Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 287015 |
| ensemblid | ENSG00000155890.4 |
| hgncid | 19014 |
| symbol | TRIM42 |
| name | tripartite motif containing 42 |
| refseq_nuc | NM_152616.5 |
| refseq_prot | NP_689829.3 |
| ensembl_nuc | ENST00000286349.4 |
| ensembl_prot | ENSP00000286349.3 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 140678064 |
| end | 140701150 |
| strand | + |
| ver | v1.2 |
| region | chr3:140678064-140701150 |
| region5000 | chr3:140673064-140706150 |
| regionname0 | TRIM42_chr3_140678064_140701150 |
| regionname5000 | TRIM42_chr3_140673064_140706150 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 723 | 248 | 68 | 40 | 111 | 3 | 25 | 83 | TRIM42_chr3_140673064_140706150 | TRIM42 | METAM others(718): Show |
chr3 | 140673064 | 140706150 |
| a0002 | 0/0 | 723 | 148 | 20 | 31 | 77 | 7 | 13 | 59 | TRIM42_chr3_140673064_140706150 | TRIM42 | METAM others(718): Show |
chr3 | 140673064 | 140706150 |
| a0003 | 0/0 | 723 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | METAM others(718): Show |
chr3 | 140673064 | 140706150 |
| a0004 | 0/0 | 723 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | METAM others(718): Show |
chr3 | 140673064 | 140706150 |
| a0005 | 0/0 | 723 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | TRIM42_chr3_140673064_140706150 | TRIM42 | METAM others(718): Show |
chr3 | 140673064 | 140706150 |
| a0006 | 0/0 | 723 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | METAM others(718): Show |
chr3 | 140673064 | 140706150 |
| a0007 | 0/0 | 723 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | METAM others(718): Show |
chr3 | 140673064 | 140706150 |
| a0008 | 0/0 | 723 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | METAM others(718): Show |
chr3 | 140673064 | 140706150 |
| a0009 | 0/0 | 723 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | METAM others(718): Show |
chr3 | 140673064 | 140706150 |
| a0010 | 0/1 | 723 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | METAM others(718): Show |
chr3 | 140673064 | 140706150 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 2169 | 231 | 55 | 37 | 111 | 3 | 24 | TRIM42_chr3_140673064_140706150 | TRIM42 | ATGGA others(2164): Show |
chr3 | 140673064 | 140706150 | ||
| a0001c0003 | 0/0 | 2169 | 15 | 12 | 3 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | ATGGA others(2164): Show |
chr3 | 140673064 | 140706150 | ||
| a0001c0013 | 0/0 | 2169 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | ATGGA others(2164): Show |
chr3 | 140673064 | 140706150 | ||
| a0001c0016 | 0/0 | 2169 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM42_chr3_140673064_140706150 | TRIM42 | ATGGA others(2164): Show |
chr3 | 140673064 | 140706150 | ||
| a0002c0002 | 0/0 | 2169 | 136 | 11 | 30 | 75 | 7 | 13 | TRIM42_chr3_140673064_140706150 | TRIM42 | ATGGA others(2164): Show |
chr3 | 140673064 | 140706150 | ||
| a0002c0004 | 0/0 | 2169 | 10 | 9 | 1 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | ATGGA others(2164): Show |
chr3 | 140673064 | 140706150 | ||
| a0002c0009 | 0/0 | 2169 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | ATGGA others(2164): Show |
chr3 | 140673064 | 140706150 | ||
| a0002c0011 | 0/0 | 2169 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | ATGGA others(2164): Show |
chr3 | 140673064 | 140706150 | ||
| a0003c0005 | 0/0 | 2169 | 5 | 5 | 0 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | ATGGA others(2164): Show |
chr3 | 140673064 | 140706150 | ||
| a0004c0006 | 0/0 | 2169 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | ATGGA others(2164): Show |
chr3 | 140673064 | 140706150 | ||
| a0005c0007 | 0/0 | 2169 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | ATGGA others(2164): Show |
chr3 | 140673064 | 140706150 | ||
| a0006c0010 | 0/0 | 2169 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | ATGGA others(2164): Show |
chr3 | 140673064 | 140706150 | ||
| a0007c0012 | 0/0 | 2169 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | ATGGA others(2164): Show |
chr3 | 140673064 | 140706150 | ||
| a0008c0014 | 0/0 | 2169 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | ATGGA others(2164): Show |
chr3 | 140673064 | 140706150 | ||
| a0009c0008 | 0/0 | 2169 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | ATGGA others(2164): Show |
chr3 | 140673064 | 140706150 | ||
| a0010c0015 | 0/1 | 2169 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | ATGGA others(2164): Show |
chr3 | 140673064 | 140706150 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2514 | 231 | 55 | 37 | 111 | 3 | 24 | TRIM42_chr3_140673064_140706150 | TRIM42 | AGGGA others(2509): Show |
chr3 | 140673064 | 140706150 |
| a0001c0003t0001 | 0/0 | 2514 | 15 | 12 | 3 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | AGGGA others(2509): Show |
chr3 | 140673064 | 140706150 |
| a0001c0013t0001 | 0/0 | 2514 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | AGGGA others(2509): Show |
chr3 | 140673064 | 140706150 |
| a0001c0016t0001 | 0/0 | 2514 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM42_chr3_140673064_140706150 | TRIM42 | AGGGA others(2509): Show |
chr3 | 140673064 | 140706150 |
| a0002c0002t0001 | 0/0 | 2514 | 136 | 11 | 30 | 75 | 7 | 13 | TRIM42_chr3_140673064_140706150 | TRIM42 | AGGGA others(2509): Show |
chr3 | 140673064 | 140706150 |
| a0002c0004t0001 | 0/0 | 2514 | 10 | 9 | 1 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | AGGGA others(2509): Show |
chr3 | 140673064 | 140706150 |
| a0002c0009t0001 | 0/0 | 2514 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | AGGGA others(2509): Show |
chr3 | 140673064 | 140706150 |
| a0002c0011t0001 | 0/0 | 2514 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | AGGGA others(2509): Show |
chr3 | 140673064 | 140706150 |
| a0003c0005t0001 | 0/0 | 2514 | 5 | 5 | 0 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | AGGGA others(2509): Show |
chr3 | 140673064 | 140706150 |
| a0004c0006t0001 | 0/0 | 2514 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | AGGGA others(2509): Show |
chr3 | 140673064 | 140706150 |
| a0005c0007t0001 | 0/0 | 2514 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | AGGGA others(2509): Show |
chr3 | 140673064 | 140706150 |
| a0006c0010t0001 | 0/0 | 2514 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | AGGGA others(2509): Show |
chr3 | 140673064 | 140706150 |
| a0007c0012t0001 | 0/0 | 2514 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | AGGGA others(2509): Show |
chr3 | 140673064 | 140706150 |
| a0008c0014t0001 | 0/0 | 2514 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | AGGGA others(2509): Show |
chr3 | 140673064 | 140706150 |
| a0009c0008t0001 | 0/0 | 2514 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | AGGGA others(2509): Show |
chr3 | 140673064 | 140706150 |
| a0010c0015t0001 | 0/1 | 2514 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | AGGGA others(2509): Show |
chr3 | 140673064 | 140706150 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 18 | 1 | 3 | 12 | 1 | 1 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0002 | 0/0 | 10 | 1 | 1 | 8 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0004 | 0/0 | 8 | 1 | 1 | 5 | 0 | 1 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0005 | 0/0 | 7 | 3 | 3 | 1 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0007 | 0/0 | 6 | 0 | 0 | 4 | 0 | 2 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0009 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0014 | 0/0 | 5 | 2 | 0 | 3 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0015 | 0/0 | 5 | 1 | 0 | 4 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0016 | 0/0 | 4 | 1 | 0 | 2 | 0 | 1 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0017 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0018 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0025 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0027 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0049 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0050 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0051 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0052 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0053 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0054 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0055 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0056 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0058 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0059 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0196 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0003t0001g0012 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0003t0001g0013 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0003t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0003t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0003t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0003t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0003t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0013t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0001c0016t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0002c0002t0001g0003 | 0/0 | 8 | 0 | 8 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0002c0002t0001g0006 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0002c0002t0001g0008 | 0/0 | 6 | 2 | 3 | 0 | 0 | 1 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0002c0002t0001g0010 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0002c0002t0001g0011 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0002c0002t0001g0019 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0002c0002t0001g0020 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0002c0002t0001g0021 | 0/0 | 4 | 0 | 0 | 2 | 0 | 2 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0002c0002t0001g0022 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0002c0002t0001g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0002c0002t0001g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0002c0002t0001g0028 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0002c0002t0001g0029 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0002c0002t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0002c0002t0001g0033 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0002c0002t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0002c0002t0001g0040 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0002c0002t0001g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0002c0002t0001g0042 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0002c0002t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0002c0002t0001g0044 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0002c0002t0001g0047 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0002c0002t0001g0060 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0002c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0002c0002t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0002c0002t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0002c0002t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0002c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0002c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0002c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0002c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0002c0002t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0002c0002t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0002c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0002c0002t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0002c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0002c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0002c0002t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0002c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0002c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0002c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0002c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0002c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0002c0002t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0002c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0002c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0002c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0002c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0002c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0002c0002t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0002c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0002c0002t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0002c0002t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0002c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0002c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0002c0002t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0002c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0002c0002t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0002c0002t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0002c0002t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0002c0002t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0002c0002t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0002c0002t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0002c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0002c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0002c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0002c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0002c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0002c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0002c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0002c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0002c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0002c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0002c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0002c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0002c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0002c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0002c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0002c0002t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0002c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0002c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0002c0004t0001g0045 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0002c0004t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0002c0004t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0002c0004t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0002c0004t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0002c0004t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0002c0004t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0002c0004t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0002c0004t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0002c0009t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0002c0011t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0003c0005t0001g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0003c0005t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0003c0005t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0003c0005t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0004c0006t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0005c0007t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0005c0007t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0006c0010t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0007c0012t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0008c0014t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0009c0008t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| a0010c0015t0001g0157 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0001 | g0042 | EUR | GBR | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG00099 | hp2 | a0002 | c0002 | t0001 | g0047 | EUR | GBR | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG00140 | hp1 | a0002 | c0002 | t0001 | g0155 | EUR | GBR | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG00140 | hp2 | a0002 | c0002 | t0001 | g0047 | EUR | GBR | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG00280 | hp1 | a0002 | c0002 | t0001 | g0044 | EUR | FIN | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0080 | EUR | FIN | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG00408 | hp1 | a0002 | c0002 | t0001 | g0010 | EAS | CHS | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG00408 | hp2 | a0002 | c0002 | t0001 | g0151 | EAS | CHS | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | CHS | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG00438 | hp1 | a0002 | c0002 | t0001 | g0032 | EAS | CHS | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | CHS | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | CHS | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | CHS | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG00558 | hp2 | a0002 | c0002 | t0001 | g0235 | EAS | CHS | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG00597 | hp2 | a0002 | c0002 | t0001 | g0139 | EAS | CHS | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | CHS | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG00609 | hp2 | a0002 | c0011 | t0001 | g0006 | EAS | CHS | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | CHS | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | CHS | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG00673 | hp2 | a0002 | c0002 | t0001 | g0247 | EAS | CHS | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG00735 | hp2 | a0002 | c0002 | t0001 | g0172 | AMR | PUR | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG00738 | hp1 | a0001 | c0003 | t0001 | g0012 | AMR | PUR | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG00738 | hp2 | a0006 | c0010 | t0001 | g0020 | AMR | PUR | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG00741 | hp1 | a0002 | c0002 | t0001 | g0147 | AMR | PUR | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG01069 | hp1 | a0002 | c0002 | t0001 | g0178 | AMR | PUR | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG01069 | hp2 | a0002 | c0002 | t0001 | g0041 | AMR | PUR | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG01071 | hp1 | a0002 | c0002 | t0001 | g0041 | AMR | PUR | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG01074 | hp1 | a0002 | c0002 | t0001 | g0154 | AMR | PUR | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG01074 | hp2 | a0002 | c0002 | t0001 | g0177 | AMR | PUR | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG01099 | hp1 | a0002 | c0002 | t0001 | g0008 | AMR | PUR | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG01109 | hp1 | a0001 | c0003 | t0001 | g0013 | AMR | PUR | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG01109 | hp2 | a0002 | c0002 | t0001 | g0020 | AMR | PUR | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG01167 | hp2 | a0002 | c0002 | t0001 | g0044 | AMR | PUR | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG01168 | hp1 | a0002 | c0002 | t0001 | g0020 | AMR | PUR | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG01243 | hp2 | a0001 | c0003 | t0001 | g0168 | AMR | PUR | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG01255 | hp1 | a0002 | c0002 | t0001 | g0003 | AMR | CLM | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG01258 | hp1 | a0002 | c0002 | t0001 | g0136 | AMR | CLM | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG01258 | hp2 | a0002 | c0002 | t0001 | g0141 | AMR | CLM | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | CLM | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | CLM | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG01346 | hp1 | a0002 | c0002 | t0001 | g0003 | AMR | CLM | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | CLM | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG01358 | hp1 | a0002 | c0002 | t0001 | g0003 | AMR | CLM | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | CLM | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG01361 | hp1 | a0002 | c0002 | t0001 | g0003 | AMR | CLM | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | CLM | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG01496 | hp2 | a0002 | c0004 | t0001 | g0045 | AMR | CLM | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0017 | EUR | IBS | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG01516 | hp2 | a0002 | c0002 | t0001 | g0173 | EUR | IBS | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG01928 | hp1 | a0002 | c0002 | t0001 | g0008 | AMR | PEL | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PEL | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG01934 | hp1 | a0002 | c0002 | t0001 | g0003 | AMR | PEL | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG01952 | hp2 | a0002 | c0002 | t0001 | g0003 | AMR | PEL | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG01975 | hp2 | a0002 | c0002 | t0001 | g0033 | AMR | PEL | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG01978 | hp1 | a0002 | c0002 | t0001 | g0135 | AMR | PEL | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PEL | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PEL | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG01981 | hp2 | a0002 | c0002 | t0001 | g0003 | AMR | PEL | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG01993 | hp1 | a0002 | c0002 | t0001 | g0096 | AMR | PEL | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PEL | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG02027 | hp1 | a0002 | c0002 | t0001 | g0252 | EAS | KHV | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | KHV | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG02055 | hp1 | a0003 | c0005 | t0001 | g0161 | AFR | ACB | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG02055 | hp2 | a0001 | c0003 | t0001 | g0061 | AFR | ACB | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG02056 | hp1 | a0002 | c0002 | t0001 | g0169 | EAS | KHV | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG02056 | hp2 | a0002 | c0002 | t0001 | g0137 | EAS | KHV | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG02071 | hp1 | a0002 | c0002 | t0001 | g0043 | EAS | KHV | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | KHV | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | KHV | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | KHV | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG02083 | hp2 | a0002 | c0002 | t0001 | g0019 | EAS | KHV | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG02129 | hp1 | a0002 | c0002 | t0001 | g0251 | EAS | KHV | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG02129 | hp2 | a0002 | c0002 | t0001 | g0248 | EAS | KHV | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | KHV | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG02132 | hp2 | a0002 | c0002 | t0001 | g0150 | EAS | KHV | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | KHV | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | ACB | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG02145 | hp2 | a0002 | c0002 | t0001 | g0156 | AFR | ACB | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG02148 | hp1 | a0002 | c0002 | t0001 | g0003 | AMR | PEL | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG02148 | hp2 | a0002 | c0002 | t0001 | g0138 | AMR | PEL | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | CDX | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG02155 | hp2 | a0002 | c0002 | t0001 | g0032 | EAS | CDX | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | CDX | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG02257 | hp1 | a0002 | c0004 | t0001 | g0164 | AFR | ACB | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | ACB | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG02273 | hp1 | a0002 | c0002 | t0001 | g0097 | AMR | PEL | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | ACB | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG02280 | hp2 | a0002 | c0004 | t0001 | g0180 | AFR | ACB | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG02293 | hp2 | a0002 | c0002 | t0001 | g0098 | AMR | PEL | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PEL | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG02300 | hp2 | a0002 | c0002 | t0001 | g0158 | AMR | PEL | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG02451 | hp1 | a0003 | c0005 | t0001 | g0046 | AFR | ACB | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | ACB | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | KHV | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG02602 | hp1 | a0002 | c0002 | t0001 | g0140 | SAS | PJL | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0187 | SAS | PJL | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | GWD | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG02622 | hp2 | a0002 | c0002 | t0001 | g0029 | AFR | GWD | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG02630 | hp2 | a0001 | c0003 | t0001 | g0013 | AFR | GWD | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG02647 | hp1 | a0001 | c0003 | t0001 | g0174 | AFR | GWD | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG02683 | hp1 | a0002 | c0002 | t0001 | g0020 | SAS | PJL | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0185 | SAS | PJL | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG02698 | hp2 | a0002 | c0002 | t0001 | g0021 | SAS | PJL | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG02717 | hp1 | a0001 | c0003 | t0001 | g0013 | AFR | GWD | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | GWD | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG02809 | hp1 | a0007 | c0012 | t0001 | g0069 | AFR | GWD | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | GWD | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | GWD | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | GWD | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG02895 | hp2 | a0004 | c0006 | t0001 | g0009 | AFR | GWD | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | GWD | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG02896 | hp2 | a0002 | c0002 | t0001 | g0008 | AFR | GWD | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG02897 | hp1 | a0002 | c0002 | t0001 | g0008 | AFR | GWD | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG02897 | hp2 | a0004 | c0006 | t0001 | g0009 | AFR | GWD | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | ESN | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG02922 | hp2 | a0003 | c0005 | t0001 | g0163 | AFR | ESN | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG02965 | hp1 | a0008 | c0014 | t0001 | g0192 | AFR | ESN | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | ESN | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG02970 | hp1 | a0001 | c0003 | t0001 | g0012 | AFR | ESN | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG02970 | hp2 | a0002 | c0002 | t0001 | g0029 | AFR | ESN | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG02976 | hp1 | a0001 | c0003 | t0001 | g0012 | AFR | ESN | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | ESN | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | GWD | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG03041 | hp2 | a0002 | c0004 | t0001 | g0182 | AFR | GWD | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG03098 | hp1 | a0002 | c0002 | t0001 | g0227 | AFR | MSL | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | ESN | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG03130 | hp2 | a0001 | c0003 | t0001 | g0167 | AFR | ESN | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ESN | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | ESN | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG03195 | hp2 | a0009 | c0008 | t0001 | g0074 | AFR | ESN | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | MSL | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG03209 | hp2 | a0003 | c0005 | t0001 | g0165 | AFR | MSL | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | MSL | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | MSL | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | MSL | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG03453 | hp2 | a0002 | c0002 | t0001 | g0228 | AFR | MSL | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | MSL | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG03486 | hp2 | a0002 | c0004 | t0001 | g0170 | AFR | MSL | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG03490 | hp1 | a0002 | c0002 | t0001 | g0040 | SAS | PJL | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG03490 | hp2 | a0001 | c0016 | t0001 | g0057 | SAS | PJL | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG03492 | hp1 | a0002 | c0002 | t0001 | g0040 | SAS | PJL | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | ESN | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | ESN | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG03540 | hp1 | a0001 | c0003 | t0001 | g0013 | AFR | GWD | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG03579 | hp1 | a0003 | c0005 | t0001 | g0046 | AFR | MSL | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG03579 | hp2 | a0002 | c0002 | t0001 | g0250 | AFR | MSL | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG03654 | hp2 | a0002 | c0002 | t0001 | g0153 | SAS | PJL | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG03669 | hp2 | a0002 | c0002 | t0001 | g0006 | SAS | PJL | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG03688 | hp1 | a0002 | c0002 | t0001 | g0042 | SAS | STU | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | STU | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0202 | SAS | PJL | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG03710 | hp1 | a0002 | c0002 | t0001 | g0134 | SAS | PJL | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0057 | SAS | BEB | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | BEB | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | BEB | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG03834 | hp2 | a0002 | c0002 | t0001 | g0008 | SAS | BEB | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | BEB | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG03927 | hp2 | a0002 | c0002 | t0001 | g0021 | SAS | BEB | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0211 | SAS | BEB | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0052 | SAS | STU | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | STU | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0213 | SAS | STU | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0179 | SAS | STU | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG04228 | hp1 | a0002 | c0002 | t0001 | g0143 | SAS | STU | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0201 | SAS | STU | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA18522 | hp1 | a0002 | c0004 | t0001 | g0166 | AFR | YRI | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA18522 | hp2 | a0001 | c0003 | t0001 | g0175 | AFR | YRI | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA18612 | hp1 | a0002 | c0002 | t0001 | g0236 | EAS | CHB | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA18612 | hp2 | a0002 | c0002 | t0001 | g0149 | EAS | CHB | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | CHB | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA18906 | hp1 | a0001 | c0003 | t0001 | g0012 | AFR | YRI | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA18906 | hp2 | a0002 | c0002 | t0001 | g0029 | AFR | YRI | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA18941 | hp2 | a0002 | c0002 | t0001 | g0146 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA18942 | hp1 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA18943 | hp2 | a0002 | c0002 | t0001 | g0021 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA18945 | hp2 | a0002 | c0002 | t0001 | g0023 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA18948 | hp1 | a0002 | c0002 | t0001 | g0033 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA18949 | hp2 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA18950 | hp2 | a0002 | c0002 | t0001 | g0245 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA18953 | hp1 | a0002 | c0002 | t0001 | g0028 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA18956 | hp1 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA18956 | hp2 | a0002 | c0002 | t0001 | g0233 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA18959 | hp1 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA18960 | hp2 | a0002 | c0009 | t0001 | g0148 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA18961 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA18963 | hp1 | a0002 | c0002 | t0001 | g0237 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA18963 | hp2 | a0002 | c0002 | t0001 | g0023 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA18964 | hp2 | a0002 | c0002 | t0001 | g0144 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA18965 | hp2 | a0002 | c0002 | t0001 | g0239 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA18966 | hp2 | a0002 | c0002 | t0001 | g0242 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA18967 | hp2 | a0002 | c0002 | t0001 | g0240 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA18968 | hp1 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA18968 | hp2 | a0002 | c0002 | t0001 | g0024 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA18970 | hp2 | a0002 | c0002 | t0001 | g0022 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA18973 | hp2 | a0002 | c0002 | t0001 | g0249 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA18974 | hp2 | a0002 | c0002 | t0001 | g0039 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA18975 | hp1 | a0002 | c0002 | t0001 | g0021 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA18975 | hp2 | a0002 | c0002 | t0001 | g0246 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA18977 | hp2 | a0002 | c0002 | t0001 | g0060 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA18979 | hp1 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA18979 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA18981 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA18982 | hp1 | a0002 | c0002 | t0001 | g0043 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA18982 | hp2 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA18983 | hp1 | a0002 | c0002 | t0001 | g0028 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA18986 | hp1 | a0002 | c0002 | t0001 | g0022 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA18986 | hp2 | a0002 | c0002 | t0001 | g0024 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA18989 | hp2 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA18990 | hp1 | a0002 | c0002 | t0001 | g0244 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA18991 | hp2 | a0002 | c0002 | t0001 | g0159 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA18993 | hp1 | a0002 | c0002 | t0001 | g0060 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA18998 | hp2 | a0002 | c0002 | t0001 | g0022 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA18999 | hp2 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA19003 | hp1 | a0002 | c0002 | t0001 | g0023 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA19006 | hp2 | a0002 | c0002 | t0001 | g0238 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA19012 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA19030 | hp1 | a0002 | c0004 | t0001 | g0162 | AFR | LWK | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA19030 | hp2 | a0001 | c0003 | t0001 | g0012 | AFR | LWK | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA19043 | hp1 | a0002 | c0002 | t0001 | g0176 | AFR | LWK | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | LWK | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA19054 | hp1 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA19056 | hp1 | a0002 | c0002 | t0001 | g0039 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA19058 | hp1 | a0002 | c0002 | t0001 | g0028 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA19058 | hp2 | a0002 | c0002 | t0001 | g0142 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA19060 | hp2 | a0002 | c0002 | t0001 | g0022 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA19064 | hp2 | a0002 | c0002 | t0001 | g0100 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA19065 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA19070 | hp1 | a0005 | c0007 | t0001 | g0241 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA19074 | hp1 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA19075 | hp1 | a0002 | c0002 | t0001 | g0024 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA19076 | hp2 | a0002 | c0002 | t0001 | g0064 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA19077 | hp2 | a0002 | c0002 | t0001 | g0145 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA19078 | hp1 | a0002 | c0002 | t0001 | g0234 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA19079 | hp1 | a0005 | c0007 | t0001 | g0243 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA19085 | hp2 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA19086 | hp2 | a0002 | c0002 | t0001 | g0099 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA19087 | hp2 | a0002 | c0002 | t0001 | g0133 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | YRI | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | YRI | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | ASW | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | ASW | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA20752 | hp2 | a0002 | c0002 | t0001 | g0152 | EUR | TSI | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | GIH | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA20905 | hp2 | a0002 | c0002 | t0001 | g0011 | SAS | GIH | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | CLM | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG01123 | hp2 | a0002 | c0002 | t0001 | g0008 | AMR | CLM | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG02109 | hp2 | a0002 | c0002 | t0001 | g0229 | AFR | ACB | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG02486 | hp1 | a0002 | c0004 | t0001 | g0045 | AFR | ACB | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG02486 | hp2 | a0001 | c0003 | t0001 | g0013 | AFR | ACB | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG02559 | hp1 | a0001 | c0013 | t0001 | g0171 | AFR | ACB | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | ACB | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | MSL | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | MSL | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG06807 | hp1 | a0002 | c0004 | t0001 | g0181 | AFR | USA | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | USA | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | USA | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | USA | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | LWK | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| NA21309 | hp2 | a0002 | c0004 | t0001 | g0160 | AFR | LWK | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| homoSapiens | chm13v2 | a0010 | c0015 | t0001 | g0157 | REF | REF | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0196 | REF | REF | TRIM42_chr3_140673064_140706150 | TRIM42 | chr3 | 140673064 | 140706150 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:140678333 | G | A | 1 | a0009 | 1 | HG03195.hp2 | missense_variant | MODERATE | c.104G>A | p.Arg35Gln | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 1/5 | 270/2514 | 104/2172 | 35/723 | chr3 | 140678333 | |||
| chr3:140683157 | C | T | 1 | a0008 | 1 | HG02965.hp1 | missense_variant&splice_region_variant | MODERATE | c.1037C>T | p.Ala346Val | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 2/5 | 1203/2514 | 1037/2172 | 346/723 | chr3 | 140683157 | |||
| chr3:140688042 | G | A | 1 | a0004 | 2 | HG02895.hp2 HG02897.hp2 |
missense_variant | MODERATE | c.1360G>A | p.Glu454Lys | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 3/5 | 1526/2514 | 1360/2172 | 454/723 | chr3 | 140688042 | |||
| chr3:140688048 | G | A | 1 | a0006 | 1 | HG00738.hp2 | missense_variant | MODERATE | c.1366G>A | p.Gly456Ser | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 3/5 | 1532/2514 | 1366/2172 | 456/723 | chr3 | 140688048 | |||
| chr3:140688105 | G | A | 5 | a0002 a0003 a0005 others(2): Show |
157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
missense_variant | MODERATE | c.1423G>A | p.Val475Met | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 3/5 | 1589/2514 | 1423/2172 | 475/723 | chr3 | 140688105 | |||
| chr3:140688172 | T | C | 1 | a0005 | 2 | NA19070.hp1 NA19079.hp1 |
missense_variant | MODERATE | c.1490T>C | p.Val497Ala | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 3/5 | 1656/2514 | 1490/2172 | 497/723 | chr3 | 140688172 | |||
| chr3:140688225 | A | G | 1 | a0007 | 1 | HG02809.hp1 | missense_variant | MODERATE | c.1543A>G | p.Met515Val | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 3/5 | 1709/2514 | 1543/2172 | 515/723 | chr3 | 140688225 | |||
| chr3:140688418 | C | A | 5 | a0002 a0003 a0005 others(2): Show |
157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
missense_variant | MODERATE | c.1736C>A | p.Ala579Glu | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 3/5 | 1902/2514 | 1736/2172 | 579/723 | chr3 | 140688418 | |||
| chr3:140700892 | T | C | 1 | a0003 | 5 | HG02055.hp1 HG02451.hp1 HG02922.hp2 others(2): Show |
missense_variant | MODERATE | c.2090T>C | p.Val697Ala | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 5/5 | 2256/2514 | 2090/2172 | 697/723 | chr3 | 140700892 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:140678247 | C | T | 1 | a0001c0016 | 1 | HG03490.hp2 | synonymous_variant | LOW | c.18C>T | p.Cys6Cys | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 1/5 | 184/2514 | 18/2172 | 6/723 | chr3 | 140678247 | |||
| chr3:140682924 | G | A | 1 | a0002c0009 | 1 | NA18960.hp2 | synonymous_variant | LOW | c.804G>A | p.Ser268Ser | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 2/5 | 970/2514 | 804/2172 | 268/723 | chr3 | 140682924 | |||
| chr3:140682945 | C | T | 5 | a0001c0003 a0001c0013 a0002c0004 others(2): Show |
32 | HG00738.hp1 HG01109.hp1 HG01243.hp2 others(29): Show |
synonymous_variant | LOW | c.825C>T | p.His275His | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 2/5 | 991/2514 | 825/2172 | 275/723 | chr3 | 140682945 | |||
| chr3:140688200 | C | T | 1 | a0002c0011 | 1 | HG00609.hp2 | synonymous_variant | LOW | c.1518C>T | p.Ser506Ser | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 3/5 | 1684/2514 | 1518/2172 | 506/723 | chr3 | 140688200 | |||
| chr3:140688455 | C | T | 1 | a0001c0013 | 1 | HG02559.hp1 | synonymous_variant | LOW | c.1773C>T | p.His591His | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 3/5 | 1939/2514 | 1773/2172 | 591/723 | chr3 | 140688455 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:140678624 | C | G | 2 | a0002c0002t0001g0251 a0002c0002t0001g0252 |
2 | HG02027.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.341+54C>G | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 1/4 | chr3 | 140678624 | |||||||
| chr3:140678771 | G | A | 1 | a0001c0003t0001g0061 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.341+201G>A | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 1/4 | chr3 | 140678771 | |||||||
| chr3:140678811 | C | A | 87 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(84): Show |
149 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(146): Show |
intron_variant | MODIFIER | c.341+241C>A | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 1/4 | chr3 | 140678811 | |||||||
| chr3:140678872 | G | A | 70 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0131 others(67): Show |
106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.341+302G>A | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 1/4 | chr3 | 140678872 | |||||||
| chr3:140678959 | C | T | 1 | a0001c0001t0001g0130 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.341+389C>T | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 1/4 | chr3 | 140678959 | |||||||
| chr3:140679021 | C | G | 5 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(2): Show |
5 | NA18949.hp1 NA18955.hp1 NA18989.hp1 others(2): Show |
intron_variant | MODIFIER | c.341+451C>G | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 1/4 | chr3 | 140679021 | |||||||
| chr3:140679054 | A | AC | 46 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(43): Show |
77 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.341+492dupC | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr3 | 140679054 | ||||||
| chr3:140679054 | A | ACC | 53 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(50): Show |
101 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.341+491_341+492dup others(2): Show |
TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr3 | 140679054 | ||||||
| chr3:140679054 | AC | A | 19 | a0001c0001t0001g0009 a0001c0001t0001g0048 a0001c0001t0001g0049 others(16): Show |
28 | HG00639.hp2 HG00733.hp1 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.341+492delC | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr3 | 140679054 | ||||||
| chr3:140679076 | T | G | 2 | a0001c0001t0001g0025 a0001c0001t0001g0053 |
5 | HG00735.hp1 HG03139.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.341+506T>G | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 1/4 | chr3 | 140679076 | |||||||
| chr3:140679206 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.341+636G>A | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 1/4 | chr3 | 140679206 | |||||||
| chr3:140679237 | T | C | 1 | a0001c0001t0001g0179 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.341+667T>C | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 1/4 | chr3 | 140679237 | |||||||
| chr3:140679280 | A | G | 2 | a0002c0002t0001g0177 a0002c0002t0001g0178 |
2 | HG01069.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.341+710A>G | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 1/4 | chr3 | 140679280 | |||||||
| chr3:140679282 | T | C | 89 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(86): Show |
151 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.341+712T>C | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 1/4 | chr3 | 140679282 | |||||||
| chr3:140679317 | C | A | 1 | a0001c0001t0001g0231 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.341+747C>A | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 1/4 | chr3 | 140679317 | |||||||
| chr3:140679540 | G | A | 1 | a0001c0001t0001g0092 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.341+970G>A | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 1/4 | chr3 | 140679540 | |||||||
| chr3:140679634 | A | C | 1 | a0001c0001t0001g0124 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.341+1064A>C | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 1/4 | chr3 | 140679634 | |||||||
| chr3:140679655 | G | A | 3 | a0002c0002t0001g0019 a0002c0002t0001g0039 a0002c0002t0001g0133 |
7 | HG02083.hp2 NA18942.hp1 NA18956.hp1 others(4): Show |
intron_variant | MODIFIER | c.341+1085G>A | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 1/4 | chr3 | 140679655 | |||||||
| chr3:140679675 | A | G | 2 | a0001c0003t0001g0174 a0001c0003t0001g0175 |
2 | HG02647.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.341+1105A>G | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 1/4 | chr3 | 140679675 | |||||||
| chr3:140679801 | T | C | 1 | a0001c0001t0001g0191 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.341+1231T>C | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 1/4 | chr3 | 140679801 | |||||||
| chr3:140679930 | A | G | 2 | a0001c0001t0001g0025 a0001c0001t0001g0053 |
5 | HG00735.hp1 HG03139.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.341+1360A>G | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 1/4 | chr3 | 140679930 | |||||||
| chr3:140679956 | C | T | 1 | a0002c0002t0001g0250 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.341+1386C>T | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 1/4 | chr3 | 140679956 | |||||||
| chr3:140680080 | G | C | 1 | a0001c0001t0001g0232 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.341+1510G>C | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 1/4 | chr3 | 140680080 | |||||||
| chr3:140680225 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.341+1655G>A | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 1/4 | chr3 | 140680225 | |||||||
| chr3:140680235 | G | T | 89 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(86): Show |
151 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.341+1665G>T | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 1/4 | chr3 | 140680235 | |||||||
| chr3:140680357 | T | C | 93 | a0001c0003t0001g0012 a0001c0003t0001g0013 a0001c0003t0001g0061 others(90): Show |
145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
intron_variant | MODIFIER | c.341+1787T>C | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 1/4 | chr3 | 140680357 | |||||||
| chr3:140680402 | C | T | 2 | a0001c0001t0001g0231 a0001c0001t0001g0232 |
2 | HG01243.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.341+1832C>T | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 1/4 | chr3 | 140680402 | |||||||
| chr3:140680634 | C | T | 1 | a0001c0001t0001g0230 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.342-1828C>T | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 1/4 | chr3 | 140680634 | |||||||
| chr3:140680767 | T | C | 23 | a0002c0002t0001g0006 a0002c0002t0001g0010 a0002c0002t0001g0022 others(20): Show |
39 | HG00408.hp1 HG00558.hp2 HG00609.hp2 others(36): Show |
intron_variant | MODIFIER | c.342-1695T>C | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 1/4 | chr3 | 140680767 | |||||||
| chr3:140680790 | A | C | 11 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(8): Show |
15 | HG00639.hp2 HG00733.hp1 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.342-1672A>C | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 1/4 | chr3 | 140680790 | |||||||
| chr3:140680839 | G | C | 1 | a0002c0002t0001g0134 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.342-1623G>C | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 1/4 | chr3 | 140680839 | |||||||
| chr3:140680863 | C | T | 2 | a0001c0001t0001g0231 a0001c0001t0001g0232 |
2 | HG01243.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.342-1599C>T | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 1/4 | chr3 | 140680863 | |||||||
| chr3:140680890 | A | G | 219 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(216): Show |
348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.342-1572A>G | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 1/4 | chr3 | 140680890 | |||||||
| chr3:140680948 | G | T | 2 | a0002c0002t0001g0029 a0002c0002t0001g0229 |
4 | HG02109.hp2 HG02622.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.342-1514G>T | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 1/4 | chr3 | 140680948 | |||||||
| chr3:140681057 | T | G | 1 | a0002c0002t0001g0233 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.342-1405T>G | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 1/4 | chr3 | 140681057 | |||||||
| chr3:140681280 | G | T | 1 | a0002c0002t0001g0173 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.342-1182G>T | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 1/4 | chr3 | 140681280 | |||||||
| chr3:140681283 | G | A | 1 | a0001c0001t0001g0193 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.342-1179G>A | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 1/4 | chr3 | 140681283 | |||||||
| chr3:140681327 | A | T | 89 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(86): Show |
151 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.342-1135A>T | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 1/4 | chr3 | 140681327 | |||||||
| chr3:140681347 | G | T | 1 | a0002c0002t0001g0172 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.342-1115G>T | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 1/4 | chr3 | 140681347 | |||||||
| chr3:140681368 | C | T | 114 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(111): Show |
192 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(189): Show |
intron_variant | MODIFIER | c.342-1094C>T | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 1/4 | chr3 | 140681368 | |||||||
| chr3:140681369 | C | T | 2 | a0001c0001t0001g0017 a0001c0001t0001g0090 |
5 | HG01081.hp1 HG01099.hp2 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.342-1093C>T | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 1/4 | chr3 | 140681369 | |||||||
| chr3:140681377 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.342-1085C>T | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 1/4 | chr3 | 140681377 | |||||||
| chr3:140681402 | T | C | 1 | a0001c0001t0001g0094 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.342-1060T>C | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 1/4 | chr3 | 140681402 | |||||||
| chr3:140681424 | T | A | 1 | a0001c0001t0001g0080 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.342-1038T>A | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 1/4 | chr3 | 140681424 | |||||||
| chr3:140681436 | C | T | 2 | a0002c0002t0001g0227 a0002c0002t0001g0228 |
2 | HG03098.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.342-1026C>T | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 1/4 | chr3 | 140681436 | |||||||
| chr3:140681443 | TGAGA | T | 23 | a0002c0002t0001g0006 a0002c0002t0001g0010 a0002c0002t0001g0022 others(20): Show |
39 | HG00408.hp1 HG00558.hp2 HG00609.hp2 others(36): Show |
intron_variant | MODIFIER | c.342-1015_342-1012d others(6): Show |
TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr3 | 140681443 | ||||||
| chr3:140681444 | G | T | 1 | a0002c0002t0001g0136 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.342-1018G>T | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 1/4 | chr3 | 140681444 | |||||||
| chr3:140681647 | G | GA | 70 | a0001c0001t0001g0025 a0001c0001t0001g0053 a0001c0001t0001g0216 others(67): Show |
109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.342-805dupA | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr3 | 140681647 | ||||||
| chr3:140681657 | A | T | 23 | a0002c0002t0001g0006 a0002c0002t0001g0010 a0002c0002t0001g0022 others(20): Show |
39 | HG00408.hp1 HG00558.hp2 HG00609.hp2 others(36): Show |
intron_variant | MODIFIER | c.342-805A>T | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 1/4 | chr3 | 140681657 | |||||||
| chr3:140681793 | C | T | 1 | a0002c0002t0001g0047 | 2 | HG00099.hp2 HG00140.hp2 |
intron_variant | MODIFIER | c.342-669C>T | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 1/4 | chr3 | 140681793 | |||||||
| chr3:140681867 | T | TA | 81 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(78): Show |
141 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.342-582dupA | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr3 | 140681867 | ||||||
| chr3:140681867 | TA | T | 55 | a0001c0001t0001g0216 a0001c0001t0001g0218 a0001c0001t0001g0219 others(52): Show |
81 | HG00408.hp1 HG00558.hp2 HG00609.hp2 others(78): Show |
intron_variant | MODIFIER | c.342-582delA | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr3 | 140681867 | ||||||
| chr3:140681899 | TA | T | 23 | a0002c0002t0001g0006 a0002c0002t0001g0010 a0002c0002t0001g0022 others(20): Show |
39 | HG00408.hp1 HG00558.hp2 HG00609.hp2 others(36): Show |
intron_variant | MODIFIER | c.342-551delA | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr3 | 140681899 | ||||||
| chr3:140681991 | T | C | 89 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(86): Show |
151 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.342-471T>C | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 1/4 | chr3 | 140681991 | |||||||
| chr3:140682013 | C | A | 89 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(86): Show |
151 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.342-449C>A | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 1/4 | chr3 | 140682013 | |||||||
| chr3:140682116 | T | C | 89 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(86): Show |
151 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.342-346T>C | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 1/4 | chr3 | 140682116 | |||||||
| chr3:140682175 | A | T | 23 | a0002c0002t0001g0006 a0002c0002t0001g0010 a0002c0002t0001g0022 others(20): Show |
39 | HG00408.hp1 HG00558.hp2 HG00609.hp2 others(36): Show |
intron_variant | MODIFIER | c.342-287A>T | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 1/4 | chr3 | 140682175 | |||||||
| chr3:140683388 | C | CAG | 22 | a0002c0002t0001g0006 a0002c0002t0001g0010 a0002c0002t0001g0022 others(19): Show |
38 | HG00408.hp1 HG00558.hp2 HG00609.hp2 others(35): Show |
intron_variant | MODIFIER | c.1039+229_1039+230i others(4): Show |
TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 2/4 | chr3 | 140683388 | |||||||
| chr3:140683533 | C | T | 1 | a0001c0001t0001g0190 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1039+374C>T | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 2/4 | chr3 | 140683533 | |||||||
| chr3:140683582 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1039+423G>A | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 2/4 | chr3 | 140683582 | |||||||
| chr3:140684024 | C | A | 1 | a0002c0002t0001g0234 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1039+865C>A | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 2/4 | chr3 | 140684024 | |||||||
| chr3:140684067 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1039+908C>T | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 2/4 | chr3 | 140684067 | |||||||
| chr3:140684104 | C | A | 183 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(180): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.1039+945C>A | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 2/4 | chr3 | 140684104 | |||||||
| chr3:140684164 | A | G | 1 | a0001c0001t0001g0231 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1039+1005A>G | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 2/4 | chr3 | 140684164 | |||||||
| chr3:140684210 | A | T | 1 | a0001c0001t0001g0120 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1039+1051A>T | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 2/4 | chr3 | 140684210 | |||||||
| chr3:140684344 | G | A | 2 | a0001c0001t0001g0125 a0001c0001t0001g0126 |
2 | NA18989.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.1039+1185G>A | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 2/4 | chr3 | 140684344 | |||||||
| chr3:140684444 | C | A | 10 | a0001c0001t0001g0216 a0001c0001t0001g0218 a0001c0001t0001g0219 others(7): Show |
10 | HG01123.hp1 HG02145.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1039+1285C>A | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 2/4 | chr3 | 140684444 | |||||||
| chr3:140684496 | G | A | 2 | a0001c0001t0001g0049 a0001c0001t0001g0185 |
3 | HG00733.hp1 HG01358.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.1039+1337G>A | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 2/4 | chr3 | 140684496 | |||||||
| chr3:140684565 | T | C | 1 | a0001c0001t0001g0095 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1039+1406T>C | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 2/4 | chr3 | 140684565 | |||||||
| chr3:140684586 | C | T | 1 | a0001c0001t0001g0076 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1039+1427C>T | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 2/4 | chr3 | 140684586 | |||||||
| chr3:140684715 | C | G | 1 | a0001c0001t0001g0122 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1039+1556C>G | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 2/4 | chr3 | 140684715 | |||||||
| chr3:140684983 | G | A | 14 | a0002c0004t0001g0045 a0002c0004t0001g0160 a0002c0004t0001g0162 others(11): Show |
16 | HG01496.hp2 HG02055.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.1039+1824G>A | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 2/4 | chr3 | 140684983 | |||||||
| chr3:140684985 | A | G | 2 | a0002c0002t0001g0029 a0002c0002t0001g0229 |
4 | HG02109.hp2 HG02622.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1039+1826A>G | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 2/4 | chr3 | 140684985 | |||||||
| chr3:140685150 | T | A | 73 | a0002c0002t0001g0003 a0002c0002t0001g0008 a0002c0002t0001g0011 others(70): Show |
112 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(109): Show |
intron_variant | MODIFIER | c.1039+1991T>A | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 2/4 | chr3 | 140685150 | |||||||
| chr3:140685251 | G | A | 1 | a0002c0002t0001g0135 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1039+2092G>A | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 2/4 | chr3 | 140685251 | |||||||
| chr3:140685295 | T | G | 1 | a0001c0001t0001g0081 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1039+2136T>G | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 2/4 | chr3 | 140685295 | |||||||
| chr3:140685303 | T | C | 1 | a0002c0002t0001g0227 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1039+2144T>C | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 2/4 | chr3 | 140685303 | |||||||
| chr3:140685314 | T | C | 73 | a0002c0002t0001g0003 a0002c0002t0001g0008 a0002c0002t0001g0011 others(70): Show |
112 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(109): Show |
intron_variant | MODIFIER | c.1039+2155T>C | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 2/4 | chr3 | 140685314 | |||||||
| chr3:140685336 | T | G | 9 | a0001c0001t0001g0025 a0001c0001t0001g0053 a0001c0003t0001g0012 others(6): Show |
20 | HG00735.hp1 HG00738.hp1 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.1039+2177T>G | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 2/4 | chr3 | 140685336 | |||||||
| chr3:140685399 | A | T | 1 | a0001c0001t0001g0231 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1039+2240A>T | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 2/4 | chr3 | 140685399 | |||||||
| chr3:140685493 | A | C | 1 | a0001c0001t0001g0215 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1040-2229A>C | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 2/4 | chr3 | 140685493 | |||||||
| chr3:140685547 | C | T | 73 | a0002c0002t0001g0003 a0002c0002t0001g0008 a0002c0002t0001g0011 others(70): Show |
112 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(109): Show |
intron_variant | MODIFIER | c.1040-2175C>T | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 2/4 | chr3 | 140685547 | |||||||
| chr3:140685664 | G | GT | 22 | a0002c0002t0001g0006 a0002c0002t0001g0010 a0002c0002t0001g0022 others(19): Show |
38 | HG00408.hp1 HG00558.hp2 HG00609.hp2 others(35): Show |
intron_variant | MODIFIER | c.1040-2049dupT | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr3 | 140685664 | ||||||
| chr3:140685811 | A | G | 95 | a0002c0002t0001g0003 a0002c0002t0001g0006 a0002c0002t0001g0008 others(92): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.1040-1911A>G | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 2/4 | chr3 | 140685811 | |||||||
| chr3:140685852 | T | C | 22 | a0002c0002t0001g0006 a0002c0002t0001g0010 a0002c0002t0001g0022 others(19): Show |
38 | HG00408.hp1 HG00558.hp2 HG00609.hp2 others(35): Show |
intron_variant | MODIFIER | c.1040-1870T>C | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 2/4 | chr3 | 140685852 | |||||||
| chr3:140685874 | A | G | 1 | a0001c0001t0001g0214 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1040-1848A>G | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 2/4 | chr3 | 140685874 | |||||||
| chr3:140686056 | C | T | 1 | a0002c0002t0001g0047 | 2 | HG00099.hp2 HG00140.hp2 |
intron_variant | MODIFIER | c.1040-1666C>T | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 2/4 | chr3 | 140686056 | |||||||
| chr3:140686098 | A | T | 1 | a0001c0001t0001g0213 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1040-1624A>T | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 2/4 | chr3 | 140686098 | |||||||
| chr3:140686208 | T | C | 73 | a0002c0002t0001g0003 a0002c0002t0001g0008 a0002c0002t0001g0011 others(70): Show |
112 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(109): Show |
intron_variant | MODIFIER | c.1040-1514T>C | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 2/4 | chr3 | 140686208 | |||||||
| chr3:140686428 | G | A | 1 | a0001c0001t0001g0191 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1040-1294G>A | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 2/4 | chr3 | 140686428 | |||||||
| chr3:140686430 | CAT | C | 29 | a0001c0001t0001g0009 a0001c0001t0001g0048 a0001c0001t0001g0049 others(26): Show |
38 | HG00639.hp2 HG00733.hp1 HG00741.hp2 others(35): Show |
intron_variant | MODIFIER | c.1040-1291_1040-129 others(6): Show |
TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 2/4 | chr3 | 140686430 | |||||||
| chr3:140686434 | C | A | 29 | a0001c0001t0001g0009 a0001c0001t0001g0048 a0001c0001t0001g0049 others(26): Show |
38 | HG00639.hp2 HG00733.hp1 HG00741.hp2 others(35): Show |
intron_variant | MODIFIER | c.1040-1288C>A | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 2/4 | chr3 | 140686434 | |||||||
| chr3:140686558 | G | A | 1 | a0002c0002t0001g0250 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1040-1164G>A | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 2/4 | chr3 | 140686558 | |||||||
| chr3:140686578 | C | T | 22 | a0002c0002t0001g0006 a0002c0002t0001g0010 a0002c0002t0001g0022 others(19): Show |
38 | HG00408.hp1 HG00558.hp2 HG00609.hp2 others(35): Show |
intron_variant | MODIFIER | c.1040-1144C>T | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 2/4 | chr3 | 140686578 | |||||||
| chr3:140686654 | G | A | 22 | a0002c0002t0001g0006 a0002c0002t0001g0010 a0002c0002t0001g0022 others(19): Show |
38 | HG00408.hp1 HG00558.hp2 HG00609.hp2 others(35): Show |
intron_variant | MODIFIER | c.1040-1068G>A | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 2/4 | chr3 | 140686654 | |||||||
| chr3:140686709 | C | G | 22 | a0002c0002t0001g0006 a0002c0002t0001g0010 a0002c0002t0001g0022 others(19): Show |
38 | HG00408.hp1 HG00558.hp2 HG00609.hp2 others(35): Show |
intron_variant | MODIFIER | c.1040-1013C>G | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 2/4 | chr3 | 140686709 | |||||||
| chr3:140686812 | C | T | 77 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(74): Show |
128 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.1040-910C>T | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 2/4 | chr3 | 140686812 | |||||||
| chr3:140686857 | C | CA | 12 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0216 others(9): Show |
12 | HG01123.hp1 HG02145.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.1040-864dupA | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr3 | 140686857 | ||||||
| chr3:140686947 | G | A | 1 | a0001c0001t0001g0131 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1040-775G>A | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 2/4 | chr3 | 140686947 | |||||||
| chr3:140686950 | G | A | 1 | a0001c0001t0001g0194 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1040-772G>A | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 2/4 | chr3 | 140686950 | |||||||
| chr3:140687060 | A | G | 3 | a0001c0001t0001g0073 a0001c0001t0001g0075 a0009c0008t0001g0074 |
3 | HG02976.hp2 HG03041.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1040-662A>G | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 2/4 | chr3 | 140687060 | |||||||
| chr3:140687075 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1040-647G>A | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 2/4 | chr3 | 140687075 | |||||||
| chr3:140687128 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1040-594G>A | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 2/4 | chr3 | 140687128 | |||||||
| chr3:140687361 | C | T | 29 | a0001c0001t0001g0009 a0001c0001t0001g0048 a0001c0001t0001g0049 others(26): Show |
38 | HG00639.hp2 HG00733.hp1 HG00741.hp2 others(35): Show |
intron_variant | MODIFIER | c.1040-361C>T | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 2/4 | chr3 | 140687361 | |||||||
| chr3:140687408 | C | T | 12 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0216 others(9): Show |
12 | HG01123.hp1 HG02145.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.1040-314C>T | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 2/4 | chr3 | 140687408 | |||||||
| chr3:140687463 | T | C | 100 | a0002c0002t0001g0003 a0002c0002t0001g0006 a0002c0002t0001g0008 others(97): Show |
157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.1040-259T>C | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 2/4 | chr3 | 140687463 | |||||||
| chr3:140687520 | G | A | 1 | a0002c0002t0001g0136 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1040-202G>A | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 2/4 | chr3 | 140687520 | |||||||
| chr3:140687682 | G | A | 1 | a0002c0002t0001g0228 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1040-40G>A | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 2/4 | chr3 | 140687682 | |||||||
| chr3:140687706 | C | T | 3 | a0001c0003t0001g0013 a0001c0003t0001g0174 a0001c0003t0001g0175 |
7 | HG01109.hp1 HG02486.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1040-16C>T | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 2/4 | chr3 | 140687706 | |||||||
| chr3:140688559 | G | T | 2 | a0002c0002t0001g0099 a0002c0002t0001g0100 |
2 | NA19064.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.1860+17G>T | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 3/4 | chr3 | 140688559 | |||||||
| chr3:140688701 | A | G | 3 | a0002c0002t0001g0227 a0002c0002t0001g0228 a0002c0002t0001g0250 |
3 | HG03098.hp1 HG03453.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1860+159A>G | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 3/4 | chr3 | 140688701 | |||||||
| chr3:140688752 | A | T | 1 | a0002c0002t0001g0159 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1860+210A>T | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 3/4 | chr3 | 140688752 | |||||||
| chr3:140688767 | T | C | 78 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(75): Show |
129 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.1860+225T>C | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 3/4 | chr3 | 140688767 | |||||||
| chr3:140688963 | G | T | 100 | a0002c0002t0001g0003 a0002c0002t0001g0006 a0002c0002t0001g0008 others(97): Show |
157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.1860+421G>T | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 3/4 | chr3 | 140688963 | |||||||
| chr3:140689160 | T | A | 1 | a0002c0002t0001g0137 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1860+618T>A | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 3/4 | chr3 | 140689160 | |||||||
| chr3:140689234 | C | T | 2 | a0001c0001t0001g0086 a0001c0001t0001g0087 |
2 | HG00642.hp1 HG00733.hp2 |
intron_variant | MODIFIER | c.1860+692C>T | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 3/4 | chr3 | 140689234 | |||||||
| chr3:140689404 | A | G | 3 | a0002c0002t0001g0227 a0002c0002t0001g0228 a0002c0002t0001g0250 |
3 | HG03098.hp1 HG03453.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1860+862A>G | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 3/4 | chr3 | 140689404 | |||||||
| chr3:140689539 | C | T | 1 | a0001c0001t0001g0189 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1860+997C>T | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 3/4 | chr3 | 140689539 | |||||||
| chr3:140689625 | T | C | 77 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(74): Show |
128 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.1860+1083T>C | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 3/4 | chr3 | 140689625 | |||||||
| chr3:140689680 | C | T | 5 | a0001c0001t0001g0009 a0001c0001t0001g0048 a0001c0001t0001g0183 others(2): Show |
10 | HG01255.hp2 HG01884.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1860+1138C>T | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 3/4 | chr3 | 140689680 | |||||||
| chr3:140689701 | C | T | 1 | a0002c0002t0001g0248 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1860+1159C>T | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 3/4 | chr3 | 140689701 | |||||||
| chr3:140689714 | C | G | 3 | a0002c0002t0001g0044 a0002c0002t0001g0156 a0002c0002t0001g0158 |
4 | HG00280.hp1 HG01167.hp2 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.1860+1172C>G | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 3/4 | chr3 | 140689714 | |||||||
| chr3:140689792 | T | C | 1 | a0002c0002t0001g0138 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1861-1176T>C | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 3/4 | chr3 | 140689792 | |||||||
| chr3:140690403 | T | C | 3 | a0002c0002t0001g0235 a0002c0002t0001g0236 a0002c0002t0001g0237 |
3 | HG00558.hp2 NA18612.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.1861-565T>C | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 3/4 | chr3 | 140690403 | |||||||
| chr3:140690414 | A | T | 1 | a0001c0001t0001g0212 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1861-554A>T | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 3/4 | chr3 | 140690414 | |||||||
| chr3:140690420 | T | A | 1 | a0001c0001t0001g0212 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1861-548T>A | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 3/4 | chr3 | 140690420 | |||||||
| chr3:140690422 | T | A | 1 | a0001c0001t0001g0212 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1861-546T>A | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 3/4 | chr3 | 140690422 | |||||||
| chr3:140690423 | G | T | 1 | a0001c0001t0001g0212 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1861-545G>T | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 3/4 | chr3 | 140690423 | |||||||
| chr3:140690424 | G | A | 1 | a0001c0001t0001g0212 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1861-544G>A | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 3/4 | chr3 | 140690424 | |||||||
| chr3:140690425 | G | T | 1 | a0001c0001t0001g0212 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1861-543G>T | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 3/4 | chr3 | 140690425 | |||||||
| chr3:140690427 | G | T | 1 | a0001c0001t0001g0212 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1861-541G>T | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 3/4 | chr3 | 140690427 | |||||||
| chr3:140690429 | A | T | 1 | a0001c0001t0001g0212 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1861-539A>T | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 3/4 | chr3 | 140690429 | |||||||
| chr3:140690432 | T | A | 1 | a0001c0001t0001g0212 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1861-536T>A | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 3/4 | chr3 | 140690432 | |||||||
| chr3:140690436 | A | T | 1 | a0001c0001t0001g0212 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1861-532A>T | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 3/4 | chr3 | 140690436 | |||||||
| chr3:140690438 | G | T | 1 | a0001c0001t0001g0212 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1861-530G>T | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 3/4 | chr3 | 140690438 | |||||||
| chr3:140690442 | G | A | 1 | a0001c0001t0001g0212 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1861-526G>A | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 3/4 | chr3 | 140690442 | |||||||
| chr3:140690445 | G | T | 1 | a0001c0001t0001g0212 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1861-523G>T | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 3/4 | chr3 | 140690445 | |||||||
| chr3:140690446 | T | A | 1 | a0001c0001t0001g0212 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1861-522T>A | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 3/4 | chr3 | 140690446 | |||||||
| chr3:140690448 | T | A | 1 | a0001c0001t0001g0212 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1861-520T>A | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 3/4 | chr3 | 140690448 | |||||||
| chr3:140690449 | A | T | 1 | a0001c0001t0001g0212 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1861-519A>T | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 3/4 | chr3 | 140690449 | |||||||
| chr3:140690450 | C | A | 1 | a0001c0001t0001g0212 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1861-518C>A | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 3/4 | chr3 | 140690450 | |||||||
| chr3:140690452 | G | A | 1 | a0001c0001t0001g0212 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1861-516G>A | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 3/4 | chr3 | 140690452 | |||||||
| chr3:140690453 | A | T | 1 | a0001c0001t0001g0212 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1861-515A>T | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 3/4 | chr3 | 140690453 | |||||||
| chr3:140690456 | T | A | 1 | a0001c0001t0001g0212 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1861-512T>A | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 3/4 | chr3 | 140690456 | |||||||
| chr3:140690458 | T | A | 1 | a0001c0001t0001g0212 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1861-510T>A | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 3/4 | chr3 | 140690458 | |||||||
| chr3:140690461 | A | T | 1 | a0001c0001t0001g0212 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1861-507A>T | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 3/4 | chr3 | 140690461 | |||||||
| chr3:140690462 | T | A | 1 | a0001c0001t0001g0212 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1861-506T>A | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 3/4 | chr3 | 140690462 | |||||||
| chr3:140690463 | G | T | 1 | a0001c0001t0001g0212 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1861-505G>T | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 3/4 | chr3 | 140690463 | |||||||
| chr3:140690466 | T | A | 1 | a0001c0001t0001g0212 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1861-502T>A | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 3/4 | chr3 | 140690466 | |||||||
| chr3:140690469 | G | T | 1 | a0001c0001t0001g0212 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1861-499G>T | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 3/4 | chr3 | 140690469 | |||||||
| chr3:140690470 | G | A | 1 | a0001c0001t0001g0212 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1861-498G>A | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 3/4 | chr3 | 140690470 | |||||||
| chr3:140690471 | A | T | 1 | a0001c0001t0001g0212 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1861-497A>T | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 3/4 | chr3 | 140690471 | |||||||
| chr3:140690473 | A | T | 1 | a0001c0001t0001g0212 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1861-495A>T | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 3/4 | chr3 | 140690473 | |||||||
| chr3:140690475 | C | T | 1 | a0001c0001t0001g0212 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1861-493C>T | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 3/4 | chr3 | 140690475 | |||||||
| chr3:140690479 | C | T | 1 | a0001c0001t0001g0212 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1861-489C>T | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 3/4 | chr3 | 140690479 | |||||||
| chr3:140690482 | C | T | 1 | a0001c0001t0001g0212 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1861-486C>T | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 3/4 | chr3 | 140690482 | |||||||
| chr3:140690486 | A | T | 1 | a0001c0001t0001g0212 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1861-482A>T | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 3/4 | chr3 | 140690486 | |||||||
| chr3:140690487 | G | A | 1 | a0001c0001t0001g0212 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1861-481G>A | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 3/4 | chr3 | 140690487 | |||||||
| chr3:140690490 | A | T | 1 | a0001c0001t0001g0212 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1861-478A>T | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 3/4 | chr3 | 140690490 | |||||||
| chr3:140690492 | A | T | 1 | a0001c0001t0001g0212 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1861-476A>T | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 3/4 | chr3 | 140690492 | |||||||
| chr3:140690493 | G | A | 1 | a0001c0001t0001g0212 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1861-475G>A | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 3/4 | chr3 | 140690493 | |||||||
| chr3:140690494 | A | T | 1 | a0001c0001t0001g0212 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1861-474A>T | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 3/4 | chr3 | 140690494 | |||||||
| chr3:140690496 | A | T | 1 | a0001c0001t0001g0212 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1861-472A>T | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 3/4 | chr3 | 140690496 | |||||||
| chr3:140690500 | G | T | 1 | a0001c0001t0001g0212 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1861-468G>T | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 3/4 | chr3 | 140690500 | |||||||
| chr3:140690502 | A | T | 1 | a0001c0001t0001g0212 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1861-466A>T | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 3/4 | chr3 | 140690502 | |||||||
| chr3:140690507 | A | T | 1 | a0001c0001t0001g0212 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1861-461A>T | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 3/4 | chr3 | 140690507 | |||||||
| chr3:140690509 | G | T | 1 | a0001c0001t0001g0212 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1861-459G>T | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 3/4 | chr3 | 140690509 | |||||||
| chr3:140690510 | C | A | 1 | a0001c0001t0001g0212 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1861-458C>A | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 3/4 | chr3 | 140690510 | |||||||
| chr3:140690513 | C | T | 1 | a0001c0001t0001g0212 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1861-455C>T | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 3/4 | chr3 | 140690513 | |||||||
| chr3:140690514 | T | A | 1 | a0001c0001t0001g0212 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1861-454T>A | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 3/4 | chr3 | 140690514 | |||||||
| chr3:140690519 | C | A | 1 | a0001c0001t0001g0212 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1861-449C>A | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 3/4 | chr3 | 140690519 | |||||||
| chr3:140690520 | C | T | 1 | a0001c0001t0001g0212 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1861-448C>T | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 3/4 | chr3 | 140690520 | |||||||
| chr3:140690522 | A | T | 1 | a0001c0001t0001g0212 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1861-446A>T | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 3/4 | chr3 | 140690522 | |||||||
| chr3:140690523 | G | A | 1 | a0001c0001t0001g0212 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1861-445G>A | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 3/4 | chr3 | 140690523 | |||||||
| chr3:140690525 | T | A | 1 | a0001c0001t0001g0212 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1861-443T>A | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 3/4 | chr3 | 140690525 | |||||||
| chr3:140690527 | T | A | 1 | a0001c0001t0001g0212 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1861-441T>A | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 3/4 | chr3 | 140690527 | |||||||
| chr3:140690531 | G | A | 1 | a0001c0001t0001g0212 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1861-437G>A | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 3/4 | chr3 | 140690531 | |||||||
| chr3:140690531 | GTATA | G | 7 | a0001c0001t0001g0034 a0001c0001t0001g0082 a0001c0001t0001g0103 others(4): Show |
8 | NA18747.hp1 NA18954.hp2 NA18957.hp1 others(5): Show |
intron_variant | MODIFIER | c.1861-385_1861-382d others(6): Show |
TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr3 | 140690531 | ||||||
| chr3:140690531 | GTATATA | G | 7 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0066 others(4): Show |
9 | HG00558.hp1 HG02698.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1861-387_1861-382d others(8): Show |
TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr3 | 140690531 | ||||||
| chr3:140690531 | GTATATAT others(1): Show |
G | 30 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0014 others(27): Show |
49 | HG00544.hp1 HG00597.hp1 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.1861-389_1861-382d others(10): Show |
TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr3 | 140690531 | ||||||
| chr3:140690531 | GTATATAT others(3): Show |
G | 34 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0016 others(31): Show |
68 | HG00544.hp2 HG00621.hp2 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.1861-391_1861-382d others(12): Show |
TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr3 | 140690531 | ||||||
| chr3:140690531 | GTATATAT others(5): Show |
G | 20 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0026 others(17): Show |
35 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(32): Show |
intron_variant | MODIFIER | c.1861-393_1861-382d others(14): Show |
TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr3 | 140690531 | ||||||
| chr3:140690531 | GTATATAT others(7): Show |
G | 13 | a0001c0001t0001g0018 a0001c0001t0001g0058 a0001c0001t0001g0063 others(10): Show |
17 | HG00438.hp2 HG00642.hp2 HG01361.hp2 others(14): Show |
intron_variant | MODIFIER | c.1861-395_1861-382d others(16): Show |
TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr3 | 140690531 | ||||||
| chr3:140690531 | GTATATAT others(9): Show |
G | 7 | a0001c0001t0001g0027 a0001c0001t0001g0053 a0001c0001t0001g0062 others(4): Show |
10 | HG00735.hp1 HG02818.hp1 HG03225.hp2 others(7): Show |
intron_variant | MODIFIER | c.1861-397_1861-382d others(18): Show |
TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr3 | 140690531 | ||||||
| chr3:140690531 | GTATATAT others(11): Show |
G | 11 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0118 others(8): Show |
13 | HG00733.hp1 HG01261.hp1 HG01358.hp2 others(10): Show |
intron_variant | MODIFIER | c.1861-399_1861-382d others(20): Show |
TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr3 | 140690531 | ||||||
| chr3:140690531 | GTATATAT others(13): Show |
G | 16 | a0001c0001t0001g0009 a0001c0001t0001g0025 a0001c0001t0001g0072 others(13): Show |
22 | HG00639.hp2 HG01255.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.1861-401_1861-382d others(22): Show |
TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr3 | 140690531 | ||||||
| chr3:140690531 | GTATATAT others(15): Show |
G | 13 | a0001c0001t0001g0048 a0001c0001t0001g0051 a0001c0001t0001g0052 others(10): Show |
25 | HG00738.hp1 HG00741.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.1861-403_1861-382d others(24): Show |
TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr3 | 140690531 | ||||||
| chr3:140690531 | GTATATAT others(17): Show |
G | 11 | a0001c0001t0001g0188 a0001c0003t0001g0175 a0002c0002t0001g0019 others(8): Show |
18 | HG02083.hp2 HG02109.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.1861-405_1861-382d others(26): Show |
TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr3 | 140690531 | ||||||
| chr3:140690531 | GTATATAT others(19): Show |
G | 16 | a0001c0001t0001g0075 a0001c0001t0001g0119 a0002c0002t0001g0040 others(13): Show |
19 | HG00280.hp1 HG00597.hp2 HG01069.hp1 others(16): Show |
intron_variant | MODIFIER | c.1861-407_1861-382d others(28): Show |
TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr3 | 140690531 | ||||||
| chr3:140690531 | GTATATAT others(21): Show |
G | 38 | a0002c0002t0001g0003 a0002c0002t0001g0008 a0002c0002t0001g0011 others(35): Show |
68 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(65): Show |
intron_variant | MODIFIER | c.1861-409_1861-382d others(30): Show |
TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr3 | 140690531 | ||||||
| chr3:140690531 | GTATATAT others(23): Show |
G | 3 | a0001c0001t0001g0232 a0002c0002t0001g0154 a0002c0002t0001g0155 |
3 | HG00140.hp1 HG01074.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.1861-411_1861-382d others(32): Show |
TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr3 | 140690531 | ||||||
| chr3:140690531 | GTATATAT others(27): Show |
G | 1 | a0001c0001t0001g0226 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1861-415_1861-382d others(36): Show |
TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr3 | 140690531 | ||||||
| chr3:140690531 | GTATATAT others(29): Show |
G | 22 | a0002c0002t0001g0006 a0002c0002t0001g0010 a0002c0002t0001g0022 others(19): Show |
38 | HG00408.hp1 HG00558.hp2 HG00609.hp2 others(35): Show |
intron_variant | MODIFIER | c.1861-417_1861-382d others(38): Show |
TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr3 | 140690531 | ||||||
| chr3:140690641 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1861-327G>A | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 3/4 | chr3 | 140690641 | |||||||
| chr3:140690650 | T | G | 208 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(205): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.1861-318T>G | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 3/4 | chr3 | 140690650 | |||||||
| chr3:140690718 | A | G | 1 | a0002c0002t0001g0137 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1861-250A>G | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 3/4 | chr3 | 140690718 | |||||||
| chr3:140690842 | G | A | 3 | a0001c0001t0001g0031 a0001c0001t0001g0037 a0001c0001t0001g0076 |
5 | HG01928.hp2 HG02135.hp2 HG02165.hp2 others(2): Show |
intron_variant | MODIFIER | c.1861-126G>A | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 3/4 | chr3 | 140690842 | |||||||
| chr3:140691293 | A | G | 2 | a0002c0002t0001g0152 a0002c0002t0001g0153 |
2 | HG03654.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.2085+101A>G | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140691293 | |||||||
| chr3:140691623 | A | C | 1 | a0001c0001t0001g0111 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.2085+431A>C | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140691623 | |||||||
| chr3:140691788 | C | A | 1 | a0002c0002t0001g0152 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2085+596C>A | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140691788 | |||||||
| chr3:140691977 | GA | G | 184 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(181): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.2085+796delA | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr3 | 140691977 | ||||||
| chr3:140692004 | C | G | 1 | a0002c0002t0001g0176 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2085+812C>G | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140692004 | |||||||
| chr3:140692064 | T | C | 100 | a0002c0002t0001g0003 a0002c0002t0001g0006 a0002c0002t0001g0008 others(97): Show |
157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.2085+872T>C | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140692064 | |||||||
| chr3:140692118 | C | G | 22 | a0002c0002t0001g0006 a0002c0002t0001g0010 a0002c0002t0001g0022 others(19): Show |
38 | HG00408.hp1 HG00558.hp2 HG00609.hp2 others(35): Show |
intron_variant | MODIFIER | c.2085+926C>G | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140692118 | |||||||
| chr3:140692202 | C | T | 1 | a0001c0001t0001g0206 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2085+1010C>T | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140692202 | |||||||
| chr3:140692226 | C | A | 98 | a0002c0002t0001g0003 a0002c0002t0001g0006 a0002c0002t0001g0008 others(95): Show |
155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.2085+1034C>A | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140692226 | |||||||
| chr3:140692530 | T | TAC | 13 | a0001c0001t0001g0056 a0001c0001t0001g0062 a0001c0001t0001g0063 others(10): Show |
14 | HG01123.hp1 HG02145.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.2085+1370_2085+137 others(6): Show |
TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr3 | 140692530 | ||||||
| chr3:140692530 | T | TACAC | 10 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0054 others(7): Show |
16 | HG00423.hp2 HG01346.hp2 HG02074.hp1 others(13): Show |
intron_variant | MODIFIER | c.2085+1368_2085+137 others(8): Show |
TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr3 | 140692530 | ||||||
| chr3:140692530 | T | TACACAC | 2 | a0001c0001t0001g0207 a0002c0002t0001g0029 |
4 | HG02027.hp2 HG02622.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.2085+1366_2085+137 others(10): Show |
TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr3 | 140692530 | ||||||
| chr3:140692530 | T | TACACACA others(1): Show |
12 | a0001c0001t0001g0030 a0001c0001t0001g0065 a0001c0001t0001g0067 others(9): Show |
13 | HG02109.hp2 HG02257.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.2085+1364_2085+137 others(12): Show |
TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr3 | 140692530 | ||||||
| chr3:140692530 | T | TACACACA others(3): Show |
1 | a0001c0001t0001g0066 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2085+1362_2085+137 others(14): Show |
TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr3 | 140692530 | ||||||
| chr3:140692530 | T | TACACACA others(5): Show |
1 | a0002c0002t0001g0176 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2085+1360_2085+137 others(16): Show |
TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr3 | 140692530 | ||||||
| chr3:140692530 | T | TACACACA others(7): Show |
1 | a0002c0002t0001g0228 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2085+1358_2085+137 others(18): Show |
TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr3 | 140692530 | ||||||
| chr3:140692530 | T | TACACACA others(9): Show |
1 | a0002c0002t0001g0250 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2085+1356_2085+137 others(20): Show |
TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr3 | 140692530 | ||||||
| chr3:140692530 | T | TACACACA others(13): Show |
1 | a0002c0002t0001g0039 | 2 | NA18974.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.2085+1352_2085+137 others(24): Show |
TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr3 | 140692530 | ||||||
| chr3:140692530 | T | TACACACA others(15): Show |
4 | a0002c0002t0001g0019 a0002c0002t0001g0024 a0002c0002t0001g0146 others(1): Show |
9 | HG00735.hp2 HG02083.hp2 NA18941.hp2 others(6): Show |
intron_variant | MODIFIER | c.2085+1350_2085+137 others(26): Show |
TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr3 | 140692530 | ||||||
| chr3:140692530 | T | TACACACA others(17): Show |
5 | a0002c0002t0001g0022 a0002c0002t0001g0133 a0002c0002t0001g0143 others(2): Show |
8 | HG04228.hp1 NA18963.hp1 NA18970.hp2 others(5): Show |
intron_variant | MODIFIER | c.2085+1348_2085+137 others(28): Show |
TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr3 | 140692530 | ||||||
| chr3:140692530 | T | TACACACA others(19): Show |
8 | a0002c0002t0001g0006 a0002c0002t0001g0028 a0002c0002t0001g0042 others(5): Show |
16 | HG00099.hp1 HG00609.hp2 HG02129.hp2 others(13): Show |
intron_variant | MODIFIER | c.2085+1346_2085+137 others(30): Show |
TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr3 | 140692530 | ||||||
| chr3:140692530 | T | TACACACA others(21): Show |
3 | a0002c0002t0001g0010 a0002c0002t0001g0236 a0005c0007t0001g0243 |
8 | HG00408.hp1 NA18612.hp1 NA18949.hp2 others(5): Show |
intron_variant | MODIFIER | c.2085+1344_2085+137 others(32): Show |
TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr3 | 140692530 | ||||||
| chr3:140692530 | T | TACACACA others(23): Show |
4 | a0002c0002t0001g0233 a0002c0002t0001g0235 a0002c0002t0001g0242 others(1): Show |
4 | HG00558.hp2 NA18956.hp2 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.2085+1342_2085+137 others(34): Show |
TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr3 | 140692530 | ||||||
| chr3:140692530 | T | TACACACA others(25): Show |
1 | a0002c0002t0001g0240 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2085+1340_2085+137 others(36): Show |
TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr3 | 140692530 | ||||||
| chr3:140692530 | T | TACACACA others(29): Show |
1 | a0002c0002t0001g0060 | 2 | NA18977.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.2085+1371_2085+137 others(40): Show |
TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr3 | 140692530 | ||||||
| chr3:140692530 | T | TACACACA others(31): Show |
1 | a0002c0002t0001g0239 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.2085+1371_2085+137 others(42): Show |
TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr3 | 140692530 | ||||||
| chr3:140692530 | T | TACACACA others(35): Show |
1 | a0002c0002t0001g0238 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.2085+1371_2085+137 others(46): Show |
TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr3 | 140692530 | ||||||
| chr3:140692530 | TAC | T | 4 | a0001c0001t0001g0059 a0001c0001t0001g0202 a0001c0001t0001g0205 others(1): Show |
5 | HG02258.hp2 HG02717.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.2085+1370_2085+137 others(6): Show |
TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr3 | 140692530 | ||||||
| chr3:140692530 | TACAC | T | 10 | a0001c0001t0001g0025 a0001c0001t0001g0053 a0001c0001t0001g0232 others(7): Show |
21 | HG00735.hp1 HG00738.hp1 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.2085+1368_2085+137 others(8): Show |
TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr3 | 140692530 | ||||||
| chr3:140692562 | C | CACACACA others(21): Show |
2 | a0002c0002t0001g0141 a0002c0002t0001g0153 |
2 | HG01258.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.2085+1371_2085+137 others(32): Show |
TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr3 | 140692562 | ||||||
| chr3:140692562 | C | CACACACA others(19): Show |
8 | a0002c0002t0001g0020 a0002c0002t0001g0032 a0002c0002t0001g0040 others(5): Show |
12 | HG00438.hp1 HG00597.hp2 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.2085+1371_2085+137 others(30): Show |
TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr3 | 140692562 | ||||||
| chr3:140692562 | C | CACACACA others(21): Show |
7 | a0002c0002t0001g0142 a0002c0002t0001g0154 a0002c0002t0001g0173 others(4): Show |
7 | HG00673.hp2 HG01074.hp1 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.2085+1371_2085+137 others(32): Show |
TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr3 | 140692562 | ||||||
| chr3:140692562 | C | CACACACA others(17): Show |
10 | a0002c0002t0001g0008 a0002c0002t0001g0023 a0002c0002t0001g0041 others(7): Show |
19 | HG00280.hp1 HG01069.hp2 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.2085+1371_2085+137 others(28): Show |
TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr3 | 140692562 | ||||||
| chr3:140692562 | C | CACACACA others(19): Show |
3 | a0002c0004t0001g0162 a0002c0004t0001g0181 a0008c0014t0001g0192 |
3 | HG02965.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2085+1371_2085+137 others(30): Show |
TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr3 | 140692562 | ||||||
| chr3:140692562 | C | CACACACA others(21): Show |
1 | a0002c0002t0001g0155 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2085+1371_2085+137 others(32): Show |
TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr3 | 140692562 | ||||||
| chr3:140692562 | C | CACACACA others(15): Show |
9 | a0002c0002t0001g0003 a0002c0002t0001g0021 a0002c0002t0001g0096 others(6): Show |
19 | HG00741.hp1 HG01255.hp1 HG01346.hp1 others(16): Show |
intron_variant | MODIFIER | c.2085+1371_2085+137 others(26): Show |
TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr3 | 140692562 | ||||||
| chr3:140692562 | C | CACACACA others(17): Show |
3 | a0002c0002t0001g0178 a0002c0004t0001g0045 a0002c0004t0001g0160 |
4 | HG01069.hp1 HG01496.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2085+1371_2085+137 others(28): Show |
TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr3 | 140692562 | ||||||
| chr3:140692562 | C | CACACACA others(13): Show |
7 | a0002c0002t0001g0011 a0002c0002t0001g0033 a0002c0002t0001g0047 others(4): Show |
13 | HG00099.hp2 HG00140.hp2 HG01975.hp2 others(10): Show |
intron_variant | MODIFIER | c.2085+1371_2085+137 others(24): Show |
TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr3 | 140692562 | ||||||
| chr3:140692562 | C | CACACACA others(15): Show |
4 | a0002c0004t0001g0166 a0002c0009t0001g0148 a0003c0005t0001g0161 others(1): Show |
4 | HG02055.hp1 HG02922.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.2085+1371_2085+137 others(26): Show |
TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr3 | 140692562 | ||||||
| chr3:140692562 | C | CACACACA others(17): Show |
1 | a0003c0005t0001g0165 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2085+1371_2085+137 others(28): Show |
TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr3 | 140692562 | ||||||
| chr3:140692562 | C | CACACACA others(11): Show |
3 | a0002c0002t0001g0098 a0002c0002t0001g0149 a0002c0002t0001g0227 |
3 | HG02293.hp2 HG03098.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.2085+1371_2085+137 others(22): Show |
TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr3 | 140692562 | ||||||
| chr3:140692562 | C | CACACACA others(13): Show |
3 | a0002c0002t0001g0043 a0002c0002t0001g0159 a0002c0004t0001g0164 |
4 | HG02071.hp1 HG02257.hp1 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.2085+1371_2085+137 others(24): Show |
TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr3 | 140692562 | ||||||
| chr3:140692562 | C | CACACACA others(15): Show |
1 | a0003c0005t0001g0046 | 2 | HG02451.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2085+1371_2085+137 others(26): Show |
TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr3 | 140692562 | ||||||
| chr3:140692562 | C | CACACACA others(9): Show |
1 | a0002c0002t0001g0158 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.2085+1371_2085+137 others(20): Show |
TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr3 | 140692562 | ||||||
| chr3:140692562 | C | CACACACA others(11): Show |
1 | a0002c0002t0001g0150 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2085+1371_2085+137 others(22): Show |
TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr3 | 140692562 | ||||||
| chr3:140692562 | C | CACACACA others(13): Show |
1 | a0002c0004t0001g0170 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2085+1371_2085+137 others(24): Show |
TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr3 | 140692562 | ||||||
| chr3:140692562 | C | CACACACA others(7): Show |
1 | a0002c0002t0001g0151 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2085+1371_2085+137 others(18): Show |
TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr3 | 140692562 | ||||||
| chr3:140692562 | C | CACACACA others(5): Show |
1 | a0001c0001t0001g0105 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2085+1371_2085+137 others(16): Show |
TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr3 | 140692562 | ||||||
| chr3:140692562 | C | CACACACA others(3): Show |
6 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0077 others(3): Show |
8 | HG00621.hp1 HG00639.hp1 HG03486.hp1 others(5): Show |
intron_variant | MODIFIER | c.2085+1371_2085+137 others(14): Show |
TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr3 | 140692562 | ||||||
| chr3:140692562 | C | CACACACA others(1): Show |
52 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(49): Show |
100 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.2085+1371_2085+137 others(12): Show |
TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr3 | 140692562 | ||||||
| chr3:140692562 | C | CACACAG | 4 | a0001c0001t0001g0083 a0001c0001t0001g0110 a0001c0001t0001g0122 others(1): Show |
4 | HG01071.hp2 HG02083.hp1 NA18949.hp1 others(1): Show |
intron_variant | MODIFIER | c.2085+1371_2085+137 others(10): Show |
TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr3 | 140692562 | ||||||
| chr3:140692562 | C | G | 5 | a0001c0001t0001g0009 a0001c0001t0001g0183 a0001c0001t0001g0198 others(2): Show |
9 | HG01255.hp2 HG01884.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.2085+1370C>G | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140692562 | |||||||
| chr3:140692564 | G | C | 20 | a0001c0001t0001g0057 a0001c0001t0001g0062 a0001c0001t0001g0063 others(17): Show |
22 | HG00621.hp2 HG01123.hp1 HG02071.hp2 others(19): Show |
intron_variant | MODIFIER | c.2085+1372G>C | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140692564 | |||||||
| chr3:140692566 | G | C | 2 | a0001c0001t0001g0220 a0001c0001t0001g0222 |
2 | HG01123.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2085+1374G>C | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140692566 | |||||||
| chr3:140692590 | G | C | 1 | a0002c0002t0001g0250 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2085+1398G>C | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140692590 | |||||||
| chr3:140692590 | G | T | 176 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(173): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.2085+1398G>T | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140692590 | |||||||
| chr3:140692732 | T | G | 1 | a0001c0001t0001g0115 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2085+1540T>G | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140692732 | |||||||
| chr3:140692737 | G | A | 1 | a0002c0002t0001g0147 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2085+1545G>A | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140692737 | |||||||
| chr3:140692908 | G | A | 3 | a0002c0002t0001g0139 a0002c0002t0001g0144 a0002c0002t0001g0151 |
3 | HG00408.hp2 HG00597.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.2085+1716G>A | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140692908 | |||||||
| chr3:140692950 | C | T | 3 | a0002c0002t0001g0227 a0002c0002t0001g0228 a0002c0002t0001g0250 |
3 | HG03098.hp1 HG03453.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2085+1758C>T | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140692950 | |||||||
| chr3:140693045 | C | T | 8 | a0001c0001t0001g0035 a0001c0001t0001g0104 a0001c0001t0001g0111 others(5): Show |
9 | HG00438.hp2 NA18955.hp2 NA18957.hp1 others(6): Show |
intron_variant | MODIFIER | c.2085+1853C>T | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140693045 | |||||||
| chr3:140693284 | T | C | 2 | a0002c0002t0001g0177 a0002c0002t0001g0178 |
2 | HG01069.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.2085+2092T>C | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140693284 | |||||||
| chr3:140693593 | C | T | 1 | a0002c0002t0001g0251 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2085+2401C>T | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140693593 | |||||||
| chr3:140693678 | A | G | 20 | a0002c0002t0001g0006 a0002c0002t0001g0010 a0002c0002t0001g0022 others(17): Show |
36 | HG00408.hp1 HG00558.hp2 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.2085+2486A>G | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140693678 | |||||||
| chr3:140693803 | T | C | 20 | a0002c0002t0001g0006 a0002c0002t0001g0010 a0002c0002t0001g0022 others(17): Show |
36 | HG00408.hp1 HG00558.hp2 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.2085+2611T>C | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140693803 | |||||||
| chr3:140693845 | A | G | 1 | a0002c0002t0001g0246 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.2085+2653A>G | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140693845 | |||||||
| chr3:140693934 | G | A | 3 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0188 |
5 | HG00741.hp2 HG01168.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.2085+2742G>A | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140693934 | |||||||
| chr3:140694368 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2085+3176G>A | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140694368 | |||||||
| chr3:140694501 | C | T | 17 | a0002c0002t0001g0029 a0002c0002t0001g0176 a0002c0002t0001g0229 others(14): Show |
21 | HG01496.hp2 HG02055.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.2085+3309C>T | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140694501 | |||||||
| chr3:140694556 | C | G | 1 | a0001c0003t0001g0168 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2085+3364C>G | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140694556 | |||||||
| chr3:140694786 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2085+3594G>A | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140694786 | |||||||
| chr3:140694956 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2085+3764C>T | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140694956 | |||||||
| chr3:140694997 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2085+3805C>T | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140694997 | |||||||
| chr3:140695106 | G | T | 3 | a0001c0001t0001g0048 a0001c0001t0001g0231 a0002c0002t0001g0227 |
4 | HG02886.hp2 HG03098.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.2085+3914G>T | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140695106 | |||||||
| chr3:140695162 | C | T | 17 | a0002c0002t0001g0029 a0002c0002t0001g0176 a0002c0002t0001g0229 others(14): Show |
21 | HG01496.hp2 HG02055.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.2085+3970C>T | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140695162 | |||||||
| chr3:140695741 | C | A | 3 | a0001c0001t0001g0048 a0001c0001t0001g0231 a0002c0002t0001g0227 |
4 | HG02886.hp2 HG03098.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.2085+4549C>A | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140695741 | |||||||
| chr3:140695888 | C | T | 60 | a0001c0001t0001g0103 a0002c0002t0001g0003 a0002c0002t0001g0008 others(57): Show |
95 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(92): Show |
intron_variant | MODIFIER | c.2085+4696C>T | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140695888 | |||||||
| chr3:140695958 | C | T | 20 | a0002c0002t0001g0006 a0002c0002t0001g0010 a0002c0002t0001g0022 others(17): Show |
36 | HG00408.hp1 HG00558.hp2 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.2085+4766C>T | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140695958 | |||||||
| chr3:140695988 | T | G | 1 | a0001c0001t0001g0051 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.2085+4796T>G | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140695988 | |||||||
| chr3:140696033 | T | G | 1 | a0002c0004t0001g0170 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2085+4841T>G | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140696033 | |||||||
| chr3:140696134 | T | C | 1 | a0001c0001t0001g0232 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2086-4754T>C | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140696134 | |||||||
| chr3:140696457 | C | T | 1 | a0002c0002t0001g0153 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2086-4431C>T | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140696457 | |||||||
| chr3:140696475 | A | C | 1 | a0002c0002t0001g0028 | 3 | NA18953.hp1 NA18983.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.2086-4413A>C | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140696475 | |||||||
| chr3:140696519 | C | G | 38 | a0001c0001t0001g0209 a0002c0002t0001g0006 a0002c0002t0001g0010 others(35): Show |
58 | HG00408.hp1 HG00558.hp2 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.2086-4369C>G | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140696519 | |||||||
| chr3:140696520 | G | A | 5 | a0001c0001t0001g0065 a0001c0001t0001g0073 a0001c0001t0001g0075 others(2): Show |
5 | HG02809.hp1 HG02895.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.2086-4368G>A | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140696520 | |||||||
| chr3:140696556 | A | G | 1 | a0001c0001t0001g0109 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.2086-4332A>G | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140696556 | |||||||
| chr3:140696649 | T | C | 1 | a0001c0001t0001g0076 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.2086-4239T>C | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140696649 | |||||||
| chr3:140697166 | G | C | 1 | a0002c0002t0001g0227 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2086-3722G>C | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140697166 | |||||||
| chr3:140697307 | T | G | 12 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0216 others(9): Show |
12 | HG01123.hp1 HG02145.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.2086-3581T>G | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140697307 | |||||||
| chr3:140697359 | A | G | 8 | a0001c0001t0001g0035 a0001c0001t0001g0104 a0001c0001t0001g0111 others(5): Show |
9 | HG00438.hp2 NA18955.hp2 NA18957.hp1 others(6): Show |
intron_variant | MODIFIER | c.2086-3529A>G | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140697359 | |||||||
| chr3:140697659 | T | C | 1 | a0001c0001t0001g0101 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2086-3229T>C | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140697659 | |||||||
| chr3:140697744 | C | A | 17 | a0002c0002t0001g0029 a0002c0002t0001g0176 a0002c0002t0001g0229 others(14): Show |
21 | HG01496.hp2 HG02055.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.2086-3144C>A | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140697744 | |||||||
| chr3:140697784 | C | A | 14 | a0002c0004t0001g0045 a0002c0004t0001g0160 a0002c0004t0001g0162 others(11): Show |
16 | HG01496.hp2 HG02055.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.2086-3104C>A | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140697784 | |||||||
| chr3:140697818 | G | T | 1 | a0001c0001t0001g0209 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2086-3070G>T | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140697818 | |||||||
| chr3:140697836 | A | C | 21 | a0001c0001t0001g0209 a0002c0002t0001g0006 a0002c0002t0001g0010 others(18): Show |
37 | HG00408.hp1 HG00558.hp2 HG00609.hp2 others(34): Show |
intron_variant | MODIFIER | c.2086-3052A>C | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140697836 | |||||||
| chr3:140697873 | C | T | 1 | a0001c0001t0001g0203 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.2086-3015C>T | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140697873 | |||||||
| chr3:140697919 | G | A | 2 | a0002c0002t0001g0244 a0002c0002t0001g0247 |
2 | HG00673.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.2086-2969G>A | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140697919 | |||||||
| chr3:140697926 | G | C | 1 | a0001c0001t0001g0123 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2086-2962G>C | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140697926 | |||||||
| chr3:140697928 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2086-2960C>T | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140697928 | |||||||
| chr3:140698011 | A | G | 1 | a0001c0001t0001g0193 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2086-2877A>G | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140698011 | |||||||
| chr3:140698018 | T | C | 36 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(33): Show |
72 | HG00423.hp2 HG00544.hp1 HG00621.hp2 others(69): Show |
intron_variant | MODIFIER | c.2086-2870T>C | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140698018 | |||||||
| chr3:140698245 | A | C | 14 | a0002c0004t0001g0045 a0002c0004t0001g0160 a0002c0004t0001g0162 others(11): Show |
16 | HG01496.hp2 HG02055.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.2086-2643A>C | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140698245 | |||||||
| chr3:140698476 | T | C | 20 | a0001c0001t0001g0009 a0001c0001t0001g0049 a0001c0001t0001g0050 others(17): Show |
29 | HG00639.hp2 HG00733.hp1 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.2086-2412T>C | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140698476 | |||||||
| chr3:140698509 | C | A | 2 | a0001c0001t0001g0201 a0002c0002t0001g0134 |
2 | HG03710.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2086-2379C>A | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140698509 | |||||||
| chr3:140698621 | CCAAAT | C | 17 | a0002c0002t0001g0029 a0002c0002t0001g0176 a0002c0002t0001g0229 others(14): Show |
21 | HG01496.hp2 HG02055.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.2086-2266_2086-226 others(9): Show |
TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140698621 | |||||||
| chr3:140698859 | T | C | 20 | a0002c0002t0001g0006 a0002c0002t0001g0010 a0002c0002t0001g0022 others(17): Show |
36 | HG00408.hp1 HG00558.hp2 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.2086-2029T>C | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140698859 | |||||||
| chr3:140698910 | A | T | 2 | a0002c0002t0001g0029 a0002c0002t0001g0176 |
4 | HG02622.hp2 HG02970.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.2086-1978A>T | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140698910 | |||||||
| chr3:140699028 | T | TTACTTC | 118 | a0001c0001t0001g0009 a0001c0001t0001g0049 a0001c0001t0001g0050 others(115): Show |
182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.2086-1857_2086-185 others(10): Show |
TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr3 | 140699028 | ||||||
| chr3:140699272 | G | A | 1 | a0001c0001t0001g0232 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2086-1616G>A | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140699272 | |||||||
| chr3:140699365 | C | T | 1 | a0002c0002t0001g0140 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2086-1523C>T | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140699365 | |||||||
| chr3:140699401 | T | G | 1 | a0002c0002t0001g0145 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2086-1487T>G | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140699401 | |||||||
| chr3:140699414 | G | T | 17 | a0001c0001t0001g0009 a0001c0001t0001g0049 a0001c0001t0001g0050 others(14): Show |
25 | HG00639.hp2 HG00733.hp1 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.2086-1474G>T | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140699414 | |||||||
| chr3:140699415 | A | C | 17 | a0001c0001t0001g0009 a0001c0001t0001g0049 a0001c0001t0001g0050 others(14): Show |
25 | HG00639.hp2 HG00733.hp1 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.2086-1473A>C | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140699415 | |||||||
| chr3:140699448 | G | A | 1 | a0001c0001t0001g0179 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2086-1440G>A | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140699448 | |||||||
| chr3:140699455 | T | C | 1 | a0001c0001t0001g0111 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.2086-1433T>C | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140699455 | |||||||
| chr3:140699523 | T | A | 1 | a0002c0002t0001g0245 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2086-1365T>A | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140699523 | |||||||
| chr3:140699524 | A | G | 21 | a0001c0001t0001g0209 a0002c0002t0001g0006 a0002c0002t0001g0010 others(18): Show |
37 | HG00408.hp1 HG00558.hp2 HG00609.hp2 others(34): Show |
intron_variant | MODIFIER | c.2086-1364A>G | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140699524 | |||||||
| chr3:140699563 | C | A | 1 | a0002c0002t0001g0245 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2086-1325C>A | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140699563 | |||||||
| chr3:140699565 | G | T | 1 | a0002c0002t0001g0245 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2086-1323G>T | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140699565 | |||||||
| chr3:140699567 | T | C | 1 | a0002c0002t0001g0245 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2086-1321T>C | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140699567 | |||||||
| chr3:140699569 | C | A | 1 | a0002c0002t0001g0245 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2086-1319C>A | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140699569 | |||||||
| chr3:140699571 | T | A | 1 | a0002c0002t0001g0245 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2086-1317T>A | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140699571 | |||||||
| chr3:140699572 | T | C | 1 | a0002c0002t0001g0245 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2086-1316T>C | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140699572 | |||||||
| chr3:140699573 | C | A | 1 | a0002c0002t0001g0245 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2086-1315C>A | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140699573 | |||||||
| chr3:140699577 | T | C | 1 | a0002c0002t0001g0245 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2086-1311T>C | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140699577 | |||||||
| chr3:140699579 | T | C | 1 | a0002c0002t0001g0245 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2086-1309T>C | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140699579 | |||||||
| chr3:140699584 | T | A | 1 | a0002c0002t0001g0245 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2086-1304T>A | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140699584 | |||||||
| chr3:140699585 | A | T | 1 | a0002c0002t0001g0245 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2086-1303A>T | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140699585 | |||||||
| chr3:140699588 | G | C | 1 | a0002c0002t0001g0245 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2086-1300G>C | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140699588 | |||||||
| chr3:140699646 | T | A | 1 | a0002c0002t0001g0245 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2086-1242T>A | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140699646 | |||||||
| chr3:140699654 | T | C | 1 | a0002c0002t0001g0245 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2086-1234T>C | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140699654 | |||||||
| chr3:140699655 | T | A | 1 | a0002c0002t0001g0245 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2086-1233T>A | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140699655 | |||||||
| chr3:140699659 | A | T | 1 | a0002c0002t0001g0245 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2086-1229A>T | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140699659 | |||||||
| chr3:140699669 | A | C | 1 | a0002c0002t0001g0245 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2086-1219A>C | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140699669 | |||||||
| chr3:140699681 | T | A | 60 | a0001c0001t0001g0103 a0002c0002t0001g0003 a0002c0002t0001g0008 others(57): Show |
95 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(92): Show |
intron_variant | MODIFIER | c.2086-1207T>A | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140699681 | |||||||
| chr3:140699690 | T | C | 1 | a0002c0002t0001g0245 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2086-1198T>C | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140699690 | |||||||
| chr3:140699800 | T | G | 60 | a0001c0001t0001g0103 a0002c0002t0001g0003 a0002c0002t0001g0008 others(57): Show |
95 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(92): Show |
intron_variant | MODIFIER | c.2086-1088T>G | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140699800 | |||||||
| chr3:140699873 | G | T | 3 | a0002c0002t0001g0029 a0002c0002t0001g0176 a0002c0002t0001g0229 |
5 | HG02109.hp2 HG02622.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.2086-1015G>T | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140699873 | |||||||
| chr3:140699919 | T | C | 1 | a0002c0002t0001g0245 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2086-969T>C | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140699919 | |||||||
| chr3:140699991 | A | C | 1 | a0002c0002t0001g0245 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2086-897A>C | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140699991 | |||||||
| chr3:140700031 | T | C | 1 | a0002c0002t0001g0245 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2086-857T>C | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140700031 | |||||||
| chr3:140700110 | G | C | 3 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0185 |
5 | HG00733.hp1 HG01358.hp2 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.2086-778G>C | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140700110 | |||||||
| chr3:140700180 | A | C | 1 | a0002c0002t0001g0245 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2086-708A>C | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140700180 | |||||||
| chr3:140700181 | G | C | 1 | a0002c0002t0001g0245 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2086-707G>C | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140700181 | |||||||
| chr3:140700182 | G | C | 1 | a0002c0002t0001g0245 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2086-706G>C | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140700182 | |||||||
| chr3:140700183 | G | C | 1 | a0002c0002t0001g0245 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2086-705G>C | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140700183 | |||||||
| chr3:140700186 | A | C | 1 | a0002c0002t0001g0245 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2086-702A>C | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140700186 | |||||||
| chr3:140700189 | T | A | 1 | a0002c0002t0001g0245 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2086-699T>A | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140700189 | |||||||
| chr3:140700200 | T | C | 1 | a0002c0002t0001g0245 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2086-688T>C | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140700200 | |||||||
| chr3:140700202 | G | A | 1 | a0002c0002t0001g0245 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2086-686G>A | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140700202 | |||||||
| chr3:140700204 | T | A | 1 | a0002c0002t0001g0245 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2086-684T>A | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140700204 | |||||||
| chr3:140700207 | G | C | 1 | a0002c0002t0001g0245 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2086-681G>C | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140700207 | |||||||
| chr3:140700208 | A | C | 1 | a0002c0002t0001g0245 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2086-680A>C | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140700208 | |||||||
| chr3:140700209 | T | C | 1 | a0002c0002t0001g0245 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2086-679T>C | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140700209 | |||||||
| chr3:140700210 | T | C | 1 | a0002c0002t0001g0245 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2086-678T>C | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140700210 | |||||||
| chr3:140700222 | T | C | 1 | a0002c0002t0001g0245 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2086-666T>C | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140700222 | |||||||
| chr3:140700227 | T | C | 1 | a0002c0002t0001g0245 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2086-661T>C | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140700227 | |||||||
| chr3:140700228 | T | A | 1 | a0002c0002t0001g0245 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2086-660T>A | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140700228 | |||||||
| chr3:140700234 | T | C | 1 | a0002c0002t0001g0245 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2086-654T>C | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140700234 | |||||||
| chr3:140700235 | C | T | 1 | a0002c0002t0001g0245 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2086-653C>T | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140700235 | |||||||
| chr3:140700236 | G | C | 1 | a0002c0002t0001g0245 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2086-652G>C | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140700236 | |||||||
| chr3:140700238 | G | T | 1 | a0002c0002t0001g0245 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2086-650G>T | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140700238 | |||||||
| chr3:140700243 | G | C | 1 | a0002c0002t0001g0245 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2086-645G>C | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140700243 | |||||||
| chr3:140700244 | T | A | 1 | a0002c0002t0001g0245 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2086-644T>A | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140700244 | |||||||
| chr3:140700248 | G | C | 1 | a0002c0002t0001g0245 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2086-640G>C | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140700248 | |||||||
| chr3:140700249 | T | C | 1 | a0002c0002t0001g0245 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2086-639T>C | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140700249 | |||||||
| chr3:140700251 | T | A | 1 | a0002c0002t0001g0245 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2086-637T>A | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140700251 | |||||||
| chr3:140700255 | T | A | 1 | a0002c0002t0001g0245 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2086-633T>A | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140700255 | |||||||
| chr3:140700256 | T | C | 1 | a0002c0002t0001g0245 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2086-632T>C | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140700256 | |||||||
| chr3:140700258 | T | A | 1 | a0002c0002t0001g0245 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2086-630T>A | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140700258 | |||||||
| chr3:140700259 | T | C | 1 | a0002c0002t0001g0245 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2086-629T>C | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140700259 | |||||||
| chr3:140700262 | G | C | 1 | a0002c0002t0001g0245 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2086-626G>C | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140700262 | |||||||
| chr3:140700263 | G | C | 1 | a0002c0002t0001g0245 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2086-625G>C | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140700263 | |||||||
| chr3:140700264 | T | C | 1 | a0002c0002t0001g0245 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2086-624T>C | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140700264 | |||||||
| chr3:140700265 | A | C | 1 | a0002c0002t0001g0245 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2086-623A>C | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140700265 | |||||||
| chr3:140700266 | G | A | 1 | a0002c0002t0001g0245 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2086-622G>A | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140700266 | |||||||
| chr3:140700268 | A | C | 1 | a0002c0002t0001g0245 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2086-620A>C | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140700268 | |||||||
| chr3:140700271 | G | A | 1 | a0002c0002t0001g0245 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2086-617G>A | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140700271 | |||||||
| chr3:140700272 | G | T | 1 | a0002c0002t0001g0245 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2086-616G>T | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140700272 | |||||||
| chr3:140700616 | C | G | 1 | a0001c0001t0001g0108 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.2086-272C>G | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140700616 | |||||||
| chr3:140700678 | A | T | 21 | a0001c0001t0001g0209 a0002c0002t0001g0006 a0002c0002t0001g0010 others(18): Show |
37 | HG00408.hp1 HG00558.hp2 HG00609.hp2 others(34): Show |
intron_variant | MODIFIER | c.2086-210A>T | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140700678 | |||||||
| chr3:140700873 | C | T | 118 | a0001c0001t0001g0009 a0001c0001t0001g0049 a0001c0001t0001g0050 others(115): Show |
182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.2086-15C>T | TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | chr3 | 140700873 |