Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 89122 |
| ensemblid | ENSG00000146833.16 |
| hgncid | 16275 |
| symbol | TRIM4 |
| name | tripartite motif containing 4 |
| refseq_nuc | NM_033091.3 |
| refseq_prot | NP_149082.1 |
| ensembl_nuc | ENST00000349062.7 |
| ensembl_prot | ENSP00000275736.4 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 99890403 |
| end | 99919530 |
| strand | - |
| ver | v1.2 |
| region | chr7:99890403-99919530 |
| region5000 | chr7:99885403-99924530 |
| regionname0 | TRIM4_chr7_99890403_99919530 |
| regionname5000 | TRIM4_chr7_99885403_99924530 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 474 | 283 | 62 | 57 | 112 | 13 | 37 | 84 | TRIM4_chr7_99885403_99924530 | TRIM4 | MEAED others(469): Show |
chr7 | 99885403 | 99924530 |
| a0002 | 0/0 | 474 | 16 | 0 | 1 | 15 | 0 | 0 | 14 | TRIM4_chr7_99885403_99924530 | TRIM4 | MEAED others(469): Show |
chr7 | 99885403 | 99924530 |
| a0003 | 0/0 | 474 | 13 | 7 | 2 | 0 | 1 | 3 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | MEAED others(469): Show |
chr7 | 99885403 | 99924530 |
| a0004 | 0/0 | 474 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | MEAED others(469): Show |
chr7 | 99885403 | 99924530 |
| a0005 | 0/0 | 474 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | MEAED others(469): Show |
chr7 | 99885403 | 99924530 |
| a0006 | 0/0 | 474 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | MEAED others(469): Show |
chr7 | 99885403 | 99924530 |
| a0007 | 0/0 | 474 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | MEAED others(469): Show |
chr7 | 99885403 | 99924530 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1422 | 121 | 5 | 28 | 65 | 5 | 16 | TRIM4_chr7_99885403_99924530 | TRIM4 | ATGGA others(1417): Show |
chr7 | 99885403 | 99924530 | ||
| a0001c0002 | 0/0 | 1422 | 101 | 11 | 23 | 45 | 6 | 16 | TRIM4_chr7_99885403_99924530 | TRIM4 | ATGGA others(1417): Show |
chr7 | 99885403 | 99924530 | ||
| a0001c0003 | 0/0 | 1422 | 56 | 45 | 6 | 0 | 2 | 3 | TRIM4_chr7_99885403_99924530 | TRIM4 | ATGGA others(1417): Show |
chr7 | 99885403 | 99924530 | ||
| a0001c0009 | 0/0 | 1422 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | ATGGA others(1417): Show |
chr7 | 99885403 | 99924530 | ||
| a0001c0011 | 0/0 | 1422 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM4_chr7_99885403_99924530 | TRIM4 | ATGGA others(1417): Show |
chr7 | 99885403 | 99924530 | ||
| a0001c0012 | 0/0 | 1422 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | ATGGA others(1417): Show |
chr7 | 99885403 | 99924530 | ||
| a0001c0013 | 0/0 | 1422 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM4_chr7_99885403_99924530 | TRIM4 | ATGGA others(1417): Show |
chr7 | 99885403 | 99924530 | ||
| a0002c0004 | 0/0 | 1422 | 16 | 0 | 1 | 15 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | ATGGA others(1417): Show |
chr7 | 99885403 | 99924530 | ||
| a0003c0005 | 0/0 | 1422 | 13 | 7 | 2 | 0 | 1 | 3 | TRIM4_chr7_99885403_99924530 | TRIM4 | ATGGA others(1417): Show |
chr7 | 99885403 | 99924530 | ||
| a0004c0008 | 0/0 | 1422 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | ATGGA others(1417): Show |
chr7 | 99885403 | 99924530 | ||
| a0005c0006 | 0/0 | 1422 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | ATGGA others(1417): Show |
chr7 | 99885403 | 99924530 | ||
| a0006c0007 | 0/0 | 1422 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | ATGGA others(1417): Show |
chr7 | 99885403 | 99924530 | ||
| a0007c0010 | 0/0 | 1422 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | ATGGA others(1417): Show |
chr7 | 99885403 | 99924530 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3314 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | GCGTT others(3309): Show |
chr7 | 99885403 | 99924530 |
| a0001c0001t0002 | 1/1 | 3314 | 110 | 4 | 24 | 60 | 4 | 16 | TRIM4_chr7_99885403_99924530 | TRIM4 | GCGTT others(3309): Show |
chr7 | 99885403 | 99924530 |
| a0001c0001t0004 | 0/0 | 3314 | 5 | 0 | 4 | 0 | 1 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | GCGTT others(3309): Show |
chr7 | 99885403 | 99924530 |
| a0001c0001t0005 | 0/0 | 3314 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | GCGTT others(3309): Show |
chr7 | 99885403 | 99924530 |
| a0001c0001t0013 | 0/0 | 3302 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | GCGTT others(3297): Show |
chr7 | 99885403 | 99924530 |
| a0001c0001t0014 | 0/0 | 3314 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | GCGTT others(3309): Show |
chr7 | 99885403 | 99924530 |
| a0001c0002t0001 | 0/0 | 3314 | 99 | 10 | 23 | 45 | 5 | 16 | TRIM4_chr7_99885403_99924530 | TRIM4 | GCGTT others(3309): Show |
chr7 | 99885403 | 99924530 |
| a0001c0002t0002 | 0/0 | 3314 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | GCGTT others(3309): Show |
chr7 | 99885403 | 99924530 |
| a0001c0002t0012 | 0/0 | 3314 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | GCGTT others(3309): Show |
chr7 | 99885403 | 99924530 |
| a0001c0003t0001 | 0/0 | 3314 | 49 | 40 | 4 | 0 | 2 | 3 | TRIM4_chr7_99885403_99924530 | TRIM4 | GCGTT others(3309): Show |
chr7 | 99885403 | 99924530 |
| a0001c0003t0003 | 0/0 | 3314 | 5 | 4 | 1 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | GCGTT others(3309): Show |
chr7 | 99885403 | 99924530 |
| a0001c0003t0009 | 0/0 | 3314 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | GCGTT others(3309): Show |
chr7 | 99885403 | 99924530 |
| a0001c0003t0015 | 0/0 | 3314 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | GCGTT others(3309): Show |
chr7 | 99885403 | 99924530 |
| a0001c0009t0002 | 0/0 | 3314 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | GCGTT others(3309): Show |
chr7 | 99885403 | 99924530 |
| a0001c0009t0005 | 0/0 | 3314 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | GCGTT others(3309): Show |
chr7 | 99885403 | 99924530 |
| a0001c0011t0010 | 0/0 | 3314 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM4_chr7_99885403_99924530 | TRIM4 | GCGTT others(3309): Show |
chr7 | 99885403 | 99924530 |
| a0001c0012t0011 | 0/0 | 3314 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | GCGTT others(3309): Show |
chr7 | 99885403 | 99924530 |
| a0001c0013t0001 | 0/0 | 3314 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM4_chr7_99885403_99924530 | TRIM4 | GCGTT others(3309): Show |
chr7 | 99885403 | 99924530 |
| a0002c0004t0001 | 0/0 | 3314 | 16 | 0 | 1 | 15 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | GCGTT others(3309): Show |
chr7 | 99885403 | 99924530 |
| a0003c0005t0001 | 0/0 | 3314 | 13 | 7 | 2 | 0 | 1 | 3 | TRIM4_chr7_99885403_99924530 | TRIM4 | GCGTT others(3309): Show |
chr7 | 99885403 | 99924530 |
| a0004c0008t0006 | 0/0 | 3314 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | GCGTT others(3309): Show |
chr7 | 99885403 | 99924530 |
| a0005c0006t0007 | 0/0 | 3314 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | GCGTT others(3309): Show |
chr7 | 99885403 | 99924530 |
| a0006c0007t0001 | 0/0 | 3314 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | GCGTT others(3309): Show |
chr7 | 99885403 | 99924530 |
| a0007c0010t0008 | 0/0 | 3314 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | GCGTT others(3309): Show |
chr7 | 99885403 | 99924530 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0001t0002g0001 | 1/1 | 50 | 2 | 10 | 28 | 1 | 7 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0001t0002g0004 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0001t0002g0006 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0001t0002g0009 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0001t0002g0012 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0001t0002g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0001t0002g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0001t0002g0037 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0001t0002g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0001t0002g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0001t0002g0041 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0001t0004g0011 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0001t0004g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0001t0005g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0001t0005g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0001t0013g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0001t0014g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0002t0001g0002 | 0/0 | 47 | 0 | 17 | 22 | 3 | 5 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0002t0001g0005 | 0/0 | 6 | 0 | 0 | 4 | 0 | 2 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0002t0001g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0002t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0002t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0002t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0002t0001g0028 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0002t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0002t0001g0030 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0002t0001g0032 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0002t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0002t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0002t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0002t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0002t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0002t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0002t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0002t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0002t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0002t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0002t0012g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0003t0001g0003 | 0/0 | 10 | 10 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0003t0001g0010 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0003t0001g0013 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0003t0001g0014 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0003t0001g0015 | 0/0 | 4 | 0 | 0 | 0 | 2 | 2 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0003t0001g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0003t0001g0025 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0003t0001g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0003t0001g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0003t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0003t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0003t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0003t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0003t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0003t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0003t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0003t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0003t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0003t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0003t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0003t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0003t0003g0016 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0003t0003g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0003t0009g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0003t0015g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0009t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0009t0005g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0011t0010g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0012t0011g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0001c0013t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0002c0004t0001g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0002c0004t0001g0008 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0002c0004t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0002c0004t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0002c0004t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0002c0004t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0002c0004t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0003c0005t0001g0022 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0003c0005t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0003c0005t0001g0035 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0003c0005t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0003c0005t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0003c0005t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0003c0005t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0003c0005t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0003c0005t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0004c0008t0006g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0004c0008t0006g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0005c0006t0007g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0006c0007t0001g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| a0007c0010t0008g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0003 | c0005 | t0001 | g0022 | EUR | GBR | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG00099 | hp2 | a0001 | c0002 | t0001 | g0002 | EUR | GBR | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG00280 | hp1 | a0001 | c0001 | t0004 | g0011 | EUR | FIN | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG00280 | hp2 | a0001 | c0002 | t0002 | g0060 | EUR | FIN | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | CHS | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG00408 | hp2 | a0002 | c0004 | t0001 | g0008 | EAS | CHS | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | CHS | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG00423 | hp2 | a0001 | c0002 | t0001 | g0020 | EAS | CHS | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG00438 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | CHS | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG00639 | hp1 | a0003 | c0005 | t0001 | g0022 | AMR | PUR | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG00639 | hp2 | a0001 | c0001 | t0004 | g0096 | AMR | PUR | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | CHS | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG00673 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | CHS | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | PUR | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG01069 | hp1 | a0001 | c0002 | t0001 | g0062 | AMR | PUR | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG01069 | hp2 | a0001 | c0001 | t0004 | g0011 | AMR | PUR | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG01070 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG01070 | hp2 | a0001 | c0001 | t0004 | g0011 | AMR | PUR | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG01074 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG01074 | hp2 | a0001 | c0001 | t0004 | g0011 | AMR | PUR | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG01081 | hp1 | a0001 | c0002 | t0001 | g0048 | AMR | PUR | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG01081 | hp2 | a0001 | c0003 | t0001 | g0025 | AMR | PUR | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0104 | AMR | PUR | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0092 | AMR | PUR | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG01109 | hp1 | a0001 | c0003 | t0015 | g0049 | AMR | PUR | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG01109 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG01167 | hp2 | a0001 | c0003 | t0001 | g0025 | AMR | PUR | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG01168 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0099 | AMR | PUR | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG01169 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG01169 | hp2 | a0001 | c0003 | t0001 | g0116 | AMR | PUR | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | PUR | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG01175 | hp2 | a0003 | c0005 | t0001 | g0022 | AMR | PUR | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG01192 | hp1 | a0001 | c0003 | t0001 | g0014 | AMR | PUR | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0109 | AMR | PUR | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG01243 | hp1 | a0001 | c0003 | t0003 | g0016 | AMR | PUR | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0064 | AMR | CLM | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG01256 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | CLM | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG01257 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | CLM | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG01261 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | CLM | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG01346 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | CLM | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | CLM | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG01358 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | CLM | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0039 | AMR | CLM | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0095 | AMR | CLM | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG01361 | hp2 | a0001 | c0002 | t0001 | g0130 | AMR | CLM | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0105 | AMR | CLM | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG01433 | hp2 | a0001 | c0002 | t0001 | g0053 | AMR | CLM | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG01515 | hp1 | a0001 | c0002 | t0001 | g0002 | EUR | IBS | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0108 | EUR | IBS | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG01516 | hp1 | a0001 | c0002 | t0001 | g0056 | EUR | IBS | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG01516 | hp2 | a0001 | c0003 | t0001 | g0015 | EUR | IBS | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG01517 | hp1 | a0001 | c0003 | t0001 | g0015 | EUR | IBS | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0041 | EUR | IBS | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG01884 | hp1 | a0001 | c0003 | t0001 | g0119 | AFR | ACB | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG01884 | hp2 | a0003 | c0005 | t0001 | g0081 | AFR | ACB | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG01891 | hp1 | a0001 | c0003 | t0001 | g0003 | AFR | ACB | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG01891 | hp2 | a0001 | c0002 | t0001 | g0029 | AFR | ACB | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG01928 | hp2 | a0001 | c0002 | t0001 | g0030 | AMR | PEL | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG01934 | hp1 | a0002 | c0004 | t0001 | g0054 | AMR | PEL | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0097 | AMR | PEL | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG01943 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0101 | AMR | PEL | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG01952 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG01952 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG02015 | hp1 | a0001 | c0002 | t0001 | g0074 | EAS | KHV | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG02027 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | KHV | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | KHV | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG02040 | hp1 | a0001 | c0001 | t0005 | g0038 | EAS | KHV | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG02055 | hp1 | a0001 | c0003 | t0001 | g0117 | AFR | ACB | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG02055 | hp2 | a0001 | c0002 | t0001 | g0018 | AFR | ACB | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG02056 | hp1 | a0001 | c0002 | t0001 | g0019 | EAS | KHV | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0094 | EAS | KHV | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG02071 | hp2 | a0007 | c0010 | t0008 | g0044 | EAS | KHV | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG02074 | hp2 | a0001 | c0002 | t0001 | g0032 | EAS | KHV | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG02080 | hp1 | a0001 | c0001 | t0005 | g0091 | EAS | KHV | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG02080 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | KHV | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG02083 | hp1 | a0001 | c0002 | t0001 | g0030 | EAS | KHV | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | KHV | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | KHV | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG02135 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | KHV | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG02165 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | CDX | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CDX | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG02257 | hp1 | a0001 | c0002 | t0001 | g0071 | AFR | ACB | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG02257 | hp2 | a0001 | c0003 | t0001 | g0013 | AFR | ACB | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG02258 | hp1 | a0001 | c0003 | t0001 | g0014 | AFR | ACB | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG02258 | hp2 | a0001 | c0003 | t0003 | g0016 | AFR | ACB | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG02273 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0039 | AMR | PEL | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG02451 | hp1 | a0001 | c0003 | t0001 | g0024 | AFR | ACB | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG02451 | hp2 | a0001 | c0003 | t0001 | g0124 | AFR | ACB | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG02602 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG02615 | hp1 | a0001 | c0003 | t0009 | g0052 | AFR | GWD | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG02615 | hp2 | a0001 | c0003 | t0001 | g0024 | AFR | GWD | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | GWD | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG02630 | hp2 | a0001 | c0003 | t0001 | g0121 | AFR | GWD | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG02647 | hp1 | a0001 | c0001 | t0013 | g0047 | AFR | GWD | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG02647 | hp2 | a0001 | c0003 | t0001 | g0126 | AFR | GWD | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0103 | SAS | PJL | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0098 | SAS | PJL | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0041 | SAS | PJL | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG02698 | hp2 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG02717 | hp1 | a0001 | c0002 | t0001 | g0018 | AFR | GWD | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG02717 | hp2 | a0001 | c0003 | t0001 | g0003 | AFR | GWD | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG02723 | hp1 | a0003 | c0005 | t0001 | g0035 | AFR | GWD | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG02723 | hp2 | a0001 | c0002 | t0001 | g0029 | AFR | GWD | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG02735 | hp1 | a0001 | c0002 | t0001 | g0080 | SAS | PJL | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG02735 | hp2 | a0001 | c0002 | t0001 | g0058 | SAS | PJL | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG02738 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG02809 | hp1 | a0001 | c0003 | t0001 | g0003 | AFR | GWD | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG02809 | hp2 | a0004 | c0008 | t0006 | g0051 | AFR | GWD | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG02818 | hp1 | a0001 | c0003 | t0001 | g0003 | AFR | GWD | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0036 | AFR | GWD | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG02895 | hp1 | a0005 | c0006 | t0007 | g0017 | AFR | GWD | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG02895 | hp2 | a0001 | c0003 | t0001 | g0013 | AFR | GWD | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG02896 | hp1 | a0006 | c0007 | t0001 | g0021 | AFR | GWD | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0036 | AFR | GWD | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG02897 | hp1 | a0006 | c0007 | t0001 | g0021 | AFR | GWD | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG02897 | hp2 | a0005 | c0006 | t0007 | g0017 | AFR | GWD | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG02965 | hp1 | a0003 | c0005 | t0001 | g0034 | AFR | ESN | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG02965 | hp2 | a0001 | c0003 | t0003 | g0016 | AFR | ESN | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG02970 | hp1 | a0001 | c0003 | t0001 | g0010 | AFR | ESN | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG02970 | hp2 | a0004 | c0008 | t0006 | g0026 | AFR | ESN | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG02976 | hp1 | a0001 | c0002 | t0001 | g0075 | AFR | ESN | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG02976 | hp2 | a0001 | c0003 | t0001 | g0042 | AFR | ESN | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0093 | SAS | PJL | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0063 | SAS | PJL | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG03041 | hp1 | a0001 | c0003 | t0001 | g0014 | AFR | GWD | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG03041 | hp2 | a0005 | c0006 | t0007 | g0017 | AFR | GWD | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG03098 | hp1 | a0001 | c0003 | t0001 | g0025 | AFR | MSL | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG03098 | hp2 | a0001 | c0012 | t0011 | g0046 | AFR | MSL | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG03130 | hp1 | a0001 | c0003 | t0001 | g0042 | AFR | ESN | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG03130 | hp2 | a0001 | c0003 | t0001 | g0043 | AFR | ESN | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG03139 | hp1 | a0001 | c0003 | t0001 | g0013 | AFR | ESN | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG03139 | hp2 | a0006 | c0007 | t0001 | g0021 | AFR | ESN | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG03195 | hp1 | a0001 | c0003 | t0001 | g0050 | AFR | ESN | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG03195 | hp2 | a0001 | c0003 | t0001 | g0003 | AFR | ESN | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG03209 | hp1 | a0001 | c0003 | t0001 | g0043 | AFR | MSL | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG03209 | hp2 | a0001 | c0003 | t0001 | g0123 | AFR | MSL | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG03225 | hp1 | a0001 | c0003 | t0003 | g0128 | AFR | MSL | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG03225 | hp2 | a0001 | c0003 | t0001 | g0003 | AFR | MSL | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG03239 | hp1 | a0001 | c0002 | t0001 | g0028 | SAS | PJL | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG03453 | hp1 | a0001 | c0003 | t0001 | g0010 | AFR | MSL | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG03453 | hp2 | a0001 | c0002 | t0001 | g0076 | AFR | MSL | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG03486 | hp1 | a0003 | c0005 | t0001 | g0115 | AFR | MSL | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG03486 | hp2 | a0001 | c0003 | t0003 | g0016 | AFR | MSL | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG03490 | hp2 | a0001 | c0002 | t0001 | g0061 | SAS | PJL | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG03491 | hp2 | a0001 | c0002 | t0001 | g0005 | SAS | PJL | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG03516 | hp1 | a0001 | c0003 | t0001 | g0024 | AFR | ESN | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG03516 | hp2 | a0001 | c0003 | t0001 | g0003 | AFR | ESN | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG03540 | hp1 | a0001 | c0002 | t0001 | g0073 | AFR | GWD | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG03540 | hp2 | a0001 | c0002 | t0001 | g0018 | AFR | GWD | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG03579 | hp1 | a0001 | c0003 | t0001 | g0010 | AFR | MSL | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG03579 | hp2 | a0003 | c0005 | t0001 | g0079 | AFR | MSL | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG03669 | hp1 | a0003 | c0005 | t0001 | g0035 | SAS | PJL | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG03669 | hp2 | a0001 | c0003 | t0001 | g0015 | SAS | PJL | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG03704 | hp1 | a0001 | c0002 | t0001 | g0005 | SAS | PJL | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0037 | SAS | PJL | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0012 | SAS | PJL | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG03710 | hp2 | a0001 | c0013 | t0001 | g0057 | SAS | PJL | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG03831 | hp1 | a0001 | c0003 | t0001 | g0015 | SAS | BEB | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG03831 | hp2 | a0001 | c0002 | t0001 | g0002 | SAS | BEB | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG03927 | hp1 | a0001 | c0002 | t0001 | g0070 | SAS | BEB | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0102 | SAS | BEB | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG04115 | hp1 | a0001 | c0002 | t0001 | g0032 | SAS | STU | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG04115 | hp2 | a0003 | c0005 | t0001 | g0084 | SAS | STU | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG04184 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | BEB | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | BEB | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG04199 | hp1 | a0001 | c0003 | t0001 | g0120 | SAS | STU | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG04199 | hp2 | a0001 | c0011 | t0010 | g0045 | SAS | STU | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG04204 | hp1 | a0001 | c0002 | t0001 | g0065 | SAS | STU | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | STU | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0012 | SAS | STU | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG04228 | hp2 | a0003 | c0005 | t0001 | g0085 | SAS | STU | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA18522 | hp1 | a0001 | c0003 | t0001 | g0013 | AFR | YRI | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA18522 | hp2 | a0001 | c0003 | t0001 | g0122 | AFR | YRI | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA18612 | hp1 | a0001 | c0009 | t0005 | g0131 | EAS | CHB | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHB | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA18906 | hp1 | a0001 | c0003 | t0001 | g0010 | AFR | YRI | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA18906 | hp2 | a0001 | c0003 | t0001 | g0010 | AFR | YRI | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA18939 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA18941 | hp1 | a0001 | c0002 | t0001 | g0020 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA18942 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA18943 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA18946 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA18948 | hp2 | a0001 | c0002 | t0001 | g0033 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA18950 | hp1 | a0001 | c0002 | t0001 | g0077 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA18951 | hp2 | a0002 | c0004 | t0001 | g0031 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA18954 | hp1 | a0002 | c0004 | t0001 | g0007 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA18956 | hp1 | a0002 | c0004 | t0001 | g0007 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA18959 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0083 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA18964 | hp1 | a0001 | c0001 | t0014 | g0089 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA18964 | hp2 | a0001 | c0002 | t0001 | g0068 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA18965 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA18966 | hp1 | a0001 | c0002 | t0001 | g0033 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA18966 | hp2 | a0001 | c0009 | t0002 | g0132 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA18969 | hp2 | a0002 | c0004 | t0001 | g0007 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA18970 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA18971 | hp1 | a0001 | c0002 | t0001 | g0069 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA18971 | hp2 | a0001 | c0001 | t0005 | g0038 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA18972 | hp2 | a0002 | c0004 | t0001 | g0066 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA18977 | hp1 | a0001 | c0002 | t0001 | g0072 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA18979 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA18981 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA18983 | hp1 | a0002 | c0004 | t0001 | g0007 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA18985 | hp1 | a0002 | c0004 | t0001 | g0067 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA18986 | hp2 | a0002 | c0004 | t0001 | g0031 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA18988 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA18990 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA18991 | hp1 | a0001 | c0002 | t0001 | g0027 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA18992 | hp1 | a0002 | c0004 | t0001 | g0008 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA18994 | hp2 | a0001 | c0002 | t0001 | g0027 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA18999 | hp2 | a0001 | c0002 | t0001 | g0019 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA19000 | hp1 | a0001 | c0002 | t0001 | g0055 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA19004 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA19011 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA19012 | hp2 | a0001 | c0002 | t0001 | g0019 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA19030 | hp1 | a0001 | c0002 | t0001 | g0059 | AFR | LWK | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA19030 | hp2 | a0001 | c0003 | t0001 | g0003 | AFR | LWK | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA19064 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA19065 | hp2 | a0002 | c0004 | t0001 | g0008 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA19066 | hp1 | a0002 | c0004 | t0001 | g0008 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA19070 | hp1 | a0002 | c0004 | t0001 | g0007 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA19072 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA19072 | hp2 | a0002 | c0004 | t0001 | g0008 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA19078 | hp2 | a0002 | c0004 | t0001 | g0127 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA19080 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA19083 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA19086 | hp1 | a0001 | c0002 | t0001 | g0020 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA19088 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA19089 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA19089 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA19090 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA19091 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0028 | EUR | TSI | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0100 | EUR | TSI | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0001 | EUR | TSI | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA20805 | hp2 | a0001 | c0002 | t0001 | g0002 | EUR | TSI | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0037 | SAS | GIH | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA20905 | hp2 | a0001 | c0002 | t0001 | g0129 | SAS | GIH | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG02486 | hp1 | a0001 | c0003 | t0001 | g0118 | AFR | ACB | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG02486 | hp2 | a0003 | c0005 | t0001 | g0034 | AFR | ACB | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG02559 | hp1 | a0001 | c0003 | t0001 | g0014 | AFR | ACB | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG02559 | hp2 | a0001 | c0003 | t0001 | g0125 | AFR | ACB | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG03471 | hp1 | a0001 | c0003 | t0001 | g0003 | AFR | MSL | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG03471 | hp2 | a0003 | c0005 | t0001 | g0078 | AFR | MSL | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG06807 | hp1 | a0001 | c0002 | t0012 | g0082 | AFR | USA | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| HG06807 | hp2 | a0004 | c0008 | t0006 | g0026 | AFR | USA | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA20300 | hp1 | a0001 | c0003 | t0001 | g0003 | AFR | USA | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | USA | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0001 | REF | REF | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0001 | REF | REF | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:99892234 | G | A | 1 | a0002 | 16 | HG00408.hp2 HG01934.hp1 NA18951.hp2 others(13): Show |
missense_variant | MODERATE | c.1354C>T | p.Arg452Cys | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 6/6 | 1483/3314 | 1354/1425 | 452/474 | chr7 | 99892234 | |||
| chr7:99892245 | G | C | 1 | a0003 | 13 | HG00099.hp1 HG00639.hp1 HG01175.hp2 others(10): Show |
missense_variant | MODERATE | c.1343C>G | p.Ser448Cys | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 6/6 | 1472/3314 | 1343/1425 | 448/474 | chr7 | 99892245 | |||
| chr7:99892567 | G | A | 2 | a0003 a0006 |
16 | HG00099.hp1 HG00639.hp1 HG01175.hp2 others(13): Show |
missense_variant | MODERATE | c.1021C>T | p.Pro341Ser | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 6/6 | 1150/3314 | 1021/1425 | 341/474 | chr7 | 99892567 | |||
| chr7:99903241 | T | G | 1 | a0004 | 3 | HG02809.hp2 HG02970.hp2 HG06807.hp2 |
missense_variant | MODERATE | c.818A>C | p.Lys273Thr | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/6 | 947/3314 | 818/1425 | 273/474 | chr7 | 99903241 | |||
| chr7:99903303 | C | G | 1 | a0005 | 3 | HG02895.hp1 HG02897.hp2 HG03041.hp2 |
missense_variant | MODERATE | c.756G>C | p.Gln252His | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/6 | 885/3314 | 756/1425 | 252/474 | chr7 | 99903303 | |||
| chr7:99919265 | G | T | 1 | a0007 | 1 | HG02071.hp2 | missense_variant | MODERATE | c.137C>A | p.Pro46Gln | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/6 | 266/3314 | 137/1425 | 46/474 | chr7 | 99919265 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:99892463 | G | T | 1 | a0005c0006 | 3 | HG02895.hp1 HG02897.hp2 HG03041.hp2 |
synonymous_variant | LOW | c.1125C>A | p.Val375Val | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 6/6 | 1254/3314 | 1125/1425 | 375/474 | chr7 | 99892463 | |||
| chr7:99903276 | T | C | 5 | a0001c0002 a0001c0011 a0001c0013 others(2): Show |
120 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(117): Show |
synonymous_variant | LOW | c.783A>G | p.Val261Val | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/6 | 912/3314 | 783/1425 | 261/474 | chr7 | 99903276 | |||
| chr7:99903288 | A | G | 11 | a0001c0002 a0001c0003 a0001c0011 others(8): Show |
199 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(196): Show |
synonymous_variant | LOW | c.771T>C | p.Ser257Ser | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/6 | 900/3314 | 771/1425 | 257/474 | chr7 | 99903288 | |||
| chr7:99908681 | A | G | 1 | a0001c0012 | 1 | HG03098.hp2 | synonymous_variant | LOW | c.621T>C | p.Asn207Asn | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 3/6 | 750/3314 | 621/1425 | 207/474 | chr7 | 99908681 | |||
| chr7:99909628 | C | A | 1 | a0001c0013 | 1 | HG03710.hp2 | synonymous_variant | LOW | c.426G>T | p.Val142Val | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 2/6 | 555/3314 | 426/1425 | 142/474 | chr7 | 99909628 | |||
| chr7:99919108 | G | A | 1 | a0001c0009 | 2 | NA18612.hp1 NA18966.hp2 |
synonymous_variant | LOW | c.294C>T | p.Cys98Cys | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/6 | 423/3314 | 294/1425 | 98/474 | chr7 | 99919108 | |||
| chr7:99919264 | C | T | 1 | a0001c0011 | 1 | HG04199.hp2 | synonymous_variant | LOW | c.138G>A | p.Pro46Pro | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/6 | 267/3314 | 138/1425 | 46/474 | chr7 | 99919264 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:99890679 | TGGACACA others(5): Show |
T | 1 | a0001c0001t0013 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1472_*1483delTTTT others(8): Show |
TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 6/6 | 1472 | chr7 | 99890679 | ||||||
| chr7:99890920 | C | T | 16 | a0001c0001t0001 a0001c0002t0001 a0001c0002t0012 others(13): Show |
199 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(196): Show |
3_prime_UTR_variant | MODIFIER | c.*1243G>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 6/6 | 1243 | chr7 | 99890920 | ||||||
| chr7:99890957 | G | A | 1 | a0001c0012t0011 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1206C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 6/6 | 1206 | chr7 | 99890957 | ||||||
| chr7:99890980 | T | C | 1 | a0001c0001t0014 | 1 | NA18964.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1183A>G | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 6/6 | 1183 | chr7 | 99890980 | ||||||
| chr7:99890987 | A | G | 1 | a0001c0011t0010 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1176T>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 6/6 | 1176 | chr7 | 99890987 | ||||||
| chr7:99890994 | A | T | 2 | a0001c0003t0009 a0004c0008t0006 |
4 | HG02615.hp1 HG02809.hp2 HG02970.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1169T>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 6/6 | 1169 | chr7 | 99890994 | ||||||
| chr7:99891122 | G | A | 1 | a0001c0002t0012 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1041C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 6/6 | 1041 | chr7 | 99891122 | ||||||
| chr7:99891134 | C | T | 1 | a0001c0003t0003 | 5 | HG01243.hp1 HG02258.hp2 HG02965.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1029G>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 6/6 | 1029 | chr7 | 99891134 | ||||||
| chr7:99891275 | C | A | 1 | a0005c0006t0007 | 3 | HG02895.hp1 HG02897.hp2 HG03041.hp2 |
3_prime_UTR_variant | MODIFIER | c.*888G>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 6/6 | 888 | chr7 | 99891275 | ||||||
| chr7:99891317 | A | T | 16 | a0001c0001t0001 a0001c0002t0001 a0001c0002t0012 others(13): Show |
199 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(196): Show |
3_prime_UTR_variant | MODIFIER | c.*846T>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 6/6 | 846 | chr7 | 99891317 | ||||||
| chr7:99891382 | A | G | 17 | a0001c0001t0001 a0001c0001t0013 a0001c0002t0001 others(14): Show |
200 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(197): Show |
3_prime_UTR_variant | MODIFIER | c.*781T>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 6/6 | 781 | chr7 | 99891382 | ||||||
| chr7:99891395 | G | A | 1 | a0001c0003t0015 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*768C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 6/6 | 768 | chr7 | 99891395 | ||||||
| chr7:99891607 | A | G | 2 | a0001c0001t0005 a0001c0009t0005 |
4 | HG02040.hp1 HG02080.hp1 NA18612.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*556T>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 6/6 | 556 | chr7 | 99891607 | ||||||
| chr7:99891827 | C | T | 1 | a0001c0003t0009 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*336G>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 6/6 | 336 | chr7 | 99891827 | ||||||
| chr7:99891948 | G | A | 1 | a0001c0001t0004 | 5 | HG00280.hp1 HG00639.hp2 HG01069.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*215C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 6/6 | 215 | chr7 | 99891948 | ||||||
| chr7:99892138 | A | T | 1 | a0007c0010t0008 | 1 | HG02071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*25T>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 6/6 | 25 | chr7 | 99892138 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:99892878 | T | A | 22 | a0001c0003t0001g0003 a0001c0003t0001g0010 a0001c0003t0001g0013 others(19): Show |
53 | HG01081.hp2 HG01167.hp2 HG01169.hp2 others(50): Show |
intron_variant | MODIFIER | c.842-132A>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99892878 | |||||||
| chr7:99893110 | C | A | 1 | a0001c0002t0001g0068 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.842-364G>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99893110 | |||||||
| chr7:99893117 | A | G | 1 | a0001c0003t0001g0024 | 3 | HG02451.hp1 HG02615.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.842-371T>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99893117 | |||||||
| chr7:99893333 | A | T | 86 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0018 others(83): Show |
198 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(195): Show |
intron_variant | MODIFIER | c.842-587T>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99893333 | |||||||
| chr7:99893368 | C | CAT | 10 | a0003c0005t0001g0022 a0003c0005t0001g0034 a0003c0005t0001g0035 others(7): Show |
16 | HG00099.hp1 HG00639.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.842-623_842-622ins others(2): Show |
TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99893368 | |||||||
| chr7:99893370 | C | CAT | 77 | a0001c0001t0013g0047 a0001c0002t0001g0002 a0001c0002t0001g0005 others(74): Show |
183 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(180): Show |
intron_variant | MODIFIER | c.842-625_842-624ins others(2): Show |
TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99893370 | |||||||
| chr7:99893370 | C | T | 10 | a0003c0005t0001g0022 a0003c0005t0001g0034 a0003c0005t0001g0035 others(7): Show |
16 | HG00099.hp1 HG00639.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.842-624G>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99893370 | |||||||
| chr7:99893432 | G | A | 1 | a0001c0001t0002g0090 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.842-686C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99893432 | |||||||
| chr7:99893455 | A | T | 1 | a0001c0012t0011g0046 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.842-709T>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99893455 | |||||||
| chr7:99893623 | T | A | 1 | a0001c0002t0001g0061 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.842-877A>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99893623 | |||||||
| chr7:99893695 | T | C | 1 | a0001c0002t0001g0062 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.842-949A>G | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99893695 | |||||||
| chr7:99893715 | T | C | 1 | a0001c0012t0011g0046 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.842-969A>G | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99893715 | |||||||
| chr7:99893967 | C | CT | 12 | a0001c0001t0002g0004 a0001c0001t0002g0009 a0001c0001t0002g0039 others(9): Show |
23 | HG00408.hp1 HG00738.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.842-1222dupA | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99893967 | |||||||
| chr7:99893967 | C | CTT | 10 | a0003c0005t0001g0022 a0003c0005t0001g0034 a0003c0005t0001g0035 others(7): Show |
16 | HG00099.hp1 HG00639.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.842-1223_842-1222d others(4): Show |
TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99893967 | |||||||
| chr7:99894414 | C | T | 4 | a0003c0005t0001g0022 a0003c0005t0001g0035 a0003c0005t0001g0084 others(1): Show |
7 | HG00099.hp1 HG00639.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.842-1668G>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99894414 | |||||||
| chr7:99894430 | C | T | 3 | a0001c0002t0001g0059 a0001c0002t0001g0075 a0001c0002t0001g0076 |
3 | HG02976.hp1 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.842-1684G>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99894430 | |||||||
| chr7:99894538 | G | A | 2 | a0002c0004t0001g0031 a0002c0004t0001g0127 |
3 | NA18951.hp2 NA18986.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.842-1792C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99894538 | |||||||
| chr7:99894637 | A | C | 1 | a0001c0002t0001g0030 | 2 | HG01928.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.842-1891T>G | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99894637 | |||||||
| chr7:99894670 | C | G | 1 | a0001c0001t0002g0099 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.842-1924G>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99894670 | |||||||
| chr7:99894673 | A | C | 76 | a0001c0001t0002g0092 a0001c0002t0001g0002 a0001c0002t0001g0005 others(73): Show |
179 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(176): Show |
intron_variant | MODIFIER | c.842-1927T>G | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99894673 | |||||||
| chr7:99894674 | A | C | 1 | a0001c0003t0001g0050 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.842-1928T>G | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99894674 | |||||||
| chr7:99895082 | A | T | 4 | a0003c0005t0001g0022 a0003c0005t0001g0035 a0003c0005t0001g0084 others(1): Show |
7 | HG00099.hp1 HG00639.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.842-2336T>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99895082 | |||||||
| chr7:99895133 | A | G | 87 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0018 others(84): Show |
199 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.842-2387T>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99895133 | |||||||
| chr7:99895493 | C | T | 1 | a0001c0001t0002g0037 | 2 | HG03704.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.842-2747G>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99895493 | |||||||
| chr7:99895536 | T | A | 1 | a0001c0003t0001g0122 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.842-2790A>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99895536 | |||||||
| chr7:99895647 | G | C | 87 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0018 others(84): Show |
199 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.842-2901C>G | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99895647 | |||||||
| chr7:99895809 | T | G | 1 | a0005c0006t0007g0017 | 3 | HG02895.hp1 HG02897.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.842-3063A>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99895809 | |||||||
| chr7:99895849 | T | C | 1 | a0001c0001t0013g0047 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.842-3103A>G | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99895849 | |||||||
| chr7:99896037 | G | A | 22 | a0001c0003t0001g0003 a0001c0003t0001g0010 a0001c0003t0001g0013 others(19): Show |
53 | HG01081.hp2 HG01167.hp2 HG01169.hp2 others(50): Show |
intron_variant | MODIFIER | c.842-3291C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99896037 | |||||||
| chr7:99896187 | T | C | 1 | a0001c0002t0001g0068 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.842-3441A>G | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99896187 | |||||||
| chr7:99896188 | G | A | 87 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0018 others(84): Show |
199 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.842-3442C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99896188 | |||||||
| chr7:99896257 | G | C | 51 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0018 others(48): Show |
124 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.842-3511C>G | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99896257 | |||||||
| chr7:99896312 | G | T | 1 | a0001c0003t0001g0123 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.842-3566C>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99896312 | |||||||
| chr7:99896407 | G | A | 87 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0018 others(84): Show |
199 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.842-3661C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99896407 | |||||||
| chr7:99896609 | G | A | 1 | a0001c0001t0002g0112 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.842-3863C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99896609 | |||||||
| chr7:99896774 | C | T | 1 | a0001c0002t0001g0080 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.842-4028G>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99896774 | |||||||
| chr7:99896840 | A | C | 1 | a0001c0001t0002g0101 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.842-4094T>G | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99896840 | |||||||
| chr7:99896882 | C | T | 5 | a0001c0003t0001g0014 a0001c0003t0001g0025 a0001c0003t0001g0042 others(2): Show |
11 | HG01081.hp2 HG01167.hp2 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.842-4136G>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99896882 | |||||||
| chr7:99896890 | C | T | 87 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0018 others(84): Show |
199 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.842-4144G>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99896890 | |||||||
| chr7:99896916 | A | G | 1 | a0001c0003t0009g0052 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.842-4170T>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99896916 | |||||||
| chr7:99896944 | G | A | 1 | a0001c0001t0002g0100 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.842-4198C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99896944 | |||||||
| chr7:99896972 | T | C | 2 | a0001c0001t0002g0039 a0001c0001t0002g0101 |
3 | HG01358.hp2 HG01943.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.842-4226A>G | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99896972 | |||||||
| chr7:99896985 | A | G | 10 | a0003c0005t0001g0022 a0003c0005t0001g0034 a0003c0005t0001g0035 others(7): Show |
16 | HG00099.hp1 HG00639.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.842-4239T>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99896985 | |||||||
| chr7:99897057 | T | C | 1 | a0001c0001t0013g0047 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.842-4311A>G | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99897057 | |||||||
| chr7:99897849 | T | G | 51 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0018 others(48): Show |
124 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.842-5103A>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99897849 | |||||||
| chr7:99897936 | C | G | 1 | a0001c0001t0002g0098 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.842-5190G>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99897936 | |||||||
| chr7:99898109 | A | G | 2 | a0001c0001t0004g0011 a0001c0001t0004g0096 |
5 | HG00280.hp1 HG00639.hp2 HG01069.hp2 others(2): Show |
intron_variant | MODIFIER | c.841+5109T>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99898109 | |||||||
| chr7:99898119 | C | T | 1 | a0001c0001t0002g0097 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.841+5099G>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99898119 | |||||||
| chr7:99898208 | A | G | 2 | a0004c0008t0006g0026 a0004c0008t0006g0051 |
3 | HG02809.hp2 HG02970.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.841+5010T>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99898208 | |||||||
| chr7:99898310 | C | T | 2 | a0001c0012t0011g0046 a0005c0006t0007g0017 |
4 | HG02895.hp1 HG02897.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.841+4908G>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99898310 | |||||||
| chr7:99898369 | C | T | 1 | a0005c0006t0007g0017 | 3 | HG02895.hp1 HG02897.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.841+4849G>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99898369 | |||||||
| chr7:99898418 | G | A | 1 | a0001c0001t0002g0102 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.841+4800C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99898418 | |||||||
| chr7:99898532 | C | G | 1 | a0001c0001t0002g0006 | 6 | HG00423.hp1 HG00673.hp1 HG02083.hp2 others(3): Show |
intron_variant | MODIFIER | c.841+4686G>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99898532 | |||||||
| chr7:99898554 | G | A | 4 | a0003c0005t0001g0022 a0003c0005t0001g0035 a0003c0005t0001g0084 others(1): Show |
7 | HG00099.hp1 HG00639.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.841+4664C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99898554 | |||||||
| chr7:99898860 | A | G | 1 | a0001c0001t0004g0096 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.841+4358T>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99898860 | |||||||
| chr7:99899044 | G | A | 10 | a0003c0005t0001g0022 a0003c0005t0001g0034 a0003c0005t0001g0035 others(7): Show |
16 | HG00099.hp1 HG00639.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.841+4174C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99899044 | |||||||
| chr7:99899118 | C | G | 1 | a0001c0001t0002g0095 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.841+4100G>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99899118 | |||||||
| chr7:99899137 | C | G | 1 | a0001c0003t0001g0123 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.841+4081G>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99899137 | |||||||
| chr7:99899156 | A | G | 1 | a0001c0001t0002g0094 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.841+4062T>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99899156 | |||||||
| chr7:99899391 | T | C | 1 | a0007c0010t0008g0044 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.841+3827A>G | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99899391 | |||||||
| chr7:99899644 | A | G | 10 | a0003c0005t0001g0022 a0003c0005t0001g0034 a0003c0005t0001g0035 others(7): Show |
16 | HG00099.hp1 HG00639.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.841+3574T>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99899644 | |||||||
| chr7:99899699 | C | T | 2 | a0001c0002t0001g0071 a0001c0002t0001g0073 |
2 | HG02257.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.841+3519G>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99899699 | |||||||
| chr7:99899878 | C | A | 4 | a0001c0003t0001g0043 a0001c0003t0001g0117 a0001c0003t0001g0123 others(1): Show |
5 | HG02055.hp1 HG02451.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.841+3340G>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99899878 | |||||||
| chr7:99899941 | C | T | 1 | a0002c0004t0001g0054 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.841+3277G>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99899941 | |||||||
| chr7:99899978 | G | T | 1 | a0001c0001t0002g0093 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.841+3240C>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99899978 | |||||||
| chr7:99900080 | C | G | 1 | a0001c0003t0001g0050 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.841+3138G>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99900080 | |||||||
| chr7:99900334 | T | A | 75 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0018 others(72): Show |
179 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(176): Show |
intron_variant | MODIFIER | c.841+2884A>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99900334 | |||||||
| chr7:99900395 | A | C | 87 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0018 others(84): Show |
199 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.841+2823T>G | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99900395 | |||||||
| chr7:99900522 | G | A | 88 | a0001c0001t0013g0047 a0001c0002t0001g0002 a0001c0002t0001g0005 others(85): Show |
200 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.841+2696C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99900522 | |||||||
| chr7:99900709 | A | AT | 51 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0018 others(48): Show |
124 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.841+2508dupA | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99900709 | |||||||
| chr7:99900876 | A | T | 87 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0018 others(84): Show |
199 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.841+2342T>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99900876 | |||||||
| chr7:99900918 | T | A | 1 | a0001c0003t0009g0052 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.841+2300A>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99900918 | |||||||
| chr7:99900929 | C | CTCAGGGT others(4): Show |
45 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0018 others(42): Show |
117 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.841+2288_841+2289i others(13): Show |
TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99900929 | |||||||
| chr7:99900934 | A | ATTTCT | 45 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0018 others(42): Show |
117 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.841+2283_841+2284i others(7): Show |
TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99900934 | |||||||
| chr7:99901105 | G | A | 1 | a0001c0001t0002g0103 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.841+2113C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99901105 | |||||||
| chr7:99901290 | G | A | 2 | a0001c0012t0011g0046 a0005c0006t0007g0017 |
4 | HG02895.hp1 HG02897.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.841+1928C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99901290 | |||||||
| chr7:99901388 | G | A | 1 | a0005c0006t0007g0017 | 3 | HG02895.hp1 HG02897.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.841+1830C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99901388 | |||||||
| chr7:99901442 | A | G | 1 | a0001c0003t0001g0050 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.841+1776T>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99901442 | |||||||
| chr7:99901486 | T | C | 1 | a0001c0003t0015g0049 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.841+1732A>G | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99901486 | |||||||
| chr7:99901583 | T | C | 1 | a0001c0002t0001g0062 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.841+1635A>G | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99901583 | |||||||
| chr7:99901733 | G | A | 1 | a0003c0005t0001g0115 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.841+1485C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99901733 | |||||||
| chr7:99902176 | T | C | 1 | a0001c0001t0002g0012 | 4 | HG00738.hp1 HG01175.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.841+1042A>G | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99902176 | |||||||
| chr7:99902249 | A | T | 87 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0018 others(84): Show |
199 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.841+969T>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99902249 | |||||||
| chr7:99902419 | T | G | 48 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0018 others(45): Show |
120 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.841+799A>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99902419 | |||||||
| chr7:99902631 | G | A | 2 | a0001c0002t0001g0063 a0001c0002t0001g0070 |
2 | HG03017.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.841+587C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99902631 | |||||||
| chr7:99902700 | C | G | 10 | a0003c0005t0001g0022 a0003c0005t0001g0034 a0003c0005t0001g0035 others(7): Show |
16 | HG00099.hp1 HG00639.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.841+518G>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99902700 | |||||||
| chr7:99902782 | T | G | 1 | a0001c0003t0015g0049 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.841+436A>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99902782 | |||||||
| chr7:99902889 | C | A | 1 | a0001c0002t0001g0064 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.841+329G>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99902889 | |||||||
| chr7:99902974 | G | A | 10 | a0003c0005t0001g0022 a0003c0005t0001g0034 a0003c0005t0001g0035 others(7): Show |
16 | HG00099.hp1 HG00639.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.841+244C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99902974 | |||||||
| chr7:99903343 | G | A | 1 | a0001c0001t0002g0111 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.744-28C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 4/5 | chr7 | 99903343 | |||||||
| chr7:99903391 | A | G | 1 | a0001c0003t0001g0050 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.744-76T>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 4/5 | chr7 | 99903391 | |||||||
| chr7:99903463 | C | T | 1 | a0001c0003t0001g0043 | 2 | HG03130.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.743+113G>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 4/5 | chr7 | 99903463 | |||||||
| chr7:99903566 | G | A | 1 | a0001c0003t0015g0049 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.743+10C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 4/5 | chr7 | 99903566 | |||||||
| chr7:99903690 | A | T | 87 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0018 others(84): Show |
199 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.721-92T>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 3/5 | chr7 | 99903690 | |||||||
| chr7:99903752 | T | C | 3 | a0003c0005t0001g0034 a0003c0005t0001g0081 a0003c0005t0001g0115 |
4 | HG01884.hp2 HG02486.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.721-154A>G | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 3/5 | chr7 | 99903752 | |||||||
| chr7:99903853 | C | T | 1 | a0001c0001t0002g0092 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.721-255G>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 3/5 | chr7 | 99903853 | |||||||
| chr7:99903899 | C | T | 1 | a0001c0003t0001g0122 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.721-301G>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 3/5 | chr7 | 99903899 | |||||||
| chr7:99904204 | T | C | 1 | a0001c0003t0001g0121 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.721-606A>G | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 3/5 | chr7 | 99904204 | |||||||
| chr7:99904245 | G | A | 1 | a0005c0006t0007g0017 | 3 | HG02895.hp1 HG02897.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.721-647C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 3/5 | chr7 | 99904245 | |||||||
| chr7:99904351 | A | T | 3 | a0001c0003t0009g0052 a0004c0008t0006g0026 a0004c0008t0006g0051 |
4 | HG02615.hp1 HG02809.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.721-753T>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 3/5 | chr7 | 99904351 | |||||||
| chr7:99904488 | A | G | 3 | a0001c0002t0001g0018 a0001c0002t0001g0029 a0001c0002t0001g0048 |
6 | HG01081.hp1 HG01891.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.721-890T>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 3/5 | chr7 | 99904488 | |||||||
| chr7:99904790 | G | A | 3 | a0001c0002t0001g0058 a0001c0002t0001g0065 a0001c0011t0010g0045 |
3 | HG02735.hp2 HG04199.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.721-1192C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 3/5 | chr7 | 99904790 | |||||||
| chr7:99904964 | G | A | 10 | a0003c0005t0001g0022 a0003c0005t0001g0034 a0003c0005t0001g0035 others(7): Show |
16 | HG00099.hp1 HG00639.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.721-1366C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 3/5 | chr7 | 99904964 | |||||||
| chr7:99905050 | TA | T | 65 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0018 others(62): Show |
150 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.721-1453delT | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 3/5 | chr7 | 99905050 | |||||||
| chr7:99905208 | T | C | 1 | a0001c0003t0001g0118 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.721-1610A>G | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 3/5 | chr7 | 99905208 | |||||||
| chr7:99905582 | G | C | 1 | a0001c0003t0001g0118 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.721-1984C>G | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 3/5 | chr7 | 99905582 | |||||||
| chr7:99905674 | A | G | 2 | a0001c0001t0002g0004 a0001c0001t0002g0114 |
8 | HG00408.hp1 HG02040.hp2 NA18945.hp2 others(5): Show |
intron_variant | MODIFIER | c.721-2076T>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 3/5 | chr7 | 99905674 | |||||||
| chr7:99905687 | A | G | 1 | a0001c0003t0009g0052 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.721-2089T>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 3/5 | chr7 | 99905687 | |||||||
| chr7:99905919 | C | T | 23 | a0001c0003t0001g0003 a0001c0003t0001g0010 a0001c0003t0001g0013 others(20): Show |
54 | HG01081.hp2 HG01167.hp2 HG01169.hp2 others(51): Show |
intron_variant | MODIFIER | c.721-2321G>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 3/5 | chr7 | 99905919 | |||||||
| chr7:99905929 | G | A | 1 | a0001c0002t0001g0080 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.721-2331C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 3/5 | chr7 | 99905929 | |||||||
| chr7:99906002 | A | G | 88 | a0001c0001t0013g0047 a0001c0002t0001g0002 a0001c0002t0001g0005 others(85): Show |
200 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.721-2404T>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 3/5 | chr7 | 99906002 | |||||||
| chr7:99906100 | G | A | 1 | a0001c0003t0009g0052 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.720+2482C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 3/5 | chr7 | 99906100 | |||||||
| chr7:99906313 | A | T | 1 | a0003c0005t0001g0081 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.720+2269T>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 3/5 | chr7 | 99906313 | |||||||
| chr7:99906453 | A | C | 1 | a0001c0002t0001g0018 | 3 | HG02055.hp2 HG02717.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.720+2129T>G | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 3/5 | chr7 | 99906453 | |||||||
| chr7:99906809 | G | A | 1 | a0001c0003t0001g0125 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.720+1773C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 3/5 | chr7 | 99906809 | |||||||
| chr7:99907340 | C | T | 1 | a0001c0012t0011g0046 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.720+1242G>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 3/5 | chr7 | 99907340 | |||||||
| chr7:99907353 | A | C | 4 | a0003c0005t0001g0022 a0003c0005t0001g0035 a0003c0005t0001g0084 others(1): Show |
7 | HG00099.hp1 HG00639.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.720+1229T>G | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 3/5 | chr7 | 99907353 | |||||||
| chr7:99907431 | G | A | 48 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0018 others(45): Show |
120 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.720+1151C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 3/5 | chr7 | 99907431 | |||||||
| chr7:99907483 | T | C | 2 | a0001c0003t0001g0025 a0001c0003t0001g0116 |
4 | HG01081.hp2 HG01167.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.720+1099A>G | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 3/5 | chr7 | 99907483 | |||||||
| chr7:99907600 | G | A | 45 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0018 others(42): Show |
117 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.720+982C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 3/5 | chr7 | 99907600 | |||||||
| chr7:99907783 | T | C | 1 | a0001c0003t0001g0126 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.720+799A>G | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 3/5 | chr7 | 99907783 | |||||||
| chr7:99907787 | A | C | 1 | a0004c0008t0006g0051 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.720+795T>G | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 3/5 | chr7 | 99907787 | |||||||
| chr7:99907857 | C | T | 1 | a0001c0001t0002g0104 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.720+725G>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 3/5 | chr7 | 99907857 | |||||||
| chr7:99907996 | G | A | 2 | a0004c0008t0006g0026 a0004c0008t0006g0051 |
3 | HG02809.hp2 HG02970.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.720+586C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 3/5 | chr7 | 99907996 | |||||||
| chr7:99908027 | G | A | 1 | a0001c0002t0001g0056 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.720+555C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 3/5 | chr7 | 99908027 | |||||||
| chr7:99908268 | T | C | 1 | a0001c0002t0001g0073 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.720+314A>G | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 3/5 | chr7 | 99908268 | |||||||
| chr7:99908282 | T | C | 3 | a0001c0012t0011g0046 a0005c0006t0007g0017 a0006c0007t0001g0021 |
7 | HG02895.hp1 HG02896.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.720+300A>G | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 3/5 | chr7 | 99908282 | |||||||
| chr7:99908525 | G | C | 2 | a0001c0003t0001g0015 a0001c0003t0001g0120 |
5 | HG01516.hp2 HG01517.hp1 HG03669.hp2 others(2): Show |
intron_variant | MODIFIER | c.720+57C>G | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 3/5 | chr7 | 99908525 | |||||||
| chr7:99908920 | G | A | 3 | a0003c0005t0001g0034 a0003c0005t0001g0081 a0003c0005t0001g0115 |
4 | HG01884.hp2 HG02486.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.490-108C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 2/5 | chr7 | 99908920 | |||||||
| chr7:99908960 | C | G | 1 | a0001c0002t0001g0058 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.490-148G>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 2/5 | chr7 | 99908960 | |||||||
| chr7:99909133 | G | GGT | 7 | a0001c0001t0013g0047 a0001c0002t0001g0071 a0001c0002t0001g0072 others(4): Show |
10 | HG02257.hp1 HG02257.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.490-323_490-322dup others(2): Show |
TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 2/5 | chr7 | 99909133 | |||||||
| chr7:99909133 | G | GGTGT | 20 | a0001c0002t0001g0019 a0001c0002t0001g0033 a0001c0002t0001g0069 others(17): Show |
33 | HG00408.hp2 HG01109.hp1 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.490-325_490-322dup others(4): Show |
TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 2/5 | chr7 | 99909133 | |||||||
| chr7:99909133 | G | GGTGTGT | 11 | a0001c0002t0001g0005 a0001c0002t0001g0020 a0001c0002t0001g0068 others(8): Show |
24 | HG00423.hp2 HG00438.hp1 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.490-327_490-322dup others(6): Show |
TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 2/5 | chr7 | 99909133 | |||||||
| chr7:99909133 | G | GGTGTGTG others(1): Show |
24 | a0001c0002t0001g0002 a0001c0002t0001g0018 a0001c0002t0001g0027 others(21): Show |
75 | HG00099.hp2 HG00280.hp2 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.490-329_490-322dup others(8): Show |
TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 2/5 | chr7 | 99909133 | |||||||
| chr7:99909133 | G | GGTGTGTG others(3): Show |
1 | a0001c0002t0001g0028 | 2 | HG03239.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.490-331_490-322dup others(10): Show |
TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 2/5 | chr7 | 99909133 | |||||||
| chr7:99909133 | G | GGTGTGTG others(5): Show |
1 | a0001c0002t0001g0075 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.490-333_490-322dup others(12): Show |
TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 2/5 | chr7 | 99909133 | |||||||
| chr7:99909157 | T | C | 1 | a0001c0001t0002g0104 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.490-345A>G | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 2/5 | chr7 | 99909157 | |||||||
| chr7:99909157 | T | TGTGC | 1 | a0003c0005t0001g0022 | 3 | HG00099.hp1 HG00639.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.490-346_490-345ins others(4): Show |
TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 2/5 | chr7 | 99909157 | |||||||
| chr7:99909159 | C | T | 1 | a0001c0002t0001g0055 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.490-347G>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 2/5 | chr7 | 99909159 | |||||||
| chr7:99909177 | T | G | 2 | a0001c0003t0001g0015 a0001c0003t0001g0120 |
5 | HG01516.hp2 HG01517.hp1 HG03669.hp2 others(2): Show |
intron_variant | MODIFIER | c.490-365A>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 2/5 | chr7 | 99909177 | |||||||
| chr7:99909358 | C | A | 1 | a0004c0008t0006g0026 | 2 | HG02970.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.489+207G>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 2/5 | chr7 | 99909358 | |||||||
| chr7:99909360 | G | A | 1 | a0001c0002t0001g0074 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.489+205C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 2/5 | chr7 | 99909360 | |||||||
| chr7:99909729 | GT | G | 70 | a0001c0001t0002g0040 a0001c0001t0002g0105 a0001c0001t0002g0108 others(67): Show |
174 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(171): Show |
intron_variant | MODIFIER | c.394-70delA | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99909729 | |||||||
| chr7:99909729 | GTT | G | 10 | a0001c0002t0001g0075 a0001c0002t0001g0076 a0003c0005t0001g0022 others(7): Show |
14 | HG00099.hp1 HG00639.hp1 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.394-71_394-70delAA | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99909729 | |||||||
| chr7:99909730 | T | G | 8 | a0001c0002t0001g0027 a0001c0002t0001g0055 a0001c0002t0001g0056 others(5): Show |
9 | HG01361.hp2 HG01516.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.394-70A>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99909730 | |||||||
| chr7:99909731 | T | G | 66 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0018 others(63): Show |
169 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.394-71A>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99909731 | |||||||
| chr7:99909732 | T | G | 10 | a0001c0002t0001g0075 a0001c0002t0001g0076 a0003c0005t0001g0022 others(7): Show |
14 | HG00099.hp1 HG00639.hp1 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.394-72A>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99909732 | |||||||
| chr7:99909733 | T | G | 2 | a0001c0012t0011g0046 a0005c0006t0007g0017 |
4 | HG02895.hp1 HG02897.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.394-73A>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99909733 | |||||||
| chr7:99909734 | T | G | 2 | a0001c0001t0002g0106 a0006c0007t0001g0021 |
4 | HG02896.hp1 HG02897.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.394-74A>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99909734 | |||||||
| chr7:99909736 | T | G | 1 | a0001c0001t0002g0107 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.394-76A>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99909736 | |||||||
| chr7:99910037 | ATTT | A | 9 | a0003c0005t0001g0022 a0003c0005t0001g0034 a0003c0005t0001g0035 others(6): Show |
13 | HG00099.hp1 HG00639.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.394-380_394-378del others(3): Show |
TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99910037 | |||||||
| chr7:99910318 | C | T | 1 | a0003c0005t0001g0079 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.394-658G>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99910318 | |||||||
| chr7:99910570 | C | T | 1 | a0001c0003t0001g0117 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.394-910G>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99910570 | |||||||
| chr7:99910716 | G | T | 1 | a0001c0003t0001g0117 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.394-1056C>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99910716 | |||||||
| chr7:99910802 | T | C | 2 | a0001c0003t0003g0016 a0001c0003t0003g0128 |
5 | HG01243.hp1 HG02258.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.394-1142A>G | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99910802 | |||||||
| chr7:99911028 | T | C | 10 | a0003c0005t0001g0022 a0003c0005t0001g0034 a0003c0005t0001g0035 others(7): Show |
16 | HG00099.hp1 HG00639.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.394-1368A>G | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99911028 | |||||||
| chr7:99911118 | A | G | 4 | a0003c0005t0001g0022 a0003c0005t0001g0035 a0003c0005t0001g0084 others(1): Show |
7 | HG00099.hp1 HG00639.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.394-1458T>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99911118 | |||||||
| chr7:99911384 | G | A | 1 | a0001c0012t0011g0046 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.394-1724C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99911384 | |||||||
| chr7:99911701 | C | T | 48 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0018 others(45): Show |
120 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.394-2041G>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99911701 | |||||||
| chr7:99911952 | C | G | 1 | a0001c0012t0011g0046 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.394-2292G>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99911952 | |||||||
| chr7:99912315 | G | A | 1 | a0001c0001t0013g0047 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.394-2655C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99912315 | |||||||
| chr7:99912530 | T | TC | 4 | a0003c0005t0001g0022 a0003c0005t0001g0035 a0003c0005t0001g0084 others(1): Show |
7 | HG00099.hp1 HG00639.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.394-2871_394-2870i others(3): Show |
TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99912530 | |||||||
| chr7:99912531 | T | A | 4 | a0003c0005t0001g0022 a0003c0005t0001g0035 a0003c0005t0001g0084 others(1): Show |
7 | HG00099.hp1 HG00639.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.394-2871A>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99912531 | |||||||
| chr7:99912531 | T | TA | 79 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0018 others(76): Show |
187 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(184): Show |
intron_variant | MODIFIER | c.394-2872dupT | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99912531 | |||||||
| chr7:99912541 | A | T | 1 | a0001c0001t0005g0091 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.394-2881T>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99912541 | |||||||
| chr7:99912543 | AT | A | 2 | a0001c0001t0002g0041 a0001c0001t0002g0108 |
3 | HG01515.hp2 HG01517.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.394-2884delA | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99912543 | |||||||
| chr7:99912544 | T | A | 87 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0018 others(84): Show |
199 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.394-2884A>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99912544 | |||||||
| chr7:99912611 | A | C | 51 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0018 others(48): Show |
124 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.394-2951T>G | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99912611 | |||||||
| chr7:99912620 | G | T | 3 | a0001c0001t0001g0088 a0001c0001t0002g0090 a0001c0001t0014g0089 |
3 | NA18964.hp1 NA18988.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.394-2960C>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99912620 | |||||||
| chr7:99912656 | G | A | 1 | a0001c0003t0009g0052 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.394-2996C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99912656 | |||||||
| chr7:99912892 | A | G | 1 | a0001c0001t0002g0110 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.394-3232T>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99912892 | |||||||
| chr7:99913227 | T | A | 87 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0018 others(84): Show |
199 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.394-3567A>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99913227 | |||||||
| chr7:99913248 | G | A | 1 | a0001c0001t0002g0109 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.394-3588C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99913248 | |||||||
| chr7:99913438 | G | A | 1 | a0001c0002t0001g0077 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.394-3778C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99913438 | |||||||
| chr7:99913594 | C | T | 1 | a0003c0005t0001g0078 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.394-3934G>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99913594 | |||||||
| chr7:99913596 | G | A | 1 | a0001c0001t0002g0110 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.394-3936C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99913596 | |||||||
| chr7:99913628 | G | A | 1 | a0001c0002t0001g0020 | 3 | HG00423.hp2 NA18941.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.394-3968C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99913628 | |||||||
| chr7:99913661 | A | T | 1 | a0004c0008t0006g0051 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.394-4001T>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99913661 | |||||||
| chr7:99913670 | C | CAAAT | 46 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0018 others(43): Show |
115 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.394-4014_394-4011d others(6): Show |
TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99913670 | |||||||
| chr7:99913670 | C | CAAATAAA others(1): Show |
6 | a0001c0002t0001g0053 a0001c0003t0009g0052 a0001c0003t0015g0049 others(3): Show |
10 | HG01109.hp1 HG01433.hp2 HG01934.hp1 others(7): Show |
intron_variant | MODIFIER | c.394-4018_394-4011d others(10): Show |
TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99913670 | |||||||
| chr7:99913723 | T | C | 1 | a0001c0002t0001g0033 | 2 | NA18948.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.394-4063A>G | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99913723 | |||||||
| chr7:99913749 | A | G | 87 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0018 others(84): Show |
199 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.394-4089T>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99913749 | |||||||
| chr7:99913940 | A | T | 48 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0018 others(45): Show |
120 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.394-4280T>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99913940 | |||||||
| chr7:99914000 | C | T | 1 | a0001c0001t0013g0047 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.394-4340G>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99914000 | |||||||
| chr7:99914086 | C | A | 1 | a0001c0002t0001g0080 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.394-4426G>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99914086 | |||||||
| chr7:99914102 | C | T | 3 | a0003c0005t0001g0034 a0003c0005t0001g0081 a0003c0005t0001g0115 |
4 | HG01884.hp2 HG02486.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.394-4442G>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99914102 | |||||||
| chr7:99914243 | G | A | 2 | a0003c0005t0001g0034 a0003c0005t0001g0081 |
3 | HG01884.hp2 HG02486.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.394-4583C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99914243 | |||||||
| chr7:99914405 | C | T | 3 | a0001c0003t0009g0052 a0004c0008t0006g0026 a0004c0008t0006g0051 |
4 | HG02615.hp1 HG02809.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.393+4604G>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99914405 | |||||||
| chr7:99914601 | G | T | 87 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0018 others(84): Show |
199 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.393+4408C>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99914601 | |||||||
| chr7:99914712 | G | A | 1 | a0007c0010t0008g0044 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.393+4297C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99914712 | |||||||
| chr7:99914965 | G | A | 1 | a0001c0002t0012g0082 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.393+4044C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99914965 | |||||||
| chr7:99915000 | G | A | 1 | a0001c0002t0001g0083 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.393+4009C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99915000 | |||||||
| chr7:99915123 | T | C | 1 | a0001c0003t0015g0049 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.393+3886A>G | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99915123 | |||||||
| chr7:99915316 | A | G | 1 | a0001c0001t0002g0113 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.393+3693T>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99915316 | |||||||
| chr7:99915504 | T | C | 1 | a0006c0007t0001g0021 | 3 | HG02896.hp1 HG02897.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.393+3505A>G | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99915504 | |||||||
| chr7:99915609 | G | C | 1 | a0005c0006t0007g0017 | 3 | HG02895.hp1 HG02897.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.393+3400C>G | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99915609 | |||||||
| chr7:99916064 | G | A | 1 | a0001c0003t0015g0049 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.393+2945C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99916064 | |||||||
| chr7:99916246 | T | G | 1 | a0001c0001t0002g0112 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.393+2763A>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99916246 | |||||||
| chr7:99916375 | C | A | 1 | a0001c0001t0002g0111 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.393+2634G>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99916375 | |||||||
| chr7:99916474 | T | C | 4 | a0003c0005t0001g0022 a0003c0005t0001g0035 a0003c0005t0001g0084 others(1): Show |
7 | HG00099.hp1 HG00639.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.393+2535A>G | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99916474 | |||||||
| chr7:99916758 | C | G | 1 | a0001c0001t0002g0087 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.393+2251G>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99916758 | |||||||
| chr7:99916794 | A | C | 86 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0018 others(83): Show |
198 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.393+2215T>G | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99916794 | |||||||
| chr7:99916883 | A | T | 1 | a0001c0001t0002g0086 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.393+2126T>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99916883 | |||||||
| chr7:99916963 | A | G | 1 | a0001c0003t0001g0050 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.393+2046T>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99916963 | |||||||
| chr7:99917024 | A | T | 1 | a0001c0001t0002g0036 | 2 | HG02818.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.393+1985T>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99917024 | |||||||
| chr7:99917476 | T | C | 1 | a0001c0001t0002g0112 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.393+1533A>G | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99917476 | |||||||
| chr7:99917477 | T | C | 88 | a0001c0001t0013g0047 a0001c0002t0001g0002 a0001c0002t0001g0005 others(85): Show |
200 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.393+1532A>G | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99917477 | |||||||
| chr7:99917478 | G | A | 1 | a0003c0005t0001g0115 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.393+1531C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99917478 | |||||||
| chr7:99917513 | A | C | 1 | a0001c0003t0015g0049 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.393+1496T>G | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99917513 | |||||||
| chr7:99917517 | C | A | 1 | a0001c0003t0003g0128 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.393+1492G>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99917517 | |||||||
| chr7:99917518 | G | GATGGGGG others(100): Show |
1 | a0001c0003t0003g0128 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.393+1490_393+1491i others(109): Show |
TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99917518 | |||||||
| chr7:99917522 | C | T | 1 | a0001c0003t0003g0128 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.393+1487G>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99917522 | |||||||
| chr7:99917523 | C | A | 1 | a0001c0003t0003g0128 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.393+1486G>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99917523 | |||||||
| chr7:99917531 | C | A | 1 | a0001c0003t0003g0128 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.393+1478G>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99917531 | |||||||
| chr7:99917532 | C | A | 1 | a0001c0003t0003g0128 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.393+1477G>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99917532 | |||||||
| chr7:99917535 | C | G | 1 | a0001c0003t0003g0128 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.393+1474G>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99917535 | |||||||
| chr7:99917537 | T | A | 1 | a0001c0003t0003g0128 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.393+1472A>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99917537 | |||||||
| chr7:99917540 | T | G | 1 | a0001c0003t0003g0128 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.393+1469A>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99917540 | |||||||
| chr7:99917544 | ACCCTGTC others(3): Show |
A | 1 | a0001c0003t0003g0128 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.393+1455_393+1464d others(12): Show |
TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99917544 | |||||||
| chr7:99917556 | C | A | 1 | a0001c0003t0003g0128 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.393+1453G>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99917556 | |||||||
| chr7:99917557 | T | A | 1 | a0001c0003t0003g0128 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.393+1452A>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99917557 | |||||||
| chr7:99917563 | T | A | 1 | a0001c0003t0003g0128 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.393+1446A>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99917563 | |||||||
| chr7:99917565 | C | G | 1 | a0001c0003t0003g0128 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.393+1444G>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99917565 | |||||||
| chr7:99917569 | ATTAGCTG others(86): Show |
A | 1 | a0001c0003t0003g0128 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.393+1347_393+1439d others(95): Show |
TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99917569 | |||||||
| chr7:99917663 | G | A | 1 | a0001c0003t0003g0128 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.393+1346C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99917663 | |||||||
| chr7:99917666 | T | A | 1 | a0001c0003t0003g0128 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.393+1343A>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99917666 | |||||||
| chr7:99917667 | T | A | 1 | a0001c0003t0003g0128 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.393+1342A>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99917667 | |||||||
| chr7:99917677 | C | T | 1 | a0001c0002t0001g0048 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.393+1332G>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99917677 | |||||||
| chr7:99917690 | G | T | 1 | a0001c0001t0013g0047 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.393+1319C>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99917690 | |||||||
| chr7:99917772 | T | TG | 2 | a0001c0001t0002g0023 a0001c0001t0002g0113 |
4 | NA18985.hp2 NA18992.hp2 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.393+1236dupC | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99917772 | |||||||
| chr7:99918040 | G | C | 1 | a0001c0001t0002g0114 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.393+969C>G | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99918040 | |||||||
| chr7:99918359 | C | G | 88 | a0001c0001t0013g0047 a0001c0002t0001g0002 a0001c0002t0001g0005 others(85): Show |
200 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.393+650G>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99918359 | |||||||
| chr7:99918381 | A | T | 2 | a0001c0012t0011g0046 a0005c0006t0007g0017 |
4 | HG02895.hp1 HG02897.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.393+628T>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99918381 | |||||||
| chr7:99918492 | G | C | 1 | a0003c0005t0001g0115 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.393+517C>G | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99918492 | |||||||
| chr7:99918566 | G | GA | 23 | a0001c0003t0001g0003 a0001c0003t0001g0010 a0001c0003t0001g0013 others(20): Show |
54 | HG01081.hp2 HG01167.hp2 HG01169.hp2 others(51): Show |
intron_variant | MODIFIER | c.393+442dupT | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99918566 | |||||||
| chr7:99918725 | G | A | 1 | a0001c0002t0001g0129 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.393+284C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99918725 | |||||||
| chr7:99919008 | C | A | 1 | a0001c0002t0001g0130 | 1 | HG01361.hp2 | splice_donor_variant&intron_variant | HIGH | c.393+1G>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99919008 |