 | |||||||
| chr11:5668569 | C | T | 4 | a0001c0002t0029g0135 a0001c0002t0029g0173 a0007c0009t0031g0075 others(1): Show |
4 | HG02145.hp2 HG02809.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.745-858G>A | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5668569 | |||||||
| chr11:5668590 | C | T | 4 | a0001c0002t0016g0241 a0001c0006t0016g0158 a0001c0006t0016g0250 others(1): Show |
4 | HG01346.hp2 HG01884.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.745-879G>A | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5668590 | |||||||
| chr11:5668594 | C | T | 2 | a0001c0002t0029g0135 a0001c0002t0029g0173 |
2 | HG02145.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.745-883G>A | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5668594 | |||||||
| chr11:5668648 | C | T | 1 | a0003c0003t0005g0273 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.745-937G>A | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5668648 | |||||||
| chr11:5668696 | T | C | 74 | a0002c0001t0002g0003 a0002c0001t0002g0011 a0002c0001t0002g0024 others(71): Show |
133 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.745-985A>G | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5668696 | |||||||
| chr11:5668745 | C | A | 33 | a0001c0002t0007g0020 a0001c0002t0007g0047 a0001c0002t0007g0048 others(30): Show |
43 | HG01109.hp1 HG01243.hp2 HG01433.hp1 others(40): Show |
intron_variant | MODIFIER | c.745-1034G>T | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5668745 | |||||||
| chr11:5668773 | C | T | 61 | a0001c0002t0006g0116 a0001c0002t0014g0069 a0001c0006t0002g0056 others(58): Show |
86 | HG00544.hp2 HG00609.hp1 HG00639.hp2 others(83): Show |
intron_variant | MODIFIER | c.745-1062G>A | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5668773 | |||||||
| chr11:5669080 | C | CT | 61 | a0001c0002t0001g0033 a0001c0002t0006g0116 a0001c0002t0014g0069 others(58): Show |
88 | HG00544.hp2 HG00609.hp1 HG00673.hp2 others(85): Show |
intron_variant | MODIFIER | c.745-1370dupA | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5669080 | |||||||
| chr11:5669080 | C | CTTT | 31 | a0001c0002t0007g0020 a0001c0002t0007g0047 a0001c0002t0007g0171 others(28): Show |
40 | HG01109.hp1 HG01243.hp2 HG01496.hp1 others(37): Show |
intron_variant | MODIFIER | c.745-1372_745-1370d others(5): Show |
TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5669080 | |||||||
| chr11:5669111 | C | A | 2 | a0001c0002t0029g0135 a0001c0002t0029g0173 |
2 | HG02145.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.745-1400G>T | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5669111 | |||||||
| chr11:5669228 | C | T | 12 | a0001c0002t0007g0020 a0001c0002t0007g0047 a0001c0002t0007g0048 others(9): Show |
17 | HG01243.hp2 HG01433.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.745-1517G>A | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5669228 | |||||||
| chr11:5669229 | G | A | 1 | a0001c0002t0001g0110 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.745-1518C>T | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5669229 | |||||||
| chr11:5669294 | G | C | 1 | a0001c0002t0007g0215 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.745-1583C>G | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5669294 | |||||||
| chr11:5669299 | T | C | 169 | a0001c0002t0006g0116 a0001c0002t0007g0020 a0001c0002t0007g0047 others(166): Show |
263 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(260): Show |
intron_variant | MODIFIER | c.745-1588A>G | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5669299 | |||||||
| chr11:5669314 | A | T | 61 | a0001c0002t0006g0116 a0001c0002t0014g0069 a0001c0006t0002g0056 others(58): Show |
86 | HG00544.hp2 HG00609.hp1 HG00639.hp2 others(83): Show |
intron_variant | MODIFIER | c.745-1603T>A | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5669314 | |||||||
| chr11:5669323 | G | A | 1 | a0001c0002t0007g0187 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.745-1612C>T | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5669323 | |||||||
| chr11:5669324 | C | G | 2 | a0001c0002t0010g0009 a0001c0002t0010g0059 |
6 | HG02615.hp1 HG02622.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.745-1613G>C | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5669324 | |||||||
| chr11:5669339 | C | G | 1 | a0001c0002t0001g0031 | 2 | HG00673.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.745-1628G>C | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5669339 | |||||||
| chr11:5669461 | A | C | 61 | a0001c0002t0006g0116 a0001c0002t0014g0069 a0001c0006t0002g0056 others(58): Show |
86 | HG00544.hp2 HG00609.hp1 HG00639.hp2 others(83): Show |
intron_variant | MODIFIER | c.745-1750T>G | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5669461 | |||||||
| chr11:5669510 | A | C | 1 | a0002c0001t0002g0050 | 2 | HG01891.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.745-1799T>G | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5669510 | |||||||
| chr11:5669511 | T | C | 61 | a0001c0002t0006g0116 a0001c0002t0014g0069 a0001c0006t0002g0056 others(58): Show |
86 | HG00544.hp2 HG00609.hp1 HG00639.hp2 others(83): Show |
intron_variant | MODIFIER | c.745-1800A>G | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5669511 | |||||||
| chr11:5669546 | C | T | 1 | a0004c0004t0002g0134 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.745-1835G>A | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5669546 | |||||||
| chr11:5669618 | T | C | 1 | a0002c0001t0003g0202 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.745-1907A>G | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5669618 | |||||||
| chr11:5669775 | A | G | 61 | a0001c0002t0006g0116 a0001c0002t0014g0069 a0001c0006t0002g0056 others(58): Show |
86 | HG00544.hp2 HG00609.hp1 HG00639.hp2 others(83): Show |
intron_variant | MODIFIER | c.745-2064T>C | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5669775 | |||||||
| chr11:5669871 | C | A | 60 | a0001c0002t0006g0116 a0001c0002t0014g0069 a0001c0006t0002g0056 others(57): Show |
85 | HG00544.hp2 HG00609.hp1 HG00639.hp2 others(82): Show |
intron_variant | MODIFIER | c.745-2160G>T | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5669871 | |||||||
| chr11:5669939 | C | T | 1 | a0002c0001t0003g0198 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.745-2228G>A | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5669939 | |||||||
| chr11:5669961 | C | T | 212 | a0001c0002t0001g0001 a0001c0002t0001g0008 a0001c0002t0001g0010 others(209): Show |
356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.745-2250G>A | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5669961 | |||||||
| chr11:5669984 | A | C | 80 | a0001c0002t0011g0021 a0001c0002t0011g0049 a0001c0002t0011g0205 others(77): Show |
143 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(140): Show |
intron_variant | MODIFIER | c.745-2273T>G | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5669984 | |||||||
| chr11:5670124 | C | T | 8 | a0001c0002t0001g0010 a0001c0002t0001g0031 a0001c0002t0001g0104 others(5): Show |
13 | HG00673.hp1 NA18939.hp1 NA18943.hp2 others(10): Show |
intron_variant | MODIFIER | c.745-2413G>A | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5670124 | |||||||
| chr11:5670170 | C | CT | 35 | a0001c0002t0001g0106 a0001c0002t0001g0118 a0001c0002t0007g0020 others(32): Show |
45 | HG00738.hp2 HG00741.hp1 HG01109.hp1 others(42): Show |
intron_variant | MODIFIER | c.745-2460dupA | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5670170 | |||||||
| chr11:5670170 | C | CTT | 6 | a0001c0002t0007g0187 a0001c0002t0028g0042 a0001c0006t0007g0260 others(3): Show |
7 | HG02145.hp1 HG02572.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.745-2461_745-2460d others(4): Show |
TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5670170 | |||||||
| chr11:5670170 | CT | C | 124 | a0001c0002t0001g0090 a0001c0002t0001g0101 a0001c0002t0001g0103 others(121): Show |
207 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.745-2460delA | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5670170 | |||||||
| chr11:5670170 | CTT | C | 9 | a0001c0002t0016g0241 a0001c0006t0016g0250 a0001c0006t0016g0254 others(6): Show |
10 | HG01515.hp2 HG01517.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.745-2461_745-2460d others(4): Show |
TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5670170 | |||||||
| chr11:5670228 | A | G | 89 | a0001c0002t0001g0094 a0001c0002t0001g0105 a0001c0002t0009g0258 others(86): Show |
152 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.745-2517T>C | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5670228 | |||||||
| chr11:5670244 | C | G | 24 | a0001c0002t0009g0032 a0001c0002t0009g0255 a0001c0002t0009g0257 others(21): Show |
32 | HG00738.hp2 HG01109.hp1 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.745-2533G>C | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5670244 | |||||||
| chr11:5670253 | C | A | 1 | a0003c0003t0006g0147 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.745-2542G>T | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5670253 | |||||||
| chr11:5670263 | T | C | 1 | a0001c0002t0015g0027 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.745-2552A>G | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5670263 | |||||||
| chr11:5670276 | C | T | 78 | a0001c0002t0001g0101 a0001c0002t0001g0104 a0001c0002t0011g0021 others(75): Show |
139 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.745-2565G>A | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5670276 | |||||||
| chr11:5670278 | T | C | 2 | a0001c0006t0002g0157 a0004c0004t0004g0161 |
2 | HG02486.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.745-2567A>G | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5670278 | |||||||
| chr11:5670298 | C | T | 81 | a0001c0002t0001g0101 a0001c0002t0001g0104 a0001c0002t0011g0021 others(78): Show |
143 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.745-2587G>A | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5670298 | |||||||
| chr11:5670323 | T | A | 1 | a0003c0003t0006g0148 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.745-2612A>T | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5670323 | |||||||
| chr11:5670327 | A | G | 146 | a0001c0002t0001g0031 a0001c0002t0001g0088 a0001c0002t0001g0097 others(143): Show |
242 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(239): Show |
intron_variant | MODIFIER | c.745-2616T>C | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5670327 | |||||||
| chr11:5670344 | A | AT | 101 | a0001c0002t0001g0001 a0001c0002t0001g0008 a0001c0002t0001g0010 others(98): Show |
174 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(171): Show |
intron_variant | MODIFIER | c.745-2634dupA | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5670344 | |||||||
| chr11:5670346 | T | C | 1 | a0001c0002t0028g0042 | 2 | HG02818.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.745-2635A>G | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5670346 | |||||||
| chr11:5670379 | T | G | 34 | a0001c0002t0007g0020 a0001c0002t0007g0047 a0001c0002t0007g0048 others(31): Show |
43 | HG00738.hp2 HG00741.hp1 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.745-2668A>C | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5670379 | |||||||
| chr11:5670391 | A | T | 108 | a0001c0002t0007g0020 a0001c0002t0007g0047 a0001c0002t0007g0048 others(105): Show |
179 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(176): Show |
intron_variant | MODIFIER | c.745-2680T>A | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5670391 | |||||||
| chr11:5670411 | C | T | 1 | a0001c0006t0007g0174 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.745-2700G>A | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5670411 | |||||||
| chr11:5670416 | G | A | 4 | a0001c0002t0029g0135 a0001c0002t0029g0173 a0007c0009t0031g0075 others(1): Show |
4 | HG02145.hp2 HG02809.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.745-2705C>T | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5670416 | |||||||
| chr11:5670421 | G | A | 1 | a0002c0001t0023g0203 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.745-2710C>T | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5670421 | |||||||
| chr11:5670460 | C | T | 1 | a0001c0006t0002g0157 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.745-2749G>A | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5670460 | |||||||
| chr11:5670508 | A | G | 14 | a0001c0002t0009g0255 a0001c0002t0009g0256 a0001c0002t0009g0257 others(11): Show |
18 | HG00738.hp2 HG00741.hp1 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.745-2797T>C | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5670508 | |||||||
| chr11:5670559 | C | A | 77 | a0001c0002t0011g0021 a0001c0002t0011g0049 a0001c0002t0011g0205 others(74): Show |
139 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(136): Show |
intron_variant | MODIFIER | c.745-2848G>T | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5670559 | |||||||
| chr11:5670594 | G | A | 8 | a0001c0007t0002g0019 a0001c0007t0002g0139 a0001c0007t0002g0153 others(5): Show |
10 | HG00639.hp2 HG01243.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.745-2883C>T | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5670594 | |||||||
| chr11:5670663 | C | T | 210 | a0001c0002t0001g0001 a0001c0002t0001g0008 a0001c0002t0001g0010 others(207): Show |
353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.745-2952G>A | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5670663 | |||||||
| chr11:5670697 | C | G | 1 | a0001c0002t0001g0100 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.745-2986G>C | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5670697 | |||||||
| chr11:5670750 | C | T | 107 | a0001c0002t0007g0020 a0001c0002t0007g0047 a0001c0002t0007g0048 others(104): Show |
178 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(175): Show |
intron_variant | MODIFIER | c.745-3039G>A | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5670750 | |||||||
| chr11:5670783 | C | A | 107 | a0001c0002t0007g0020 a0001c0002t0007g0047 a0001c0002t0007g0048 others(104): Show |
178 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(175): Show |
intron_variant | MODIFIER | c.745-3072G>T | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5670783 | |||||||
| chr11:5670784 | A | AGC | 107 | a0001c0002t0007g0020 a0001c0002t0007g0047 a0001c0002t0007g0048 others(104): Show |
178 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(175): Show |
intron_variant | MODIFIER | c.745-3074_745-3073i others(4): Show |
TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5670784 | |||||||
| chr11:5670785 | C | T | 107 | a0001c0002t0007g0020 a0001c0002t0007g0047 a0001c0002t0007g0048 others(104): Show |
178 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(175): Show |
intron_variant | MODIFIER | c.745-3074G>A | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5670785 | |||||||
| chr11:5670789 | A | G | 106 | a0001c0002t0007g0020 a0001c0002t0007g0047 a0001c0002t0007g0048 others(103): Show |
176 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(173): Show |
intron_variant | MODIFIER | c.745-3078T>C | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5670789 | |||||||
| chr11:5670802 | C | G | 107 | a0001c0002t0007g0020 a0001c0002t0007g0047 a0001c0002t0007g0048 others(104): Show |
178 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(175): Show |
intron_variant | MODIFIER | c.745-3091G>C | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5670802 | |||||||
| chr11:5670818 | A | C | 2 | a0006c0008t0001g0149 a0006c0008t0001g0150 |
2 | HG03710.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.745-3107T>G | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5670818 | |||||||
| chr11:5670914 | G | A | 74 | a0001c0002t0011g0021 a0001c0002t0011g0049 a0001c0002t0011g0205 others(71): Show |
136 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.745-3203C>T | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5670914 | |||||||
| chr11:5671019 | G | A | 2 | a0001c0007t0002g0019 a0001c0007t0002g0194 |
4 | HG01243.hp1 HG02970.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.745-3308C>T | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5671019 | |||||||
| chr11:5671209 | G | C | 102 | a0001c0002t0001g0001 a0001c0002t0001g0008 a0001c0002t0001g0010 others(99): Show |
174 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(171): Show |
intron_variant | MODIFIER | c.745-3498C>G | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5671209 | |||||||
| chr11:5671285 | T | C | 74 | a0001c0002t0011g0021 a0001c0002t0011g0049 a0001c0002t0011g0205 others(71): Show |
136 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.745-3574A>G | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5671285 | |||||||
| chr11:5671304 | T | TA | 103 | a0001c0002t0001g0001 a0001c0002t0001g0008 a0001c0002t0001g0010 others(100): Show |
175 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(172): Show |
intron_variant | MODIFIER | c.745-3594dupT | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5671304 | |||||||
| chr11:5671304 | TA | T | 9 | a0001c0007t0002g0019 a0001c0007t0002g0139 a0001c0007t0002g0152 others(6): Show |
11 | HG00639.hp2 HG01243.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.745-3594delT | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5671304 | |||||||
| chr11:5671313 | A | AAC | 20 | a0001c0002t0009g0255 a0001c0002t0009g0256 a0001c0002t0009g0257 others(17): Show |
24 | HG00738.hp2 HG00741.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.745-3604_745-3603d others(4): Show |
TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5671313 | |||||||
| chr11:5671313 | A | AC | 13 | a0001c0002t0007g0020 a0001c0002t0007g0047 a0001c0002t0007g0048 others(10): Show |
18 | HG01243.hp2 HG01433.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.745-3603_745-3602i others(3): Show |
TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5671313 | |||||||
| chr11:5671315 | C | A | 72 | a0001c0002t0011g0021 a0001c0002t0011g0049 a0001c0002t0011g0205 others(69): Show |
134 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.745-3604G>T | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5671315 | |||||||
| chr11:5671317 | C | CACA | 73 | a0001c0002t0011g0021 a0001c0002t0011g0049 a0001c0002t0011g0205 others(70): Show |
135 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.745-3607_745-3606i others(5): Show |
TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5671317 | |||||||
| chr11:5671321 | A | G | 9 | a0001c0002t0007g0020 a0001c0002t0007g0047 a0001c0002t0007g0048 others(6): Show |
13 | HG01243.hp2 HG01433.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.745-3610T>C | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5671321 | |||||||
| chr11:5671325 | C | A | 2 | a0001c0002t0001g0017 a0003c0003t0005g0276 |
4 | HG02015.hp2 HG02056.hp1 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.745-3614G>T | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5671325 | |||||||
| chr11:5671359 | T | C | 102 | a0001c0002t0001g0001 a0001c0002t0001g0008 a0001c0002t0001g0010 others(99): Show |
174 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(171): Show |
intron_variant | MODIFIER | c.745-3648A>G | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5671359 | |||||||
| chr11:5671385 | T | C | 34 | a0001c0002t0007g0020 a0001c0002t0007g0047 a0001c0002t0007g0048 others(31): Show |
43 | HG00738.hp2 HG00741.hp1 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.745-3674A>G | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5671385 | |||||||
| chr11:5671595 | C | T | 74 | a0001c0002t0011g0021 a0001c0002t0011g0049 a0001c0002t0011g0205 others(71): Show |
136 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.745-3884G>A | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5671595 | |||||||
| chr11:5671608 | A | T | 74 | a0001c0002t0011g0021 a0001c0002t0011g0049 a0001c0002t0011g0205 others(71): Show |
136 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.745-3897T>A | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5671608 | |||||||
| chr11:5671649 | G | A | 102 | a0001c0002t0001g0001 a0001c0002t0001g0008 a0001c0002t0001g0010 others(99): Show |
174 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(171): Show |
intron_variant | MODIFIER | c.745-3938C>T | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5671649 | |||||||
| chr11:5671704 | G | A | 1 | a0001c0002t0001g0117 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.745-3993C>T | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5671704 | |||||||
| chr11:5671704 | G | T | 1 | a0002c0012t0002g0224 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.745-3993C>A | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5671704 | |||||||
| chr11:5671823 | T | C | 109 | a0001c0002t0001g0001 a0001c0002t0001g0008 a0001c0002t0001g0010 others(106): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.745-4112A>G | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5671823 | |||||||
| chr11:5671825 | G | GT | 209 | a0001c0002t0001g0001 a0001c0002t0001g0008 a0001c0002t0001g0010 others(206): Show |
352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.745-4115dupA | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5671825 | |||||||
| chr11:5671951 | G | A | 209 | a0001c0002t0001g0001 a0001c0002t0001g0008 a0001c0002t0001g0010 others(206): Show |
352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.745-4240C>T | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5671951 | |||||||
| chr11:5672317 | G | T | 222 | a0001c0002t0001g0001 a0001c0002t0001g0008 a0001c0002t0001g0010 others(219): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.745-4606C>A | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5672317 | |||||||
| chr11:5672541 | G | T | 101 | a0001c0002t0001g0001 a0001c0002t0001g0008 a0001c0002t0001g0010 others(98): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.745-4830C>A | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5672541 | |||||||
| chr11:5672765 | T | C | 1 | a0002c0001t0002g0235 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.745-5054A>G | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5672765 | |||||||
| chr11:5672816 | T | C | 2 | a0001c0002t0010g0009 a0001c0002t0010g0059 |
6 | HG02615.hp1 HG02622.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.745-5105A>G | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5672816 | |||||||
| chr11:5673147 | G | C | 101 | a0001c0002t0001g0001 a0001c0002t0001g0008 a0001c0002t0001g0010 others(98): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.744+5057C>G | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5673147 | |||||||
| chr11:5673320 | A | T | 1 | a0004c0004t0002g0134 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.744+4884T>A | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5673320 | |||||||
| chr11:5673460 | C | T | 1 | a0001c0002t0001g0099 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.744+4744G>A | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5673460 | |||||||
| chr11:5673544 | A | G | 1 | a0003c0003t0024g0262 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.744+4660T>C | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5673544 | |||||||
| chr11:5673765 | A | G | 10 | a0001c0002t0001g0097 a0001c0002t0007g0020 a0001c0002t0007g0047 others(7): Show |
15 | HG01243.hp2 HG01433.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.744+4439T>C | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5673765 | |||||||
| chr11:5673892 | T | C | 1 | a0002c0001t0003g0204 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.744+4312A>G | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5673892 | |||||||
| chr11:5673910 | C | T | 3 | a0004c0004t0002g0074 a0004c0004t0017g0076 a0004c0004t0017g0240 |
3 | HG02818.hp2 HG02922.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.744+4294G>A | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5673910 | |||||||
| chr11:5674078 | C | T | 1 | a0002c0001t0003g0022 | 3 | NA18945.hp2 NA18952.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.744+4126G>A | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5674078 | |||||||
| chr11:5674101 | A | G | 209 | a0001c0002t0001g0001 a0001c0002t0001g0008 a0001c0002t0001g0010 others(206): Show |
352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.744+4103T>C | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5674101 | |||||||
| chr11:5674356 | A | G | 1 | a0001c0002t0033g0070 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.744+3848T>C | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5674356 | |||||||
| chr11:5674513 | T | C | 210 | a0001c0002t0001g0001 a0001c0002t0001g0008 a0001c0002t0001g0010 others(207): Show |
353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.744+3691A>G | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5674513 | |||||||
| chr11:5674519 | C | T | 1 | a0001c0002t0007g0171 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.744+3685G>A | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5674519 | |||||||
| chr11:5674532 | A | T | 1 | a0001c0002t0028g0042 | 2 | HG02818.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.744+3672T>A | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5674532 | |||||||
| chr11:5674592 | G | A | 1 | a0004c0004t0004g0045 | 2 | HG01255.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.744+3612C>T | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5674592 | |||||||
| chr11:5674628 | C | G | 4 | a0001c0002t0011g0021 a0001c0002t0011g0049 a0001c0002t0011g0205 others(1): Show |
11 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(8): Show |
intron_variant | MODIFIER | c.744+3576G>C | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5674628 | |||||||
| chr11:5674646 | G | A | 2 | a0001c0006t0016g0250 a0001c0006t0016g0254 |
2 | HG01884.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.744+3558C>T | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5674646 | |||||||
| chr11:5674650 | T | G | 2 | a0001c0006t0016g0250 a0001c0006t0016g0254 |
2 | HG01884.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.744+3554A>C | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5674650 | |||||||
| chr11:5674802 | T | C | 1 | a0003c0003t0005g0277 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.744+3402A>G | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5674802 | |||||||
| chr11:5674826 | T | C | 14 | a0001c0002t0009g0255 a0001c0002t0009g0256 a0001c0002t0009g0257 others(11): Show |
18 | HG00738.hp2 HG00741.hp1 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.744+3378A>G | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5674826 | |||||||
| chr11:5674874 | G | T | 105 | a0001c0002t0001g0001 a0001c0002t0001g0008 a0001c0002t0001g0010 others(102): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.744+3330C>A | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5674874 | |||||||
| chr11:5675016 | A | C | 3 | a0003c0003t0006g0237 a0003c0003t0008g0025 a0003c0003t0008g0238 |
5 | NA18954.hp1 NA18985.hp2 NA19006.hp2 others(2): Show |
intron_variant | MODIFIER | c.744+3188T>G | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5675016 | |||||||
| chr11:5675024 | A | G | 127 | a0001c0002t0001g0001 a0001c0002t0001g0008 a0001c0002t0001g0010 others(124): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.744+3180T>C | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5675024 | |||||||
| chr11:5675036 | C | CT | 72 | a0001c0002t0011g0021 a0001c0002t0011g0049 a0001c0002t0011g0205 others(69): Show |
134 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.744+3167dupA | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5675036 | |||||||
| chr11:5675145 | C | T | 4 | a0007c0009t0019g0252 a0007c0009t0019g0253 a0007c0009t0031g0075 others(1): Show |
4 | HG01109.hp1 HG02145.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.744+3059G>A | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5675145 | |||||||
| chr11:5675178 | G | A | 113 | a0001c0002t0001g0001 a0001c0002t0001g0008 a0001c0002t0001g0010 others(110): Show |
185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.744+3026C>T | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5675178 | |||||||
| chr11:5675180 | C | G | 1 | a0001c0002t0001g0098 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.744+3024G>C | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5675180 | |||||||
| chr11:5675184 | A | G | 1 | a0001c0002t0028g0042 | 2 | HG02818.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.744+3020T>C | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5675184 | |||||||
| chr11:5675205 | TTA | T | 67 | a0001c0002t0011g0021 a0001c0002t0011g0049 a0001c0002t0011g0205 others(64): Show |
126 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.744+2997_744+2998d others(4): Show |
TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5675205 | |||||||
| chr11:5675206 | TA | T | 24 | a0001c0002t0001g0111 a0001c0002t0009g0255 a0001c0002t0009g0256 others(21): Show |
31 | HG00733.hp1 HG00738.hp2 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.744+2997delT | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5675206 | |||||||
| chr11:5675207 | A | T | 118 | a0001c0002t0001g0001 a0001c0002t0001g0008 a0001c0002t0001g0010 others(115): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.744+2997T>A | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5675207 | |||||||
| chr11:5675256 | T | C | 2 | a0001c0002t0029g0135 a0001c0002t0029g0173 |
2 | HG02145.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.744+2948A>G | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5675256 | |||||||
| chr11:5675296 | G | C | 1 | a0001c0002t0009g0257 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.744+2908C>G | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5675296 | |||||||
| chr11:5675350 | G | A | 113 | a0001c0002t0001g0001 a0001c0002t0001g0008 a0001c0002t0001g0010 others(110): Show |
185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.744+2854C>T | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5675350 | |||||||
| chr11:5675371 | T | G | 1 | a0002c0001t0002g0212 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.744+2833A>C | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5675371 | |||||||
| chr11:5675456 | G | C | 1 | a0002c0001t0003g0190 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.744+2748C>G | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5675456 | |||||||
| chr11:5675560 | C | T | 2 | a0002c0001t0034g0071 a0002c0001t0041g0136 |
2 | HG02647.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.744+2644G>A | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5675560 | |||||||
| chr11:5675568 | C | T | 3 | a0002c0001t0003g0018 a0002c0001t0003g0246 a0002c0001t0032g0061 |
5 | HG02486.hp1 HG02886.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.744+2636G>A | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5675568 | |||||||
| chr11:5675662 | CT | C | 16 | a0001c0002t0007g0020 a0001c0002t0007g0047 a0001c0002t0007g0048 others(13): Show |
21 | HG01243.hp2 HG01433.hp1 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.744+2541delA | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5675662 | |||||||
| chr11:5675662 | CTT | C | 108 | a0001c0002t0001g0001 a0001c0002t0001g0008 a0001c0002t0001g0010 others(105): Show |
180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.744+2540_744+2541d others(4): Show |
TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5675662 | |||||||
| chr11:5675699 | T | C | 1 | a0001c0002t0016g0241 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.744+2505A>G | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5675699 | |||||||
| chr11:5675835 | G | A | 224 | a0001c0002t0001g0001 a0001c0002t0001g0008 a0001c0002t0001g0010 others(221): Show |
369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.744+2369C>T | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5675835 | |||||||
| chr11:5675858 | C | CG | 73 | a0001c0002t0011g0021 a0001c0002t0011g0049 a0001c0002t0011g0205 others(70): Show |
135 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.744+2345_744+2346i others(3): Show |
TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5675858 | |||||||
| chr11:5675868 | T | C | 113 | a0001c0002t0001g0001 a0001c0002t0001g0008 a0001c0002t0001g0010 others(110): Show |
185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.744+2336A>G | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5675868 | |||||||
| chr11:5675922 | A | C | 73 | a0001c0002t0011g0021 a0001c0002t0011g0049 a0001c0002t0011g0205 others(70): Show |
135 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.744+2282T>G | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5675922 | |||||||
| chr11:5675925 | C | G | 1 | a0001c0002t0001g0247 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.744+2279G>C | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5675925 | |||||||
| chr11:5675929 | C | T | 9 | a0001c0002t0007g0020 a0001c0002t0007g0047 a0001c0002t0007g0048 others(6): Show |
14 | HG01243.hp2 HG01433.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.744+2275G>A | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5675929 | |||||||
| chr11:5675948 | G | A | 1 | a0004c0004t0002g0134 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.744+2256C>T | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5675948 | |||||||
| chr11:5675956 | A | G | 113 | a0001c0002t0001g0001 a0001c0002t0001g0008 a0001c0002t0001g0010 others(110): Show |
185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.744+2248T>C | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5675956 | |||||||
| chr11:5675965 | T | G | 1 | a0004c0004t0002g0091 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.744+2239A>C | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5675965 | |||||||
| chr11:5676036 | A | AT | 7 | a0001c0002t0017g0178 a0001c0002t0029g0135 a0001c0002t0029g0173 others(4): Show |
7 | HG01109.hp1 HG02145.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.744+2167dupA | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5676036 | |||||||
| chr11:5676071 | C | T | 113 | a0001c0002t0001g0001 a0001c0002t0001g0008 a0001c0002t0001g0010 others(110): Show |
185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.744+2133G>A | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5676071 | |||||||
| chr11:5676101 | T | C | 69 | a0001c0002t0001g0001 a0001c0002t0001g0008 a0001c0002t0001g0010 others(66): Show |
123 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.744+2103A>G | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5676101 | |||||||
| chr11:5676310 | C | T | 1 | a0002c0001t0002g0229 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.744+1894G>A | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5676310 | |||||||
| chr11:5676341 | G | C | 49 | a0001c0002t0011g0021 a0001c0002t0011g0049 a0001c0002t0011g0205 others(46): Show |
90 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.744+1863C>G | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5676341 | |||||||
| chr11:5676403 | C | T | 9 | a0001c0002t0007g0020 a0001c0002t0007g0047 a0001c0002t0007g0048 others(6): Show |
14 | HG01243.hp2 HG01433.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.744+1801G>A | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5676403 | |||||||
| chr11:5676509 | A | G | 4 | a0001c0002t0007g0020 a0001c0002t0007g0047 a0001c0002t0007g0048 others(1): Show |
8 | HG01243.hp2 HG01433.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.744+1695T>C | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5676509 | |||||||
| chr11:5676528 | T | G | 14 | a0001c0002t0009g0255 a0001c0002t0009g0256 a0001c0002t0009g0257 others(11): Show |
18 | HG00738.hp2 HG00741.hp1 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.744+1676A>C | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5676528 | |||||||
| chr11:5676544 | C | T | 1 | a0002c0001t0003g0197 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.744+1660G>A | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5676544 | |||||||
| chr11:5676582 | C | G | 1 | a0002c0001t0003g0196 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.744+1622G>C | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5676582 | |||||||
| chr11:5676640 | A | G | 113 | a0001c0002t0001g0001 a0001c0002t0001g0008 a0001c0002t0001g0010 others(110): Show |
185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.744+1564T>C | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5676640 | |||||||
| chr11:5676646 | G | T | 14 | a0001c0002t0009g0255 a0001c0002t0009g0256 a0001c0002t0009g0257 others(11): Show |
18 | HG00738.hp2 HG00741.hp1 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.744+1558C>A | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5676646 | |||||||
| chr11:5676684 | A | G | 1 | a0002c0001t0002g0228 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.744+1520T>C | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5676684 | |||||||
| chr11:5676764 | A | G | 113 | a0001c0002t0001g0001 a0001c0002t0001g0008 a0001c0002t0001g0010 others(110): Show |
185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.744+1440T>C | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5676764 | |||||||
| chr11:5676796 | A | C | 2 | a0001c0002t0007g0215 a0002c0001t0002g0227 |
2 | HG01978.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.744+1408T>G | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5676796 | |||||||
| chr11:5676797 | C | T | 1 | a0001c0002t0007g0215 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.744+1407G>A | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5676797 | |||||||
| chr11:5676830 | C | T | 1 | a0001c0002t0007g0020 | 3 | HG01243.hp2 HG03579.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.744+1374G>A | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5676830 | |||||||
| chr11:5676896 | C | A | 1 | a0008c0010t0002g0208 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.744+1308G>T | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5676896 | |||||||
| chr11:5676899 | T | G | 1 | a0008c0010t0002g0208 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.744+1305A>C | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5676899 | |||||||
| chr11:5676901 | T | C | 1 | a0001c0006t0002g0157 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.744+1303A>G | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5676901 | |||||||
| chr11:5677088 | A | C | 108 | a0001c0002t0001g0001 a0001c0002t0001g0008 a0001c0002t0001g0010 others(105): Show |
180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.744+1116T>G | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5677088 | |||||||
| chr11:5677198 | C | T | 1 | a0002c0001t0006g0214 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.744+1006G>A | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5677198 | |||||||
| chr11:5677225 | G | A | 35 | a0001c0002t0018g0209 a0002c0001t0003g0219 a0004c0004t0002g0091 others(32): Show |
53 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(50): Show |
intron_variant | MODIFIER | c.744+979C>T | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5677225 | |||||||
| chr11:5677243 | A | C | 9 | a0001c0002t0007g0020 a0001c0002t0007g0047 a0001c0002t0007g0048 others(6): Show |
14 | HG01243.hp2 HG01433.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.744+961T>G | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5677243 | |||||||
| chr11:5677290 | G | A | 1 | a0001c0002t0015g0073 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.744+914C>T | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5677290 | |||||||
| chr11:5677308 | C | T | 9 | a0001c0002t0007g0020 a0001c0002t0007g0047 a0001c0002t0007g0048 others(6): Show |
14 | HG01243.hp2 HG01433.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.744+896G>A | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5677308 | |||||||
| chr11:5677434 | C | T | 105 | a0001c0002t0001g0001 a0001c0002t0001g0008 a0001c0002t0001g0010 others(102): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.744+770G>A | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5677434 | |||||||
| chr11:5677491 | T | C | 1 | a0004c0004t0004g0170 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.744+713A>G | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5677491 | |||||||
| chr11:5677546 | C | T | 1 | a0001c0006t0004g0191 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.744+658G>A | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5677546 | |||||||
| chr11:5677600 | C | T | 2 | a0002c0001t0002g0051 a0002c0001t0002g0195 |
3 | NA18974.hp2 NA18997.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.744+604G>A | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5677600 | |||||||
| chr11:5677720 | C | T | 7 | a0001c0006t0016g0158 a0001c0006t0016g0250 a0001c0006t0016g0254 others(4): Show |
7 | HG01109.hp1 HG01346.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.744+484G>A | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5677720 | |||||||
| chr11:5677725 | A | G | 210 | a0001c0002t0001g0001 a0001c0002t0001g0008 a0001c0002t0001g0010 others(207): Show |
353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.744+479T>C | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5677725 | |||||||
| chr11:5677727 | C | A | 3 | a0001c0002t0001g0034 a0001c0002t0001g0118 a0001c0002t0001g0119 |
4 | HG01123.hp1 HG02293.hp2 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.744+477G>T | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5677727 | |||||||
| chr11:5677817 | C | G | 1 | a0001c0002t0040g0210 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.744+387G>C | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5677817 | |||||||
| chr11:5677965 | A | T | 1 | a0005c0005t0001g0121 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.744+239T>A | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5677965 | |||||||
| chr11:5677989 | C | G | 1 | a0001c0002t0028g0042 | 2 | HG02818.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.744+215G>C | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5677989 | |||||||
| chr11:5678031 | G | A | 1 | a0002c0001t0003g0218 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.744+173C>T | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5678031 | |||||||
| chr11:5678094 | C | T | 1 | a0001c0002t0017g0178 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.744+110G>A | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5678094 | |||||||
| chr11:5678141 | A | C | 9 | a0001c0002t0001g0097 a0001c0002t0007g0020 a0001c0002t0007g0047 others(6): Show |
13 | HG01243.hp2 HG01433.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.744+63T>G | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5678141 | |||||||
| chr11:5678194 | C | T | 1 | a0001c0002t0028g0042 | 2 | HG02818.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.744+10G>A | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 4/7 | chr11 | 5678194 | |||||||
| chr11:5678571 | C | A | 231 | a0001c0002t0001g0001 a0001c0002t0001g0008 a0001c0002t0001g0010 others(228): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.514-137G>T | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 3/7 | chr11 | 5678571 | |||||||
| chr11:5678663 | G | C | 2 | a0001c0007t0002g0019 a0001c0007t0002g0194 |
4 | HG01243.hp1 HG02970.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.514-229C>G | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 3/7 | chr11 | 5678663 | |||||||
| chr11:5678820 | A | T | 14 | a0001c0002t0009g0255 a0001c0002t0009g0256 a0001c0002t0009g0257 others(11): Show |
18 | HG00738.hp2 HG00741.hp1 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.513+254T>A | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 3/7 | chr11 | 5678820 | |||||||
| chr11:5678854 | C | A | 2 | a0005c0005t0001g0126 a0011c0019t0001g0125 |
2 | HG00140.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.513+220G>T | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 3/7 | chr11 | 5678854 | |||||||
| chr11:5678873 | C | A | 3 | a0001c0002t0017g0178 a0001c0002t0029g0135 a0001c0002t0029g0173 |
3 | HG02145.hp2 HG02615.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.513+201G>T | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 3/7 | chr11 | 5678873 | |||||||
| chr11:5678922 | C | T | 1 | a0001c0002t0001g0030 | 2 | NA18962.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.513+152G>A | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 3/7 | chr11 | 5678922 | |||||||
| chr11:5679032 | C | G | 1 | a0002c0001t0003g0077 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.513+42G>C | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 3/7 | chr11 | 5679032 | |||||||
| chr11:5679382 | G | A | 1 | a0001c0002t0001g0120 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.418-213C>T | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 2/7 | chr11 | 5679382 | |||||||
| chr11:5679401 | G | A | 21 | a0001c0002t0009g0255 a0001c0002t0009g0256 a0001c0002t0009g0257 others(18): Show |
25 | HG00738.hp2 HG00741.hp1 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.418-232C>T | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 2/7 | chr11 | 5679401 | |||||||
| chr11:5679419 | A | G | 135 | a0001c0002t0001g0001 a0001c0002t0001g0008 a0001c0002t0001g0010 others(132): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.418-250T>C | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 2/7 | chr11 | 5679419 | |||||||
| chr11:5679609 | T | C | 1 | a0002c0001t0003g0206 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.417+152A>G | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 2/7 | chr11 | 5679609 | |||||||
| chr11:5680314 | A | G | 2 | a0001c0006t0016g0158 a0001c0006t0016g0254 |
2 | HG01346.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.-61-76T>C | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5680314 | |||||||
| chr11:5680480 | T | A | 1 | a0004c0004t0004g0176 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-61-242A>T | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5680480 | |||||||
| chr11:5680528 | G | C | 8 | a0001c0002t0028g0042 a0001c0002t0029g0135 a0002c0001t0003g0077 others(5): Show |
9 | HG01109.hp1 HG02145.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.-61-290C>G | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5680528 | |||||||
| chr11:5680533 | T | G | 8 | a0001c0002t0028g0042 a0001c0002t0029g0135 a0002c0001t0003g0077 others(5): Show |
9 | HG01109.hp1 HG02145.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.-61-295A>C | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5680533 | |||||||
| chr11:5680579 | C | G | 3 | a0001c0002t0001g0029 a0001c0002t0001g0094 a0001c0002t0019g0095 |
4 | NA18966.hp1 NA18989.hp1 NA19086.hp2 others(1): Show |
intron_variant | MODIFIER | c.-61-341G>C | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5680579 | |||||||
| chr11:5680589 | G | A | 240 | a0001c0002t0001g0001 a0001c0002t0001g0008 a0001c0002t0001g0010 others(237): Show |
385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
intron_variant | MODIFIER | c.-61-351C>T | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5680589 | |||||||
| chr11:5680606 | C | G | 3 | a0002c0001t0003g0188 a0002c0001t0003g0189 a0002c0001t0003g0190 |
3 | NA18747.hp2 NA19010.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.-61-368G>C | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5680606 | |||||||
| chr11:5680616 | C | T | 3 | a0001c0002t0012g0065 a0001c0002t0012g0066 a0001c0002t0012g0067 |
3 | HG02895.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-61-378G>A | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5680616 | |||||||
| chr11:5680640 | C | A | 2 | a0001c0006t0007g0260 a0001c0006t0016g0254 |
2 | HG01884.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.-61-402G>T | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5680640 | |||||||
| chr11:5680653 | A | G | 108 | a0001c0002t0001g0247 a0001c0002t0007g0020 a0001c0002t0007g0047 others(105): Show |
173 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.-61-415T>C | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5680653 | |||||||
| chr11:5680656 | T | G | 57 | a0001c0002t0001g0247 a0001c0002t0007g0215 a0001c0002t0011g0021 others(54): Show |
101 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.-61-418A>C | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5680656 | |||||||
| chr11:5680674 | G | A | 2 | a0001c0002t0007g0215 a0002c0001t0002g0181 |
2 | HG02257.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-61-436C>T | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5680674 | |||||||
| chr11:5680712 | A | G | 3 | a0007c0009t0019g0252 a0007c0009t0019g0253 a0007c0009t0031g0251 |
3 | HG01109.hp1 HG02145.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-61-474T>C | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5680712 | |||||||
| chr11:5680760 | T | C | 143 | a0001c0002t0001g0247 a0001c0002t0007g0020 a0001c0002t0007g0047 others(140): Show |
232 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(229): Show |
intron_variant | MODIFIER | c.-61-522A>G | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5680760 | |||||||
| chr11:5680761 | G | T | 143 | a0001c0002t0001g0247 a0001c0002t0007g0020 a0001c0002t0007g0047 others(140): Show |
232 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(229): Show |
intron_variant | MODIFIER | c.-61-523C>A | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5680761 | |||||||
| chr11:5680764 | C | A | 1 | a0002c0001t0026g0064 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-61-526G>T | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5680764 | |||||||
| chr11:5680770 | G | A | 139 | a0001c0002t0001g0247 a0001c0002t0007g0020 a0001c0002t0007g0047 others(136): Show |
228 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.-61-532C>T | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5680770 | |||||||
| chr11:5680869 | G | A | 145 | a0001c0002t0001g0138 a0001c0002t0007g0020 a0001c0002t0007g0047 others(142): Show |
234 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(231): Show |
intron_variant | MODIFIER | c.-61-631C>T | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5680869 | |||||||
| chr11:5680910 | C | G | 3 | a0007c0009t0019g0252 a0007c0009t0019g0253 a0007c0009t0031g0251 |
3 | HG01109.hp1 HG02145.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-61-672G>C | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5680910 | |||||||
| chr11:5680940 | T | C | 6 | a0001c0007t0002g0152 a0001c0007t0002g0153 a0001c0007t0002g0154 others(3): Show |
8 | HG00639.hp2 HG02280.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.-61-702A>G | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5680940 | |||||||
| chr11:5680981 | C | T | 142 | a0001c0002t0001g0138 a0001c0002t0007g0020 a0001c0002t0007g0047 others(139): Show |
231 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(228): Show |
intron_variant | MODIFIER | c.-61-743G>A | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5680981 | |||||||
| chr11:5680983 | A | C | 142 | a0001c0002t0001g0138 a0001c0002t0007g0020 a0001c0002t0007g0047 others(139): Show |
231 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(228): Show |
intron_variant | MODIFIER | c.-61-745T>G | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5680983 | |||||||
| chr11:5681009 | G | C | 1 | a0001c0002t0016g0241 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-61-771C>G | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5681009 | |||||||
| chr11:5681071 | T | C | 4 | a0002c0001t0003g0077 a0004c0004t0002g0074 a0004c0004t0017g0076 others(1): Show |
4 | HG02809.hp1 HG02818.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-61-833A>G | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5681071 | |||||||
| chr11:5681103 | G | A | 148 | a0001c0002t0001g0138 a0001c0002t0007g0020 a0001c0002t0007g0047 others(145): Show |
239 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.-61-865C>T | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5681103 | |||||||
| chr11:5681113 | G | C | 75 | a0001c0002t0007g0020 a0001c0002t0007g0047 a0001c0002t0007g0048 others(72): Show |
118 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.-61-875C>G | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5681113 | |||||||
| chr11:5681140 | T | C | 148 | a0001c0002t0001g0138 a0001c0002t0007g0020 a0001c0002t0007g0047 others(145): Show |
239 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.-61-902A>G | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5681140 | |||||||
| chr11:5681160 | G | A | 148 | a0001c0002t0001g0138 a0001c0002t0007g0020 a0001c0002t0007g0047 others(145): Show |
239 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.-61-922C>T | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5681160 | |||||||
| chr11:5681212 | G | A | 60 | a0001c0002t0001g0138 a0001c0002t0007g0187 a0001c0002t0007g0215 others(57): Show |
106 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.-61-974C>T | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5681212 | |||||||
| chr11:5681232 | A | C | 233 | a0001c0002t0001g0001 a0001c0002t0001g0008 a0001c0002t0001g0010 others(230): Show |
378 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(375): Show |
intron_variant | MODIFIER | c.-61-994T>G | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5681232 | |||||||
| chr11:5681259 | T | C | 148 | a0001c0002t0001g0138 a0001c0002t0007g0020 a0001c0002t0007g0047 others(145): Show |
239 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.-61-1021A>G | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5681259 | |||||||
| chr11:5681262 | G | A | 5 | a0001c0002t0007g0020 a0001c0002t0007g0047 a0001c0002t0007g0048 others(2): Show |
9 | HG01243.hp2 HG01433.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.-61-1024C>T | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5681262 | |||||||
| chr11:5681269 | T | C | 60 | a0001c0002t0001g0138 a0001c0002t0007g0187 a0001c0002t0007g0215 others(57): Show |
106 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.-61-1031A>G | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5681269 | |||||||
| chr11:5681299 | C | G | 148 | a0001c0002t0001g0138 a0001c0002t0007g0020 a0001c0002t0007g0047 others(145): Show |
239 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.-61-1061G>C | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5681299 | |||||||
| chr11:5681300 | G | A | 1 | a0001c0006t0016g0254 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-61-1062C>T | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5681300 | |||||||
| chr11:5681328 | G | A | 2 | a0001c0002t0029g0135 a0002c0001t0041g0136 |
2 | HG02145.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-61-1090C>T | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5681328 | |||||||
| chr11:5681333 | A | G | 233 | a0001c0002t0001g0001 a0001c0002t0001g0008 a0001c0002t0001g0010 others(230): Show |
378 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(375): Show |
intron_variant | MODIFIER | c.-61-1095T>C | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5681333 | |||||||
| chr11:5681342 | C | T | 1 | a0004c0004t0002g0091 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-61-1104G>A | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5681342 | |||||||
| chr11:5681364 | A | G | 60 | a0001c0002t0001g0138 a0001c0002t0007g0187 a0001c0002t0007g0215 others(57): Show |
106 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.-61-1126T>C | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5681364 | |||||||
| chr11:5681406 | C | T | 1 | a0002c0001t0003g0186 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-61-1168G>A | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5681406 | |||||||
| chr11:5681439 | A | G | 4 | a0001c0006t0016g0250 a0007c0009t0019g0252 a0007c0009t0019g0253 others(1): Show |
4 | HG01109.hp1 HG02145.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-61-1201T>C | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5681439 | |||||||
| chr11:5681461 | A | G | 1 | a0002c0001t0003g0185 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-61-1223T>C | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5681461 | |||||||
| chr11:5681496 | T | C | 144 | a0001c0002t0001g0138 a0001c0002t0007g0020 a0001c0002t0007g0047 others(141): Show |
235 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(232): Show |
intron_variant | MODIFIER | c.-61-1258A>G | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5681496 | |||||||
| chr11:5681578 | A | C | 5 | a0001c0006t0002g0157 a0001c0006t0016g0158 a0004c0004t0002g0074 others(2): Show |
5 | HG01346.hp2 HG02486.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.-61-1340T>G | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5681578 | |||||||
| chr11:5681614 | G | A | 6 | a0001c0007t0002g0152 a0001c0007t0002g0153 a0001c0007t0002g0154 others(3): Show |
8 | HG00639.hp2 HG02280.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.-61-1376C>T | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5681614 | |||||||
| chr11:5681756 | A | ATTCCAGC others(65): Show |
17 | a0001c0002t0001g0138 a0001c0002t0007g0215 a0001c0002t0018g0209 others(14): Show |
29 | HG00323.hp1 HG01069.hp2 HG01515.hp2 others(26): Show |
intron_variant | MODIFIER | c.-61-1519_-61-1518i others(74): Show |
TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5681756 | |||||||
| chr11:5681756 | A | ATTCCAGC others(65): Show |
53 | a0001c0002t0007g0187 a0001c0002t0010g0009 a0001c0002t0010g0059 others(50): Show |
89 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.-61-1590_-61-1519d others(74): Show |
TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5681756 | |||||||
| chr11:5681838 | G | A | 5 | a0001c0002t0009g0255 a0001c0002t0009g0256 a0001c0002t0009g0257 others(2): Show |
5 | HG00738.hp2 HG00741.hp1 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.-61-1600C>T | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5681838 | |||||||
| chr11:5681884 | T | C | 140 | a0001c0002t0001g0138 a0001c0002t0007g0020 a0001c0002t0007g0047 others(137): Show |
231 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(228): Show |
intron_variant | MODIFIER | c.-61-1646A>G | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5681884 | |||||||
| chr11:5681924 | G | A | 3 | a0001c0002t0033g0070 a0002c0001t0014g0016 a0002c0001t0034g0071 |
5 | HG02647.hp1 HG02965.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-61-1686C>T | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5681924 | |||||||
| chr11:5681945 | C | T | 2 | a0001c0007t0002g0152 a0003c0003t0005g0265 |
2 | NA18953.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-61-1707G>A | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5681945 | |||||||
| chr11:5682002 | T | C | 6 | a0005c0005t0001g0006 a0005c0005t0001g0036 a0005c0005t0001g0037 others(3): Show |
14 | HG01981.hp1 HG01981.hp2 HG02004.hp1 others(11): Show |
intron_variant | MODIFIER | c.-61-1764A>G | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5682002 | |||||||
| chr11:5682093 | G | A | 140 | a0001c0002t0001g0138 a0001c0002t0007g0020 a0001c0002t0007g0047 others(137): Show |
231 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(228): Show |
intron_variant | MODIFIER | c.-61-1855C>T | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5682093 | |||||||
| chr11:5682178 | C | T | 87 | a0001c0002t0001g0001 a0001c0002t0001g0008 a0001c0002t0001g0010 others(84): Show |
141 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.-61-1940G>A | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5682178 | |||||||
| chr11:5682192 | C | T | 2 | a0001c0006t0007g0260 a0001c0006t0016g0254 |
2 | HG01884.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.-61-1954G>A | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5682192 | |||||||
| chr11:5682217 | A | C | 140 | a0001c0002t0001g0138 a0001c0002t0007g0020 a0001c0002t0007g0047 others(137): Show |
231 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(228): Show |
intron_variant | MODIFIER | c.-61-1979T>G | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5682217 | |||||||
| chr11:5682276 | G | A | 1 | a0006c0008t0001g0151 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-61-2038C>T | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5682276 | |||||||
| chr11:5682294 | T | C | 2 | a0001c0006t0002g0248 a0001c0006t0002g0249 |
2 | HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-61-2056A>G | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5682294 | |||||||
| chr11:5682328 | C | G | 140 | a0001c0002t0001g0138 a0001c0002t0007g0020 a0001c0002t0007g0047 others(137): Show |
231 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(228): Show |
intron_variant | MODIFIER | c.-61-2090G>C | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5682328 | |||||||
| chr11:5682343 | C | G | 2 | a0003c0003t0006g0039 a0003c0003t0006g0137 |
3 | NA18975.hp1 NA18991.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.-61-2105G>C | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5682343 | |||||||
| chr11:5682369 | C | T | 1 | a0002c0001t0003g0184 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.-61-2131G>A | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5682369 | |||||||
| chr11:5682459 | A | T | 5 | a0001c0002t0001g0088 a0001c0002t0001g0089 a0001c0002t0001g0090 others(2): Show |
5 | NA18942.hp2 NA18981.hp1 NA18992.hp1 others(2): Show |
intron_variant | MODIFIER | c.-61-2221T>A | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5682459 | |||||||
| chr11:5682538 | T | C | 73 | a0001c0002t0001g0138 a0001c0002t0007g0020 a0001c0002t0007g0047 others(70): Show |
116 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.-61-2300A>G | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5682538 | |||||||
| chr11:5682544 | A | G | 140 | a0001c0002t0001g0138 a0001c0002t0007g0020 a0001c0002t0007g0047 others(137): Show |
231 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(228): Show |
intron_variant | MODIFIER | c.-61-2306T>C | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5682544 | |||||||
| chr11:5682600 | C | T | 1 | a0002c0001t0003g0219 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-62+2268G>A | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5682600 | |||||||
| chr11:5682640 | T | A | 141 | a0001c0002t0001g0130 a0001c0002t0001g0138 a0001c0002t0007g0020 others(138): Show |
232 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(229): Show |
intron_variant | MODIFIER | c.-62+2228A>T | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5682640 | |||||||
| chr11:5682662 | T | C | 3 | a0006c0008t0001g0149 a0006c0008t0001g0150 a0006c0008t0001g0151 |
3 | HG01099.hp2 HG03710.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.-62+2206A>G | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5682662 | |||||||
| chr11:5682681 | A | G | 2 | a0001c0007t0002g0019 a0002c0001t0003g0159 |
4 | HG02257.hp2 HG02970.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-62+2187T>C | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5682681 | |||||||
| chr11:5682778 | C | T | 2 | a0001c0002t0029g0135 a0002c0001t0041g0136 |
2 | HG02145.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-62+2090G>A | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5682778 | |||||||
| chr11:5682779 | A | G | 140 | a0001c0002t0001g0138 a0001c0002t0007g0020 a0001c0002t0007g0047 others(137): Show |
231 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(228): Show |
intron_variant | MODIFIER | c.-62+2089T>C | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5682779 | |||||||
| chr11:5682785 | G | A | 1 | a0002c0001t0002g0242 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-62+2083C>T | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5682785 | |||||||
| chr11:5682812 | T | C | 141 | a0001c0002t0001g0138 a0001c0002t0007g0020 a0001c0002t0007g0047 others(138): Show |
233 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(230): Show |
intron_variant | MODIFIER | c.-62+2056A>G | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5682812 | |||||||
| chr11:5682816 | G | A | 1 | a0002c0001t0003g0219 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-62+2052C>T | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5682816 | |||||||
| chr11:5682850 | T | G | 1 | a0004c0004t0002g0134 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-62+2018A>C | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5682850 | |||||||
| chr11:5682851 | TGAG | T | 6 | a0001c0007t0002g0152 a0001c0007t0002g0153 a0001c0007t0002g0154 others(3): Show |
8 | HG00639.hp2 HG02280.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.-62+2014_-62+2016d others(5): Show |
TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5682851 | |||||||
| chr11:5682916 | T | C | 74 | a0001c0002t0001g0138 a0001c0002t0007g0020 a0001c0002t0007g0047 others(71): Show |
122 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.-62+1952A>G | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5682916 | |||||||
| chr11:5682980 | C | G | 140 | a0001c0002t0001g0138 a0001c0002t0007g0020 a0001c0002t0007g0047 others(137): Show |
231 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(228): Show |
intron_variant | MODIFIER | c.-62+1888G>C | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5682980 | |||||||
| chr11:5682982 | C | T | 140 | a0001c0002t0001g0138 a0001c0002t0007g0020 a0001c0002t0007g0047 others(137): Show |
231 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(228): Show |
intron_variant | MODIFIER | c.-62+1886G>A | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5682982 | |||||||
| chr11:5682990 | G | C | 140 | a0001c0002t0001g0138 a0001c0002t0007g0020 a0001c0002t0007g0047 others(137): Show |
231 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(228): Show |
intron_variant | MODIFIER | c.-62+1878C>G | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5682990 | |||||||
| chr11:5683007 | G | A | 2 | a0001c0006t0002g0157 a0001c0006t0016g0158 |
2 | HG01346.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.-62+1861C>T | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5683007 | |||||||
| chr11:5683076 | G | A | 141 | a0001c0002t0001g0138 a0001c0002t0007g0020 a0001c0002t0007g0047 others(138): Show |
232 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(229): Show |
intron_variant | MODIFIER | c.-62+1792C>T | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5683076 | |||||||
| chr11:5683116 | C | T | 1 | a0013c0018t0001g0085 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-62+1752G>A | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5683116 | |||||||
| chr11:5683138 | C | T | 4 | a0002c0001t0003g0077 a0004c0004t0002g0074 a0004c0004t0017g0076 others(1): Show |
4 | HG02809.hp1 HG02818.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-62+1730G>A | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5683138 | |||||||
| chr11:5683150 | C | G | 1 | a0001c0006t0002g0056 | 2 | HG02055.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.-62+1718G>C | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5683150 | |||||||
| chr11:5683153 | A | G | 140 | a0001c0002t0001g0138 a0001c0002t0007g0020 a0001c0002t0007g0047 others(137): Show |
231 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(228): Show |
intron_variant | MODIFIER | c.-62+1715T>C | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5683153 | |||||||
| chr11:5683167 | A | G | 144 | a0001c0002t0001g0138 a0001c0002t0007g0020 a0001c0002t0007g0047 others(141): Show |
235 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(232): Show |
intron_variant | MODIFIER | c.-62+1701T>C | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5683167 | |||||||
| chr11:5683168 | C | G | 6 | a0001c0007t0002g0152 a0001c0007t0002g0153 a0001c0007t0002g0154 others(3): Show |
8 | HG00639.hp2 HG02280.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.-62+1700G>C | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5683168 | |||||||
| chr11:5683196 | G | A | 54 | a0001c0002t0007g0187 a0001c0002t0007g0215 a0001c0002t0011g0021 others(51): Show |
95 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.-62+1672C>T | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5683196 | |||||||
| chr11:5683210 | C | T | 1 | a0004c0004t0002g0134 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-62+1658G>A | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5683210 | |||||||
| chr11:5683217 | G | C | 233 | a0001c0002t0001g0001 a0001c0002t0001g0008 a0001c0002t0001g0010 others(230): Show |
378 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(375): Show |
intron_variant | MODIFIER | c.-62+1651C>G | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5683217 | |||||||
| chr11:5683234 | C | T | 139 | a0001c0002t0001g0138 a0001c0002t0007g0020 a0001c0002t0007g0047 others(136): Show |
230 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(227): Show |
intron_variant | MODIFIER | c.-62+1634G>A | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5683234 | |||||||
| chr11:5683246 | C | T | 2 | a0005c0005t0001g0083 a0005c0005t0001g0084 |
2 | HG03669.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.-62+1622G>A | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5683246 | |||||||
| chr11:5683292 | G | A | 8 | a0001c0006t0002g0157 a0001c0006t0016g0158 a0001c0007t0002g0152 others(5): Show |
10 | HG00639.hp2 HG01346.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.-62+1576C>T | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5683292 | |||||||
| chr11:5683328 | C | A | 1 | a0002c0001t0038g0220 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.-62+1540G>T | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5683328 | |||||||
| chr11:5683333 | C | T | 140 | a0001c0002t0001g0138 a0001c0002t0007g0020 a0001c0002t0007g0047 others(137): Show |
231 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(228): Show |
intron_variant | MODIFIER | c.-62+1535G>A | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5683333 | |||||||
| chr11:5683350 | C | G | 233 | a0001c0002t0001g0001 a0001c0002t0001g0008 a0001c0002t0001g0010 others(230): Show |
378 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(375): Show |
intron_variant | MODIFIER | c.-62+1518G>C | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5683350 | |||||||
| chr11:5683362 | G | C | 1 | a0001c0002t0028g0042 | 2 | HG02818.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-62+1506C>G | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5683362 | |||||||
| chr11:5683400 | T | C | 1 | a0001c0006t0007g0260 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-62+1468A>G | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5683400 | |||||||
| chr11:5683454 | G | A | 1 | a0005c0005t0001g0131 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-62+1414C>T | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5683454 | |||||||
| chr11:5683464 | G | A | 2 | a0001c0007t0002g0019 a0002c0001t0003g0159 |
4 | HG02257.hp2 HG02970.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-62+1404C>T | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5683464 | |||||||
| chr11:5683481 | A | G | 144 | a0001c0002t0001g0138 a0001c0002t0007g0020 a0001c0002t0007g0047 others(141): Show |
235 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(232): Show |
intron_variant | MODIFIER | c.-62+1387T>C | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5683481 | |||||||
| chr11:5683506 | T | G | 144 | a0001c0002t0001g0138 a0001c0002t0007g0020 a0001c0002t0007g0047 others(141): Show |
235 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(232): Show |
intron_variant | MODIFIER | c.-62+1362A>C | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5683506 | |||||||
| chr11:5683512 | A | G | 144 | a0001c0002t0001g0138 a0001c0002t0007g0020 a0001c0002t0007g0047 others(141): Show |
235 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(232): Show |
intron_variant | MODIFIER | c.-62+1356T>C | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5683512 | |||||||
| chr11:5683516 | TTA | T | 4 | a0001c0006t0016g0250 a0007c0009t0019g0252 a0007c0009t0019g0253 others(1): Show |
4 | HG01109.hp1 HG02145.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-62+1350_-62+1351d others(4): Show |
TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5683516 | |||||||
| chr11:5683527 | G | A | 1 | a0004c0004t0004g0132 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-62+1341C>T | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5683527 | |||||||
| chr11:5683589 | A | G | 144 | a0001c0002t0001g0138 a0001c0002t0007g0020 a0001c0002t0007g0047 others(141): Show |
235 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(232): Show |
intron_variant | MODIFIER | c.-62+1279T>C | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5683589 | |||||||
| chr11:5683722 | C | T | 2 | a0002c0001t0003g0182 a0002c0001t0003g0183 |
2 | HG02071.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.-62+1146G>A | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5683722 | |||||||
| chr11:5683806 | A | G | 1 | a0012c0016t0002g0222 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-62+1062T>C | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5683806 | |||||||
| chr11:5683846 | C | A | 1 | a0001c0002t0001g0133 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-62+1022G>T | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5683846 | |||||||
| chr11:5683901 | C | A | 144 | a0001c0002t0001g0138 a0001c0002t0007g0020 a0001c0002t0007g0047 others(141): Show |
235 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(232): Show |
intron_variant | MODIFIER | c.-62+967G>T | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5683901 | |||||||
| chr11:5683915 | C | G | 144 | a0001c0002t0001g0138 a0001c0002t0007g0020 a0001c0002t0007g0047 others(141): Show |
235 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(232): Show |
intron_variant | MODIFIER | c.-62+953G>C | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5683915 | |||||||
| chr11:5683934 | A | G | 144 | a0001c0002t0001g0138 a0001c0002t0007g0020 a0001c0002t0007g0047 others(141): Show |
235 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(232): Show |
intron_variant | MODIFIER | c.-62+934T>C | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5683934 | |||||||
| chr11:5684006 | C | T | 1 | a0002c0001t0022g0221 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-62+862G>A | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5684006 | |||||||
| chr11:5684027 | G | T | 1 | a0002c0001t0002g0181 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-62+841C>A | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5684027 | |||||||
| chr11:5684077 | G | C | 233 | a0001c0002t0001g0001 a0001c0002t0001g0008 a0001c0002t0001g0010 others(230): Show |
378 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(375): Show |
intron_variant | MODIFIER | c.-62+791C>G | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5684077 | |||||||
| chr11:5684090 | T | C | 241 | a0001c0002t0001g0001 a0001c0002t0001g0008 a0001c0002t0001g0010 others(238): Show |
387 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(384): Show |
intron_variant | MODIFIER | c.-62+778A>G | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5684090 | |||||||
| chr11:5684124 | C | T | 140 | a0001c0002t0001g0138 a0001c0002t0007g0020 a0001c0002t0007g0047 others(137): Show |
231 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(228): Show |
intron_variant | MODIFIER | c.-62+744G>A | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5684124 | |||||||
| chr11:5684174 | C | T | 1 | a0005c0005t0019g0078 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.-62+694G>A | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5684174 | |||||||
| chr11:5684260 | G | A | 29 | a0001c0002t0007g0020 a0001c0002t0007g0047 a0001c0002t0007g0048 others(26): Show |
49 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(46): Show |
intron_variant | MODIFIER | c.-62+608C>T | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5684260 | |||||||
| chr11:5684324 | C | A | 52 | a0001c0002t0007g0187 a0001c0002t0007g0215 a0001c0002t0011g0021 others(49): Show |
88 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.-62+544G>T | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5684324 | |||||||
| chr11:5684420 | A | AC | 140 | a0001c0002t0001g0138 a0001c0002t0007g0020 a0001c0002t0007g0047 others(137): Show |
231 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(228): Show |
intron_variant | MODIFIER | c.-62+447dupG | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5684420 | |||||||
| chr11:5684445 | A | G | 140 | a0001c0002t0001g0138 a0001c0002t0007g0020 a0001c0002t0007g0047 others(137): Show |
231 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(228): Show |
intron_variant | MODIFIER | c.-62+423T>C | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5684445 | |||||||
| chr11:5684471 | C | T | 90 | a0001c0002t0001g0001 a0001c0002t0001g0008 a0001c0002t0001g0010 others(87): Show |
144 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.-62+397G>A | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5684471 | |||||||
| chr11:5684521 | T | C | 3 | a0001c0006t0002g0261 a0003c0003t0024g0262 a0003c0003t0024g0263 |
3 | HG01255.hp1 HG02451.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-62+347A>G | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5684521 | |||||||
| chr11:5684711 | C | T | 4 | a0002c0001t0003g0077 a0004c0004t0002g0074 a0004c0004t0017g0076 others(1): Show |
4 | HG02809.hp1 HG02818.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-62+157G>A | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5684711 | |||||||
| chr11:5684834 | C | A | 1 | a0003c0003t0008g0264 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-62+34G>T | TRIM5 | ENSG00000132256.20 | transcript | ENST00000380034.8 | protein_coding | 1/7 | chr11 | 5684834 |