Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 10612 |
| ensemblid | ENSG00000110171.21 |
| hgncid | 10064 |
| symbol | TRIM3 |
| name | tripartite motif containing 3 |
| refseq_nuc | NM_033278.4 |
| refseq_prot | NP_150594.2 |
| ensembl_nuc | ENST00000345851.8 |
| ensembl_prot | ENSP00000340797.3 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 6448613 |
| end | 6473941 |
| strand | - |
| ver | v1.2 |
| region | chr11:6448613-6473941 |
| region5000 | chr11:6443613-6478941 |
| regionname0 | TRIM3_chr11_6448613_6473941 |
| regionname5000 | TRIM3_chr11_6443613_6478941 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 744 | 377 | 90 | 80 | 138 | 18 | 49 | 102 | TRIM3_chr11_6443613_6478941 | TRIM3 | MAKRE others(739): Show |
chr11 | 6443613 | 6478941 |
| a0002 | 0/0 | 744 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | MAKRE others(739): Show |
chr11 | 6443613 | 6478941 |
| a0003 | 0/0 | 744 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | MAKRE others(739): Show |
chr11 | 6443613 | 6478941 |
| a0004 | 0/0 | 744 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TRIM3_chr11_6443613_6478941 | TRIM3 | MAKRE others(739): Show |
chr11 | 6443613 | 6478941 |
| a0005 | 0/0 | 744 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TRIM3_chr11_6443613_6478941 | TRIM3 | MAKRE others(739): Show |
chr11 | 6443613 | 6478941 |
| a0006 | 0/0 | 744 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TRIM3_chr11_6443613_6478941 | TRIM3 | MAKRE others(739): Show |
chr11 | 6443613 | 6478941 |
| a0007 | 0/0 | 744 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | MAKRE others(739): Show |
chr11 | 6443613 | 6478941 |
| a0008 | 0/0 | 744 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TRIM3_chr11_6443613_6478941 | TRIM3 | MAKRE others(739): Show |
chr11 | 6443613 | 6478941 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2232 | 306 | 61 | 61 | 133 | 13 | 36 | TRIM3_chr11_6443613_6478941 | TRIM3 | ATGGC others(2227): Show |
chr11 | 6443613 | 6478941 | ||
| a0001c0002 | 0/0 | 2232 | 60 | 26 | 16 | 5 | 4 | 9 | TRIM3_chr11_6443613_6478941 | TRIM3 | ATGGC others(2227): Show |
chr11 | 6443613 | 6478941 | ||
| a0001c0003 | 0/0 | 2232 | 4 | 1 | 1 | 0 | 0 | 2 | TRIM3_chr11_6443613_6478941 | TRIM3 | ATGGC others(2227): Show |
chr11 | 6443613 | 6478941 | ||
| a0001c0004 | 0/0 | 2232 | 2 | 1 | 1 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | ATGGC others(2227): Show |
chr11 | 6443613 | 6478941 | ||
| a0001c0005 | 0/0 | 2232 | 2 | 0 | 0 | 0 | 1 | 1 | TRIM3_chr11_6443613_6478941 | TRIM3 | ATGGC others(2227): Show |
chr11 | 6443613 | 6478941 | ||
| a0001c0011 | 0/0 | 2232 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | ATGGC others(2227): Show |
chr11 | 6443613 | 6478941 | ||
| a0001c0014 | 0/0 | 2232 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM3_chr11_6443613_6478941 | TRIM3 | ATGGC others(2227): Show |
chr11 | 6443613 | 6478941 | ||
| a0001c0015 | 0/0 | 2232 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | ATGGC others(2227): Show |
chr11 | 6443613 | 6478941 | ||
| a0002c0009 | 0/0 | 2232 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | ATGGC others(2227): Show |
chr11 | 6443613 | 6478941 | ||
| a0003c0013 | 0/0 | 2232 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM3_chr11_6443613_6478941 | TRIM3 | ATGGC others(2227): Show |
chr11 | 6443613 | 6478941 | ||
| a0004c0010 | 0/0 | 2232 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | ATGGC others(2227): Show |
chr11 | 6443613 | 6478941 | ||
| a0005c0006 | 0/0 | 2232 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | ATGGC others(2227): Show |
chr11 | 6443613 | 6478941 | ||
| a0006c0008 | 0/0 | 2232 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | ATGGC others(2227): Show |
chr11 | 6443613 | 6478941 | ||
| a0007c0007 | 0/0 | 2232 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | ATGGC others(2227): Show |
chr11 | 6443613 | 6478941 | ||
| a0008c0012 | 0/0 | 2232 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | ATGGC others(2227): Show |
chr11 | 6443613 | 6478941 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2838 | 257 | 43 | 49 | 125 | 10 | 28 | TRIM3_chr11_6443613_6478941 | TRIM3 | CTGTG others(2833): Show |
chr11 | 6443613 | 6478941 |
| a0001c0001t0002 | 0/0 | 2838 | 3 | 1 | 0 | 2 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | CTGTG others(2833): Show |
chr11 | 6443613 | 6478941 |
| a0001c0001t0003 | 0/0 | 2838 | 36 | 12 | 11 | 4 | 3 | 6 | TRIM3_chr11_6443613_6478941 | TRIM3 | CTGTG others(2833): Show |
chr11 | 6443613 | 6478941 |
| a0001c0001t0004 | 0/0 | 2838 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | CTGTG others(2833): Show |
chr11 | 6443613 | 6478941 |
| a0001c0001t0005 | 0/0 | 2838 | 5 | 5 | 0 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | CTGTG others(2833): Show |
chr11 | 6443613 | 6478941 |
| a0001c0001t0006 | 0/0 | 2838 | 2 | 0 | 1 | 0 | 0 | 1 | TRIM3_chr11_6443613_6478941 | TRIM3 | CTGTG others(2833): Show |
chr11 | 6443613 | 6478941 |
| a0001c0001t0007 | 0/0 | 2838 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | CTGTG others(2833): Show |
chr11 | 6443613 | 6478941 |
| a0001c0001t0008 | 0/0 | 2838 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM3_chr11_6443613_6478941 | TRIM3 | CTGTG others(2833): Show |
chr11 | 6443613 | 6478941 |
| a0001c0002t0001 | 0/0 | 2838 | 3 | 0 | 1 | 0 | 0 | 2 | TRIM3_chr11_6443613_6478941 | TRIM3 | CTGTG others(2833): Show |
chr11 | 6443613 | 6478941 |
| a0001c0002t0002 | 0/0 | 2838 | 38 | 17 | 10 | 2 | 3 | 6 | TRIM3_chr11_6443613_6478941 | TRIM3 | CTGTG others(2833): Show |
chr11 | 6443613 | 6478941 |
| a0001c0002t0003 | 0/0 | 2838 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | CTGTG others(2833): Show |
chr11 | 6443613 | 6478941 |
| a0001c0002t0004 | 0/0 | 2838 | 18 | 8 | 5 | 3 | 1 | 1 | TRIM3_chr11_6443613_6478941 | TRIM3 | CTGTG others(2833): Show |
chr11 | 6443613 | 6478941 |
| a0001c0003t0001 | 0/0 | 2838 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | CTGTG others(2833): Show |
chr11 | 6443613 | 6478941 |
| a0001c0003t0003 | 0/0 | 2838 | 3 | 1 | 0 | 0 | 0 | 2 | TRIM3_chr11_6443613_6478941 | TRIM3 | CTGTG others(2833): Show |
chr11 | 6443613 | 6478941 |
| a0001c0004t0001 | 0/0 | 2838 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | CTGTG others(2833): Show |
chr11 | 6443613 | 6478941 |
| a0001c0004t0002 | 0/0 | 2838 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | CTGTG others(2833): Show |
chr11 | 6443613 | 6478941 |
| a0001c0005t0002 | 0/0 | 2838 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM3_chr11_6443613_6478941 | TRIM3 | CTGTG others(2833): Show |
chr11 | 6443613 | 6478941 |
| a0001c0005t0004 | 0/0 | 2838 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | CTGTG others(2833): Show |
chr11 | 6443613 | 6478941 |
| a0001c0011t0001 | 0/0 | 2838 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | CTGTG others(2833): Show |
chr11 | 6443613 | 6478941 |
| a0001c0014t0001 | 0/0 | 2838 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM3_chr11_6443613_6478941 | TRIM3 | CTGTG others(2833): Show |
chr11 | 6443613 | 6478941 |
| a0001c0015t0002 | 0/0 | 2838 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | CTGTG others(2833): Show |
chr11 | 6443613 | 6478941 |
| a0002c0009t0001 | 0/0 | 2838 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | CTGTG others(2833): Show |
chr11 | 6443613 | 6478941 |
| a0003c0013t0001 | 0/0 | 2838 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM3_chr11_6443613_6478941 | TRIM3 | CTGTG others(2833): Show |
chr11 | 6443613 | 6478941 |
| a0004c0010t0001 | 0/0 | 2838 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | CTGTG others(2833): Show |
chr11 | 6443613 | 6478941 |
| a0005c0006t0001 | 0/0 | 2838 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | CTGTG others(2833): Show |
chr11 | 6443613 | 6478941 |
| a0006c0008t0003 | 0/0 | 2838 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | CTGTG others(2833): Show |
chr11 | 6443613 | 6478941 |
| a0007c0007t0002 | 0/0 | 2838 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | CTGTG others(2833): Show |
chr11 | 6443613 | 6478941 |
| a0008c0012t0001 | 0/0 | 2838 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | CTGTG others(2833): Show |
chr11 | 6443613 | 6478941 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 1/0 | 14 | 0 | 0 | 13 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0002 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0003 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0006 | 0/0 | 5 | 0 | 1 | 2 | 2 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0008 | 0/0 | 4 | 0 | 1 | 0 | 0 | 3 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0009 | 0/0 | 4 | 3 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0010 | 0/0 | 4 | 0 | 2 | 1 | 1 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0031 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0038 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0215 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0002g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0003g0019 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0003g0039 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0003g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0003g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0003g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0003g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0003g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0003g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0003g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0003g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0003g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0003g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0003g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0003g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0003g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0003g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0003g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0003g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0003g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0003g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0003g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0003g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0003g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0003g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0003g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0004g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0005g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0005g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0005g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0006g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0006g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0007g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0001t0008g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0002t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0002t0002g0004 | 0/0 | 6 | 0 | 1 | 0 | 2 | 3 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0002t0002g0011 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0002t0002g0040 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0002t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0002t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0002t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0002t0002g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0002t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0002t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0002t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0002t0002g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0002t0002g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0002t0002g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0002t0002g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0002t0002g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0002t0002g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0002t0002g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0002t0002g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0002t0002g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0002t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0002t0002g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0002t0002g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0002t0002g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0002t0002g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0002t0002g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0002t0002g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0002t0002g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0002t0002g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0002t0002g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0002t0003g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0002t0004g0012 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0002t0004g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0002t0004g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0002t0004g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0002t0004g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0002t0004g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0002t0004g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0002t0004g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0002t0004g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0002t0004g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0002t0004g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0002t0004g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0002t0004g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0002t0004g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0002t0004g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0003t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0003t0003g0036 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0003t0003g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0004t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0004t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0005t0002g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0005t0004g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0011t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0014t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0001c0015t0002g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0002c0009t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0003c0013t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0004c0010t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0005c0006t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0006c0008t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0007c0007t0002g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| a0008c0012t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | GBR | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0143 | EUR | GBR | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0230 | EUR | GBR | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG00140 | hp2 | a0001 | c0005 | t0004 | g0276 | EUR | GBR | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0225 | EUR | FIN | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0034 | EUR | FIN | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0128 | EUR | FIN | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG00323 | hp2 | a0001 | c0002 | t0002 | g0274 | EUR | FIN | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | CHS | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | CHS | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | CHS | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | CHS | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | CHS | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | CHS | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | CHS | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | CHS | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | CHS | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | CHS | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | CHS | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG00639 | hp1 | a0001 | c0002 | t0004 | g0291 | AMR | PUR | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0019 | AMR | PUR | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0062 | AMR | PUR | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | CHS | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | CHS | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG00733 | hp1 | a0001 | c0002 | t0002 | g0277 | AMR | PUR | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0141 | AMR | PUR | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG00738 | hp2 | a0001 | c0002 | t0002 | g0243 | AMR | PUR | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG01069 | hp2 | a0001 | c0002 | t0002 | g0011 | AMR | PUR | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0142 | AMR | PUR | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | PUR | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG01106 | hp1 | a0001 | c0001 | t0006 | g0199 | AMR | PUR | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG01109 | hp1 | a0001 | c0002 | t0002 | g0283 | AMR | PUR | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG01109 | hp2 | a0001 | c0004 | t0001 | g0133 | AMR | PUR | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG01169 | hp2 | a0001 | c0002 | t0002 | g0004 | AMR | PUR | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG01175 | hp2 | a0001 | c0015 | t0002 | g0272 | AMR | PUR | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0139 | AMR | PUR | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG01243 | hp1 | a0001 | c0002 | t0004 | g0286 | AMR | PUR | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG01243 | hp2 | a0001 | c0003 | t0001 | g0184 | AMR | PUR | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG01255 | hp1 | a0001 | c0002 | t0001 | g0151 | AMR | CLM | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0254 | AMR | CLM | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG01256 | hp2 | a0001 | c0002 | t0002 | g0278 | AMR | CLM | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG01257 | hp1 | a0001 | c0002 | t0004 | g0012 | AMR | CLM | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | CLM | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG01258 | hp1 | a0001 | c0002 | t0004 | g0012 | AMR | CLM | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | CLM | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | CLM | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0112 | AMR | CLM | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | CLM | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | CLM | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | CLM | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0120 | AMR | CLM | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG01515 | hp2 | a0001 | c0002 | t0002 | g0004 | EUR | IBS | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0144 | EUR | IBS | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0039 | EUR | IBS | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG01517 | hp1 | a0001 | c0002 | t0002 | g0004 | EUR | IBS | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG01517 | hp2 | a0001 | c0001 | t0003 | g0039 | EUR | IBS | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0089 | AFR | ACB | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG01884 | hp2 | a0001 | c0002 | t0002 | g0040 | AFR | ACB | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG01891 | hp1 | a0001 | c0002 | t0002 | g0242 | AFR | ACB | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | PEL | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG01928 | hp2 | a0001 | c0002 | t0002 | g0011 | AMR | PEL | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG01934 | hp1 | a0001 | c0002 | t0002 | g0257 | AMR | PEL | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG01943 | hp1 | a0001 | c0001 | t0003 | g0125 | AMR | PEL | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0233 | AMR | PEL | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG01952 | hp1 | a0001 | c0002 | t0002 | g0011 | AMR | PEL | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PEL | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG01975 | hp1 | a0001 | c0002 | t0004 | g0012 | AMR | PEL | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PEL | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | PEL | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PEL | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PEL | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | PEL | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PEL | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PEL | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | KHV | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG02040 | hp1 | a0001 | c0001 | t0003 | g0107 | EAS | KHV | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | ACB | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG02055 | hp2 | a0001 | c0002 | t0002 | g0282 | AFR | ACB | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | KHV | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | KHV | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | KHV | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | KHV | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | KHV | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | KHV | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | KHV | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | ACB | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | ACB | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PEL | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CDX | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | CDX | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0056 | AFR | ACB | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG02257 | hp2 | a0001 | c0002 | t0002 | g0265 | AFR | ACB | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0058 | AFR | ACB | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG02258 | hp2 | a0002 | c0009 | t0001 | g0171 | AFR | ACB | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG02273 | hp1 | a0001 | c0001 | t0003 | g0145 | AMR | PEL | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | PEL | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | ACB | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | ACB | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG02293 | hp1 | a0001 | c0001 | t0003 | g0148 | AMR | PEL | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PEL | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG02300 | hp1 | a0001 | c0002 | t0002 | g0011 | AMR | PEL | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG02300 | hp2 | a0001 | c0001 | t0003 | g0147 | AMR | PEL | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG02451 | hp1 | a0001 | c0002 | t0002 | g0292 | AFR | ACB | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | ACB | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG02572 | hp1 | a0001 | c0002 | t0002 | g0241 | AFR | GWD | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0229 | SAS | PJL | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0222 | SAS | PJL | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG02615 | hp1 | a0001 | c0002 | t0004 | g0244 | AFR | GWD | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG02615 | hp2 | a0001 | c0002 | t0002 | g0270 | AFR | GWD | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0019 | AFR | GWD | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG02622 | hp2 | a0001 | c0002 | t0004 | g0296 | AFR | GWD | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG02630 | hp1 | a0001 | c0002 | t0002 | g0295 | AFR | GWD | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG02630 | hp2 | a0001 | c0002 | t0004 | g0245 | AFR | GWD | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG02647 | hp1 | a0001 | c0011 | t0001 | g0203 | AFR | GWD | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0253 | AFR | GWD | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG02683 | hp1 | a0001 | c0001 | t0006 | g0085 | SAS | PJL | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG02698 | hp1 | a0001 | c0002 | t0002 | g0273 | SAS | PJL | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | GWD | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0061 | AFR | GWD | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG02723 | hp1 | a0001 | c0002 | t0003 | g0155 | AFR | GWD | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0121 | AFR | GWD | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG02738 | hp2 | a0001 | c0001 | t0008 | g0168 | SAS | PJL | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG02809 | hp2 | a0001 | c0002 | t0002 | g0268 | AFR | GWD | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG02818 | hp1 | a0001 | c0001 | t0005 | g0054 | AFR | GWD | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG02818 | hp2 | a0001 | c0002 | t0002 | g0246 | AFR | GWD | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | GWD | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | GWD | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0161 | AFR | GWD | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG02922 | hp1 | a0001 | c0001 | t0005 | g0017 | AFR | ESN | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | ESN | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG02965 | hp1 | a0001 | c0003 | t0003 | g0183 | AFR | ESN | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG02965 | hp2 | a0001 | c0002 | t0004 | g0290 | AFR | ESN | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | ESN | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | ESN | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0269 | AFR | ESN | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | ESN | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG03041 | hp1 | a0001 | c0001 | t0005 | g0017 | AFR | GWD | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG03041 | hp2 | a0001 | c0002 | t0004 | g0293 | AFR | GWD | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0202 | AFR | MSL | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG03098 | hp2 | a0001 | c0002 | t0002 | g0285 | AFR | MSL | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG03130 | hp1 | a0001 | c0002 | t0002 | g0288 | AFR | ESN | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG03139 | hp1 | a0001 | c0002 | t0004 | g0287 | AFR | ESN | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | ESN | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | ESN | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG03209 | hp1 | a0001 | c0001 | t0005 | g0017 | AFR | MSL | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | MSL | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG03225 | hp1 | a0001 | c0002 | t0002 | g0294 | AFR | MSL | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0173 | SAS | PJL | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG03239 | hp2 | a0001 | c0002 | t0001 | g0118 | SAS | PJL | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | MSL | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0064 | AFR | MSL | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | MSL | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG03490 | hp1 | a0001 | c0001 | t0003 | g0228 | SAS | PJL | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG03516 | hp1 | a0001 | c0002 | t0002 | g0289 | AFR | ESN | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | ESN | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG03540 | hp1 | a0001 | c0002 | t0004 | g0261 | AFR | GWD | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG03540 | hp2 | a0001 | c0002 | t0002 | g0255 | AFR | GWD | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | MSL | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG03669 | hp1 | a0001 | c0002 | t0002 | g0004 | SAS | PJL | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0126 | SAS | PJL | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | STU | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG03688 | hp2 | a0001 | c0002 | t0001 | g0134 | SAS | STU | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0156 | SAS | PJL | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0152 | SAS | BEB | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0240 | SAS | BEB | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG03834 | hp1 | a0001 | c0002 | t0004 | g0266 | SAS | BEB | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG03834 | hp2 | a0001 | c0005 | t0002 | g0275 | SAS | BEB | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG03927 | hp1 | a0001 | c0002 | t0002 | g0040 | SAS | BEB | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | BEB | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG03942 | hp1 | a0001 | c0003 | t0003 | g0036 | SAS | BEB | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0101 | SAS | BEB | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG04115 | hp1 | a0001 | c0002 | t0002 | g0004 | SAS | STU | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0041 | SAS | STU | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG04184 | hp1 | a0001 | c0001 | t0003 | g0175 | SAS | BEB | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG04184 | hp2 | a0001 | c0002 | t0002 | g0004 | SAS | BEB | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0214 | SAS | STU | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG04199 | hp2 | a0001 | c0014 | t0001 | g0157 | SAS | STU | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | STU | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0165 | SAS | STU | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG04228 | hp1 | a0003 | c0013 | t0001 | g0167 | SAS | STU | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG04228 | hp2 | a0001 | c0002 | t0002 | g0267 | SAS | STU | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | CHB | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0122 | AFR | YRI | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | YRI | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA18944 | hp1 | a0001 | c0001 | t0003 | g0113 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA18946 | hp1 | a0004 | c0010 | t0001 | g0201 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA18950 | hp1 | a0001 | c0002 | t0004 | g0258 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA18952 | hp1 | a0001 | c0002 | t0004 | g0271 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA18952 | hp2 | a0001 | c0001 | t0004 | g0263 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA18954 | hp2 | a0001 | c0002 | t0002 | g0281 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA18968 | hp2 | a0001 | c0002 | t0004 | g0279 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA18969 | hp1 | a0005 | c0006 | t0001 | g0158 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA18970 | hp2 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA18982 | hp1 | a0001 | c0002 | t0002 | g0259 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA18994 | hp2 | a0001 | c0001 | t0003 | g0047 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA19002 | hp1 | a0006 | c0008 | t0003 | g0044 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | LWK | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | LWK | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | LWK | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA19043 | hp2 | a0007 | c0007 | t0002 | g0264 | AFR | LWK | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0262 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA19077 | hp2 | a0001 | c0001 | t0007 | g0072 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA19080 | hp2 | a0008 | c0012 | t0001 | g0182 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | YRI | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0237 | AFR | YRI | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA20129 | hp1 | a0001 | c0002 | t0002 | g0284 | AFR | ASW | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA20129 | hp2 | a0001 | c0004 | t0002 | g0248 | AFR | ASW | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0010 | EUR | TSI | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0094 | EUR | TSI | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0227 | EUR | TSI | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA20805 | hp2 | a0001 | c0002 | t0004 | g0012 | EUR | TSI | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | GIH | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA20905 | hp2 | a0001 | c0003 | t0003 | g0036 | SAS | GIH | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | CLM | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | CLM | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG02109 | hp1 | a0001 | c0001 | t0005 | g0124 | AFR | ACB | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | ACB | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0050 | AFR | ACB | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | ACB | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0252 | AFR | ACB | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | MSL | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | MSL | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG06807 | hp1 | a0001 | c0002 | t0002 | g0280 | AFR | USA | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | USA | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA20300 | hp1 | a0001 | c0002 | t0004 | g0247 | AFR | USA | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | USA | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0215 | REF | REF | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0001 | REF | REF | TRIM3_chr11_6443613_6478941 | TRIM3 | chr11 | 6443613 | 6478941 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:6449047 | G | C | 1 | a0006 | 1 | NA19002.hp1 | missense_variant | MODERATE | c.2216C>G | p.Ala739Gly | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 12/12 | 2404/2838 | 2216/2235 | 739/744 | chr11 | 6449047 | |||
| chr11:6449134 | G | A | 1 | a0005 | 1 | NA18969.hp1 | missense_variant | MODERATE | c.2129C>T | p.Ala710Val | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 12/12 | 2317/2838 | 2129/2235 | 710/744 | chr11 | 6449134 | |||
| chr11:6449349 | T | C | 1 | a0002 | 1 | HG02258.hp2 | missense_variant | MODERATE | c.2039A>G | p.Asn680Ser | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 11/12 | 2227/2838 | 2039/2235 | 680/744 | chr11 | 6449349 | |||
| chr11:6450903 | C | A | 1 | a0004 | 1 | NA18946.hp1 | missense_variant | MODERATE | c.1859G>T | p.Arg620Leu | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 9/12 | 2047/2838 | 1859/2235 | 620/744 | chr11 | 6450903 | |||
| chr11:6456780 | G | C | 1 | a0008 | 1 | NA19080.hp2 | missense_variant | MODERATE | c.946C>G | p.Leu316Val | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 6/12 | 1134/2838 | 946/2235 | 316/744 | chr11 | 6456780 | |||
| chr11:6456875 | T | C | 1 | a0003 | 1 | HG04228.hp1 | missense_variant | MODERATE | c.851A>G | p.Gln284Arg | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 6/12 | 1039/2838 | 851/2235 | 284/744 | chr11 | 6456875 | |||
| chr11:6457712 | C | T | 1 | a0007 | 1 | NA19043.hp2 | missense_variant | MODERATE | c.499G>A | p.Glu167Lys | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 4/12 | 687/2838 | 499/2235 | 167/744 | chr11 | 6457712 | |||
| chr11:6465613 | C | T | 1 | a0005 | 1 | NA18969.hp1 | missense_variant | MODERATE | c.83G>A | p.Arg28Gln | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/12 | 271/2838 | 83/2235 | 28/744 | chr11 | 6465613 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:6451016 | G | A | 1 | a0001c0015 | 1 | HG01175.hp2 | synonymous_variant | LOW | c.1746C>T | p.Ala582Ala | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 9/12 | 1934/2838 | 1746/2235 | 582/744 | chr11 | 6451016 | |||
| chr11:6456586 | G | A | 1 | a0001c0011 | 1 | HG02647.hp1 | synonymous_variant | LOW | c.1140C>T | p.Asp380Asp | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 6/12 | 1328/2838 | 1140/2235 | 380/744 | chr11 | 6456586 | |||
| chr11:6456601 | C | T | 4 | a0001c0002 a0001c0005 a0001c0015 others(1): Show |
64 | HG00140.hp2 HG00323.hp2 HG00639.hp1 others(61): Show |
synonymous_variant | LOW | c.1125G>A | p.Pro375Pro | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 6/12 | 1313/2838 | 1125/2235 | 375/744 | chr11 | 6456601 | |||
| chr11:6456787 | G | C | 2 | a0001c0003 a0008c0012 |
5 | HG01243.hp2 HG02965.hp1 HG03942.hp1 others(2): Show |
synonymous_variant | LOW | c.939C>G | p.Gly313Gly | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 6/12 | 1127/2838 | 939/2235 | 313/744 | chr11 | 6456787 | |||
| chr11:6457370 | G | A | 1 | a0001c0014 | 1 | HG04199.hp2 | synonymous_variant | LOW | c.622C>T | p.Leu208Leu | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 5/12 | 810/2838 | 622/2235 | 208/744 | chr11 | 6457370 | |||
| chr11:6457389 | G | A | 4 | a0001c0002 a0001c0005 a0001c0015 others(1): Show |
64 | HG00140.hp2 HG00323.hp2 HG00639.hp1 others(61): Show |
synonymous_variant | LOW | c.603C>T | p.Ile201Ile | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 5/12 | 791/2838 | 603/2235 | 201/744 | chr11 | 6457389 | |||
| chr11:6457443 | G | A | 1 | a0001c0004 | 2 | HG01109.hp2 NA20129.hp2 |
synonymous_variant | LOW | c.549C>T | p.Val183Val | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 5/12 | 737/2838 | 549/2235 | 183/744 | chr11 | 6457443 | |||
| chr11:6458257 | T | C | 1 | a0001c0005 | 2 | HG00140.hp2 HG03834.hp2 |
synonymous_variant | LOW | c.171A>G | p.Leu57Leu | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 3/12 | 359/2838 | 171/2235 | 57/744 | chr11 | 6458257 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:6448680 | G | A | 1 | a0001c0001t0008 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*348C>T | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 12/12 | 348 | chr11 | 6448680 | ||||||
| chr11:6448827 | G | A | 7 | a0001c0001t0003 a0001c0001t0004 a0001c0002t0003 others(4): Show |
61 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*201C>T | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 12/12 | 201 | chr11 | 6448827 | ||||||
| chr11:6448857 | T | C | 1 | a0001c0001t0006 | 2 | HG01106.hp1 HG02683.hp1 |
3_prime_UTR_variant | MODIFIER | c.*171A>G | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 12/12 | 171 | chr11 | 6448857 | ||||||
| chr11:6448881 | G | A | 1 | a0001c0001t0005 | 5 | HG02109.hp1 HG02818.hp1 HG02922.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*147C>T | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 12/12 | 147 | chr11 | 6448881 | ||||||
| chr11:6465713 | C | T | 1 | a0001c0001t0007 | 1 | NA19077.hp2 | 5_prime_UTR_variant | MODIFIER | c.-18G>A | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/12 | 18 | chr11 | 6465713 | ||||||
| chr11:6465715 | C | T | 9 | a0001c0001t0002 a0001c0001t0004 a0001c0002t0002 others(6): Show |
65 | HG00140.hp2 HG00323.hp2 HG00639.hp1 others(62): Show |
5_prime_UTR_variant | MODIFIER | c.-20G>A | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/12 | 20 | chr11 | 6465715 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:6449189 | G | C | 1 | a0001c0001t0001g0207 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2083-9C>G | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 11/11 | chr11 | 6449189 | |||||||
| chr11:6449248 | G | A | 1 | a0001c0011t0001g0203 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2082+58C>T | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 11/11 | chr11 | 6449248 | |||||||
| chr11:6449292 | C | A | 1 | a0001c0001t0001g0111 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2082+14G>T | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 11/11 | chr11 | 6449292 | |||||||
| chr11:6449293 | A | G | 1 | a0001c0001t0001g0111 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2082+13T>C | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 11/11 | chr11 | 6449293 | |||||||
| chr11:6449991 | T | C | 5 | a0001c0001t0001g0035 a0001c0001t0001g0055 a0001c0001t0001g0057 others(2): Show |
6 | HG02809.hp1 HG02886.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1942-545A>G | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 10/11 | chr11 | 6449991 | |||||||
| chr11:6450016 | G | A | 2 | a0001c0002t0002g0285 a0001c0003t0001g0184 |
2 | HG01243.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1941+535C>T | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 10/11 | chr11 | 6450016 | |||||||
| chr11:6450202 | T | C | 1 | a0001c0001t0003g0056 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1941+349A>G | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 10/11 | chr11 | 6450202 | |||||||
| chr11:6450210 | T | C | 1 | a0001c0002t0002g0243 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1941+341A>G | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 10/11 | chr11 | 6450210 | |||||||
| chr11:6450360 | C | T | 7 | a0001c0001t0001g0170 a0001c0001t0001g0208 a0001c0001t0001g0233 others(4): Show |
7 | HG01943.hp2 HG02451.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1941+191G>A | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 10/11 | chr11 | 6450360 | |||||||
| chr11:6450492 | T | G | 43 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0023 others(40): Show |
52 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(49): Show |
intron_variant | MODIFIER | c.1941+59A>C | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 10/11 | chr11 | 6450492 | |||||||
| chr11:6450805 | G | A | 1 | a0001c0001t0003g0141 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1870+87C>T | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 9/11 | chr11 | 6450805 | |||||||
| chr11:6451469 | G | T | 1 | a0001c0001t0001g0150 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1534-31C>A | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 7/11 | chr11 | 6451469 | |||||||
| chr11:6451657 | G | A | 2 | a0001c0002t0002g0241 a0001c0002t0002g0242 |
2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1534-219C>T | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 7/11 | chr11 | 6451657 | |||||||
| chr11:6451684 | T | A | 1 | a0001c0001t0001g0222 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1534-246A>T | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 7/11 | chr11 | 6451684 | |||||||
| chr11:6451783 | C | T | 2 | a0001c0001t0001g0096 a0001c0001t0001g0146 |
2 | HG00741.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.1534-345G>A | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 7/11 | chr11 | 6451783 | |||||||
| chr11:6451821 | A | G | 1 | a0001c0001t0002g0269 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1534-383T>C | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 7/11 | chr11 | 6451821 | |||||||
| chr11:6451823 | T | G | 7 | a0001c0001t0001g0170 a0001c0001t0001g0208 a0001c0001t0001g0233 others(4): Show |
7 | HG01943.hp2 HG02451.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1534-385A>C | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 7/11 | chr11 | 6451823 | |||||||
| chr11:6451856 | A | C | 1 | a0001c0001t0001g0225 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1534-418T>G | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 7/11 | chr11 | 6451856 | |||||||
| chr11:6451897 | T | C | 7 | a0001c0001t0001g0204 a0001c0001t0001g0249 a0001c0001t0001g0252 others(4): Show |
9 | HG02109.hp1 HG02559.hp2 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.1534-459A>G | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 7/11 | chr11 | 6451897 | |||||||
| chr11:6451943 | T | C | 1 | a0001c0001t0008g0168 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1534-505A>G | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 7/11 | chr11 | 6451943 | |||||||
| chr11:6452176 | G | C | 3 | a0001c0001t0005g0017 a0001c0001t0005g0054 a0001c0001t0005g0124 |
5 | HG02109.hp1 HG02818.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1534-738C>G | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 7/11 | chr11 | 6452176 | |||||||
| chr11:6452308 | T | C | 2 | a0001c0001t0001g0204 a0001c0001t0001g0252 |
2 | HG02559.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1534-870A>G | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 7/11 | chr11 | 6452308 | |||||||
| chr11:6452338 | T | C | 6 | a0001c0001t0001g0204 a0001c0001t0001g0249 a0001c0001t0001g0252 others(3): Show |
8 | HG02109.hp1 HG02559.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1534-900A>G | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 7/11 | chr11 | 6452338 | |||||||
| chr11:6452423 | G | C | 2 | a0001c0001t0003g0064 a0001c0002t0004g0296 |
2 | HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1534-985C>G | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 7/11 | chr11 | 6452423 | |||||||
| chr11:6452600 | T | TGGA | 7 | a0001c0001t0001g0170 a0001c0001t0001g0208 a0001c0001t0001g0233 others(4): Show |
7 | HG01943.hp2 HG02451.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1534-1165_1534-116 others(7): Show |
TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 7/11 | chr11 | 6452600 | |||||||
| chr11:6452623 | C | T | 7 | a0001c0001t0001g0170 a0001c0001t0001g0208 a0001c0001t0001g0233 others(4): Show |
7 | HG01943.hp2 HG02451.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1534-1185G>A | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 7/11 | chr11 | 6452623 | |||||||
| chr11:6452665 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1534-1227C>T | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 7/11 | chr11 | 6452665 | |||||||
| chr11:6452705 | A | G | 1 | a0001c0001t0001g0088 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1534-1267T>C | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 7/11 | chr11 | 6452705 | |||||||
| chr11:6452715 | C | T | 1 | a0001c0001t0001g0249 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1534-1277G>A | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 7/11 | chr11 | 6452715 | |||||||
| chr11:6452740 | G | A | 1 | a0001c0001t0001g0212 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1534-1302C>T | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 7/11 | chr11 | 6452740 | |||||||
| chr11:6452762 | G | A | 6 | a0001c0001t0001g0204 a0001c0001t0001g0249 a0001c0001t0001g0252 others(3): Show |
8 | HG02109.hp1 HG02559.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1534-1324C>T | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 7/11 | chr11 | 6452762 | |||||||
| chr11:6452762 | G | T | 2 | a0001c0002t0002g0241 a0001c0002t0002g0242 |
2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1534-1324C>A | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 7/11 | chr11 | 6452762 | |||||||
| chr11:6452765 | G | A | 1 | a0001c0001t0001g0154 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1534-1327C>T | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 7/11 | chr11 | 6452765 | |||||||
| chr11:6452943 | A | G | 92 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0023 others(89): Show |
104 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.1534-1505T>C | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 7/11 | chr11 | 6452943 | |||||||
| chr11:6452949 | C | T | 3 | a0001c0001t0003g0062 a0001c0001t0003g0120 a0001c0001t0003g0121 |
3 | HG00642.hp1 HG01433.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1534-1511G>A | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 7/11 | chr11 | 6452949 | |||||||
| chr11:6453050 | G | A | 1 | a0001c0002t0002g0281 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1534-1612C>T | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 7/11 | chr11 | 6453050 | |||||||
| chr11:6453187 | C | G | 41 | a0001c0001t0001g0159 a0001c0001t0001g0170 a0001c0001t0001g0207 others(38): Show |
42 | HG00639.hp1 HG00639.hp2 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.1534-1749G>C | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 7/11 | chr11 | 6453187 | |||||||
| chr11:6453364 | C | T | 5 | a0001c0001t0001g0249 a0001c0001t0001g0252 a0001c0001t0005g0017 others(2): Show |
7 | HG02109.hp1 HG02559.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1534-1926G>A | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 7/11 | chr11 | 6453364 | |||||||
| chr11:6453459 | C | A | 5 | a0001c0001t0001g0035 a0001c0001t0001g0055 a0001c0001t0001g0057 others(2): Show |
6 | HG02809.hp1 HG02886.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1534-2021G>T | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 7/11 | chr11 | 6453459 | |||||||
| chr11:6453478 | A | G | 4 | a0001c0001t0001g0159 a0001c0001t0001g0207 a0001c0001t0001g0253 others(1): Show |
4 | HG02647.hp2 HG02717.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1534-2040T>C | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 7/11 | chr11 | 6453478 | |||||||
| chr11:6453481 | C | T | 1 | a0001c0002t0004g0291 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1534-2043G>A | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 7/11 | chr11 | 6453481 | |||||||
| chr11:6453519 | A | G | 1 | a0001c0001t0001g0188 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1534-2081T>C | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 7/11 | chr11 | 6453519 | |||||||
| chr11:6453539 | A | G | 1 | a0001c0001t0001g0252 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1534-2101T>C | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 7/11 | chr11 | 6453539 | |||||||
| chr11:6453542 | C | T | 1 | a0001c0001t0003g0237 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1534-2104G>A | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 7/11 | chr11 | 6453542 | |||||||
| chr11:6453647 | A | G | 2 | a0001c0002t0002g0285 a0001c0003t0001g0184 |
2 | HG01243.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1534-2209T>C | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 7/11 | chr11 | 6453647 | |||||||
| chr11:6453817 | A | G | 1 | a0001c0001t0001g0083 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1533+2255T>C | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 7/11 | chr11 | 6453817 | |||||||
| chr11:6453821 | G | A | 4 | a0001c0001t0003g0120 a0001c0001t0005g0017 a0001c0001t0005g0054 others(1): Show |
6 | HG01433.hp2 HG02109.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1533+2251C>T | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 7/11 | chr11 | 6453821 | |||||||
| chr11:6453826 | T | C | 3 | a0001c0001t0001g0204 a0001c0002t0002g0242 a0001c0002t0002g0284 |
3 | HG01891.hp1 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1533+2246A>G | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 7/11 | chr11 | 6453826 | |||||||
| chr11:6453870 | A | G | 178 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(175): Show |
221 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.1533+2202T>C | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 7/11 | chr11 | 6453870 | |||||||
| chr11:6453973 | C | T | 1 | a0001c0001t0001g0035 | 2 | HG02809.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1533+2099G>A | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 7/11 | chr11 | 6453973 | |||||||
| chr11:6454059 | G | A | 1 | a0001c0001t0001g0103 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1533+2013C>T | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 7/11 | chr11 | 6454059 | |||||||
| chr11:6454076 | C | T | 4 | a0001c0001t0001g0191 a0001c0001t0001g0194 a0001c0002t0002g0011 others(1): Show |
7 | HG01069.hp2 HG01928.hp2 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.1533+1996G>A | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 7/11 | chr11 | 6454076 | |||||||
| chr11:6454097 | G | A | 21 | a0001c0001t0001g0035 a0001c0001t0001g0051 a0001c0001t0001g0055 others(18): Show |
23 | HG01099.hp2 HG01884.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.1533+1975C>T | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 7/11 | chr11 | 6454097 | |||||||
| chr11:6454228 | T | G | 1 | a0001c0001t0003g0058 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1533+1844A>C | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 7/11 | chr11 | 6454228 | |||||||
| chr11:6454259 | C | T | 1 | a0001c0002t0004g0296 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1533+1813G>A | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 7/11 | chr11 | 6454259 | |||||||
| chr11:6454261 | T | A | 1 | a0001c0001t0001g0109 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1533+1811A>T | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 7/11 | chr11 | 6454261 | |||||||
| chr11:6454298 | G | A | 1 | a0001c0002t0002g0295 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1533+1774C>T | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 7/11 | chr11 | 6454298 | |||||||
| chr11:6454378 | C | T | 1 | a0001c0003t0001g0184 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1533+1694G>A | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 7/11 | chr11 | 6454378 | |||||||
| chr11:6454386 | C | CA | 22 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0060 others(19): Show |
24 | HG00323.hp1 HG00741.hp2 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.1533+1685dupT | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 7/11 | chr11 | 6454386 | |||||||
| chr11:6454386 | C | CAA | 106 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(103): Show |
136 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(133): Show |
intron_variant | MODIFIER | c.1533+1684_1533+168 others(6): Show |
TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 7/11 | chr11 | 6454386 | |||||||
| chr11:6454386 | C | CAAA | 19 | a0001c0001t0001g0046 a0001c0001t0001g0053 a0001c0001t0001g0129 others(16): Show |
19 | HG01243.hp2 HG01346.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.1533+1683_1533+168 others(7): Show |
TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 7/11 | chr11 | 6454386 | |||||||
| chr11:6454386 | CA | C | 31 | a0001c0001t0001g0028 a0001c0001t0001g0057 a0001c0001t0001g0095 others(28): Show |
34 | HG00639.hp1 HG00639.hp2 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.1533+1685delT | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 7/11 | chr11 | 6454386 | |||||||
| chr11:6454386 | CAA | C | 9 | a0001c0001t0001g0055 a0001c0001t0001g0169 a0001c0001t0001g0181 others(6): Show |
10 | HG00642.hp1 HG01433.hp2 HG01516.hp2 others(7): Show |
intron_variant | MODIFIER | c.1533+1684_1533+168 others(6): Show |
TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 7/11 | chr11 | 6454386 | |||||||
| chr11:6454619 | A | G | 1 | a0001c0001t0003g0061 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1533+1453T>C | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 7/11 | chr11 | 6454619 | |||||||
| chr11:6454646 | C | T | 4 | a0001c0001t0001g0213 a0001c0001t0001g0216 a0001c0001t0001g0217 others(1): Show |
4 | HG01074.hp2 HG01123.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.1533+1426G>A | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 7/11 | chr11 | 6454646 | |||||||
| chr11:6454709 | A | T | 63 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0049 others(60): Show |
73 | HG00639.hp1 HG00639.hp2 HG00642.hp1 others(70): Show |
intron_variant | MODIFIER | c.1533+1363T>A | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 7/11 | chr11 | 6454709 | |||||||
| chr11:6454718 | C | T | 2 | a0001c0001t0001g0100 a0001c0001t0001g0106 |
2 | HG00544.hp1 HG00673.hp2 |
intron_variant | MODIFIER | c.1533+1354G>A | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 7/11 | chr11 | 6454718 | |||||||
| chr11:6454719 | G | A | 2 | a0001c0001t0001g0114 a0001c0001t0001g0160 |
2 | HG00408.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.1533+1353C>T | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 7/11 | chr11 | 6454719 | |||||||
| chr11:6454879 | G | A | 2 | a0001c0002t0002g0280 a0001c0002t0002g0283 |
2 | HG01109.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1533+1193C>T | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 7/11 | chr11 | 6454879 | |||||||
| chr11:6454939 | C | T | 1 | a0001c0001t0001g0074 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1533+1133G>A | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 7/11 | chr11 | 6454939 | |||||||
| chr11:6454958 | G | C | 1 | a0001c0001t0001g0212 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1533+1114C>G | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 7/11 | chr11 | 6454958 | |||||||
| chr11:6455161 | A | T | 1 | a0001c0001t0001g0099 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1533+911T>A | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 7/11 | chr11 | 6455161 | |||||||
| chr11:6455231 | C | T | 36 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0049 others(33): Show |
44 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.1533+841G>A | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 7/11 | chr11 | 6455231 | |||||||
| chr11:6455267 | CAT | C | 91 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0049 others(88): Show |
112 | HG00140.hp2 HG00323.hp2 HG00639.hp1 others(109): Show |
intron_variant | MODIFIER | c.1533+803_1533+804d others(4): Show |
TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 7/11 | chr11 | 6455267 | |||||||
| chr11:6455465 | A | G | 1 | a0001c0001t0001g0252 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1533+607T>C | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 7/11 | chr11 | 6455465 | |||||||
| chr11:6455642 | T | A | 1 | a0001c0001t0001g0132 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1533+430A>T | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 7/11 | chr11 | 6455642 | |||||||
| chr11:6455742 | G | A | 1 | a0001c0005t0004g0276 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1533+330C>T | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 7/11 | chr11 | 6455742 | |||||||
| chr11:6455901 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1533+171C>T | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 7/11 | chr11 | 6455901 | |||||||
| chr11:6455946 | TTAAGGAA others(12): Show |
T | 53 | a0001c0001t0001g0256 a0001c0002t0001g0118 a0001c0002t0001g0134 others(50): Show |
65 | HG00140.hp2 HG00323.hp2 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.1533+107_1533+125d others(21): Show |
TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 7/11 | chr11 | 6455946 | |||||||
| chr11:6455954 | C | T | 1 | a0001c0001t0001g0132 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1533+118G>A | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 7/11 | chr11 | 6455954 | |||||||
| chr11:6455970 | G | A | 1 | a0001c0002t0002g0274 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1533+102C>T | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 7/11 | chr11 | 6455970 | |||||||
| chr11:6456213 | T | C | 41 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0049 others(38): Show |
50 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.1430-38A>G | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 6/11 | chr11 | 6456213 | |||||||
| chr11:6456225 | C | T | 55 | a0001c0001t0001g0132 a0001c0001t0001g0250 a0001c0001t0001g0253 others(52): Show |
67 | HG00140.hp2 HG00323.hp2 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.1430-50G>A | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 6/11 | chr11 | 6456225 | |||||||
| chr11:6456246 | C | A | 1 | a0001c0001t0001g0132 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1429+51G>T | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 6/11 | chr11 | 6456246 | |||||||
| chr11:6457151 | T | G | 37 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0049 others(34): Show |
45 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.697-122A>C | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 5/11 | chr11 | 6457151 | |||||||
| chr11:6457154 | C | T | 52 | a0001c0002t0001g0118 a0001c0002t0001g0134 a0001c0002t0001g0151 others(49): Show |
64 | HG00140.hp2 HG00323.hp2 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.697-125G>A | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 5/11 | chr11 | 6457154 | |||||||
| chr11:6457533 | C | A | 13 | a0001c0001t0001g0051 a0001c0001t0001g0055 a0001c0001t0001g0057 others(10): Show |
14 | HG00639.hp2 HG02145.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.516-57G>T | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 4/11 | chr11 | 6457533 | |||||||
| chr11:6457539 | C | T | 1 | a0001c0001t0005g0054 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.516-63G>A | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 4/11 | chr11 | 6457539 | |||||||
| chr11:6457680 | C | G | 1 | a0001c0001t0001g0181 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.515+16G>C | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 4/11 | chr11 | 6457680 | |||||||
| chr11:6457870 | G | A | 1 | a0001c0001t0001g0088 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.364-23C>T | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 3/11 | chr11 | 6457870 | |||||||
| chr11:6457891 | C | T | 7 | a0001c0001t0001g0035 a0001c0001t0001g0159 a0001c0001t0001g0179 others(4): Show |
8 | HG02280.hp1 HG02486.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.364-44G>A | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 3/11 | chr11 | 6457891 | |||||||
| chr11:6457918 | C | G | 1 | a0001c0001t0005g0124 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.364-71G>C | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 3/11 | chr11 | 6457918 | |||||||
| chr11:6458449 | C | T | 1 | a0001c0001t0001g0105 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.132-153G>A | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6458449 | |||||||
| chr11:6458514 | G | C | 2 | a0001c0001t0001g0135 a0001c0001t0003g0039 |
3 | HG01516.hp2 HG01517.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.132-218C>G | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6458514 | |||||||
| chr11:6458554 | T | G | 1 | a0001c0001t0001g0149 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.132-258A>C | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6458554 | |||||||
| chr11:6458581 | T | C | 1 | a0001c0001t0001g0229 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.132-285A>G | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6458581 | |||||||
| chr11:6458794 | G | A | 1 | a0001c0001t0001g0249 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.132-498C>T | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6458794 | |||||||
| chr11:6458812 | G | A | 1 | a0001c0002t0002g0277 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.132-516C>T | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6458812 | |||||||
| chr11:6458814 | T | TG | 8 | a0001c0001t0001g0035 a0001c0001t0001g0159 a0001c0001t0001g0179 others(5): Show |
9 | HG02280.hp1 HG02486.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.132-519dupC | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6458814 | |||||||
| chr11:6458833 | A | G | 105 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0035 others(102): Show |
127 | HG00140.hp2 HG00323.hp2 HG00639.hp1 others(124): Show |
intron_variant | MODIFIER | c.132-537T>C | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6458833 | |||||||
| chr11:6458908 | C | G | 2 | a0001c0001t0001g0250 a0001c0001t0001g0253 |
2 | HG02647.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.132-612G>C | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6458908 | |||||||
| chr11:6459065 | C | T | 2 | a0001c0001t0001g0117 a0001c0001t0003g0152 |
2 | HG02698.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.132-769G>A | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6459065 | |||||||
| chr11:6459147 | C | T | 4 | a0001c0003t0001g0184 a0001c0003t0003g0036 a0001c0003t0003g0183 others(1): Show |
5 | HG01243.hp2 HG02965.hp1 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.132-851G>A | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6459147 | |||||||
| chr11:6459366 | C | A | 4 | a0001c0003t0001g0184 a0001c0003t0003g0036 a0001c0003t0003g0183 others(1): Show |
5 | HG01243.hp2 HG02965.hp1 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.132-1070G>T | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6459366 | |||||||
| chr11:6459524 | C | G | 29 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0022 others(26): Show |
39 | HG00438.hp1 HG00673.hp1 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.132-1228G>C | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6459524 | |||||||
| chr11:6459661 | T | C | 1 | a0001c0003t0003g0036 | 2 | HG03942.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.132-1365A>G | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6459661 | |||||||
| chr11:6459674 | T | C | 1 | a0001c0001t0001g0195 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.132-1378A>G | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6459674 | |||||||
| chr11:6459906 | C | T | 1 | a0001c0001t0003g0237 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.132-1610G>A | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6459906 | |||||||
| chr11:6459987 | G | A | 1 | a0001c0001t0006g0085 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.132-1691C>T | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6459987 | |||||||
| chr11:6460040 | G | C | 1 | a0001c0001t0001g0115 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.132-1744C>G | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6460040 | |||||||
| chr11:6460132 | C | G | 4 | a0001c0003t0001g0184 a0001c0003t0003g0036 a0001c0003t0003g0183 others(1): Show |
5 | HG01243.hp2 HG02965.hp1 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.132-1836G>C | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6460132 | |||||||
| chr11:6460278 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.132-1982G>A | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6460278 | |||||||
| chr11:6460332 | C | T | 4 | a0001c0003t0001g0184 a0001c0003t0003g0036 a0001c0003t0003g0183 others(1): Show |
5 | HG01243.hp2 HG02965.hp1 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.132-2036G>A | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6460332 | |||||||
| chr11:6460333 | C | G | 4 | a0001c0003t0001g0184 a0001c0003t0003g0036 a0001c0003t0003g0183 others(1): Show |
5 | HG01243.hp2 HG02965.hp1 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.132-2037G>C | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6460333 | |||||||
| chr11:6460370 | AAG | A | 3 | a0001c0001t0001g0005 a0001c0001t0001g0116 a0001c0001t0001g0163 |
7 | HG02040.hp2 HG02155.hp1 NA18981.hp1 others(4): Show |
intron_variant | MODIFIER | c.132-2076_132-2075d others(4): Show |
TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6460370 | |||||||
| chr11:6460469 | G | A | 4 | a0001c0003t0001g0184 a0001c0003t0003g0036 a0001c0003t0003g0183 others(1): Show |
5 | HG01243.hp2 HG02965.hp1 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.132-2173C>T | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6460469 | |||||||
| chr11:6460665 | C | A | 4 | a0001c0003t0001g0184 a0001c0003t0003g0036 a0001c0003t0003g0183 others(1): Show |
5 | HG01243.hp2 HG02965.hp1 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.132-2369G>T | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6460665 | |||||||
| chr11:6460797 | A | C | 4 | a0001c0003t0001g0184 a0001c0003t0003g0036 a0001c0003t0003g0183 others(1): Show |
5 | HG01243.hp2 HG02965.hp1 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.132-2501T>G | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6460797 | |||||||
| chr11:6460851 | T | C | 7 | a0001c0002t0002g0241 a0001c0002t0002g0242 a0001c0002t0002g0243 others(4): Show |
7 | HG00738.hp2 HG01891.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.132-2555A>G | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6460851 | |||||||
| chr11:6460875 | C | T | 4 | a0001c0003t0001g0184 a0001c0003t0003g0036 a0001c0003t0003g0183 others(1): Show |
5 | HG01243.hp2 HG02965.hp1 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.132-2579G>A | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6460875 | |||||||
| chr11:6460898 | C | CT | 28 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0026 others(25): Show |
31 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(28): Show |
intron_variant | MODIFIER | c.132-2603dupA | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6460898 | |||||||
| chr11:6460898 | CT | C | 51 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0018 others(48): Show |
62 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(59): Show |
intron_variant | MODIFIER | c.132-2603delA | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6460898 | |||||||
| chr11:6460898 | CTTTT | C | 80 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0035 others(77): Show |
101 | HG00140.hp2 HG00323.hp2 HG00639.hp1 others(98): Show |
intron_variant | MODIFIER | c.132-2606_132-2603d others(6): Show |
TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6460898 | |||||||
| chr11:6460898 | CTTTTT | C | 10 | a0001c0001t0001g0095 a0001c0001t0001g0159 a0001c0001t0001g0181 others(7): Show |
10 | HG00642.hp1 HG01168.hp2 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.132-2607_132-2603d others(7): Show |
TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6460898 | |||||||
| chr11:6460898 | CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0001g0207 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.132-2616_132-2603d others(16): Show |
TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6460898 | |||||||
| chr11:6460991 | C | T | 1 | a0001c0001t0001g0132 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.132-2695G>A | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6460991 | |||||||
| chr11:6460999 | G | A | 4 | a0001c0002t0002g0280 a0001c0002t0002g0282 a0001c0002t0002g0283 others(1): Show |
4 | HG01109.hp1 HG02055.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.132-2703C>T | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6460999 | |||||||
| chr11:6461009 | G | A | 1 | a0001c0001t0003g0064 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.132-2713C>T | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6461009 | |||||||
| chr11:6461080 | A | G | 1 | a0001c0001t0001g0052 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.132-2784T>C | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6461080 | |||||||
| chr11:6461218 | T | C | 1 | a0001c0001t0001g0249 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.132-2922A>G | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6461218 | |||||||
| chr11:6461243 | C | T | 4 | a0001c0003t0001g0184 a0001c0003t0003g0036 a0001c0003t0003g0183 others(1): Show |
5 | HG01243.hp2 HG02965.hp1 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.132-2947G>A | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6461243 | |||||||
| chr11:6461265 | T | C | 1 | a0001c0001t0001g0236 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.132-2969A>G | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6461265 | |||||||
| chr11:6461296 | G | T | 4 | a0001c0003t0001g0184 a0001c0003t0003g0036 a0001c0003t0003g0183 others(1): Show |
5 | HG01243.hp2 HG02965.hp1 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.132-3000C>A | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6461296 | |||||||
| chr11:6461297 | TG | T | 24 | a0001c0002t0002g0040 a0001c0002t0002g0241 a0001c0002t0002g0242 others(21): Show |
25 | HG00639.hp1 HG00738.hp2 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.132-3002delC | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6461297 | |||||||
| chr11:6461361 | A | T | 1 | a0001c0001t0001g0098 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.132-3065T>A | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6461361 | |||||||
| chr11:6461482 | C | A | 2 | a0001c0003t0003g0036 a0008c0012t0001g0182 |
3 | HG03942.hp1 NA19080.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.132-3186G>T | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6461482 | |||||||
| chr11:6461483 | G | C | 151 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0009 others(148): Show |
191 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.132-3187C>G | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6461483 | |||||||
| chr11:6461634 | C | G | 1 | a0001c0001t0001g0144 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.132-3338G>C | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6461634 | |||||||
| chr11:6461641 | A | T | 2 | a0001c0003t0001g0184 a0001c0003t0003g0183 |
2 | HG01243.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.132-3345T>A | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6461641 | |||||||
| chr11:6461691 | C | T | 5 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0001g0208 others(2): Show |
5 | HG01346.hp1 HG02896.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.132-3395G>A | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6461691 | |||||||
| chr11:6461980 | A | T | 3 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0123 |
5 | HG01070.hp2 HG01123.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.131+3585T>A | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6461980 | |||||||
| chr11:6461999 | C | T | 4 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0252 others(1): Show |
4 | HG02486.hp2 HG02559.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.131+3566G>A | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6461999 | |||||||
| chr11:6462030 | G | A | 2 | a0001c0001t0001g0204 a0001c0011t0001g0203 |
2 | HG02647.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.131+3535C>T | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6462030 | |||||||
| chr11:6462046 | C | T | 1 | a0001c0002t0004g0290 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.131+3519G>A | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6462046 | |||||||
| chr11:6462059 | G | A | 2 | a0001c0001t0001g0251 a0001c0001t0001g0252 |
2 | HG02486.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.131+3506C>T | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6462059 | |||||||
| chr11:6462062 | C | A | 1 | a0001c0002t0002g0281 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.131+3503G>T | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6462062 | |||||||
| chr11:6462127 | C | G | 1 | a0001c0001t0001g0041 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.131+3438G>C | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6462127 | |||||||
| chr11:6462211 | A | T | 4 | a0001c0003t0001g0184 a0001c0003t0003g0036 a0001c0003t0003g0183 others(1): Show |
5 | HG01243.hp2 HG02965.hp1 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.131+3354T>A | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6462211 | |||||||
| chr11:6462235 | T | C | 2 | a0001c0001t0001g0051 a0001c0001t0001g0063 |
2 | HG02145.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.131+3330A>G | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6462235 | |||||||
| chr11:6462236 | C | CTT | 120 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0013 others(117): Show |
147 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.131+3328_131+3329i others(4): Show |
TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6462236 | |||||||
| chr11:6462280 | C | A | 156 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0010 others(153): Show |
190 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(187): Show |
intron_variant | MODIFIER | c.131+3285G>T | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6462280 | |||||||
| chr11:6462533 | G | A | 54 | a0001c0001t0001g0256 a0001c0001t0002g0260 a0001c0001t0002g0262 others(51): Show |
66 | HG00140.hp2 HG00323.hp2 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.131+3032C>T | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6462533 | |||||||
| chr11:6462660 | C | T | 5 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0001g0208 others(2): Show |
5 | HG01346.hp1 HG02896.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.131+2905G>A | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6462660 | |||||||
| chr11:6462669 | C | G | 1 | a0001c0001t0001g0181 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.131+2896G>C | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6462669 | |||||||
| chr11:6462700 | C | T | 2 | a0001c0001t0001g0140 a0001c0001t0001g0143 |
2 | HG00099.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.131+2865G>A | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6462700 | |||||||
| chr11:6462799 | G | A | 3 | a0001c0001t0001g0069 a0001c0001t0001g0087 a0001c0001t0001g0088 |
3 | HG02071.hp1 NA18947.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.131+2766C>T | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6462799 | |||||||
| chr11:6462910 | T | C | 2 | a0001c0001t0001g0075 a0001c0001t0001g0096 |
2 | HG00741.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.131+2655A>G | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6462910 | |||||||
| chr11:6462935 | G | A | 54 | a0001c0001t0001g0256 a0001c0001t0002g0260 a0001c0001t0002g0262 others(51): Show |
66 | HG00140.hp2 HG00323.hp2 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.131+2630C>T | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6462935 | |||||||
| chr11:6462972 | T | C | 1 | a0001c0003t0003g0036 | 2 | HG03942.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.131+2593A>G | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6462972 | |||||||
| chr11:6462979 | G | C | 3 | a0001c0001t0001g0008 a0001c0001t0001g0042 a0001c0001t0001g0048 |
6 | HG01069.hp1 HG01070.hp1 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.131+2586C>G | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6462979 | |||||||
| chr11:6463049 | G | A | 119 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0018 others(116): Show |
144 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.131+2516C>T | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6463049 | |||||||
| chr11:6463076 | G | T | 1 | a0001c0001t0001g0097 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.131+2489C>A | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6463076 | |||||||
| chr11:6463078 | G | A | 56 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0018 others(53): Show |
68 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.131+2487C>T | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6463078 | |||||||
| chr11:6463085 | G | A | 4 | a0001c0003t0001g0184 a0001c0003t0003g0036 a0001c0003t0003g0183 others(1): Show |
5 | HG01243.hp2 HG02965.hp1 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.131+2480C>T | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6463085 | |||||||
| chr11:6463113 | G | A | 3 | a0001c0001t0001g0035 a0001c0001t0001g0179 a0001c0001t0001g0180 |
4 | HG02280.hp1 HG02809.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.131+2452C>T | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6463113 | |||||||
| chr11:6463257 | G | A | 119 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0018 others(116): Show |
144 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.131+2308C>T | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6463257 | |||||||
| chr11:6463270 | A | T | 1 | a0001c0001t0001g0186 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.131+2295T>A | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6463270 | |||||||
| chr11:6463290 | T | C | 8 | a0001c0002t0002g0241 a0001c0002t0002g0242 a0001c0002t0002g0243 others(5): Show |
8 | HG00738.hp2 HG01891.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.131+2275A>G | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6463290 | |||||||
| chr11:6463472 | A | G | 1 | a0001c0001t0002g0260 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.131+2093T>C | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6463472 | |||||||
| chr11:6463553 | AG | A | 3 | a0001c0001t0001g0249 a0001c0003t0003g0036 a0008c0012t0001g0182 |
4 | HG03195.hp1 HG03942.hp1 NA19080.hp2 others(1): Show |
intron_variant | MODIFIER | c.131+2011delC | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6463553 | |||||||
| chr11:6463578 | T | C | 1 | a0001c0001t0003g0237 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.131+1987A>G | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6463578 | |||||||
| chr11:6463610 | C | T | 2 | a0001c0003t0003g0036 a0008c0012t0001g0182 |
3 | HG03942.hp1 NA19080.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.131+1955G>A | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6463610 | |||||||
| chr11:6463629 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.131+1936C>T | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6463629 | |||||||
| chr11:6463835 | G | A | 1 | a0001c0001t0003g0089 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.131+1730C>T | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6463835 | |||||||
| chr11:6463881 | A | G | 54 | a0001c0001t0001g0256 a0001c0001t0002g0260 a0001c0001t0002g0262 others(51): Show |
66 | HG00140.hp2 HG00323.hp2 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.131+1684T>C | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6463881 | |||||||
| chr11:6464030 | G | A | 14 | a0001c0001t0001g0009 a0001c0001t0001g0164 a0001c0001t0001g0165 others(11): Show |
19 | HG02258.hp2 HG02451.hp2 HG02738.hp2 others(16): Show |
intron_variant | MODIFIER | c.131+1535C>T | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6464030 | |||||||
| chr11:6464167 | G | A | 1 | a0001c0001t0001g0205 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.131+1398C>T | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6464167 | |||||||
| chr11:6464420 | T | G | 2 | a0001c0003t0003g0036 a0008c0012t0001g0182 |
3 | HG03942.hp1 NA19080.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.131+1145A>C | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6464420 | |||||||
| chr11:6464439 | A | G | 56 | a0001c0001t0001g0181 a0001c0001t0001g0249 a0001c0001t0001g0256 others(53): Show |
68 | HG00140.hp2 HG00323.hp2 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.131+1126T>C | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6464439 | |||||||
| chr11:6464594 | T | A | 1 | a0001c0001t0001g0208 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.131+971A>T | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6464594 | |||||||
| chr11:6464660 | T | G | 2 | a0001c0003t0003g0036 a0008c0012t0001g0182 |
3 | HG03942.hp1 NA19080.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.131+905A>C | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6464660 | |||||||
| chr11:6464852 | C | T | 1 | a0001c0001t0001g0249 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.131+713G>A | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6464852 | |||||||
| chr11:6464856 | G | A | 1 | a0001c0001t0003g0064 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.131+709C>T | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6464856 | |||||||
| chr11:6464881 | G | A | 2 | a0001c0003t0003g0036 a0008c0012t0001g0182 |
3 | HG03942.hp1 NA19080.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.131+684C>T | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6464881 | |||||||
| chr11:6464939 | A | G | 2 | a0001c0003t0003g0036 a0008c0012t0001g0182 |
3 | HG03942.hp1 NA19080.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.131+626T>C | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6464939 | |||||||
| chr11:6464941 | C | T | 54 | a0001c0001t0001g0249 a0001c0001t0002g0260 a0001c0001t0002g0262 others(51): Show |
66 | HG00140.hp2 HG00323.hp2 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.131+624G>A | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6464941 | |||||||
| chr11:6464944 | G | A | 3 | a0001c0001t0001g0035 a0001c0001t0001g0179 a0001c0001t0001g0180 |
4 | HG02280.hp1 HG02809.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.131+621C>T | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6464944 | |||||||
| chr11:6464986 | C | CA | 25 | a0001c0001t0001g0002 a0001c0001t0001g0031 a0001c0001t0001g0067 others(22): Show |
31 | HG00323.hp1 HG01074.hp2 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.131+578dupT | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6464986 | |||||||
| chr11:6464986 | C | CAA | 44 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0018 others(41): Show |
56 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(53): Show |
intron_variant | MODIFIER | c.131+577_131+578dup others(2): Show |
TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6464986 | |||||||
| chr11:6464986 | C | CAAA | 7 | a0001c0001t0001g0190 a0001c0001t0001g0211 a0001c0001t0001g0212 others(4): Show |
7 | HG00741.hp2 HG01099.hp2 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.131+576_131+578dup others(3): Show |
TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6464986 | |||||||
| chr11:6464986 | CA | C | 16 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0094 others(13): Show |
17 | HG00738.hp2 HG00741.hp1 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.131+578delT | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6464986 | |||||||
| chr11:6464986 | CAA | C | 49 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0252 others(46): Show |
61 | HG00140.hp2 HG00323.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.131+577_131+578del others(2): Show |
TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6464986 | |||||||
| chr11:6465201 | A | T | 2 | a0001c0001t0001g0032 a0001c0001t0001g0137 |
3 | HG00735.hp1 HG01099.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.131+364T>A | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6465201 | |||||||
| chr11:6465409 | C | A | 2 | a0001c0003t0001g0184 a0001c0003t0003g0183 |
2 | HG01243.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.131+156G>T | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6465409 | |||||||
| chr11:6465479 | T | C | 2 | a0001c0003t0001g0184 a0001c0003t0003g0183 |
2 | HG01243.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.131+86A>G | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6465479 | |||||||
| chr11:6465483 | CCCTCACC others(21): Show |
C | 1 | a0001c0001t0003g0064 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.131+54_131+81delAT others(26): Show |
TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | 6465483 | |||||||
| chr11:6465944 | T | C | 2 | a0001c0001t0001g0132 a0001c0004t0001g0133 |
2 | HG01109.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-37-212A>G | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 1/11 | chr11 | 6465944 | |||||||
| chr11:6465959 | C | G | 2 | a0001c0001t0003g0141 a0001c0001t0003g0142 |
2 | HG00735.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.-37-227G>C | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 1/11 | chr11 | 6465959 | |||||||
| chr11:6465983 | C | T | 1 | a0001c0001t0001g0181 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-37-251G>A | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 1/11 | chr11 | 6465983 | |||||||
| chr11:6466067 | C | T | 1 | a0001c0001t0001g0071 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-37-335G>A | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 1/11 | chr11 | 6466067 | |||||||
| chr11:6466362 | G | T | 1 | a0001c0001t0001g0140 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-37-630C>A | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 1/11 | chr11 | 6466362 | |||||||
| chr11:6466423 | A | C | 1 | a0001c0001t0001g0091 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-37-691T>G | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 1/11 | chr11 | 6466423 | |||||||
| chr11:6466476 | C | T | 2 | a0001c0003t0003g0036 a0008c0012t0001g0182 |
3 | HG03942.hp1 NA19080.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.-37-744G>A | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 1/11 | chr11 | 6466476 | |||||||
| chr11:6466538 | A | G | 2 | a0001c0001t0001g0070 a0001c0001t0001g0090 |
2 | HG02027.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.-37-806T>C | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 1/11 | chr11 | 6466538 | |||||||
| chr11:6466570 | C | G | 27 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0022 others(24): Show |
36 | HG00438.hp1 HG00673.hp1 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.-37-838G>C | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 1/11 | chr11 | 6466570 | |||||||
| chr11:6466592 | G | GT | 7 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 others(4): Show |
7 | HG01255.hp2 HG01361.hp1 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.-37-861_-37-860ins others(1): Show |
TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 1/11 | chr11 | 6466592 | |||||||
| chr11:6466593 | G | GT | 62 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0018 others(59): Show |
77 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.-37-862dupA | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 1/11 | chr11 | 6466593 | |||||||
| chr11:6466593 | G | GTT | 62 | a0001c0001t0001g0035 a0001c0001t0001g0159 a0001c0001t0001g0179 others(59): Show |
75 | HG00140.hp2 HG00323.hp2 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.-37-863_-37-862dup others(2): Show |
TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 1/11 | chr11 | 6466593 | |||||||
| chr11:6466593 | G | GTTT | 8 | a0001c0002t0002g0241 a0001c0002t0002g0259 a0001c0002t0002g0282 others(5): Show |
8 | HG01109.hp1 HG01243.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.-37-864_-37-862dup others(3): Show |
TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 1/11 | chr11 | 6466593 | |||||||
| chr11:6466593 | G | T | 7 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 others(4): Show |
7 | HG01255.hp2 HG01361.hp1 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.-37-861C>A | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 1/11 | chr11 | 6466593 | |||||||
| chr11:6466871 | G | C | 56 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0018 others(53): Show |
68 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.-37-1139C>G | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 1/11 | chr11 | 6466871 | |||||||
| chr11:6466985 | T | C | 1 | a0001c0002t0001g0134 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-37-1253A>G | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 1/11 | chr11 | 6466985 | |||||||
| chr11:6467127 | A | G | 3 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 |
3 | NA18962.hp1 NA18997.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.-37-1395T>C | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 1/11 | chr11 | 6467127 | |||||||
| chr11:6467316 | T | C | 1 | a0001c0003t0003g0036 | 2 | HG03942.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-37-1584A>G | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 1/11 | chr11 | 6467316 | |||||||
| chr11:6467318 | G | A | 1 | a0001c0001t0001g0135 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-37-1586C>T | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 1/11 | chr11 | 6467318 | |||||||
| chr11:6467341 | G | T | 1 | a0001c0001t0001g0159 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-37-1609C>A | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 1/11 | chr11 | 6467341 | |||||||
| chr11:6467546 | G | A | 2 | a0001c0001t0001g0136 a0001c0001t0001g0176 |
2 | HG00738.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.-37-1814C>T | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 1/11 | chr11 | 6467546 | |||||||
| chr11:6467698 | G | A | 1 | a0001c0001t0003g0064 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-37-1966C>T | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 1/11 | chr11 | 6467698 | |||||||
| chr11:6467790 | C | T | 4 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0003g0202 others(1): Show |
4 | HG02647.hp1 HG03098.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-37-2058G>A | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 1/11 | chr11 | 6467790 | |||||||
| chr11:6467804 | G | A | 2 | a0001c0001t0001g0032 a0001c0001t0001g0137 |
3 | HG00735.hp1 HG01099.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.-37-2072C>T | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 1/11 | chr11 | 6467804 | |||||||
| chr11:6468049 | T | C | 1 | a0008c0012t0001g0182 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.-37-2317A>G | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 1/11 | chr11 | 6468049 | |||||||
| chr11:6468309 | C | T | 6 | a0001c0001t0001g0035 a0001c0001t0001g0159 a0001c0001t0001g0179 others(3): Show |
7 | HG02280.hp1 HG02723.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.-37-2577G>A | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 1/11 | chr11 | 6468309 | |||||||
| chr11:6468363 | A | G | 2 | a0001c0001t0001g0256 a0001c0002t0004g0258 |
2 | NA18942.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.-37-2631T>C | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 1/11 | chr11 | 6468363 | |||||||
| chr11:6468422 | G | A | 1 | a0004c0010t0001g0201 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-37-2690C>T | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 1/11 | chr11 | 6468422 | |||||||
| chr11:6468489 | G | C | 17 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0041 others(14): Show |
19 | HG00099.hp2 HG00280.hp2 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.-37-2757C>G | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 1/11 | chr11 | 6468489 | |||||||
| chr11:6468520 | G | GAACCCAG others(14): Show |
1 | a0001c0001t0003g0237 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-37-2809_-37-2789d others(23): Show |
TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 1/11 | chr11 | 6468520 | |||||||
| chr11:6468611 | C | T | 33 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0049 others(30): Show |
41 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.-37-2879G>A | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 1/11 | chr11 | 6468611 | |||||||
| chr11:6468680 | T | A | 1 | a0001c0001t0003g0152 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-37-2948A>T | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 1/11 | chr11 | 6468680 | |||||||
| chr11:6468742 | G | A | 1 | a0001c0001t0001g0181 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-37-3010C>T | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 1/11 | chr11 | 6468742 | |||||||
| chr11:6468805 | C | T | 1 | a0001c0001t0001g0185 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-37-3073G>A | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 1/11 | chr11 | 6468805 | |||||||
| chr11:6468854 | G | GTGAA | 62 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0018 others(59): Show |
75 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(72): Show |
intron_variant | MODIFIER | c.-37-3126_-37-3123d others(6): Show |
TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 1/11 | chr11 | 6468854 | |||||||
| chr11:6468854 | G | GTGAATGA others(1): Show |
51 | a0001c0001t0001g0035 a0001c0001t0001g0179 a0001c0001t0001g0180 others(48): Show |
64 | HG00140.hp2 HG00323.hp2 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.-37-3130_-37-3123d others(10): Show |
TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 1/11 | chr11 | 6468854 | |||||||
| chr11:6468854 | G | GTGAATGA others(5): Show |
9 | a0001c0001t0001g0249 a0001c0001t0001g0250 a0001c0001t0001g0253 others(6): Show |
9 | HG01109.hp1 HG01243.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.-37-3134_-37-3123d others(14): Show |
TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 1/11 | chr11 | 6468854 | |||||||
| chr11:6468854 | GTGAATGA others(1): Show |
G | 35 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0049 others(32): Show |
43 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(40): Show |
intron_variant | MODIFIER | c.-37-3130_-37-3123d others(10): Show |
TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 1/11 | chr11 | 6468854 | |||||||
| chr11:6468925 | C | G | 1 | a0001c0001t0001g0048 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-37-3193G>C | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 1/11 | chr11 | 6468925 | |||||||
| chr11:6468992 | G | A | 2 | a0001c0001t0003g0156 a0001c0014t0001g0157 |
2 | HG03710.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.-37-3260C>T | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 1/11 | chr11 | 6468992 | |||||||
| chr11:6469131 | G | A | 1 | a0001c0002t0002g0285 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-37-3399C>T | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 1/11 | chr11 | 6469131 | |||||||
| chr11:6469276 | C | A | 1 | a0001c0001t0001g0249 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-37-3544G>T | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 1/11 | chr11 | 6469276 | |||||||
| chr11:6469463 | A | G | 1 | a0001c0001t0001g0181 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-37-3731T>C | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 1/11 | chr11 | 6469463 | |||||||
| chr11:6469734 | C | T | 1 | a0001c0001t0001g0196 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.-37-4002G>A | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 1/11 | chr11 | 6469734 | |||||||
| chr11:6469880 | A | T | 1 | a0001c0001t0001g0250 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-38+3911T>A | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 1/11 | chr11 | 6469880 | |||||||
| chr11:6469949 | A | T | 2 | a0001c0003t0003g0036 a0008c0012t0001g0182 |
3 | HG03942.hp1 NA19080.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.-38+3842T>A | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 1/11 | chr11 | 6469949 | |||||||
| chr11:6470015 | C | T | 4 | a0001c0003t0001g0184 a0001c0003t0003g0036 a0001c0003t0003g0183 others(1): Show |
5 | HG01243.hp2 HG02965.hp1 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.-38+3776G>A | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 1/11 | chr11 | 6470015 | |||||||
| chr11:6470028 | T | C | 1 | a0001c0001t0001g0042 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-38+3763A>G | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 1/11 | chr11 | 6470028 | |||||||
| chr11:6470323 | A | C | 4 | a0001c0001t0001g0046 a0001c0001t0003g0045 a0001c0001t0003g0047 others(1): Show |
4 | NA18969.hp2 NA18970.hp2 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.-38+3468T>G | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 1/11 | chr11 | 6470323 | |||||||
| chr11:6470422 | G | A | 1 | a0008c0012t0001g0182 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.-38+3369C>T | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 1/11 | chr11 | 6470422 | |||||||
| chr11:6470460 | G | A | 1 | a0001c0002t0004g0286 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-38+3331C>T | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 1/11 | chr11 | 6470460 | |||||||
| chr11:6470575 | C | T | 2 | a0001c0003t0003g0036 a0008c0012t0001g0182 |
3 | HG03942.hp1 NA19080.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.-38+3216G>A | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 1/11 | chr11 | 6470575 | |||||||
| chr11:6470630 | G | A | 4 | a0001c0002t0002g0246 a0001c0002t0004g0245 a0001c0002t0004g0247 others(1): Show |
4 | HG02630.hp2 HG02818.hp2 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.-38+3161C>T | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 1/11 | chr11 | 6470630 | |||||||
| chr11:6470733 | C | T | 2 | a0001c0002t0002g0241 a0001c0002t0002g0242 |
2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.-38+3058G>A | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 1/11 | chr11 | 6470733 | |||||||
| chr11:6470846 | T | C | 6 | a0001c0001t0001g0181 a0001c0001t0001g0249 a0001c0001t0001g0250 others(3): Show |
6 | HG02486.hp2 HG02559.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.-38+2945A>G | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 1/11 | chr11 | 6470846 | |||||||
| chr11:6470922 | G | A | 1 | a0001c0001t0001g0240 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-38+2869C>T | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 1/11 | chr11 | 6470922 | |||||||
| chr11:6471283 | T | C | 1 | a0005c0006t0001g0158 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-38+2508A>G | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 1/11 | chr11 | 6471283 | |||||||
| chr11:6471447 | A | G | 1 | a0001c0001t0001g0249 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-38+2344T>C | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 1/11 | chr11 | 6471447 | |||||||
| chr11:6471473 | A | G | 1 | a0001c0001t0001g0043 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-38+2318T>C | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 1/11 | chr11 | 6471473 | |||||||
| chr11:6471486 | C | T | 54 | a0001c0001t0001g0256 a0001c0001t0002g0260 a0001c0001t0002g0262 others(51): Show |
66 | HG00140.hp2 HG00323.hp2 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.-38+2305G>A | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 1/11 | chr11 | 6471486 | |||||||
| chr11:6471545 | C | T | 13 | a0001c0001t0001g0018 a0001c0001t0001g0185 a0001c0001t0001g0186 others(10): Show |
15 | HG00408.hp2 HG00544.hp2 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.-38+2246G>A | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 1/11 | chr11 | 6471545 | |||||||
| chr11:6471692 | T | C | 1 | a0001c0001t0001g0159 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-38+2099A>G | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 1/11 | chr11 | 6471692 | |||||||
| chr11:6471717 | G | A | 54 | a0001c0001t0001g0256 a0001c0001t0002g0260 a0001c0001t0002g0262 others(51): Show |
66 | HG00140.hp2 HG00323.hp2 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.-38+2074C>T | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 1/11 | chr11 | 6471717 | |||||||
| chr11:6471900 | A | G | 8 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0252 others(5): Show |
9 | HG01243.hp2 HG02486.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.-38+1891T>C | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 1/11 | chr11 | 6471900 | |||||||
| chr11:6471923 | T | C | 54 | a0001c0001t0001g0256 a0001c0001t0002g0260 a0001c0001t0002g0262 others(51): Show |
66 | HG00140.hp2 HG00323.hp2 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.-38+1868A>G | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 1/11 | chr11 | 6471923 | |||||||
| chr11:6471975 | A | G | 1 | a0001c0001t0001g0042 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-38+1816T>C | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 1/11 | chr11 | 6471975 | |||||||
| chr11:6472141 | G | A | 1 | a0001c0001t0001g0176 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-38+1650C>T | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 1/11 | chr11 | 6472141 | |||||||
| chr11:6472241 | G | A | 1 | a0001c0001t0001g0160 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-38+1550C>T | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 1/11 | chr11 | 6472241 | |||||||
| chr11:6472376 | G | A | 1 | a0001c0001t0003g0161 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-38+1415C>T | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 1/11 | chr11 | 6472376 | |||||||
| chr11:6472397 | G | A | 3 | a0001c0001t0001g0005 a0001c0001t0001g0162 a0001c0001t0001g0163 |
7 | HG02040.hp2 HG02155.hp1 NA18981.hp1 others(4): Show |
intron_variant | MODIFIER | c.-38+1394C>T | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 1/11 | chr11 | 6472397 | |||||||
| chr11:6472579 | C | T | 1 | a0001c0001t0001g0041 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-38+1212G>A | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 1/11 | chr11 | 6472579 | |||||||
| chr11:6472590 | T | C | 11 | a0001c0001t0001g0181 a0001c0001t0001g0249 a0001c0002t0002g0288 others(8): Show |
11 | HG00639.hp1 HG02451.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.-38+1201A>G | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 1/11 | chr11 | 6472590 | |||||||
| chr11:6472618 | G | C | 1 | a0001c0002t0004g0296 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-38+1173C>G | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 1/11 | chr11 | 6472618 | |||||||
| chr11:6472623 | T | C | 1 | a0001c0001t0001g0249 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-38+1168A>G | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 1/11 | chr11 | 6472623 | |||||||
| chr11:6472770 | T | C | 15 | a0001c0001t0001g0009 a0001c0001t0001g0164 a0001c0001t0001g0165 others(12): Show |
20 | HG00738.hp1 HG02258.hp2 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.-38+1021A>G | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 1/11 | chr11 | 6472770 | |||||||
| chr11:6472874 | A | ATTCTGCA others(13): Show |
1 | a0001c0001t0001g0181 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-38+897_-38+916dup others(20): Show |
TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 1/11 | chr11 | 6472874 | |||||||
| chr11:6473102 | G | A | 2 | a0001c0001t0001g0177 a0001c0001t0001g0178 |
2 | HG03017.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.-38+689C>T | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 1/11 | chr11 | 6473102 | |||||||
| chr11:6473230 | G | A | 4 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0252 others(1): Show |
4 | HG02486.hp2 HG02559.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.-38+561C>T | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 1/11 | chr11 | 6473230 | |||||||
| chr11:6473239 | G | C | 3 | a0001c0001t0001g0035 a0001c0001t0001g0179 a0001c0001t0001g0180 |
4 | HG02280.hp1 HG02809.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-38+552C>G | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 1/11 | chr11 | 6473239 | |||||||
| chr11:6473310 | GGGTGTCC others(37): Show |
G | 1 | a0001c0001t0001g0254 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-38+437_-38+480del others(44): Show |
TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 1/11 | chr11 | 6473310 | |||||||
| chr11:6473550 | C | T | 1 | a0001c0002t0002g0255 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-38+241G>A | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 1/11 | chr11 | 6473550 | |||||||
| chr11:6473556 | T | C | 127 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(124): Show |
157 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.-38+235A>G | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 1/11 | chr11 | 6473556 | |||||||
| chr11:6473678 | G | C | 46 | a0001c0001t0001g0256 a0001c0001t0002g0260 a0001c0001t0002g0262 others(43): Show |
58 | HG00140.hp2 HG00323.hp2 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.-38+113C>G | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 1/11 | chr11 | 6473678 | |||||||
| chr11:6473685 | G | A | 46 | a0001c0001t0001g0256 a0001c0001t0002g0260 a0001c0001t0002g0262 others(43): Show |
58 | HG00140.hp2 HG00323.hp2 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.-38+106C>T | TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 1/11 | chr11 | 6473685 |