Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 9830 |
| ensemblid | ENSG00000106785.15 |
| hgncid | 16283 |
| symbol | TRIM14 |
| name | tripartite motif containing 14 |
| refseq_nuc | NM_014788.4 |
| refseq_prot | NP_055603.2 |
| ensembl_nuc | ENST00000341469.7 |
| ensembl_prot | ENSP00000344208.2 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 98084353 |
| end | 98119222 |
| strand | - |
| ver | v1.2 |
| region | chr9:98084353-98119222 |
| region5000 | chr9:98079353-98124222 |
| regionname0 | TRIM14_chr9_98084353_98119222 |
| regionname5000 | TRIM14_chr9_98079353_98124222 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 442 | 337 | 63 | 59 | 161 | 14 | 38 | 121 | TRIM14_chr9_98079353_98124222 | TRIM14 | MAGAA others(437): Show |
chr9 | 98079353 | 98124222 |
| a0002 | 0/0 | 442 | 12 | 11 | 1 | 0 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | MAGAA others(437): Show |
chr9 | 98079353 | 98124222 |
| a0003 | 0/0 | 442 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | MAGAA others(437): Show |
chr9 | 98079353 | 98124222 |
| a0004 | 0/0 | 442 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | MAGAA others(437): Show |
chr9 | 98079353 | 98124222 |
| a0005 | 0/0 | 442 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TRIM14_chr9_98079353_98124222 | TRIM14 | MAGAA others(437): Show |
chr9 | 98079353 | 98124222 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1326 | 324 | 51 | 58 | 161 | 14 | 38 | TRIM14_chr9_98079353_98124222 | TRIM14 | ATGGC others(1321): Show |
chr9 | 98079353 | 98124222 | ||
| a0001c0002 | 0/0 | 1326 | 7 | 7 | 0 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | ATGGC others(1321): Show |
chr9 | 98079353 | 98124222 | ||
| a0001c0005 | 0/0 | 1326 | 4 | 3 | 1 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | ATGGC others(1321): Show |
chr9 | 98079353 | 98124222 | ||
| a0001c0006 | 0/0 | 1326 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | ATGGC others(1321): Show |
chr9 | 98079353 | 98124222 | ||
| a0002c0003 | 0/0 | 1326 | 7 | 6 | 1 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | ATGGC others(1321): Show |
chr9 | 98079353 | 98124222 | ||
| a0002c0004 | 0/0 | 1326 | 5 | 5 | 0 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | ATGGC others(1321): Show |
chr9 | 98079353 | 98124222 | ||
| a0003c0007 | 0/0 | 1326 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | ATGGC others(1321): Show |
chr9 | 98079353 | 98124222 | ||
| a0004c0009 | 0/0 | 1326 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | ATGGC others(1321): Show |
chr9 | 98079353 | 98124222 | ||
| a0005c0008 | 0/0 | 1326 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | ATGGC others(1321): Show |
chr9 | 98079353 | 98124222 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 4480 | 94 | 4 | 14 | 54 | 8 | 12 | TRIM14_chr9_98079353_98124222 | TRIM14 | CTGTG others(4475): Show |
chr9 | 98079353 | 98124222 |
| a0001c0001t0002 | 0/0 | 4480 | 72 | 13 | 17 | 41 | 0 | 1 | TRIM14_chr9_98079353_98124222 | TRIM14 | CTGTG others(4475): Show |
chr9 | 98079353 | 98124222 |
| a0001c0001t0003 | 0/0 | 4480 | 66 | 26 | 6 | 13 | 3 | 18 | TRIM14_chr9_98079353_98124222 | TRIM14 | CTGTG others(4475): Show |
chr9 | 98079353 | 98124222 |
| a0001c0001t0004 | 0/0 | 4480 | 41 | 0 | 4 | 33 | 0 | 4 | TRIM14_chr9_98079353_98124222 | TRIM14 | CTGTG others(4475): Show |
chr9 | 98079353 | 98124222 |
| a0001c0001t0005 | 0/0 | 4480 | 23 | 2 | 11 | 6 | 2 | 2 | TRIM14_chr9_98079353_98124222 | TRIM14 | CTGTG others(4475): Show |
chr9 | 98079353 | 98124222 |
| a0001c0001t0006 | 0/0 | 4480 | 2 | 1 | 1 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | CTGTG others(4475): Show |
chr9 | 98079353 | 98124222 |
| a0001c0001t0008 | 0/0 | 4480 | 4 | 0 | 0 | 4 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | CTGTG others(4475): Show |
chr9 | 98079353 | 98124222 |
| a0001c0001t0009 | 0/0 | 4480 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | CTGTG others(4475): Show |
chr9 | 98079353 | 98124222 |
| a0001c0001t0010 | 0/0 | 4480 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | CTGTG others(4475): Show |
chr9 | 98079353 | 98124222 |
| a0001c0001t0012 | 0/0 | 4480 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | CTGTG others(4475): Show |
chr9 | 98079353 | 98124222 |
| a0001c0001t0013 | 0/0 | 4480 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | CTGTG others(4475): Show |
chr9 | 98079353 | 98124222 |
| a0001c0001t0014 | 0/0 | 4480 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | CTGTG others(4475): Show |
chr9 | 98079353 | 98124222 |
| a0001c0001t0016 | 0/0 | 4480 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | CTGTG others(4475): Show |
chr9 | 98079353 | 98124222 |
| a0001c0001t0017 | 0/0 | 4480 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | CTGTG others(4475): Show |
chr9 | 98079353 | 98124222 |
| a0001c0001t0019 | 0/0 | 4480 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | CTGTG others(4475): Show |
chr9 | 98079353 | 98124222 |
| a0001c0001t0020 | 0/0 | 4480 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | CTGTG others(4475): Show |
chr9 | 98079353 | 98124222 |
| a0001c0001t0021 | 0/0 | 4480 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | CTGTG others(4475): Show |
chr9 | 98079353 | 98124222 |
| a0001c0001t0022 | 0/0 | 4480 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | CTGTG others(4475): Show |
chr9 | 98079353 | 98124222 |
| a0001c0001t0023 | 0/0 | 4480 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | CTGTG others(4475): Show |
chr9 | 98079353 | 98124222 |
| a0001c0001t0024 | 0/0 | 4480 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | CTGTG others(4475): Show |
chr9 | 98079353 | 98124222 |
| a0001c0001t0025 | 0/0 | 4480 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | CTGTG others(4475): Show |
chr9 | 98079353 | 98124222 |
| a0001c0001t0026 | 0/0 | 4481 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM14_chr9_98079353_98124222 | TRIM14 | CTGTG others(4476): Show |
chr9 | 98079353 | 98124222 |
| a0001c0001t0027 | 0/0 | 4480 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | CTGTG others(4475): Show |
chr9 | 98079353 | 98124222 |
| a0001c0001t0028 | 0/0 | 4480 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | CTGTG others(4475): Show |
chr9 | 98079353 | 98124222 |
| a0001c0001t0029 | 0/0 | 4480 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | CTGTG others(4475): Show |
chr9 | 98079353 | 98124222 |
| a0001c0002t0007 | 0/0 | 4481 | 6 | 6 | 0 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | CTGTG others(4476): Show |
chr9 | 98079353 | 98124222 |
| a0001c0002t0015 | 0/0 | 4481 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | CTGTG others(4476): Show |
chr9 | 98079353 | 98124222 |
| a0001c0005t0002 | 0/0 | 4480 | 4 | 3 | 1 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | CTGTG others(4475): Show |
chr9 | 98079353 | 98124222 |
| a0001c0006t0011 | 0/0 | 4480 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | CTGTG others(4475): Show |
chr9 | 98079353 | 98124222 |
| a0002c0003t0002 | 0/0 | 4480 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | CTGTG others(4475): Show |
chr9 | 98079353 | 98124222 |
| a0002c0003t0003 | 0/0 | 4480 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | CTGTG others(4475): Show |
chr9 | 98079353 | 98124222 |
| a0002c0003t0006 | 0/0 | 4480 | 2 | 1 | 1 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | CTGTG others(4475): Show |
chr9 | 98079353 | 98124222 |
| a0002c0003t0018 | 0/0 | 4480 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | CTGTG others(4475): Show |
chr9 | 98079353 | 98124222 |
| a0002c0004t0002 | 0/0 | 4480 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | CTGTG others(4475): Show |
chr9 | 98079353 | 98124222 |
| a0002c0004t0006 | 0/0 | 4480 | 4 | 4 | 0 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | CTGTG others(4475): Show |
chr9 | 98079353 | 98124222 |
| a0003c0007t0001 | 0/0 | 4480 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | CTGTG others(4475): Show |
chr9 | 98079353 | 98124222 |
| a0004c0009t0002 | 0/0 | 4480 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | CTGTG others(4475): Show |
chr9 | 98079353 | 98124222 |
| a0005c0008t0001 | 0/0 | 4480 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | CTGTG others(4475): Show |
chr9 | 98079353 | 98124222 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0006 | 0/0 | 3 | 1 | 0 | 0 | 2 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0001g0021 | 1/0 | 2 | 0 | 0 | 0 | 0 | 1 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0001g0229 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0002g0001 | 0/0 | 6 | 0 | 4 | 2 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0002g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0002g0004 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0002g0008 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0002g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0002g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0002g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0003g0005 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0003g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0003g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0003g0018 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0003g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0003g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0003g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0003g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0003g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0003g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0003g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0003g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0003g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0003g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0003g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0003g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0003g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0003g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0003g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0003g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0003g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0003g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0003g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0003g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0003g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0003g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0003g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0003g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0003g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0004g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0004g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0004g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0004g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0004g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0004g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0004g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0004g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0004g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0004g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0004g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0004g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0004g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0004g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0004g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0004g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0004g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0004g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0004g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0004g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0004g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0004g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0004g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0004g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0004g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0004g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0004g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0004g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0004g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0004g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0004g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0004g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0004g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0004g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0004g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0004g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0005g0013 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0005g0015 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0005g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0005g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0005g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0005g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0005g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0005g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0005g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0005g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0005g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0005g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0005g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0005g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0005g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0005g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0005g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0005g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0005g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0005g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0006g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0006g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0008g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0008g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0008g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0008g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0009g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0009g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0009g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0010g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0010g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0012g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0012g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0013g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0014g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0016g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0017g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0019g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0020g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0021g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0022g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0023g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0024g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0025g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0026g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0027g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0028g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0001t0029g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0002t0007g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0002t0007g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0002t0007g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0002t0007g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0002t0007g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0002t0007g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0002t0015g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0005t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0005t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0005t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0005t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0006t0011g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0001c0006t0011g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0002c0003t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0002c0003t0003g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0002c0003t0003g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0002c0003t0003g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0002c0003t0006g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0002c0003t0006g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0002c0003t0018g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0002c0004t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0002c0004t0006g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0002c0004t0006g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0002c0004t0006g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0002c0004t0006g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0003c0007t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0004c0009t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| a0005c0008t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0014 | EUR | GBR | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG00099 | hp2 | a0001 | c0001 | t0005 | g0015 | EUR | GBR | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG00323 | hp1 | a0001 | c0001 | t0005 | g0129 | EUR | FIN | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0128 | EUR | FIN | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | CHS | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG00408 | hp2 | a0003 | c0007 | t0001 | g0113 | EAS | CHS | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG00423 | hp1 | a0001 | c0001 | t0005 | g0207 | EAS | CHS | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | CHS | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | CHS | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG00438 | hp2 | a0004 | c0009 | t0002 | g0050 | EAS | CHS | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0178 | EAS | CHS | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG00558 | hp1 | a0001 | c0001 | t0004 | g0160 | EAS | CHS | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0145 | EAS | CHS | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG00597 | hp1 | a0001 | c0001 | t0004 | g0173 | EAS | CHS | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | CHS | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | CHS | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | CHS | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | CHS | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | CHS | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0054 | AMR | PUR | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG00642 | hp2 | a0001 | c0005 | t0002 | g0114 | AMR | PUR | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | CHS | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG00673 | hp2 | a0001 | c0001 | t0008 | g0158 | EAS | CHS | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG00738 | hp1 | a0001 | c0001 | t0004 | g0165 | AMR | PUR | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG00738 | hp2 | a0001 | c0001 | t0005 | g0015 | AMR | PUR | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG00741 | hp1 | a0001 | c0001 | t0004 | g0057 | AMR | PUR | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0175 | AMR | PUR | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG01069 | hp1 | a0001 | c0001 | t0010 | g0186 | AMR | PUR | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG01069 | hp2 | a0001 | c0001 | t0005 | g0234 | AMR | PUR | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG01070 | hp2 | a0001 | c0001 | t0005 | g0029 | AMR | PUR | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG01071 | hp1 | a0001 | c0001 | t0010 | g0180 | AMR | PUR | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG01074 | hp2 | a0001 | c0001 | t0005 | g0130 | AMR | PUR | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG01081 | hp2 | a0001 | c0001 | t0005 | g0112 | AMR | PUR | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0294 | AMR | PUR | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0210 | AMR | PUR | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0061 | AMR | PUR | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0257 | AMR | PUR | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0290 | AMR | PUR | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG01168 | hp2 | a0001 | c0001 | t0014 | g0224 | AMR | PUR | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0248 | AMR | PUR | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0091 | AMR | PUR | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0140 | AMR | PUR | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG01243 | hp2 | a0002 | c0003 | t0006 | g0044 | AMR | PUR | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG01255 | hp1 | a0001 | c0001 | t0013 | g0045 | AMR | CLM | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | CLM | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG01256 | hp1 | a0001 | c0001 | t0006 | g0181 | AMR | CLM | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | CLM | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | CLM | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0121 | AMR | CLM | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG01261 | hp1 | a0001 | c0001 | t0004 | g0077 | AMR | CLM | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0078 | AMR | CLM | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG01358 | hp1 | a0001 | c0001 | t0004 | g0170 | AMR | CLM | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG01358 | hp2 | a0001 | c0001 | t0005 | g0022 | AMR | CLM | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG01433 | hp2 | a0001 | c0001 | t0005 | g0013 | AMR | CLM | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0280 | AMR | CLM | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG01496 | hp2 | a0001 | c0001 | t0005 | g0204 | AMR | CLM | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG01515 | hp2 | a0001 | c0001 | t0003 | g0233 | EUR | IBS | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0163 | EUR | IBS | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0055 | EUR | IBS | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0161 | EUR | IBS | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG01884 | hp1 | a0001 | c0005 | t0002 | g0142 | AFR | ACB | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0012 | AFR | ACB | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG01891 | hp1 | a0001 | c0002 | t0007 | g0052 | AFR | ACB | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG01891 | hp2 | a0001 | c0002 | t0007 | g0212 | AFR | ACB | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG01943 | hp1 | a0001 | c0001 | t0005 | g0205 | AMR | PEL | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0075 | AMR | PEL | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG01952 | hp1 | a0001 | c0001 | t0019 | g0225 | AMR | PEL | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0034 | AMR | PEL | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0080 | AMR | PEL | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG01978 | hp2 | a0001 | c0001 | t0003 | g0228 | AMR | PEL | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0071 | AMR | PEL | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG01981 | hp2 | a0001 | c0001 | t0003 | g0005 | AMR | PEL | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | PEL | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG02004 | hp2 | a0001 | c0001 | t0005 | g0208 | AMR | PEL | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | KHV | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG02015 | hp2 | a0001 | c0001 | t0027 | g0249 | EAS | KHV | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG02040 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | KHV | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | KHV | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0062 | AFR | ACB | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | KHV | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG02074 | hp1 | a0001 | c0001 | t0004 | g0254 | EAS | KHV | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | KHV | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0299 | EAS | KHV | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | KHV | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | KHV | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0108 | EAS | KHV | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0153 | EAS | KHV | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | KHV | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | KHV | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG02135 | hp2 | a0001 | c0001 | t0004 | g0010 | EAS | KHV | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0132 | AFR | ACB | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | CDX | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG02155 | hp2 | a0001 | c0001 | t0004 | g0056 | EAS | CDX | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | CDX | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG02165 | hp2 | a0001 | c0001 | t0028 | g0123 | EAS | CDX | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0117 | AFR | ACB | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG02257 | hp2 | a0001 | c0002 | t0015 | g0086 | AFR | ACB | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG02258 | hp1 | a0002 | c0003 | t0003 | g0150 | AFR | ACB | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0102 | AFR | ACB | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG02273 | hp1 | a0001 | c0001 | t0003 | g0005 | AMR | PEL | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0072 | AMR | PEL | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG02300 | hp1 | a0001 | c0001 | t0005 | g0022 | AMR | PEL | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG02451 | hp1 | a0002 | c0004 | t0006 | g0216 | AFR | ACB | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0137 | AFR | ACB | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | KHV | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG02523 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | KHV | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG02572 | hp1 | a0001 | c0001 | t0005 | g0219 | AFR | GWD | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0041 | AFR | GWD | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0152 | SAS | PJL | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0151 | SAS | PJL | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG02615 | hp1 | a0002 | c0003 | t0003 | g0176 | AFR | GWD | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0125 | AFR | GWD | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0146 | AFR | GWD | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0039 | AFR | GWD | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0103 | AFR | GWD | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | GWD | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0147 | AFR | GWD | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG02717 | hp2 | a0001 | c0001 | t0005 | g0105 | AFR | GWD | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0035 | AFR | GWD | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0118 | AFR | GWD | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0223 | SAS | PJL | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0260 | SAS | PJL | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG02738 | hp1 | a0001 | c0001 | t0003 | g0131 | SAS | PJL | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG02738 | hp2 | a0001 | c0001 | t0005 | g0272 | SAS | PJL | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG02809 | hp1 | a0002 | c0004 | t0006 | g0218 | AFR | GWD | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG02809 | hp2 | a0001 | c0005 | t0002 | g0099 | AFR | GWD | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG02818 | hp1 | a0001 | c0006 | t0011 | g0042 | AFR | GWD | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0104 | AFR | GWD | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG02886 | hp1 | a0002 | c0003 | t0018 | g0217 | AFR | GWD | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG02886 | hp2 | a0001 | c0001 | t0003 | g0115 | AFR | GWD | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0134 | AFR | GWD | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0111 | AFR | GWD | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG02922 | hp1 | a0002 | c0003 | t0006 | g0138 | AFR | ESN | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0141 | AFR | ESN | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG02965 | hp1 | a0001 | c0001 | t0009 | g0177 | AFR | ESN | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0059 | AFR | ESN | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0211 | AFR | ESN | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0148 | AFR | ESN | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG03041 | hp1 | a0001 | c0002 | t0007 | g0154 | AFR | GWD | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0040 | AFR | GWD | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG03098 | hp1 | a0001 | c0006 | t0011 | g0043 | AFR | MSL | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG03098 | hp2 | a0001 | c0001 | t0006 | g0143 | AFR | MSL | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG03130 | hp1 | a0002 | c0004 | t0002 | g0085 | AFR | ESN | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | ESN | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG03209 | hp1 | a0001 | c0001 | t0009 | g0097 | AFR | MSL | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0012 | AFR | MSL | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG03225 | hp1 | a0001 | c0002 | t0007 | g0213 | AFR | MSL | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG03225 | hp2 | a0002 | c0004 | t0006 | g0215 | AFR | MSL | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG03239 | hp1 | a0001 | c0001 | t0004 | g0193 | SAS | PJL | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0246 | SAS | PJL | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0009 | AFR | MSL | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0033 | AFR | MSL | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG03490 | hp1 | a0001 | c0001 | t0004 | g0190 | SAS | PJL | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG03490 | hp2 | a0001 | c0001 | t0026 | g0247 | SAS | PJL | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0279 | SAS | PJL | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG03491 | hp2 | a0001 | c0001 | t0003 | g0120 | SAS | PJL | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG03492 | hp1 | a0001 | c0001 | t0004 | g0191 | SAS | PJL | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0255 | SAS | PJL | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0019 | AFR | GWD | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG03540 | hp2 | a0001 | c0001 | t0022 | g0124 | AFR | GWD | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0171 | SAS | STU | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | STU | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0087 | SAS | PJL | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0238 | SAS | PJL | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0018 | SAS | PJL | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0230 | SAS | BEB | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0149 | SAS | BEB | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0032 | SAS | BEB | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG03834 | hp2 | a0001 | c0001 | t0003 | g0232 | SAS | BEB | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG03927 | hp1 | a0001 | c0001 | t0004 | g0236 | SAS | BEB | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0199 | SAS | BEB | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG03942 | hp1 | a0001 | c0001 | t0003 | g0098 | SAS | BEB | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | BEB | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0227 | SAS | STU | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG04115 | hp2 | a0001 | c0001 | t0003 | g0182 | SAS | STU | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG04184 | hp1 | a0001 | c0001 | t0003 | g0197 | SAS | BEB | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0300 | SAS | BEB | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG04204 | hp1 | a0001 | c0001 | t0005 | g0013 | SAS | STU | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0262 | SAS | STU | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0226 | SAS | STU | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0222 | SAS | STU | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CHB | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA18747 | hp2 | a0001 | c0001 | t0008 | g0189 | EAS | CHB | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0116 | AFR | YRI | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0135 | AFR | YRI | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA18939 | hp2 | a0001 | c0001 | t0003 | g0194 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0293 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA18943 | hp1 | a0001 | c0001 | t0005 | g0206 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA18944 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA18945 | hp1 | a0001 | c0001 | t0021 | g0060 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA18946 | hp1 | a0001 | c0001 | t0004 | g0011 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA18947 | hp1 | a0001 | c0001 | t0003 | g0266 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA18949 | hp2 | a0001 | c0001 | t0003 | g0196 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA18950 | hp1 | a0001 | c0001 | t0005 | g0286 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA18950 | hp2 | a0001 | c0001 | t0004 | g0011 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA18951 | hp1 | a0001 | c0001 | t0004 | g0264 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA18951 | hp2 | a0001 | c0001 | t0003 | g0195 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA18953 | hp1 | a0001 | c0001 | t0004 | g0275 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA18957 | hp1 | a0001 | c0001 | t0005 | g0203 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA18957 | hp2 | a0001 | c0001 | t0003 | g0198 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA18959 | hp1 | a0001 | c0001 | t0012 | g0183 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA18962 | hp2 | a0001 | c0001 | t0004 | g0096 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA18964 | hp2 | a0001 | c0001 | t0004 | g0296 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA18966 | hp2 | a0001 | c0001 | t0004 | g0297 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA18968 | hp1 | a0001 | c0001 | t0023 | g0067 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0298 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA18970 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA18975 | hp2 | a0001 | c0001 | t0005 | g0127 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA18980 | hp1 | a0001 | c0001 | t0003 | g0093 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA18980 | hp2 | a0001 | c0001 | t0004 | g0166 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA18984 | hp1 | a0001 | c0001 | t0004 | g0159 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0284 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA18985 | hp1 | a0001 | c0001 | t0004 | g0263 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA18986 | hp1 | a0001 | c0001 | t0029 | g0094 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0305 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA18988 | hp1 | a0001 | c0001 | t0004 | g0184 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA18992 | hp2 | a0001 | c0001 | t0004 | g0283 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA18998 | hp1 | a0001 | c0001 | t0003 | g0301 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA19000 | hp1 | a0001 | c0001 | t0020 | g0209 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA19002 | hp2 | a0001 | c0001 | t0004 | g0187 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA19003 | hp2 | a0001 | c0001 | t0004 | g0174 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA19007 | hp2 | a0001 | c0001 | t0004 | g0168 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0037 | AFR | LWK | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA19030 | hp2 | a0001 | c0001 | t0009 | g0101 | AFR | LWK | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA19043 | hp1 | a0001 | c0002 | t0007 | g0220 | AFR | LWK | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA19043 | hp2 | a0001 | c0001 | t0024 | g0109 | AFR | LWK | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA19055 | hp1 | a0001 | c0001 | t0008 | g0192 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA19055 | hp2 | a0001 | c0001 | t0002 | g0288 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA19057 | hp1 | a0001 | c0001 | t0004 | g0088 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA19057 | hp2 | a0005 | c0008 | t0001 | g0270 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA19060 | hp2 | a0001 | c0001 | t0003 | g0267 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA19062 | hp1 | a0001 | c0001 | t0004 | g0239 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA19064 | hp2 | a0001 | c0001 | t0004 | g0084 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA19065 | hp2 | a0001 | c0001 | t0004 | g0100 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA19066 | hp2 | a0001 | c0001 | t0003 | g0256 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA19067 | hp2 | a0001 | c0001 | t0004 | g0169 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA19068 | hp1 | a0001 | c0001 | t0008 | g0095 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA19068 | hp2 | a0001 | c0001 | t0025 | g0049 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA19070 | hp1 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA19075 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA19075 | hp2 | a0001 | c0001 | t0002 | g0289 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA19077 | hp1 | a0001 | c0001 | t0004 | g0287 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA19077 | hp2 | a0001 | c0001 | t0003 | g0200 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0274 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA19080 | hp1 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA19081 | hp1 | a0001 | c0001 | t0004 | g0081 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0292 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA19087 | hp1 | a0001 | c0001 | t0012 | g0282 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA19087 | hp2 | a0001 | c0001 | t0017 | g0065 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA19088 | hp1 | a0001 | c0001 | t0004 | g0265 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0261 | EUR | TSI | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0020 | EUR | TSI | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0119 | EUR | TSI | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA20805 | hp2 | a0001 | c0001 | t0016 | g0291 | EUR | TSI | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | GIH | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA20905 | hp2 | a0001 | c0001 | t0003 | g0167 | SAS | GIH | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG02109 | hp1 | a0001 | c0001 | t0003 | g0009 | AFR | ACB | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG02109 | hp2 | a0002 | c0003 | t0003 | g0155 | AFR | ACB | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0133 | AFR | ACB | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0139 | AFR | ACB | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG02559 | hp1 | a0001 | c0002 | t0007 | g0089 | AFR | ACB | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0126 | AFR | ACB | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG03471 | hp1 | a0002 | c0004 | t0006 | g0092 | AFR | MSL | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0036 | AFR | MSL | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0019 | AFR | USA | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0136 | AFR | USA | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA18955 | hp1 | a0001 | c0001 | t0005 | g0162 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | USA | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA20300 | hp2 | a0002 | c0003 | t0002 | g0214 | AFR | USA | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA21309 | hp1 | a0001 | c0001 | t0003 | g0038 | AFR | LWK | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| NA21309 | hp2 | a0001 | c0005 | t0002 | g0053 | AFR | LWK | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0229 | REF | REF | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0021 | REF | REF | TRIM14_chr9_98079353_98124222 | TRIM14 | chr9 | 98079353 | 98124222 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:98087490 | T | C | 1 | a0005 | 1 | NA19057.hp2 | missense_variant | MODERATE | c.1309A>G | p.Ser437Gly | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 6/6 | 1343/4480 | 1309/1329 | 437/442 | chr9 | 98087490 | |||
| chr9:98087844 | T | C | 1 | a0004 | 1 | HG00438.hp2 | missense_variant | MODERATE | c.955A>G | p.Thr319Ala | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 6/6 | 989/4480 | 955/1329 | 319/442 | chr9 | 98087844 | |||
| chr9:98094893 | G | A | 1 | a0002 | 12 | HG01243.hp2 HG02109.hp2 HG02258.hp1 others(9): Show |
missense_variant | MODERATE | c.674C>T | p.Thr225Met | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 4/6 | 708/4480 | 674/1329 | 225/442 | chr9 | 98094893 | |||
| chr9:98094912 | C | T | 1 | a0003 | 1 | HG00408.hp2 | missense_variant | MODERATE | c.655G>A | p.Val219Met | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 4/6 | 689/4480 | 655/1329 | 219/442 | chr9 | 98094912 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:98087806 | C | T | 1 | a0001c0002 | 7 | HG01891.hp1 HG01891.hp2 HG02257.hp2 others(4): Show |
synonymous_variant | LOW | c.993G>A | p.Ala331Ala | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 6/6 | 1027/4480 | 993/1329 | 331/442 | chr9 | 98087806 | |||
| chr9:98087944 | A | G | 1 | a0001c0006 | 2 | HG02818.hp1 HG03098.hp1 |
synonymous_variant | LOW | c.855T>C | p.Asp285Asp | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 6/6 | 889/4480 | 855/1329 | 285/442 | chr9 | 98087944 | |||
| chr9:98091937 | G | A | 1 | a0002c0004 | 5 | HG02451.hp1 HG02809.hp1 HG03130.hp1 others(2): Show |
synonymous_variant | LOW | c.765C>T | p.Pro255Pro | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 5/6 | 799/4480 | 765/1329 | 255/442 | chr9 | 98091937 | |||
| chr9:98100057 | C | A | 1 | a0001c0005 | 4 | HG00642.hp2 HG01884.hp1 HG02809.hp2 others(1): Show |
synonymous_variant | LOW | c.411G>T | p.Thr137Thr | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 3/6 | 445/4480 | 411/1329 | 137/442 | chr9 | 98100057 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:98084377 | T | C | 1 | a0001c0001t0027 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3093A>G | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 6/6 | 3093 | chr9 | 98084377 | ||||||
| chr9:98084378 | A | T | 1 | a0001c0001t0027 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3092T>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 6/6 | 3092 | chr9 | 98084378 | ||||||
| chr9:98084380 | T | A | 1 | a0001c0001t0027 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3090A>T | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 6/6 | 3090 | chr9 | 98084380 | ||||||
| chr9:98084395 | A | T | 1 | a0001c0001t0027 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3075T>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 6/6 | 3075 | chr9 | 98084395 | ||||||
| chr9:98084398 | A | T | 1 | a0001c0001t0027 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3072T>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 6/6 | 3072 | chr9 | 98084398 | ||||||
| chr9:98084429 | T | C | 1 | a0001c0001t0019 | 1 | HG01952.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3041A>G | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 6/6 | 3041 | chr9 | 98084429 | ||||||
| chr9:98084512 | A | G | 1 | a0001c0001t0027 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2958T>C | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 6/6 | 2958 | chr9 | 98084512 | ||||||
| chr9:98084595 | C | G | 1 | a0001c0001t0008 | 4 | HG00673.hp2 NA18747.hp2 NA19055.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2875G>C | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 6/6 | 2875 | chr9 | 98084595 | ||||||
| chr9:98084609 | A | T | 1 | a0001c0001t0027 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2861T>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 6/6 | 2861 | chr9 | 98084609 | ||||||
| chr9:98084628 | T | C | 1 | a0001c0001t0027 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2842A>G | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 6/6 | 2842 | chr9 | 98084628 | ||||||
| chr9:98084693 | A | T | 1 | a0001c0001t0027 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2777T>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 6/6 | 2777 | chr9 | 98084693 | ||||||
| chr9:98084730 | T | G | 4 | a0001c0001t0005 a0001c0001t0024 a0001c0002t0007 others(1): Show |
31 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*2740A>C | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 6/6 | 2740 | chr9 | 98084730 | ||||||
| chr9:98084733 | A | C | 1 | a0001c0001t0027 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2737T>G | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 6/6 | 2737 | chr9 | 98084733 | ||||||
| chr9:98084740 | G | A | 1 | a0001c0001t0012 | 2 | NA18959.hp1 NA19087.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2730C>T | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 6/6 | 2730 | chr9 | 98084740 | ||||||
| chr9:98084762 | T | A | 1 | a0001c0001t0020 | 1 | NA19000.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2708A>T | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 6/6 | 2708 | chr9 | 98084762 | ||||||
| chr9:98084827 | G | A | 4 | a0001c0001t0005 a0001c0001t0024 a0001c0002t0007 others(1): Show |
31 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*2643C>T | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 6/6 | 2643 | chr9 | 98084827 | ||||||
| chr9:98084986 | G | A | 1 | a0001c0006t0011 | 2 | HG02818.hp1 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2484C>T | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 6/6 | 2484 | chr9 | 98084986 | ||||||
| chr9:98084999 | G | A | 1 | a0001c0001t0028 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2471C>T | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 6/6 | 2471 | chr9 | 98084999 | ||||||
| chr9:98085015 | G | A | 7 | a0001c0001t0002 a0001c0001t0021 a0001c0001t0025 others(4): Show |
81 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*2455C>T | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 6/6 | 2455 | chr9 | 98085015 | ||||||
| chr9:98085015 | G | C | 1 | a0001c0001t0029 | 1 | NA18986.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2455C>G | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 6/6 | 2455 | chr9 | 98085015 | ||||||
| chr9:98085022 | G | T | 1 | a0001c0001t0029 | 1 | NA18986.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2448C>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 6/6 | 2448 | chr9 | 98085022 | ||||||
| chr9:98085032 | G | C | 1 | a0001c0001t0029 | 1 | NA18986.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2438C>G | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 6/6 | 2438 | chr9 | 98085032 | ||||||
| chr9:98085049 | T | C | 1 | a0002c0003t0018 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2421A>G | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 6/6 | 2421 | chr9 | 98085049 | ||||||
| chr9:98085209 | C | T | 1 | a0001c0006t0011 | 2 | HG02818.hp1 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2261G>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 6/6 | 2261 | chr9 | 98085209 | ||||||
| chr9:98085269 | G | T | 13 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0006 others(10): Show |
114 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(111): Show |
3_prime_UTR_variant | MODIFIER | c.*2201C>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 6/6 | 2201 | chr9 | 98085269 | ||||||
| chr9:98085275 | G | A | 1 | a0001c0001t0021 | 1 | NA18945.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2195C>T | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 6/6 | 2195 | chr9 | 98085275 | ||||||
| chr9:98085297 | G | C | 1 | a0001c0001t0022 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2173C>G | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 6/6 | 2173 | chr9 | 98085297 | ||||||
| chr9:98085387 | A | G | 1 | a0001c0001t0017 | 1 | NA19087.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2083T>C | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 6/6 | 2083 | chr9 | 98085387 | ||||||
| chr9:98085408 | T | C | 1 | a0001c0006t0011 | 2 | HG02818.hp1 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2062A>G | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 6/6 | 2062 | chr9 | 98085408 | ||||||
| chr9:98085433 | G | A | 1 | a0001c0001t0023 | 1 | NA18968.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2037C>T | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 6/6 | 2037 | chr9 | 98085433 | ||||||
| chr9:98085574 | C | T | 1 | a0001c0001t0016 | 1 | NA20805.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1896G>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 6/6 | 1896 | chr9 | 98085574 | ||||||
| chr9:98085596 | G | A | 1 | a0001c0001t0024 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1874C>T | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 6/6 | 1874 | chr9 | 98085596 | ||||||
| chr9:98085627 | A | G | 1 | a0001c0006t0011 | 2 | HG02818.hp1 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1843T>C | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 6/6 | 1843 | chr9 | 98085627 | ||||||
| chr9:98085646 | T | G | 1 | a0001c0002t0015 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1824A>C | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 6/6 | 1824 | chr9 | 98085646 | ||||||
| chr9:98085667 | T | C | 1 | a0001c0001t0025 | 1 | NA19068.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1803A>G | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 6/6 | 1803 | chr9 | 98085667 | ||||||
| chr9:98085798 | T | G | 1 | a0001c0001t0013 | 1 | HG01255.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1672A>C | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 6/6 | 1672 | chr9 | 98085798 | ||||||
| chr9:98085856 | C | A | 2 | a0001c0002t0007 a0001c0002t0015 |
7 | HG01891.hp1 HG01891.hp2 HG02257.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1614G>T | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 6/6 | 1614 | chr9 | 98085856 | ||||||
| chr9:98085970 | C | T | 1 | a0001c0001t0009 | 3 | HG02965.hp1 HG03209.hp1 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1500G>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 6/6 | 1500 | chr9 | 98085970 | ||||||
| chr9:98086014 | C | A | 1 | a0001c0006t0011 | 2 | HG02818.hp1 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1456G>T | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 6/6 | 1456 | chr9 | 98086014 | ||||||
| chr9:98086080 | A | G | 1 | a0001c0006t0011 | 2 | HG02818.hp1 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1390T>C | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 6/6 | 1390 | chr9 | 98086080 | ||||||
| chr9:98086218 | G | A | 1 | a0001c0006t0011 | 2 | HG02818.hp1 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1252C>T | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 6/6 | 1252 | chr9 | 98086218 | ||||||
| chr9:98086816 | A | AT | 3 | a0001c0001t0026 a0001c0002t0007 a0001c0002t0015 |
8 | HG01891.hp1 HG01891.hp2 HG02257.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*653dupA | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 6/6 | 653 | chr9 | 98086816 | ||||||
| chr9:98086843 | C | T | 1 | a0001c0001t0014 | 1 | HG01168.hp2 | 3_prime_UTR_variant | MODIFIER | c.*627G>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 6/6 | 627 | chr9 | 98086843 | ||||||
| chr9:98086920 | A | T | 1 | a0001c0001t0010 | 2 | HG01069.hp1 HG01071.hp1 |
3_prime_UTR_variant | MODIFIER | c.*550T>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 6/6 | 550 | chr9 | 98086920 | ||||||
| chr9:98087183 | G | A | 7 | a0001c0001t0004 a0001c0001t0008 a0001c0001t0012 others(4): Show |
51 | HG00558.hp1 HG00597.hp1 HG00673.hp2 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*287C>T | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 6/6 | 287 | chr9 | 98087183 | ||||||
| chr9:98087218 | G | T | 4 | a0001c0001t0003 a0001c0001t0009 a0001c0001t0013 others(1): Show |
73 | HG00741.hp2 HG01109.hp1 HG01192.hp1 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*252C>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 6/6 | 252 | chr9 | 98087218 | ||||||
| chr9:98087400 | T | G | 7 | a0001c0001t0004 a0001c0001t0008 a0001c0001t0012 others(4): Show |
51 | HG00558.hp1 HG00597.hp1 HG00673.hp2 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*70A>C | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 6/6 | 70 | chr9 | 98087400 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:98088346 | T | TTTTC | 179 | a0001c0001t0001g0028 a0001c0001t0001g0310 a0001c0001t0001g0311 others(176): Show |
201 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.794-345_794-342dup others(4): Show |
TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 5/5 | chr9 | 98088346 | |||||||
| chr9:98088511 | C | T | 1 | a0002c0004t0006g0216 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.794-506G>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 5/5 | chr9 | 98088511 | |||||||
| chr9:98088685 | A | G | 70 | a0001c0001t0001g0310 a0001c0001t0001g0311 a0001c0001t0001g0312 others(67): Show |
84 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.794-680T>C | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 5/5 | chr9 | 98088685 | |||||||
| chr9:98088810 | T | C | 1 | a0001c0001t0012g0183 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.794-805A>G | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 5/5 | chr9 | 98088810 | |||||||
| chr9:98088865 | T | C | 179 | a0001c0001t0001g0028 a0001c0001t0001g0310 a0001c0001t0001g0311 others(176): Show |
201 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.794-860A>G | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 5/5 | chr9 | 98088865 | |||||||
| chr9:98088916 | T | G | 118 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0024 others(115): Show |
131 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.794-911A>C | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 5/5 | chr9 | 98088916 | |||||||
| chr9:98088919 | G | T | 160 | a0001c0001t0001g0028 a0001c0001t0001g0310 a0001c0001t0001g0311 others(157): Show |
179 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(176): Show |
intron_variant | MODIFIER | c.794-914C>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 5/5 | chr9 | 98088919 | |||||||
| chr9:98088922 | G | T | 3 | a0001c0005t0002g0114 a0001c0006t0011g0042 a0001c0006t0011g0043 |
3 | HG00642.hp2 HG02818.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.794-917C>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 5/5 | chr9 | 98088922 | |||||||
| chr9:98089022 | C | T | 7 | a0001c0002t0007g0052 a0001c0002t0007g0089 a0001c0002t0007g0154 others(4): Show |
7 | HG01891.hp1 HG01891.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.794-1017G>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 5/5 | chr9 | 98089022 | |||||||
| chr9:98089138 | C | T | 78 | a0001c0001t0003g0005 a0001c0001t0003g0009 a0001c0001t0003g0012 others(75): Show |
83 | HG00741.hp2 HG01109.hp1 HG01192.hp1 others(80): Show |
intron_variant | MODIFIER | c.794-1133G>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 5/5 | chr9 | 98089138 | |||||||
| chr9:98089337 | T | C | 7 | a0001c0002t0007g0052 a0001c0002t0007g0089 a0001c0002t0007g0154 others(4): Show |
7 | HG01891.hp1 HG01891.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.794-1332A>G | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 5/5 | chr9 | 98089337 | |||||||
| chr9:98089378 | T | G | 71 | a0001c0001t0001g0028 a0001c0001t0001g0310 a0001c0001t0001g0311 others(68): Show |
85 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.794-1373A>C | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 5/5 | chr9 | 98089378 | |||||||
| chr9:98089440 | G | A | 1 | a0001c0001t0002g0062 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.794-1435C>T | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 5/5 | chr9 | 98089440 | |||||||
| chr9:98089714 | T | C | 1 | a0001c0001t0004g0236 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.794-1709A>G | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 5/5 | chr9 | 98089714 | |||||||
| chr9:98089850 | C | CG | 3 | a0001c0001t0001g0258 a0001c0001t0001g0302 a0001c0001t0002g0061 |
3 | HG01109.hp2 NA18955.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.794-1846dupC | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 5/5 | chr9 | 98089850 | |||||||
| chr9:98089850 | C | T | 4 | a0001c0001t0004g0056 a0001c0001t0004g0077 a0001c0001t0004g0096 others(1): Show |
4 | HG01261.hp1 HG02155.hp2 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.794-1845G>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 5/5 | chr9 | 98089850 | |||||||
| chr9:98089856 | C | T | 1 | a0001c0001t0022g0124 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.794-1851G>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 5/5 | chr9 | 98089856 | |||||||
| chr9:98089875 | C | A | 1 | a0001c0002t0015g0086 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.794-1870G>T | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 5/5 | chr9 | 98089875 | |||||||
| chr9:98089886 | C | T | 1 | a0001c0001t0001g0028 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.794-1881G>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 5/5 | chr9 | 98089886 | |||||||
| chr9:98089942 | T | C | 1 | a0001c0002t0007g0052 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.794-1937A>G | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 5/5 | chr9 | 98089942 | |||||||
| chr9:98089962 | G | A | 7 | a0001c0001t0006g0143 a0002c0003t0006g0138 a0002c0004t0002g0085 others(4): Show |
7 | HG02451.hp1 HG02809.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.793+1947C>T | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 5/5 | chr9 | 98089962 | |||||||
| chr9:98090133 | C | T | 2 | a0001c0006t0011g0042 a0001c0006t0011g0043 |
2 | HG02818.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.793+1776G>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 5/5 | chr9 | 98090133 | |||||||
| chr9:98090304 | T | C | 1 | a0001c0001t0004g0236 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.793+1605A>G | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 5/5 | chr9 | 98090304 | |||||||
| chr9:98090456 | G | T | 1 | a0001c0005t0002g0053 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.793+1453C>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 5/5 | chr9 | 98090456 | |||||||
| chr9:98090524 | T | C | 1 | a0001c0001t0002g0058 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.793+1385A>G | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 5/5 | chr9 | 98090524 | |||||||
| chr9:98090560 | C | CT | 21 | a0001c0001t0001g0006 a0001c0001t0001g0188 a0001c0001t0001g0226 others(18): Show |
23 | HG01069.hp1 HG01071.hp1 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.793+1348dupA | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 5/5 | chr9 | 98090560 | |||||||
| chr9:98090560 | CT | C | 33 | a0001c0001t0001g0024 a0001c0001t0001g0110 a0001c0001t0001g0259 others(30): Show |
36 | HG01070.hp2 HG02109.hp1 HG02109.hp2 others(33): Show |
intron_variant | MODIFIER | c.793+1348delA | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 5/5 | chr9 | 98090560 | |||||||
| chr9:98090560 | CTT | C | 104 | a0001c0001t0001g0028 a0001c0001t0002g0001 a0001c0001t0002g0003 others(101): Show |
121 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(118): Show |
intron_variant | MODIFIER | c.793+1347_793+1348d others(4): Show |
TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 5/5 | chr9 | 98090560 | |||||||
| chr9:98090560 | CTTT | C | 11 | a0001c0001t0002g0072 a0001c0001t0002g0108 a0001c0001t0003g0211 others(8): Show |
11 | HG01256.hp1 HG01891.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.793+1346_793+1348d others(5): Show |
TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 5/5 | chr9 | 98090560 | |||||||
| chr9:98090632 | C | T | 2 | a0001c0006t0011g0042 a0001c0006t0011g0043 |
2 | HG02818.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.793+1277G>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 5/5 | chr9 | 98090632 | |||||||
| chr9:98090778 | G | A | 46 | a0001c0001t0004g0002 a0001c0001t0004g0010 a0001c0001t0004g0011 others(43): Show |
51 | HG00558.hp1 HG00597.hp1 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.793+1131C>T | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 5/5 | chr9 | 98090778 | |||||||
| chr9:98090819 | T | C | 2 | a0001c0006t0011g0042 a0001c0006t0011g0043 |
2 | HG02818.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.793+1090A>G | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 5/5 | chr9 | 98090819 | |||||||
| chr9:98091273 | A | G | 1 | a0001c0001t0001g0281 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.793+636T>C | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 5/5 | chr9 | 98091273 | |||||||
| chr9:98091377 | T | A | 2 | a0001c0006t0011g0042 a0001c0006t0011g0043 |
2 | HG02818.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.793+532A>T | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 5/5 | chr9 | 98091377 | |||||||
| chr9:98091386 | G | A | 1 | a0001c0001t0003g0148 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.793+523C>T | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 5/5 | chr9 | 98091386 | |||||||
| chr9:98091387 | G | C | 2 | a0001c0006t0011g0042 a0001c0006t0011g0043 |
2 | HG02818.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.793+522C>G | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 5/5 | chr9 | 98091387 | |||||||
| chr9:98091395 | T | G | 2 | a0001c0001t0004g0190 a0001c0001t0004g0191 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.793+514A>C | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 5/5 | chr9 | 98091395 | |||||||
| chr9:98091550 | C | G | 1 | a0001c0001t0001g0024 | 2 | NA18944.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.793+359G>C | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 5/5 | chr9 | 98091550 | |||||||
| chr9:98091630 | T | G | 1 | a0001c0001t0003g0197 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.793+279A>C | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 5/5 | chr9 | 98091630 | |||||||
| chr9:98091660 | T | C | 71 | a0001c0001t0001g0310 a0001c0001t0001g0311 a0001c0001t0001g0312 others(68): Show |
85 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.793+249A>G | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 5/5 | chr9 | 98091660 | |||||||
| chr9:98091747 | C | T | 1 | a0001c0001t0001g0238 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.793+162G>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 5/5 | chr9 | 98091747 | |||||||
| chr9:98091784 | A | AAAAT | 178 | a0001c0001t0001g0028 a0001c0001t0001g0309 a0001c0001t0001g0310 others(175): Show |
200 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(197): Show |
intron_variant | MODIFIER | c.793+121_793+124dup others(4): Show |
TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 5/5 | chr9 | 98091784 | |||||||
| chr9:98091784 | A | AAAATAAA others(1): Show |
6 | a0001c0001t0004g0165 a0001c0002t0015g0086 a0001c0005t0002g0053 others(3): Show |
6 | HG00642.hp2 HG00738.hp1 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.793+117_793+124dup others(8): Show |
TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 5/5 | chr9 | 98091784 | |||||||
| chr9:98092142 | A | T | 1 | a0001c0001t0003g0262 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.701-141T>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 4/5 | chr9 | 98092142 | |||||||
| chr9:98092201 | G | C | 1 | a0002c0004t0006g0216 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.701-200C>G | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 4/5 | chr9 | 98092201 | |||||||
| chr9:98092435 | AC | A | 10 | a0001c0001t0006g0143 a0002c0003t0003g0150 a0002c0003t0003g0155 others(7): Show |
10 | HG01243.hp2 HG02109.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.701-435delG | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 4/5 | chr9 | 98092435 | |||||||
| chr9:98092483 | C | G | 139 | a0001c0001t0001g0028 a0001c0001t0001g0310 a0001c0001t0001g0311 others(136): Show |
158 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(155): Show |
intron_variant | MODIFIER | c.701-482G>C | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 4/5 | chr9 | 98092483 | |||||||
| chr9:98092506 | A | T | 1 | a0001c0001t0003g0119 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.701-505T>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 4/5 | chr9 | 98092506 | |||||||
| chr9:98092514 | T | C | 2 | a0001c0001t0001g0020 a0001c0001t0001g0221 |
3 | HG00642.hp1 HG01255.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.701-513A>G | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 4/5 | chr9 | 98092514 | |||||||
| chr9:98092638 | C | A | 182 | a0001c0001t0001g0028 a0001c0001t0001g0310 a0001c0001t0001g0311 others(179): Show |
204 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(201): Show |
intron_variant | MODIFIER | c.701-637G>T | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 4/5 | chr9 | 98092638 | |||||||
| chr9:98092904 | G | T | 1 | a0001c0001t0002g0034 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.701-903C>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 4/5 | chr9 | 98092904 | |||||||
| chr9:98093115 | T | C | 1 | a0001c0001t0002g0016 | 2 | HG02071.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.701-1114A>G | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 4/5 | chr9 | 98093115 | |||||||
| chr9:98093734 | T | TTTA | 107 | a0001c0001t0001g0028 a0001c0001t0001g0226 a0001c0001t0002g0035 others(104): Show |
115 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.700+1130_700+1132d others(5): Show |
TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 4/5 | chr9 | 98093734 | |||||||
| chr9:98093896 | C | A | 12 | a0002c0003t0002g0214 a0002c0003t0003g0150 a0002c0003t0003g0155 others(9): Show |
12 | HG01243.hp2 HG02109.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.700+971G>T | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 4/5 | chr9 | 98093896 | |||||||
| chr9:98093896 | C | T | 5 | a0001c0002t0007g0052 a0001c0002t0007g0089 a0001c0002t0007g0154 others(2): Show |
5 | HG01891.hp1 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.700+971G>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 4/5 | chr9 | 98093896 | |||||||
| chr9:98093988 | C | G | 1 | a0001c0001t0002g0075 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.700+879G>C | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 4/5 | chr9 | 98093988 | |||||||
| chr9:98094114 | A | G | 1 | a0004c0009t0002g0050 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.700+753T>C | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 4/5 | chr9 | 98094114 | |||||||
| chr9:98094165 | C | T | 69 | a0001c0001t0001g0310 a0001c0001t0001g0311 a0001c0001t0001g0312 others(66): Show |
83 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(80): Show |
intron_variant | MODIFIER | c.700+702G>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 4/5 | chr9 | 98094165 | |||||||
| chr9:98094813 | G | T | 1 | a0001c0001t0003g0300 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.700+54C>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 4/5 | chr9 | 98094813 | |||||||
| chr9:98094856 | C | T | 1 | a0001c0001t0003g0199 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.700+11G>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 4/5 | chr9 | 98094856 | |||||||
| chr9:98095085 | C | A | 1 | a0001c0001t0003g0036 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.538-56G>T | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 3/5 | chr9 | 98095085 | |||||||
| chr9:98095202 | C | T | 1 | a0001c0006t0011g0043 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.538-173G>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 3/5 | chr9 | 98095202 | |||||||
| chr9:98095232 | G | A | 1 | a0001c0001t0002g0075 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.538-203C>T | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 3/5 | chr9 | 98095232 | |||||||
| chr9:98095418 | T | C | 1 | a0001c0001t0002g0108 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.538-389A>G | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 3/5 | chr9 | 98095418 | |||||||
| chr9:98095511 | C | T | 2 | a0001c0001t0004g0190 a0001c0001t0004g0191 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.538-482G>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 3/5 | chr9 | 98095511 | |||||||
| chr9:98095559 | G | C | 1 | a0001c0006t0011g0043 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.538-530C>G | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 3/5 | chr9 | 98095559 | |||||||
| chr9:98095610 | A | G | 11 | a0001c0001t0001g0028 a0001c0001t0005g0112 a0001c0001t0005g0219 others(8): Show |
11 | HG01081.hp2 HG01891.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.538-581T>C | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 3/5 | chr9 | 98095610 | |||||||
| chr9:98095616 | T | C | 3 | a0001c0001t0009g0097 a0001c0001t0009g0101 a0001c0001t0009g0177 |
3 | HG02965.hp1 HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.538-587A>G | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 3/5 | chr9 | 98095616 | |||||||
| chr9:98095678 | A | C | 1 | a0001c0001t0002g0135 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.538-649T>G | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 3/5 | chr9 | 98095678 | |||||||
| chr9:98095690 | G | A | 1 | a0001c0001t0001g0313 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.538-661C>T | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 3/5 | chr9 | 98095690 | |||||||
| chr9:98095710 | C | T | 1 | a0001c0001t0005g0272 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.538-681G>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 3/5 | chr9 | 98095710 | |||||||
| chr9:98095837 | G | A | 1 | a0001c0001t0002g0292 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.538-808C>T | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 3/5 | chr9 | 98095837 | |||||||
| chr9:98095999 | T | G | 2 | a0001c0001t0003g0195 a0001c0001t0003g0200 |
2 | NA18951.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.538-970A>C | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 3/5 | chr9 | 98095999 | |||||||
| chr9:98096114 | G | A | 1 | a0001c0001t0004g0184 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.538-1085C>T | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 3/5 | chr9 | 98096114 | |||||||
| chr9:98096183 | G | A | 9 | a0001c0001t0002g0008 a0001c0001t0002g0019 a0001c0001t0002g0033 others(6): Show |
11 | HG01081.hp1 HG01243.hp1 HG01952.hp2 others(8): Show |
intron_variant | MODIFIER | c.538-1154C>T | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 3/5 | chr9 | 98096183 | |||||||
| chr9:98096327 | C | T | 1 | a0001c0005t0002g0114 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.538-1298G>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 3/5 | chr9 | 98096327 | |||||||
| chr9:98096395 | G | A | 1 | a0001c0001t0001g0240 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.538-1366C>T | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 3/5 | chr9 | 98096395 | |||||||
| chr9:98096395 | G | C | 3 | a0001c0001t0009g0097 a0001c0001t0009g0101 a0001c0001t0009g0177 |
3 | HG02965.hp1 HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.538-1366C>G | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 3/5 | chr9 | 98096395 | |||||||
| chr9:98096402 | C | T | 4 | a0001c0001t0002g0035 a0001c0001t0002g0102 a0001c0001t0002g0141 others(1): Show |
4 | HG02258.hp2 HG02723.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.538-1373G>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 3/5 | chr9 | 98096402 | |||||||
| chr9:98096581 | C | CTTTCTGC others(8): Show |
1 | a0001c0001t0005g0112 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.538-1553_538-1552i others(17): Show |
TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 3/5 | chr9 | 98096581 | |||||||
| chr9:98096585 | G | T | 1 | a0001c0001t0005g0112 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.538-1556C>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 3/5 | chr9 | 98096585 | |||||||
| chr9:98096587 | A | T | 1 | a0001c0001t0005g0112 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.538-1558T>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 3/5 | chr9 | 98096587 | |||||||
| chr9:98096589 | A | C | 1 | a0001c0001t0005g0112 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.538-1560T>G | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 3/5 | chr9 | 98096589 | |||||||
| chr9:98096624 | A | C | 17 | a0001c0001t0005g0013 a0001c0001t0005g0015 a0001c0001t0005g0022 others(14): Show |
20 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(17): Show |
intron_variant | MODIFIER | c.538-1595T>G | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 3/5 | chr9 | 98096624 | |||||||
| chr9:98096762 | C | G | 1 | a0001c0001t0022g0124 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.538-1733G>C | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 3/5 | chr9 | 98096762 | |||||||
| chr9:98097327 | T | TAAAA | 3 | a0001c0001t0003g0111 a0001c0001t0003g0115 a0001c0001t0003g0118 |
3 | HG02723.hp2 HG02886.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.538-2299_538-2298i others(6): Show |
TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 3/5 | chr9 | 98097327 | |||||||
| chr9:98097420 | C | T | 1 | a0001c0001t0003g0232 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.538-2391G>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 3/5 | chr9 | 98097420 | |||||||
| chr9:98097424 | C | T | 1 | a0001c0001t0022g0124 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.538-2395G>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 3/5 | chr9 | 98097424 | |||||||
| chr9:98097602 | T | C | 1 | a0001c0001t0001g0070 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.537+2329A>G | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 3/5 | chr9 | 98097602 | |||||||
| chr9:98097629 | T | G | 1 | a0001c0001t0001g0242 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.537+2302A>C | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 3/5 | chr9 | 98097629 | |||||||
| chr9:98097986 | C | T | 1 | a0001c0001t0001g0179 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.537+1945G>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 3/5 | chr9 | 98097986 | |||||||
| chr9:98098319 | A | G | 4 | a0001c0001t0005g0112 a0001c0001t0024g0109 a0001c0002t0007g0212 others(1): Show |
4 | HG01081.hp2 HG01891.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.537+1612T>C | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 3/5 | chr9 | 98098319 | |||||||
| chr9:98098343 | G | A | 2 | a0001c0001t0002g0058 a0001c0001t0002g0063 |
2 | NA18953.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.537+1588C>T | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 3/5 | chr9 | 98098343 | |||||||
| chr9:98098423 | C | T | 1 | a0001c0001t0005g0112 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.537+1508G>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 3/5 | chr9 | 98098423 | |||||||
| chr9:98098507 | G | C | 191 | a0001c0001t0001g0025 a0001c0001t0001g0028 a0001c0001t0001g0226 others(188): Show |
214 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(211): Show |
intron_variant | MODIFIER | c.537+1424C>G | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 3/5 | chr9 | 98098507 | |||||||
| chr9:98098547 | T | TA | 72 | a0001c0001t0001g0245 a0001c0001t0001g0253 a0001c0001t0001g0278 others(69): Show |
86 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.537+1383dupT | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 3/5 | chr9 | 98098547 | |||||||
| chr9:98098795 | C | T | 3 | a0001c0001t0024g0109 a0001c0002t0007g0212 a0001c0002t0007g0213 |
3 | HG01891.hp2 HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.537+1136G>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 3/5 | chr9 | 98098795 | |||||||
| chr9:98098826 | C | T | 1 | a0001c0001t0004g0187 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.537+1105G>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 3/5 | chr9 | 98098826 | |||||||
| chr9:98098969 | G | A | 1 | a0001c0001t0022g0124 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.537+962C>T | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 3/5 | chr9 | 98098969 | |||||||
| chr9:98099024 | G | A | 3 | a0001c0001t0024g0109 a0001c0002t0007g0212 a0001c0002t0007g0213 |
3 | HG01891.hp2 HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.537+907C>T | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 3/5 | chr9 | 98099024 | |||||||
| chr9:98099065 | G | A | 1 | a0001c0001t0005g0112 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.537+866C>T | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 3/5 | chr9 | 98099065 | |||||||
| chr9:98099105 | T | G | 17 | a0001c0001t0005g0013 a0001c0001t0005g0015 a0001c0001t0005g0022 others(14): Show |
20 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(17): Show |
intron_variant | MODIFIER | c.537+826A>C | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 3/5 | chr9 | 98099105 | |||||||
| chr9:98099171 | G | A | 1 | a0001c0001t0022g0124 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.537+760C>T | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 3/5 | chr9 | 98099171 | |||||||
| chr9:98099411 | C | T | 1 | a0001c0001t0003g0256 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.537+520G>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 3/5 | chr9 | 98099411 | |||||||
| chr9:98099452 | C | CA | 19 | a0001c0001t0001g0110 a0001c0001t0001g0243 a0001c0001t0001g0302 others(16): Show |
19 | HG00597.hp1 HG00741.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.537+478dupT | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 3/5 | chr9 | 98099452 | |||||||
| chr9:98099452 | CA | C | 8 | a0001c0001t0001g0030 a0001c0001t0001g0073 a0001c0001t0002g0058 others(5): Show |
8 | HG00558.hp1 HG01256.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.537+478delT | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 3/5 | chr9 | 98099452 | |||||||
| chr9:98099520 | G | C | 1 | a0001c0001t0003g0137 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.537+411C>G | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 3/5 | chr9 | 98099520 | |||||||
| chr9:98099539 | A | C | 3 | a0001c0001t0024g0109 a0001c0002t0007g0212 a0001c0002t0007g0213 |
3 | HG01891.hp2 HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.537+392T>G | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 3/5 | chr9 | 98099539 | |||||||
| chr9:98099711 | G | A | 1 | a0001c0001t0004g0011 | 2 | NA18946.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.537+220C>T | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 3/5 | chr9 | 98099711 | |||||||
| chr9:98099924 | G | T | 1 | a0001c0001t0005g0112 | 1 | HG01081.hp2 | splice_region_variant&intron_variant | LOW | c.537+7C>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 3/5 | chr9 | 98099924 | |||||||
| chr9:98100207 | C | G | 1 | a0001c0001t0004g0011 | 2 | NA18946.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.304-43G>C | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98100207 | |||||||
| chr9:98100259 | G | C | 3 | a0001c0001t0006g0143 a0002c0003t0006g0044 a0002c0003t0006g0138 |
3 | HG01243.hp2 HG02922.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.304-95C>G | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98100259 | |||||||
| chr9:98100319 | C | G | 1 | a0001c0001t0006g0143 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.304-155G>C | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98100319 | |||||||
| chr9:98100375 | G | A | 5 | a0001c0002t0007g0052 a0001c0002t0007g0089 a0001c0002t0007g0154 others(2): Show |
5 | HG01891.hp1 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.304-211C>T | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98100375 | |||||||
| chr9:98100515 | A | C | 5 | a0001c0002t0007g0052 a0001c0002t0007g0089 a0001c0002t0007g0154 others(2): Show |
5 | HG01891.hp1 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.304-351T>G | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98100515 | |||||||
| chr9:98100620 | G | A | 1 | a0001c0001t0005g0112 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.304-456C>T | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98100620 | |||||||
| chr9:98100864 | G | A | 3 | a0001c0001t0024g0109 a0001c0002t0007g0212 a0001c0002t0007g0213 |
3 | HG01891.hp2 HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.304-700C>T | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98100864 | |||||||
| chr9:98101219 | C | T | 2 | a0001c0001t0004g0275 a0001c0001t0004g0287 |
2 | NA18953.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.304-1055G>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98101219 | |||||||
| chr9:98101241 | C | T | 3 | a0001c0001t0024g0109 a0001c0002t0007g0212 a0001c0002t0007g0213 |
3 | HG01891.hp2 HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.304-1077G>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98101241 | |||||||
| chr9:98101245 | G | C | 71 | a0001c0001t0001g0226 a0001c0001t0002g0274 a0001c0001t0003g0005 others(68): Show |
76 | HG00642.hp2 HG00741.hp2 HG01069.hp1 others(73): Show |
intron_variant | MODIFIER | c.304-1081C>G | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98101245 | |||||||
| chr9:98101260 | A | C | 11 | a0001c0001t0001g0028 a0001c0001t0005g0112 a0001c0001t0005g0219 others(8): Show |
11 | HG01081.hp2 HG01891.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.304-1096T>G | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98101260 | |||||||
| chr9:98101395 | G | A | 1 | a0001c0001t0002g0064 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.304-1231C>T | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98101395 | |||||||
| chr9:98101412 | C | T | 1 | a0001c0001t0004g0084 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.304-1248G>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98101412 | |||||||
| chr9:98101427 | A | AT | 17 | a0001c0001t0001g0269 a0001c0001t0005g0013 a0001c0001t0005g0015 others(14): Show |
20 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(17): Show |
intron_variant | MODIFIER | c.304-1264dupA | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98101427 | |||||||
| chr9:98101427 | A | T | 1 | a0001c0001t0022g0124 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.304-1263T>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98101427 | |||||||
| chr9:98101427 | AT | A | 8 | a0001c0001t0001g0028 a0001c0001t0003g0175 a0001c0001t0004g0193 others(5): Show |
8 | HG00741.hp2 HG01081.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.304-1264delA | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98101427 | |||||||
| chr9:98101448 | G | A | 1 | a0001c0001t0003g0055 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.304-1284C>T | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98101448 | |||||||
| chr9:98101450 | A | T | 2 | a0001c0001t0001g0028 a0001c0001t0005g0219 |
2 | HG02145.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.304-1286T>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98101450 | |||||||
| chr9:98101512 | G | A | 13 | a0001c0001t0006g0143 a0002c0003t0002g0214 a0002c0003t0003g0150 others(10): Show |
13 | HG01243.hp2 HG02109.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.304-1348C>T | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98101512 | |||||||
| chr9:98101542 | C | T | 17 | a0001c0001t0005g0013 a0001c0001t0005g0015 a0001c0001t0005g0022 others(14): Show |
20 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(17): Show |
intron_variant | MODIFIER | c.304-1378G>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98101542 | |||||||
| chr9:98101659 | G | T | 71 | a0001c0001t0001g0226 a0001c0001t0002g0274 a0001c0001t0003g0005 others(68): Show |
76 | HG00642.hp2 HG00741.hp2 HG01069.hp1 others(73): Show |
intron_variant | MODIFIER | c.304-1495C>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98101659 | |||||||
| chr9:98101690 | G | GA | 6 | a0001c0001t0001g0028 a0001c0001t0005g0112 a0001c0001t0005g0219 others(3): Show |
6 | HG01081.hp2 HG01891.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.304-1527dupT | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98101690 | |||||||
| chr9:98101705 | C | A | 2 | a0001c0001t0001g0028 a0001c0001t0005g0219 |
2 | HG02145.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.304-1541G>T | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98101705 | |||||||
| chr9:98101707 | A | C | 64 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(61): Show |
78 | HG00438.hp2 HG00558.hp2 HG00609.hp2 others(75): Show |
intron_variant | MODIFIER | c.304-1543T>G | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98101707 | |||||||
| chr9:98101722 | A | G | 1 | a0001c0001t0002g0016 | 2 | HG02071.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.304-1558T>C | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98101722 | |||||||
| chr9:98101912 | GCTTGAGA others(4): Show |
G | 3 | a0001c0001t0024g0109 a0001c0002t0007g0212 a0001c0002t0007g0213 |
3 | HG01891.hp2 HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.304-1759_304-1749d others(13): Show |
TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98101912 | |||||||
| chr9:98101932 | C | T | 1 | a0001c0002t0007g0052 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.304-1768G>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98101932 | |||||||
| chr9:98101933 | G | A | 2 | a0001c0001t0001g0028 a0001c0001t0005g0219 |
2 | HG02145.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.304-1769C>T | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98101933 | |||||||
| chr9:98101967 | C | T | 71 | a0001c0001t0001g0226 a0001c0001t0002g0274 a0001c0001t0003g0005 others(68): Show |
76 | HG00642.hp2 HG00741.hp2 HG01069.hp1 others(73): Show |
intron_variant | MODIFIER | c.304-1803G>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98101967 | |||||||
| chr9:98101975 | C | T | 3 | a0001c0001t0024g0109 a0001c0002t0007g0212 a0001c0002t0007g0213 |
3 | HG01891.hp2 HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.304-1811G>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98101975 | |||||||
| chr9:98102007 | C | CA | 6 | a0001c0001t0001g0028 a0001c0001t0001g0110 a0001c0001t0002g0051 others(3): Show |
6 | HG02145.hp1 HG02738.hp1 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.304-1844dupT | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98102007 | |||||||
| chr9:98102007 | CA | C | 26 | a0001c0001t0001g0107 a0001c0001t0001g0163 a0001c0001t0001g0221 others(23): Show |
30 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(27): Show |
intron_variant | MODIFIER | c.304-1844delT | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98102007 | |||||||
| chr9:98102028 | A | C | 1 | a0001c0001t0005g0203 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.304-1864T>G | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98102028 | |||||||
| chr9:98102090 | C | T | 172 | a0001c0001t0001g0226 a0001c0001t0002g0001 a0001c0001t0002g0003 others(169): Show |
194 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(191): Show |
intron_variant | MODIFIER | c.304-1926G>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98102090 | |||||||
| chr9:98102456 | T | C | 5 | a0001c0002t0007g0052 a0001c0002t0007g0089 a0001c0002t0007g0154 others(2): Show |
5 | HG01891.hp1 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.304-2292A>G | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98102456 | |||||||
| chr9:98102474 | C | T | 17 | a0001c0001t0005g0013 a0001c0001t0005g0015 a0001c0001t0005g0022 others(14): Show |
20 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(17): Show |
intron_variant | MODIFIER | c.304-2310G>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98102474 | |||||||
| chr9:98102539 | T | C | 2 | a0001c0001t0004g0160 a0001c0001t0004g0174 |
2 | HG00558.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.304-2375A>G | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98102539 | |||||||
| chr9:98102540 | G | A | 3 | a0001c0001t0024g0109 a0001c0002t0007g0212 a0001c0002t0007g0213 |
3 | HG01891.hp2 HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.304-2376C>T | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98102540 | |||||||
| chr9:98102606 | G | A | 1 | a0001c0001t0004g0236 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.304-2442C>T | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98102606 | |||||||
| chr9:98102624 | G | A | 1 | a0001c0001t0004g0011 | 2 | NA18946.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.304-2460C>T | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98102624 | |||||||
| chr9:98102637 | T | C | 77 | a0001c0001t0001g0226 a0001c0001t0002g0274 a0001c0001t0003g0005 others(74): Show |
82 | HG00642.hp2 HG00741.hp2 HG01069.hp1 others(79): Show |
intron_variant | MODIFIER | c.304-2473A>G | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98102637 | |||||||
| chr9:98102690 | G | C | 2 | a0002c0003t0003g0150 a0002c0003t0003g0155 |
2 | HG02109.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.304-2526C>G | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98102690 | |||||||
| chr9:98102728 | G | A | 2 | a0001c0006t0011g0042 a0001c0006t0011g0043 |
2 | HG02818.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.304-2564C>T | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98102728 | |||||||
| chr9:98102837 | A | G | 14 | a0001c0001t0006g0143 a0001c0001t0022g0124 a0002c0003t0002g0214 others(11): Show |
14 | HG01243.hp2 HG02109.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.304-2673T>C | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98102837 | |||||||
| chr9:98103013 | T | C | 1 | a0001c0001t0005g0112 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.304-2849A>G | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98103013 | |||||||
| chr9:98103107 | C | T | 3 | a0001c0001t0003g0111 a0001c0001t0003g0115 a0001c0001t0003g0118 |
3 | HG02723.hp2 HG02886.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.304-2943G>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98103107 | |||||||
| chr9:98103180 | A | G | 178 | a0001c0001t0001g0226 a0001c0001t0001g0245 a0001c0001t0001g0253 others(175): Show |
200 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(197): Show |
intron_variant | MODIFIER | c.304-3016T>C | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98103180 | |||||||
| chr9:98103192 | A | AAAC | 4 | a0001c0001t0005g0112 a0001c0001t0024g0109 a0001c0002t0007g0212 others(1): Show |
4 | HG01081.hp2 HG01891.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.304-3031_304-3029d others(5): Show |
TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98103192 | |||||||
| chr9:98103347 | T | C | 1 | a0001c0005t0002g0142 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.304-3183A>G | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98103347 | |||||||
| chr9:98103516 | A | C | 175 | a0001c0001t0001g0226 a0001c0001t0002g0001 a0001c0001t0002g0003 others(172): Show |
197 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(194): Show |
intron_variant | MODIFIER | c.304-3352T>G | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98103516 | |||||||
| chr9:98103560 | T | G | 4 | a0001c0005t0002g0053 a0001c0005t0002g0099 a0001c0005t0002g0114 others(1): Show |
4 | HG00642.hp2 HG01884.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.304-3396A>C | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98103560 | |||||||
| chr9:98103836 | C | CA | 17 | a0001c0001t0001g0241 a0001c0001t0001g0244 a0001c0001t0001g0250 others(14): Show |
17 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(14): Show |
intron_variant | MODIFIER | c.304-3673dupT | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98103836 | |||||||
| chr9:98103836 | C | CAAAAAA | 50 | a0001c0001t0003g0005 a0001c0001t0003g0009 a0001c0001t0003g0012 others(47): Show |
55 | HG00642.hp2 HG00741.hp2 HG01069.hp1 others(52): Show |
intron_variant | MODIFIER | c.304-3678_304-3673d others(8): Show |
TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98103836 | |||||||
| chr9:98103836 | C | CAAAAAAA | 10 | a0001c0001t0001g0226 a0001c0001t0003g0117 a0001c0001t0003g0120 others(7): Show |
10 | HG01109.hp1 HG01515.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.304-3679_304-3673d others(9): Show |
TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98103836 | |||||||
| chr9:98103882 | C | T | 3 | a0001c0001t0024g0109 a0001c0002t0007g0212 a0001c0002t0007g0213 |
3 | HG01891.hp2 HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.304-3718G>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98103882 | |||||||
| chr9:98103919 | A | C | 68 | a0001c0001t0001g0226 a0001c0001t0003g0005 a0001c0001t0003g0009 others(65): Show |
73 | HG00642.hp2 HG00741.hp2 HG01069.hp1 others(70): Show |
intron_variant | MODIFIER | c.304-3755T>G | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98103919 | |||||||
| chr9:98103939 | C | T | 5 | a0001c0002t0007g0052 a0001c0002t0007g0089 a0001c0002t0007g0154 others(2): Show |
5 | HG01891.hp1 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.304-3775G>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98103939 | |||||||
| chr9:98103952 | G | A | 3 | a0001c0001t0024g0109 a0001c0002t0007g0212 a0001c0002t0007g0213 |
3 | HG01891.hp2 HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.304-3788C>T | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98103952 | |||||||
| chr9:98104023 | A | G | 1 | a0001c0001t0022g0124 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.304-3859T>C | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98104023 | |||||||
| chr9:98104283 | C | T | 1 | a0001c0001t0005g0112 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.304-4119G>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98104283 | |||||||
| chr9:98104303 | T | C | 1 | a0001c0002t0015g0086 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.304-4139A>G | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98104303 | |||||||
| chr9:98104357 | C | T | 45 | a0001c0001t0001g0025 a0001c0001t0001g0157 a0001c0001t0001g0172 others(42): Show |
51 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.304-4193G>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98104357 | |||||||
| chr9:98104410 | C | T | 3 | a0001c0001t0003g0222 a0001c0001t0003g0227 a0001c0001t0003g0230 |
3 | HG03831.hp1 HG04115.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.304-4246G>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98104410 | |||||||
| chr9:98104510 | G | A | 2 | a0001c0006t0011g0042 a0001c0006t0011g0043 |
2 | HG02818.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.304-4346C>T | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98104510 | |||||||
| chr9:98104521 | G | C | 3 | a0001c0001t0024g0109 a0001c0002t0007g0212 a0001c0002t0007g0213 |
3 | HG01891.hp2 HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.304-4357C>G | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98104521 | |||||||
| chr9:98104523 | T | TAGAGAGA others(15): Show |
1 | a0001c0001t0022g0124 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.304-4381_304-4360d others(24): Show |
TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98104523 | |||||||
| chr9:98104590 | T | C | 73 | a0001c0001t0001g0226 a0001c0001t0003g0005 a0001c0001t0003g0009 others(70): Show |
78 | HG00642.hp2 HG00741.hp2 HG01069.hp1 others(75): Show |
intron_variant | MODIFIER | c.304-4426A>G | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98104590 | |||||||
| chr9:98104621 | C | T | 68 | a0001c0001t0001g0226 a0001c0001t0003g0005 a0001c0001t0003g0009 others(65): Show |
73 | HG00642.hp2 HG00741.hp2 HG01069.hp1 others(70): Show |
intron_variant | MODIFIER | c.304-4457G>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98104621 | |||||||
| chr9:98104754 | A | C | 1 | a0001c0001t0003g0139 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.304-4590T>G | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98104754 | |||||||
| chr9:98104755 | G | A | 1 | a0001c0001t0004g0081 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.304-4591C>T | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98104755 | |||||||
| chr9:98104944 | TG | T | 71 | a0001c0001t0001g0031 a0001c0001t0001g0066 a0001c0001t0001g0156 others(68): Show |
85 | HG00438.hp2 HG00558.hp2 HG00609.hp2 others(82): Show |
intron_variant | MODIFIER | c.304-4781delC | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98104944 | |||||||
| chr9:98105008 | CA | C | 65 | a0001c0001t0001g0226 a0001c0001t0003g0005 a0001c0001t0003g0009 others(62): Show |
70 | HG00642.hp2 HG00741.hp2 HG01069.hp1 others(67): Show |
intron_variant | MODIFIER | c.304-4845delT | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98105008 | |||||||
| chr9:98105186 | C | CGG | 8 | a0001c0001t0001g0006 a0001c0001t0001g0238 a0001c0001t0001g0246 others(5): Show |
10 | HG01099.hp1 HG01167.hp1 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.303+4701_303+4702d others(4): Show |
TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98105186 | |||||||
| chr9:98105593 | C | A | 17 | a0001c0001t0005g0013 a0001c0001t0005g0015 a0001c0001t0005g0022 others(14): Show |
20 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(17): Show |
intron_variant | MODIFIER | c.303+4296G>T | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98105593 | |||||||
| chr9:98105727 | G | A | 1 | a0001c0005t0002g0053 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.303+4162C>T | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98105727 | |||||||
| chr9:98105818 | T | C | 1 | a0001c0001t0003g0148 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.303+4071A>G | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98105818 | |||||||
| chr9:98105865 | C | A | 15 | a0001c0001t0005g0013 a0001c0001t0005g0015 a0001c0001t0005g0022 others(12): Show |
18 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(15): Show |
intron_variant | MODIFIER | c.303+4024G>T | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98105865 | |||||||
| chr9:98105907 | T | C | 74 | a0001c0001t0001g0025 a0001c0001t0001g0161 a0001c0001t0001g0163 others(71): Show |
80 | HG00642.hp2 HG00741.hp2 HG01069.hp1 others(77): Show |
intron_variant | MODIFIER | c.303+3982A>G | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98105907 | |||||||
| chr9:98105922 | G | A | 70 | a0001c0001t0001g0025 a0001c0001t0001g0161 a0001c0001t0001g0163 others(67): Show |
76 | HG00642.hp2 HG00741.hp2 HG01069.hp1 others(73): Show |
intron_variant | MODIFIER | c.303+3967C>T | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98105922 | |||||||
| chr9:98106036 | A | G | 3 | a0001c0001t0003g0012 a0001c0001t0003g0117 a0001c0001t0003g0125 |
4 | HG01884.hp2 HG02257.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.303+3853T>C | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98106036 | |||||||
| chr9:98106250 | T | A | 113 | a0001c0001t0001g0028 a0001c0001t0001g0031 a0001c0001t0001g0066 others(110): Show |
130 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.303+3639A>T | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98106250 | |||||||
| chr9:98106305 | T | A | 117 | a0001c0001t0001g0028 a0001c0001t0001g0031 a0001c0001t0001g0066 others(114): Show |
134 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.303+3584A>T | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98106305 | |||||||
| chr9:98106458 | C | G | 1 | a0001c0001t0001g0306 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.303+3431G>C | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98106458 | |||||||
| chr9:98106513 | T | A | 79 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0024 others(76): Show |
87 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.303+3376A>T | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98106513 | |||||||
| chr9:98106618 | G | A | 175 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(172): Show |
194 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.303+3271C>T | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98106618 | |||||||
| chr9:98106818 | C | CT | 188 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(185): Show |
208 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.303+3070dupA | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98106818 | |||||||
| chr9:98106825 | C | CT | 6 | a0001c0001t0002g0046 a0001c0001t0002g0082 a0001c0001t0003g0087 others(3): Show |
6 | HG01192.hp1 HG02818.hp1 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.303+3063dupA | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98106825 | |||||||
| chr9:98106826 | T | TTC | 68 | a0001c0001t0001g0157 a0001c0001t0001g0164 a0001c0001t0001g0172 others(65): Show |
75 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.303+3062_303+3063i others(4): Show |
TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98106826 | |||||||
| chr9:98106827 | T | TC | 24 | a0001c0001t0001g0028 a0001c0001t0005g0013 a0001c0001t0005g0015 others(21): Show |
26 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(23): Show |
intron_variant | MODIFIER | c.303+3061_303+3062i others(3): Show |
TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98106827 | |||||||
| chr9:98107222 | G | A | 1 | a0001c0001t0005g0219 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.303+2667C>T | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98107222 | |||||||
| chr9:98107254 | G | A | 2 | a0001c0001t0001g0030 a0001c0001t0001g0152 |
2 | HG02602.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.303+2635C>T | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98107254 | |||||||
| chr9:98107260 | A | G | 2 | a0001c0001t0001g0255 a0001c0001t0001g0279 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.303+2629T>C | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98107260 | |||||||
| chr9:98107307 | A | C | 1 | a0001c0001t0001g0179 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.303+2582T>G | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98107307 | |||||||
| chr9:98107314 | T | C | 1 | a0001c0001t0001g0028 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.303+2575A>G | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98107314 | |||||||
| chr9:98107501 | T | G | 1 | a0001c0001t0004g0165 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.303+2388A>C | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98107501 | |||||||
| chr9:98107638 | A | G | 184 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(181): Show |
203 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.303+2251T>C | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98107638 | |||||||
| chr9:98107668 | G | A | 1 | a0001c0001t0002g0132 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.303+2221C>T | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98107668 | |||||||
| chr9:98107673 | A | AT | 93 | a0001c0001t0001g0128 a0001c0001t0001g0157 a0001c0001t0001g0161 others(90): Show |
101 | HG00323.hp2 HG00423.hp1 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.303+2215dupA | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98107673 | |||||||
| chr9:98107690 | G | A | 8 | a0001c0001t0006g0143 a0001c0001t0013g0045 a0001c0001t0022g0124 others(5): Show |
8 | HG01243.hp2 HG01255.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.303+2199C>T | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98107690 | |||||||
| chr9:98107837 | A | AT | 21 | a0001c0001t0001g0014 a0001c0001t0005g0013 a0001c0001t0005g0015 others(18): Show |
24 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(21): Show |
intron_variant | MODIFIER | c.303+2051dupA | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98107837 | |||||||
| chr9:98107837 | AT | A | 105 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0024 others(102): Show |
116 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.303+2051delA | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98107837 | |||||||
| chr9:98107887 | C | T | 1 | a0001c0002t0007g0213 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.303+2002G>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98107887 | |||||||
| chr9:98107926 | C | T | 8 | a0001c0001t0006g0143 a0001c0001t0013g0045 a0001c0001t0024g0109 others(5): Show |
8 | HG01243.hp2 HG01255.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.303+1963G>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98107926 | |||||||
| chr9:98107936 | G | A | 1 | a0001c0001t0003g0039 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.303+1953C>T | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98107936 | |||||||
| chr9:98108081 | C | CT | 42 | a0001c0001t0001g0128 a0001c0001t0001g0157 a0001c0001t0001g0161 others(39): Show |
47 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.303+1807dupA | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98108081 | |||||||
| chr9:98108219 | G | C | 112 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0024 others(109): Show |
123 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.303+1670C>G | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98108219 | |||||||
| chr9:98108243 | A | G | 5 | a0001c0001t0004g0166 a0001c0001t0008g0095 a0001c0001t0008g0158 others(2): Show |
5 | HG00673.hp2 NA18747.hp2 NA18980.hp2 others(2): Show |
intron_variant | MODIFIER | c.303+1646T>C | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98108243 | |||||||
| chr9:98108376 | A | AACATCAT others(9): Show |
1 | a0002c0004t0002g0085 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.303+1497_303+1512d others(18): Show |
TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98108376 | |||||||
| chr9:98108397 | A | G | 1 | a0001c0002t0015g0086 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.303+1492T>C | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98108397 | |||||||
| chr9:98108463 | A | G | 1 | a0001c0001t0002g0268 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.303+1426T>C | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98108463 | |||||||
| chr9:98108735 | T | A | 3 | a0001c0001t0013g0045 a0001c0002t0007g0220 a0002c0003t0006g0044 |
3 | HG01243.hp2 HG01255.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.303+1154A>T | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98108735 | |||||||
| chr9:98108737 | A | AGTTGTC | 3 | a0001c0001t0013g0045 a0001c0002t0007g0220 a0002c0003t0006g0044 |
3 | HG01243.hp2 HG01255.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.303+1151_303+1152i others(8): Show |
TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98108737 | |||||||
| chr9:98108738 | T | A | 3 | a0001c0001t0013g0045 a0001c0002t0007g0220 a0002c0003t0006g0044 |
3 | HG01243.hp2 HG01255.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.303+1151A>T | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98108738 | |||||||
| chr9:98108746 | A | C | 25 | a0001c0001t0001g0028 a0001c0001t0002g0008 a0001c0001t0002g0019 others(22): Show |
28 | HG01081.hp1 HG01243.hp1 HG01952.hp2 others(25): Show |
intron_variant | MODIFIER | c.303+1143T>G | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98108746 | |||||||
| chr9:98108786 | T | C | 22 | a0001c0001t0001g0028 a0001c0001t0002g0008 a0001c0001t0002g0019 others(19): Show |
25 | HG01081.hp1 HG01243.hp1 HG01952.hp2 others(22): Show |
intron_variant | MODIFIER | c.303+1103A>G | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98108786 | |||||||
| chr9:98108879 | C | CT | 91 | a0001c0001t0001g0014 a0001c0001t0001g0028 a0001c0001t0001g0128 others(88): Show |
99 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.303+1009dupA | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98108879 | |||||||
| chr9:98108879 | C | CTT | 28 | a0001c0001t0002g0008 a0001c0001t0002g0019 a0001c0001t0002g0033 others(25): Show |
31 | HG01081.hp1 HG01243.hp1 HG01952.hp2 others(28): Show |
intron_variant | MODIFIER | c.303+1008_303+1009d others(4): Show |
TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98108879 | |||||||
| chr9:98109190 | A | T | 1 | a0001c0001t0001g0250 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.303+699T>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98109190 | |||||||
| chr9:98109206 | C | T | 2 | a0001c0001t0003g0195 a0001c0001t0003g0200 |
2 | NA18951.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.303+683G>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98109206 | |||||||
| chr9:98109244 | G | A | 24 | a0001c0001t0001g0028 a0001c0001t0002g0008 a0001c0001t0002g0019 others(21): Show |
27 | HG01081.hp1 HG01243.hp1 HG01952.hp2 others(24): Show |
intron_variant | MODIFIER | c.303+645C>T | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98109244 | |||||||
| chr9:98109247 | GA | G | 24 | a0001c0001t0001g0028 a0001c0001t0002g0008 a0001c0001t0002g0019 others(21): Show |
27 | HG01081.hp1 HG01243.hp1 HG01952.hp2 others(24): Show |
intron_variant | MODIFIER | c.303+641delT | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98109247 | |||||||
| chr9:98109262 | GAGGATGA others(17): Show |
G | 24 | a0001c0001t0001g0028 a0001c0001t0002g0008 a0001c0001t0002g0019 others(21): Show |
27 | HG01081.hp1 HG01243.hp1 HG01952.hp2 others(24): Show |
intron_variant | MODIFIER | c.303+603_303+626del others(24): Show |
TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98109262 | |||||||
| chr9:98109271 | A | C | 54 | a0001c0001t0001g0157 a0001c0001t0001g0161 a0001c0001t0001g0163 others(51): Show |
59 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.303+618T>G | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98109271 | |||||||
| chr9:98109276 | G | T | 2 | a0001c0002t0007g0089 a0001c0002t0007g0154 |
2 | HG02559.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.303+613C>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98109276 | |||||||
| chr9:98109277 | A | G | 1 | a0005c0008t0001g0270 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.303+612T>C | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98109277 | |||||||
| chr9:98109296 | G | C | 25 | a0001c0001t0001g0027 a0001c0001t0001g0110 a0001c0001t0001g0237 others(22): Show |
26 | HG00438.hp2 HG00621.hp2 HG02015.hp1 others(23): Show |
intron_variant | MODIFIER | c.303+593C>G | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98109296 | |||||||
| chr9:98109297 | G | C | 2 | a0001c0001t0003g0040 a0001c0001t0003g0041 |
2 | HG02572.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.303+592C>G | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98109297 | |||||||
| chr9:98109435 | C | T | 256 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(253): Show |
287 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(284): Show |
intron_variant | MODIFIER | c.303+454G>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98109435 | |||||||
| chr9:98109445 | A | G | 9 | a0001c0001t0002g0008 a0001c0001t0002g0019 a0001c0001t0002g0033 others(6): Show |
11 | HG01081.hp1 HG01243.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.303+444T>C | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98109445 | |||||||
| chr9:98109481 | G | C | 2 | a0001c0002t0007g0089 a0001c0002t0007g0154 |
2 | HG02559.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.303+408C>G | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98109481 | |||||||
| chr9:98109638 | T | C | 1 | a0001c0001t0001g0188 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.303+251A>G | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 2/5 | chr9 | 98109638 | |||||||
| chr9:98110172 | G | A | 27 | a0001c0001t0001g0028 a0001c0001t0002g0008 a0001c0001t0002g0019 others(24): Show |
30 | HG01081.hp1 HG01243.hp1 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.208-188C>T | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98110172 | |||||||
| chr9:98110307 | C | T | 27 | a0001c0001t0001g0028 a0001c0001t0002g0008 a0001c0001t0002g0019 others(24): Show |
30 | HG01081.hp1 HG01243.hp1 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.208-323G>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98110307 | |||||||
| chr9:98110331 | A | G | 1 | a0001c0001t0004g0170 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.208-347T>C | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98110331 | |||||||
| chr9:98110431 | C | T | 6 | a0002c0003t0002g0214 a0002c0003t0018g0217 a0002c0004t0002g0085 others(3): Show |
6 | HG02451.hp1 HG02809.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.208-447G>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98110431 | |||||||
| chr9:98110557 | A | G | 1 | a0001c0001t0004g0169 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.208-573T>C | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98110557 | |||||||
| chr9:98110645 | C | A | 1 | a0001c0001t0002g0108 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.208-661G>T | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98110645 | |||||||
| chr9:98110713 | T | G | 1 | a0001c0001t0004g0165 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.208-729A>C | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98110713 | |||||||
| chr9:98110805 | G | A | 12 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0002g0001 others(9): Show |
17 | HG01099.hp2 HG01106.hp2 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.208-821C>T | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98110805 | |||||||
| chr9:98110848 | A | AAAAAT | 74 | a0001c0001t0001g0020 a0001c0001t0001g0110 a0001c0001t0001g0122 others(71): Show |
81 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.208-869_208-865dup others(5): Show |
TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98110848 | |||||||
| chr9:98110848 | A | AAAAATAA others(3): Show |
20 | a0001c0001t0002g0078 a0001c0001t0002g0102 a0001c0001t0003g0103 others(17): Show |
20 | HG00408.hp2 HG00673.hp2 HG01261.hp2 others(17): Show |
intron_variant | MODIFIER | c.208-874_208-865dup others(10): Show |
TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98110848 | |||||||
| chr9:98110848 | A | AAAAATAA others(8): Show |
8 | a0001c0001t0001g0028 a0001c0001t0001g0161 a0001c0001t0001g0163 others(5): Show |
8 | HG00738.hp1 HG01106.hp1 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.208-879_208-865dup others(15): Show |
TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98110848 | |||||||
| chr9:98110848 | A | AAAAATAA others(13): Show |
13 | a0001c0001t0002g0035 a0001c0001t0002g0132 a0001c0001t0002g0135 others(10): Show |
14 | HG01243.hp2 HG02109.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.208-884_208-865dup others(20): Show |
TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98110848 | |||||||
| chr9:98110848 | A | AAAAATAA others(18): Show |
9 | a0001c0001t0002g0008 a0001c0001t0002g0033 a0001c0001t0002g0034 others(6): Show |
10 | HG01081.hp1 HG01243.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.208-889_208-865dup others(25): Show |
TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98110848 | |||||||
| chr9:98110848 | A | AAAAATAA others(23): Show |
1 | a0001c0001t0002g0019 | 2 | HG03540.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.208-894_208-865dup others(30): Show |
TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98110848 | |||||||
| chr9:98110848 | A | AAAAATAA others(33): Show |
1 | a0001c0006t0011g0042 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.208-904_208-865dup others(40): Show |
TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98110848 | |||||||
| chr9:98110848 | AAAAATAA others(3): Show |
A | 1 | a0001c0001t0028g0123 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.208-874_208-865del others(10): Show |
TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98110848 | |||||||
| chr9:98110933 | A | G | 27 | a0001c0001t0001g0028 a0001c0001t0002g0008 a0001c0001t0002g0019 others(24): Show |
30 | HG01081.hp1 HG01243.hp1 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.208-949T>C | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98110933 | |||||||
| chr9:98110959 | C | T | 1 | a0001c0001t0002g0133 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.208-975G>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98110959 | |||||||
| chr9:98111048 | TC | T | 32 | a0001c0001t0001g0028 a0001c0001t0002g0008 a0001c0001t0002g0019 others(29): Show |
35 | HG01081.hp1 HG01243.hp1 HG01884.hp1 others(32): Show |
intron_variant | MODIFIER | c.208-1065delG | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98111048 | |||||||
| chr9:98111049 | C | A | 2 | a0001c0001t0002g0132 a0001c0001t0003g0039 |
2 | HG02145.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.208-1065G>T | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98111049 | |||||||
| chr9:98111050 | C | A | 25 | a0001c0001t0001g0028 a0001c0001t0002g0008 a0001c0001t0002g0019 others(22): Show |
28 | HG01081.hp1 HG01243.hp1 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.208-1066G>T | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98111050 | |||||||
| chr9:98111054 | C | G | 1 | a0001c0001t0001g0276 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.208-1070G>C | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98111054 | |||||||
| chr9:98111056 | C | G | 17 | a0001c0001t0001g0014 a0001c0001t0001g0128 a0001c0001t0003g0195 others(14): Show |
20 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(17): Show |
intron_variant | MODIFIER | c.208-1072G>C | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98111056 | |||||||
| chr9:98111058 | C | A | 54 | a0001c0001t0001g0157 a0001c0001t0001g0161 a0001c0001t0001g0163 others(51): Show |
59 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.208-1074G>T | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98111058 | |||||||
| chr9:98111058 | C | CA | 7 | a0001c0001t0001g0188 a0001c0001t0001g0202 a0001c0001t0001g0307 others(4): Show |
7 | HG01074.hp1 HG02615.hp2 HG04184.hp1 others(4): Show |
intron_variant | MODIFIER | c.208-1075dupT | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98111058 | |||||||
| chr9:98111183 | TGGTGAAT others(23): Show |
T | 1 | a0001c0001t0002g0048 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.208-1229_208-1200d others(32): Show |
TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98111183 | |||||||
| chr9:98111320 | C | T | 1 | a0001c0001t0005g0112 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.208-1336G>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98111320 | |||||||
| chr9:98111373 | G | T | 1 | a0001c0001t0006g0143 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.208-1389C>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98111373 | |||||||
| chr9:98111420 | C | CAAACA | 27 | a0001c0001t0001g0028 a0001c0001t0002g0008 a0001c0001t0002g0019 others(24): Show |
30 | HG01081.hp1 HG01243.hp1 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.208-1441_208-1437d others(7): Show |
TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98111420 | |||||||
| chr9:98111649 | T | C | 27 | a0001c0001t0001g0028 a0001c0001t0002g0008 a0001c0001t0002g0019 others(24): Show |
30 | HG01081.hp1 HG01243.hp1 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.208-1665A>G | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98111649 | |||||||
| chr9:98111782 | T | G | 1 | a0001c0001t0004g0287 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.208-1798A>C | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98111782 | |||||||
| chr9:98111803 | T | C | 20 | a0001c0001t0002g0008 a0001c0001t0002g0019 a0001c0001t0002g0033 others(17): Show |
23 | HG01081.hp1 HG01243.hp1 HG01952.hp2 others(20): Show |
intron_variant | MODIFIER | c.208-1819A>G | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98111803 | |||||||
| chr9:98111855 | T | C | 2 | a0001c0002t0007g0212 a0001c0002t0007g0213 |
2 | HG01891.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.208-1871A>G | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98111855 | |||||||
| chr9:98111982 | G | A | 27 | a0001c0001t0001g0028 a0001c0001t0002g0008 a0001c0001t0002g0019 others(24): Show |
30 | HG01081.hp1 HG01243.hp1 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.208-1998C>T | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98111982 | |||||||
| chr9:98112350 | T | C | 1 | a0001c0001t0003g0139 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.208-2366A>G | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98112350 | |||||||
| chr9:98112522 | A | C | 27 | a0001c0001t0001g0028 a0001c0001t0002g0008 a0001c0001t0002g0019 others(24): Show |
30 | HG01081.hp1 HG01243.hp1 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.208-2538T>G | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98112522 | |||||||
| chr9:98112582 | C | T | 2 | a0001c0002t0007g0089 a0001c0002t0007g0154 |
2 | HG02559.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.208-2598G>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98112582 | |||||||
| chr9:98112754 | C | T | 2 | a0001c0001t0013g0045 a0002c0003t0006g0044 |
2 | HG01243.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.208-2770G>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98112754 | |||||||
| chr9:98112797 | CA | C | 207 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(204): Show |
237 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(234): Show |
intron_variant | MODIFIER | c.208-2814delT | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98112797 | |||||||
| chr9:98112797 | CAA | C | 14 | a0001c0001t0001g0161 a0001c0001t0001g0246 a0001c0001t0001g0290 others(11): Show |
14 | HG01168.hp1 HG01517.hp2 HG01943.hp1 others(11): Show |
intron_variant | MODIFIER | c.208-2815_208-2814d others(4): Show |
TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98112797 | |||||||
| chr9:98112839 | C | T | 27 | a0001c0001t0001g0028 a0001c0001t0002g0008 a0001c0001t0002g0019 others(24): Show |
30 | HG01081.hp1 HG01243.hp1 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.208-2855G>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98112839 | |||||||
| chr9:98112844 | T | C | 146 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0024 others(143): Show |
166 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(163): Show |
intron_variant | MODIFIER | c.208-2860A>G | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98112844 | |||||||
| chr9:98112970 | T | A | 1 | a0001c0002t0007g0154 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.208-2986A>T | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98112970 | |||||||
| chr9:98113113 | C | CA | 24 | a0001c0001t0001g0235 a0001c0001t0001g0273 a0001c0001t0001g0285 others(21): Show |
25 | HG00423.hp2 HG01891.hp1 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.208-3130dupT | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98113113 | |||||||
| chr9:98113113 | CA | C | 42 | a0001c0001t0001g0201 a0001c0001t0001g0237 a0001c0001t0001g0245 others(39): Show |
45 | HG00558.hp1 HG00639.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.208-3130delT | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98113113 | |||||||
| chr9:98113142 | G | GA | 175 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0024 others(172): Show |
198 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(195): Show |
intron_variant | MODIFIER | c.208-3159dupT | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98113142 | |||||||
| chr9:98113485 | G | C | 1 | a0001c0001t0001g0235 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.208-3501C>G | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98113485 | |||||||
| chr9:98113540 | A | G | 153 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0024 others(150): Show |
173 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(170): Show |
intron_variant | MODIFIER | c.208-3556T>C | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98113540 | |||||||
| chr9:98113568 | T | A | 1 | a0002c0004t0006g0092 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.208-3584A>T | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98113568 | |||||||
| chr9:98113574 | T | G | 1 | a0002c0004t0006g0092 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.208-3590A>C | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98113574 | |||||||
| chr9:98113652 | G | A | 20 | a0001c0001t0002g0008 a0001c0001t0002g0019 a0001c0001t0002g0033 others(17): Show |
23 | HG01081.hp1 HG01243.hp1 HG01952.hp2 others(20): Show |
intron_variant | MODIFIER | c.208-3668C>T | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98113652 | |||||||
| chr9:98114002 | T | C | 20 | a0001c0001t0002g0008 a0001c0001t0002g0019 a0001c0001t0002g0033 others(17): Show |
23 | HG01081.hp1 HG01243.hp1 HG01952.hp2 others(20): Show |
intron_variant | MODIFIER | c.208-4018A>G | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98114002 | |||||||
| chr9:98114044 | A | T | 149 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0024 others(146): Show |
169 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.208-4060T>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98114044 | |||||||
| chr9:98114050 | A | G | 2 | a0001c0002t0007g0089 a0001c0002t0007g0154 |
2 | HG02559.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.208-4066T>C | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98114050 | |||||||
| chr9:98114150 | C | T | 1 | a0001c0005t0002g0053 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.208-4166G>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98114150 | |||||||
| chr9:98114230 | A | T | 3 | a0001c0001t0003g0222 a0001c0001t0003g0230 a0001c0001t0004g0236 |
3 | HG03831.hp1 HG03927.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.208-4246T>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98114230 | |||||||
| chr9:98114291 | T | G | 1 | a0001c0001t0004g0084 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.208-4307A>C | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98114291 | |||||||
| chr9:98114341 | G | GT | 6 | a0001c0001t0001g0110 a0001c0001t0001g0243 a0001c0001t0001g0244 others(3): Show |
6 | HG00438.hp1 HG01891.hp1 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.208-4358dupA | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98114341 | |||||||
| chr9:98114350 | T | C | 1 | a0001c0001t0008g0189 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.208-4366A>G | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98114350 | |||||||
| chr9:98114386 | T | C | 172 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0024 others(169): Show |
195 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(192): Show |
intron_variant | MODIFIER | c.208-4402A>G | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98114386 | |||||||
| chr9:98114403 | G | A | 1 | a0001c0001t0003g0153 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.208-4419C>T | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98114403 | |||||||
| chr9:98114456 | C | G | 20 | a0001c0001t0002g0008 a0001c0001t0002g0019 a0001c0001t0002g0033 others(17): Show |
23 | HG01081.hp1 HG01243.hp1 HG01952.hp2 others(20): Show |
intron_variant | MODIFIER | c.208-4472G>C | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98114456 | |||||||
| chr9:98114495 | G | A | 1 | a0001c0001t0004g0236 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.207+4487C>T | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98114495 | |||||||
| chr9:98114592 | G | C | 1 | a0001c0001t0004g0275 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.207+4390C>G | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98114592 | |||||||
| chr9:98114597 | C | T | 20 | a0001c0001t0002g0008 a0001c0001t0002g0019 a0001c0001t0002g0033 others(17): Show |
23 | HG01081.hp1 HG01243.hp1 HG01952.hp2 others(20): Show |
intron_variant | MODIFIER | c.207+4385G>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98114597 | |||||||
| chr9:98114621 | C | T | 8 | a0001c0001t0006g0143 a0001c0001t0013g0045 a0001c0001t0024g0109 others(5): Show |
8 | HG01243.hp2 HG01255.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.207+4361G>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98114621 | |||||||
| chr9:98114660 | C | T | 20 | a0001c0001t0002g0008 a0001c0001t0002g0019 a0001c0001t0002g0033 others(17): Show |
23 | HG01081.hp1 HG01243.hp1 HG01952.hp2 others(20): Show |
intron_variant | MODIFIER | c.207+4322G>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98114660 | |||||||
| chr9:98114900 | T | C | 1 | a0001c0001t0003g0300 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.207+4082A>G | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98114900 | |||||||
| chr9:98114981 | T | C | 1 | a0001c0001t0003g0198 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.207+4001A>G | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98114981 | |||||||
| chr9:98115007 | A | C | 1 | a0001c0001t0003g0087 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.207+3975T>G | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98115007 | |||||||
| chr9:98115197 | T | C | 253 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(250): Show |
284 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(281): Show |
intron_variant | MODIFIER | c.207+3785A>G | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98115197 | |||||||
| chr9:98115237 | A | G | 7 | a0001c0001t0006g0143 a0001c0001t0013g0045 a0001c0002t0007g0212 others(4): Show |
7 | HG01243.hp2 HG01255.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.207+3745T>C | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98115237 | |||||||
| chr9:98115246 | C | T | 9 | a0001c0001t0002g0003 a0001c0001t0002g0046 a0001c0001t0002g0047 others(6): Show |
11 | HG00438.hp2 HG00558.hp2 HG02165.hp1 others(8): Show |
intron_variant | MODIFIER | c.207+3736G>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98115246 | |||||||
| chr9:98115684 | A | G | 3 | a0001c0001t0005g0219 a0001c0002t0015g0086 a0002c0004t0002g0085 |
3 | HG02257.hp2 HG02572.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.207+3298T>C | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98115684 | |||||||
| chr9:98115940 | T | C | 5 | a0001c0001t0006g0143 a0001c0001t0013g0045 a0001c0002t0007g0220 others(2): Show |
5 | HG01243.hp2 HG01255.hp1 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.207+3042A>G | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98115940 | |||||||
| chr9:98115951 | A | T | 1 | a0001c0001t0002g0108 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.207+3031T>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98115951 | |||||||
| chr9:98115994 | C | T | 49 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0001g0164 others(46): Show |
54 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.207+2988G>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98115994 | |||||||
| chr9:98115995 | G | T | 2 | a0001c0001t0001g0157 a0001c0001t0001g0303 |
2 | NA18964.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.207+2987C>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98115995 | |||||||
| chr9:98116301 | C | CA | 11 | a0001c0001t0001g0128 a0001c0001t0003g0131 a0001c0001t0003g0200 others(8): Show |
11 | HG00323.hp1 HG00323.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.207+2680dupT | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98116301 | |||||||
| chr9:98116301 | CA | C | 179 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0024 others(176): Show |
204 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(201): Show |
intron_variant | MODIFIER | c.207+2680delT | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98116301 | |||||||
| chr9:98116574 | C | T | 2 | a0001c0001t0001g0020 a0001c0001t0001g0221 |
3 | HG00642.hp1 HG01255.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.207+2408G>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98116574 | |||||||
| chr9:98116845 | CA | C | 141 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0024 others(138): Show |
160 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(157): Show |
intron_variant | MODIFIER | c.207+2136delT | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98116845 | |||||||
| chr9:98116845 | CAA | C | 12 | a0001c0001t0001g0237 a0001c0001t0001g0238 a0001c0001t0001g0240 others(9): Show |
12 | HG00621.hp2 HG01243.hp2 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.207+2135_207+2136d others(4): Show |
TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98116845 | |||||||
| chr9:98116951 | G | T | 2 | a0001c0006t0011g0042 a0001c0006t0011g0043 |
2 | HG02818.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.207+2031C>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98116951 | |||||||
| chr9:98117017 | A | T | 23 | a0001c0001t0002g0008 a0001c0001t0002g0019 a0001c0001t0002g0033 others(20): Show |
26 | HG01081.hp1 HG01243.hp1 HG01952.hp2 others(23): Show |
intron_variant | MODIFIER | c.207+1965T>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98117017 | |||||||
| chr9:98117030 | C | T | 1 | a0001c0001t0003g0131 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.207+1952G>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98117030 | |||||||
| chr9:98117113 | C | CTAAATCC others(47): Show |
1 | a0001c0001t0002g0126 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.207+1815_207+1868d others(56): Show |
TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98117113 | |||||||
| chr9:98117199 | G | A | 2 | a0001c0001t0001g0201 a0001c0001t0001g0202 |
2 | NA18949.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.207+1783C>T | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98117199 | |||||||
| chr9:98117267 | G | C | 14 | a0001c0001t0001g0014 a0001c0001t0001g0128 a0001c0001t0005g0013 others(11): Show |
17 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(14): Show |
intron_variant | MODIFIER | c.207+1715C>G | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98117267 | |||||||
| chr9:98117276 | T | TTTTA | 115 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0152 others(112): Show |
123 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(120): Show |
intron_variant | MODIFIER | c.207+1702_207+1705d others(6): Show |
TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98117276 | |||||||
| chr9:98117276 | T | TTTTATTT others(1): Show |
6 | a0001c0001t0001g0309 a0001c0001t0001g0310 a0001c0001t0001g0311 others(3): Show |
7 | HG01109.hp1 HG02976.hp1 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.207+1698_207+1705d others(10): Show |
TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98117276 | |||||||
| chr9:98117276 | T | TTTTATTT others(5): Show |
2 | a0001c0001t0001g0312 a0001c0001t0001g0313 |
2 | NA18989.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.207+1694_207+1705d others(14): Show |
TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98117276 | |||||||
| chr9:98117505 | G | A | 8 | a0001c0001t0005g0219 a0001c0002t0007g0212 a0001c0002t0007g0213 others(5): Show |
8 | HG01891.hp2 HG02451.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.207+1477C>T | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98117505 | |||||||
| chr9:98117575 | A | C | 1 | a0001c0001t0001g0031 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.207+1407T>G | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98117575 | |||||||
| chr9:98117822 | G | A | 1 | a0001c0001t0001g0314 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.207+1160C>T | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98117822 | |||||||
| chr9:98117983 | G | A | 1 | a0001c0002t0007g0220 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.207+999C>T | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98117983 | |||||||
| chr9:98118258 | TG | T | 293 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(290): Show |
326 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(323): Show |
intron_variant | MODIFIER | c.207+723delC | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98118258 | |||||||
| chr9:98118277 | T | G | 85 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0024 others(82): Show |
94 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.207+705A>C | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98118277 | |||||||
| chr9:98118537 | C | T | 1 | a0001c0001t0001g0030 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.207+445G>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98118537 | |||||||
| chr9:98118664 | C | T | 1 | a0001c0001t0005g0029 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.207+318G>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98118664 | |||||||
| chr9:98118921 | G | T | 1 | a0001c0001t0001g0028 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.207+61C>A | TRIM14 | ENSG00000106785.15 | transcript | ENST00000341469.7 | protein_coding | 1/5 | chr9 | 98118921 |