Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 55223 |
| ensemblid | ENSG00000116525.14 |
| hgncid | 25574 |
| symbol | TRIM62 |
| name | tripartite motif containing 62 |
| refseq_nuc | NM_018207.3 |
| refseq_prot | NP_060677.2 |
| ensembl_nuc | ENST00000291416.10 |
| ensembl_prot | ENSP00000291416.5 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 33145399 |
| end | 33182043 |
| strand | - |
| ver | v1.2 |
| region | chr1:33145399-33182043 |
| region5000 | chr1:33140399-33187043 |
| regionname0 | TRIM62_chr1_33145399_33182043 |
| regionname5000 | TRIM62_chr1_33140399_33187043 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 475 | 325 | 78 | 52 | 149 | 10 | 34 | 109 | TRIM62_chr1_33140399_33187043 | TRIM62 | MACSL others(470): Show |
chr1 | 33140399 | 33187043 |
| a0002 | 0/0 | 475 | 12 | 12 | 0 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | MACSL others(470): Show |
chr1 | 33140399 | 33187043 |
| a0003 | 0/0 | 475 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | TRIM62_chr1_33140399_33187043 | TRIM62 | MACSL others(470): Show |
chr1 | 33140399 | 33187043 |
| a0004 | 0/0 | 475 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TRIM62_chr1_33140399_33187043 | TRIM62 | MACSL others(470): Show |
chr1 | 33140399 | 33187043 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1425 | 224 | 53 | 37 | 104 | 6 | 23 | TRIM62_chr1_33140399_33187043 | TRIM62 | ATGGC others(1420): Show |
chr1 | 33140399 | 33187043 | ||
| a0001c0002 | 1/0 | 1425 | 87 | 14 | 15 | 43 | 4 | 10 | TRIM62_chr1_33140399_33187043 | TRIM62 | ATGGC others(1420): Show |
chr1 | 33140399 | 33187043 | ||
| a0001c0004 | 0/0 | 1425 | 6 | 6 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | ATGGC others(1420): Show |
chr1 | 33140399 | 33187043 | ||
| a0001c0006 | 0/0 | 1425 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | ATGGC others(1420): Show |
chr1 | 33140399 | 33187043 | ||
| a0001c0007 | 0/0 | 1425 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | ATGGC others(1420): Show |
chr1 | 33140399 | 33187043 | ||
| a0001c0008 | 0/0 | 1425 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM62_chr1_33140399_33187043 | TRIM62 | ATGGC others(1420): Show |
chr1 | 33140399 | 33187043 | ||
| a0001c0009 | 0/0 | 1425 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | ATGGC others(1420): Show |
chr1 | 33140399 | 33187043 | ||
| a0001c0011 | 0/0 | 1425 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | ATGGC others(1420): Show |
chr1 | 33140399 | 33187043 | ||
| a0001c0012 | 0/0 | 1425 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | ATGGC others(1420): Show |
chr1 | 33140399 | 33187043 | ||
| a0001c0013 | 0/0 | 1425 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | ATGGC others(1420): Show |
chr1 | 33140399 | 33187043 | ||
| a0001c0014 | 0/0 | 1425 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | ATGGC others(1420): Show |
chr1 | 33140399 | 33187043 | ||
| a0002c0003 | 0/0 | 1425 | 12 | 12 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | ATGGC others(1420): Show |
chr1 | 33140399 | 33187043 | ||
| a0003c0005 | 0/0 | 1425 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | ATGGC others(1420): Show |
chr1 | 33140399 | 33187043 | ||
| a0004c0010 | 0/0 | 1425 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | ATGGC others(1420): Show |
chr1 | 33140399 | 33187043 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3817 | 182 | 46 | 36 | 73 | 6 | 20 | TRIM62_chr1_33140399_33187043 | TRIM62 | GGGTT others(3812): Show |
chr1 | 33140399 | 33187043 |
| a0001c0001t0002 | 0/0 | 3817 | 3 | 0 | 1 | 2 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | GGGTT others(3812): Show |
chr1 | 33140399 | 33187043 |
| a0001c0001t0003 | 0/0 | 3817 | 28 | 4 | 0 | 21 | 0 | 3 | TRIM62_chr1_33140399_33187043 | TRIM62 | GGGTT others(3812): Show |
chr1 | 33140399 | 33187043 |
| a0001c0001t0005 | 0/0 | 3817 | 4 | 0 | 0 | 4 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | GGGTT others(3812): Show |
chr1 | 33140399 | 33187043 |
| a0001c0001t0006 | 0/0 | 3817 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | GGGTT others(3812): Show |
chr1 | 33140399 | 33187043 |
| a0001c0001t0007 | 0/0 | 3817 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | GGGTT others(3812): Show |
chr1 | 33140399 | 33187043 |
| a0001c0001t0008 | 0/0 | 3817 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | GGGTT others(3812): Show |
chr1 | 33140399 | 33187043 |
| a0001c0001t0011 | 0/0 | 3817 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | GGGTT others(3812): Show |
chr1 | 33140399 | 33187043 |
| a0001c0001t0012 | 0/0 | 3817 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | GGGTT others(3812): Show |
chr1 | 33140399 | 33187043 |
| a0001c0002t0001 | 0/0 | 3817 | 3 | 1 | 2 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | GGGTT others(3812): Show |
chr1 | 33140399 | 33187043 |
| a0001c0002t0002 | 0/0 | 3817 | 58 | 1 | 10 | 33 | 4 | 10 | TRIM62_chr1_33140399_33187043 | TRIM62 | GGGTT others(3812): Show |
chr1 | 33140399 | 33187043 |
| a0001c0002t0003 | 1/0 | 3817 | 19 | 6 | 2 | 10 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | GGGTT others(3812): Show |
chr1 | 33140399 | 33187043 |
| a0001c0002t0009 | 0/0 | 3817 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | GGGTT others(3812): Show |
chr1 | 33140399 | 33187043 |
| a0001c0002t0010 | 0/0 | 3817 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | GGGTT others(3812): Show |
chr1 | 33140399 | 33187043 |
| a0001c0002t0016 | 0/0 | 3817 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | GGGTT others(3812): Show |
chr1 | 33140399 | 33187043 |
| a0001c0002t0017 | 0/0 | 3817 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | GGGTT others(3812): Show |
chr1 | 33140399 | 33187043 |
| a0001c0002t0018 | 0/0 | 3817 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | GGGTT others(3812): Show |
chr1 | 33140399 | 33187043 |
| a0001c0004t0003 | 0/0 | 3817 | 5 | 5 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | GGGTT others(3812): Show |
chr1 | 33140399 | 33187043 |
| a0001c0004t0007 | 0/0 | 3817 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | GGGTT others(3812): Show |
chr1 | 33140399 | 33187043 |
| a0001c0006t0003 | 0/0 | 3817 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | GGGTT others(3812): Show |
chr1 | 33140399 | 33187043 |
| a0001c0007t0014 | 0/0 | 3817 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | GGGTT others(3812): Show |
chr1 | 33140399 | 33187043 |
| a0001c0008t0001 | 0/0 | 3817 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM62_chr1_33140399_33187043 | TRIM62 | GGGTT others(3812): Show |
chr1 | 33140399 | 33187043 |
| a0001c0009t0001 | 0/0 | 3817 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | GGGTT others(3812): Show |
chr1 | 33140399 | 33187043 |
| a0001c0011t0001 | 0/0 | 3817 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | GGGTT others(3812): Show |
chr1 | 33140399 | 33187043 |
| a0001c0012t0015 | 0/0 | 3817 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | GGGTT others(3812): Show |
chr1 | 33140399 | 33187043 |
| a0001c0013t0002 | 0/0 | 3817 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | GGGTT others(3812): Show |
chr1 | 33140399 | 33187043 |
| a0001c0014t0002 | 0/0 | 3817 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | GGGTT others(3812): Show |
chr1 | 33140399 | 33187043 |
| a0002c0003t0003 | 0/0 | 3817 | 4 | 4 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | GGGTT others(3812): Show |
chr1 | 33140399 | 33187043 |
| a0002c0003t0004 | 0/0 | 3817 | 7 | 7 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | GGGTT others(3812): Show |
chr1 | 33140399 | 33187043 |
| a0002c0003t0013 | 0/0 | 3817 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | GGGTT others(3812): Show |
chr1 | 33140399 | 33187043 |
| a0003c0005t0001 | 0/0 | 3817 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | GGGTT others(3812): Show |
chr1 | 33140399 | 33187043 |
| a0004c0010t0001 | 0/0 | 3817 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | GGGTT others(3812): Show |
chr1 | 33140399 | 33187043 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 10 | 1 | 3 | 5 | 0 | 1 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0003 | 0/0 | 7 | 0 | 3 | 3 | 1 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0004 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0009 | 0/0 | 4 | 1 | 1 | 1 | 0 | 1 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0014 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0017 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0035 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0074 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0003g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0003g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0003g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0003g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0003g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0003g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0003g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0003g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0005g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0005g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0005g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0006g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0006g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0007g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0008g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0011g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0001t0012g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0002t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0002t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0002t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0002t0002g0001 | 0/0 | 28 | 1 | 3 | 18 | 3 | 3 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0002t0002g0008 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0002t0002g0043 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0002t0002g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0002t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0002t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0002t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0002t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0002t0002g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0002t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0002t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0002t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0002t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0002t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0002t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0002t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0002t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0002t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0002t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0002t0003g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0002t0003g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0002t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0002t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0002t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0002t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0002t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0002t0003g0209 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0002t0003g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0002t0003g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0002t0003g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0002t0003g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0002t0003g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0002t0003g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0002t0009g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0002t0009g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0002t0010g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0002t0010g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0002t0016g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0002t0017g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0002t0018g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0004t0003g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0004t0003g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0004t0003g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0004t0007g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0006t0003g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0007t0014g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0008t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0009t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0011t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0012t0015g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0013t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0001c0014t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0002c0003t0003g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0002c0003t0003g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0002c0003t0003g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0002c0003t0003g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0002c0003t0004g0005 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0002c0003t0004g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0002c0003t0013g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0003c0005t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| a0004c0010t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0088 | EUR | GBR | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0125 | EUR | GBR | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG00323 | hp1 | a0001 | c0002 | t0002 | g0001 | EUR | FIN | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | FIN | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | CHS | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG00408 | hp2 | a0001 | c0013 | t0002 | g0205 | EAS | CHS | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | CHS | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG00544 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | CHS | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG00544 | hp2 | a0001 | c0001 | t0011 | g0147 | EAS | CHS | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0161 | EAS | CHS | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | CHS | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | CHS | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG00639 | hp1 | a0001 | c0002 | t0003 | g0213 | AMR | PUR | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0167 | EAS | CHS | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0100 | AMR | PUR | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG00735 | hp2 | a0001 | c0002 | t0002 | g0202 | AMR | PUR | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0211 | AMR | PUR | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0210 | AMR | PUR | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG01074 | hp1 | a0001 | c0002 | t0002 | g0197 | AMR | PUR | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG01099 | hp1 | a0001 | c0002 | t0002 | g0188 | AMR | PUR | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG01106 | hp1 | a0001 | c0002 | t0002 | g0189 | AMR | PUR | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG01109 | hp2 | a0001 | c0002 | t0018 | g0230 | AMR | PUR | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG01167 | hp2 | a0001 | c0002 | t0002 | g0206 | AMR | PUR | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG01243 | hp1 | a0001 | c0002 | t0003 | g0214 | AMR | PUR | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG01255 | hp2 | a0001 | c0002 | t0002 | g0001 | AMR | CLM | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG01256 | hp2 | a0001 | c0002 | t0002 | g0001 | AMR | CLM | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG01261 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | CLM | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | CLM | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG01346 | hp2 | a0001 | c0002 | t0002 | g0190 | AMR | CLM | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | CLM | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0027 | EUR | IBS | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG01515 | hp2 | a0001 | c0002 | t0002 | g0186 | EUR | IBS | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG01517 | hp1 | a0001 | c0002 | t0002 | g0001 | EUR | IBS | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0027 | EUR | IBS | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG01884 | hp1 | a0001 | c0002 | t0016 | g0228 | AFR | ACB | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG01884 | hp2 | a0001 | c0002 | t0003 | g0212 | AFR | ACB | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG01891 | hp2 | a0002 | c0003 | t0004 | g0005 | AFR | ACB | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG01978 | hp1 | a0001 | c0002 | t0002 | g0198 | AMR | PEL | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | KHV | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG02015 | hp2 | a0001 | c0002 | t0002 | g0225 | EAS | KHV | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | KHV | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0149 | AFR | ACB | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | ACB | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | KHV | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG02071 | hp2 | a0001 | c0002 | t0002 | g0044 | EAS | KHV | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | KHV | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG02074 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | KHV | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG02080 | hp2 | a0001 | c0001 | t0003 | g0066 | EAS | KHV | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0111 | EAS | KHV | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0176 | EAS | KHV | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG02135 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | KHV | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | KHV | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | ACB | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | CDX | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG02165 | hp2 | a0001 | c0002 | t0002 | g0044 | EAS | CDX | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | ACB | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | ACB | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0138 | AFR | ACB | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG02451 | hp1 | a0001 | c0002 | t0009 | g0181 | AFR | ACB | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | GWD | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG02622 | hp2 | a0001 | c0002 | t0017 | g0229 | AFR | GWD | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG02630 | hp1 | a0002 | c0003 | t0003 | g0217 | AFR | GWD | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG02698 | hp1 | a0001 | c0002 | t0002 | g0001 | SAS | PJL | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG02723 | hp2 | a0001 | c0002 | t0003 | g0045 | AFR | GWD | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0157 | AFR | GWD | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG02818 | hp1 | a0001 | c0002 | t0003 | g0218 | AFR | GWD | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG02818 | hp2 | a0001 | c0004 | t0003 | g0010 | AFR | GWD | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG02886 | hp1 | a0001 | c0002 | t0002 | g0001 | AFR | GWD | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG02886 | hp2 | a0001 | c0001 | t0003 | g0160 | AFR | GWD | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG02896 | hp1 | a0001 | c0002 | t0010 | g0232 | AFR | GWD | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG02897 | hp1 | a0001 | c0002 | t0010 | g0231 | AFR | GWD | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG02922 | hp1 | a0001 | c0004 | t0003 | g0072 | AFR | ESN | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG02922 | hp2 | a0001 | c0006 | t0003 | g0174 | AFR | ESN | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | ESN | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG02965 | hp2 | a0001 | c0001 | t0008 | g0016 | AFR | ESN | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | ESN | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG03017 | hp2 | a0001 | c0002 | t0002 | g0001 | SAS | PJL | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | MSL | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | MSL | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG03130 | hp1 | a0002 | c0003 | t0013 | g0223 | AFR | ESN | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | ESN | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG03139 | hp1 | a0001 | c0004 | t0003 | g0073 | AFR | ESN | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | ESN | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | ESN | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG03195 | hp2 | a0002 | c0003 | t0004 | g0005 | AFR | ESN | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG03209 | hp1 | a0002 | c0003 | t0004 | g0005 | AFR | MSL | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | MSL | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | MSL | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG03239 | hp1 | a0001 | c0002 | t0002 | g0185 | SAS | PJL | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG03453 | hp1 | a0001 | c0002 | t0003 | g0045 | AFR | MSL | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | MSL | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG03486 | hp1 | a0001 | c0002 | t0001 | g0179 | AFR | MSL | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | MSL | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG03490 | hp1 | a0001 | c0002 | t0002 | g0043 | SAS | PJL | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG03540 | hp1 | a0001 | c0011 | t0001 | g0220 | AFR | GWD | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG03540 | hp2 | a0002 | c0003 | t0004 | g0005 | AFR | GWD | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG03669 | hp1 | a0001 | c0002 | t0002 | g0187 | SAS | PJL | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0126 | SAS | PJL | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0071 | SAS | PJL | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG03710 | hp2 | a0001 | c0008 | t0001 | g0130 | SAS | PJL | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG03831 | hp1 | a0001 | c0002 | t0002 | g0199 | SAS | BEB | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG03834 | hp1 | a0001 | c0002 | t0002 | g0184 | SAS | BEB | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG03834 | hp2 | a0001 | c0002 | t0002 | g0183 | SAS | BEB | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0079 | SAS | BEB | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG03927 | hp2 | a0001 | c0002 | t0002 | g0001 | SAS | BEB | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG03942 | hp1 | a0001 | c0002 | t0002 | g0043 | SAS | BEB | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | BEB | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | STU | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | STU | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | BEB | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0087 | SAS | BEB | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | STU | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | STU | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA18522 | hp1 | a0001 | c0007 | t0014 | g0226 | AFR | YRI | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA18522 | hp2 | a0002 | c0003 | t0004 | g0005 | AFR | YRI | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA18747 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | CHB | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA18747 | hp2 | a0001 | c0001 | t0012 | g0136 | EAS | CHB | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA18906 | hp1 | a0002 | c0003 | t0003 | g0216 | AFR | YRI | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA18906 | hp2 | a0001 | c0002 | t0009 | g0180 | AFR | YRI | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA18941 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA18945 | hp2 | a0001 | c0002 | t0003 | g0007 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA18946 | hp2 | a0001 | c0002 | t0002 | g0208 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA18947 | hp1 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA18948 | hp1 | a0001 | c0001 | t0005 | g0170 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA18948 | hp2 | a0001 | c0001 | t0003 | g0036 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA18949 | hp2 | a0001 | c0002 | t0002 | g0191 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA18950 | hp2 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA18951 | hp2 | a0001 | c0002 | t0003 | g0195 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA18953 | hp1 | a0001 | c0001 | t0003 | g0037 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA18954 | hp1 | a0001 | c0001 | t0003 | g0039 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA18954 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA18957 | hp1 | a0001 | c0002 | t0003 | g0207 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA18960 | hp1 | a0003 | c0005 | t0001 | g0029 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA18960 | hp2 | a0001 | c0002 | t0002 | g0203 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA18961 | hp1 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA18963 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA18965 | hp2 | a0001 | c0001 | t0003 | g0036 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA18966 | hp2 | a0001 | c0002 | t0003 | g0007 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA18967 | hp1 | a0001 | c0001 | t0005 | g0041 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA18974 | hp1 | a0001 | c0001 | t0003 | g0166 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA18979 | hp1 | a0001 | c0001 | t0003 | g0164 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA18979 | hp2 | a0001 | c0002 | t0003 | g0007 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA18980 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA18980 | hp2 | a0001 | c0001 | t0003 | g0163 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA18982 | hp2 | a0001 | c0002 | t0003 | g0192 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA18983 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA18988 | hp1 | a0001 | c0001 | t0005 | g0041 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA18988 | hp2 | a0001 | c0002 | t0003 | g0194 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA18989 | hp2 | a0001 | c0001 | t0003 | g0037 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA18991 | hp1 | a0001 | c0002 | t0002 | g0201 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA18998 | hp2 | a0001 | c0002 | t0003 | g0007 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA19000 | hp2 | a0001 | c0001 | t0003 | g0064 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA19002 | hp2 | a0001 | c0002 | t0003 | g0007 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA19003 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA19004 | hp1 | a0001 | c0009 | t0001 | g0095 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA19004 | hp2 | a0001 | c0002 | t0002 | g0204 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA19006 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA19012 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA19030 | hp1 | a0002 | c0003 | t0003 | g0222 | AFR | LWK | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | LWK | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA19043 | hp1 | a0001 | c0014 | t0002 | g0182 | AFR | LWK | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | LWK | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA19054 | hp2 | a0001 | c0002 | t0003 | g0193 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA19057 | hp1 | a0001 | c0001 | t0003 | g0038 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA19057 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA19058 | hp1 | a0001 | c0001 | t0003 | g0162 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA19062 | hp2 | a0001 | c0002 | t0002 | g0200 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA19064 | hp1 | a0001 | c0001 | t0003 | g0038 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA19065 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0039 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA19067 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA19074 | hp1 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA19079 | hp1 | a0001 | c0001 | t0006 | g0152 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA19080 | hp2 | a0001 | c0001 | t0003 | g0159 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA19081 | hp1 | a0001 | c0001 | t0006 | g0140 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA19081 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA19083 | hp2 | a0001 | c0002 | t0002 | g0196 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA19084 | hp1 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA19084 | hp2 | a0001 | c0001 | t0003 | g0065 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA19085 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA19085 | hp2 | a0001 | c0001 | t0005 | g0171 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA19086 | hp1 | a0001 | c0001 | t0003 | g0165 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA19090 | hp1 | a0003 | c0005 | t0001 | g0029 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA19090 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA19091 | hp1 | a0001 | c0001 | t0003 | g0168 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA19091 | hp2 | a0004 | c0010 | t0001 | g0178 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA19240 | hp1 | a0002 | c0003 | t0004 | g0005 | AFR | YRI | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA19240 | hp2 | a0001 | c0004 | t0003 | g0010 | AFR | YRI | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA20129 | hp1 | a0001 | c0002 | t0003 | g0219 | AFR | ASW | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ASW | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0177 | EUR | TSI | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA20752 | hp2 | a0001 | c0002 | t0002 | g0001 | EUR | TSI | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | CLM | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG02109 | hp1 | a0001 | c0004 | t0007 | g0156 | AFR | ACB | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG02109 | hp2 | a0001 | c0004 | t0003 | g0010 | AFR | ACB | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | ACB | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG02486 | hp2 | a0002 | c0003 | t0003 | g0224 | AFR | ACB | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG02559 | hp1 | a0001 | c0001 | t0007 | g0068 | AFR | ACB | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | ACB | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | MSL | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG03471 | hp2 | a0001 | c0002 | t0003 | g0215 | AFR | MSL | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG06807 | hp1 | a0001 | c0001 | t0008 | g0016 | AFR | USA | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| HG06807 | hp2 | a0001 | c0012 | t0015 | g0227 | AFR | USA | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | USA | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | USA | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | LWK | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| NA21309 | hp2 | a0002 | c0003 | t0004 | g0221 | AFR | LWK | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0074 | REF | REF | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0003 | g0209 | REF | REF | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:33147188 | C | T | 1 | a0002 | 12 | HG01891.hp2 HG02486.hp2 HG02630.hp1 others(9): Show |
missense_variant | MODERATE | c.1417G>A | p.Val473Ile | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 5/5 | 2028/3817 | 1417/1428 | 473/475 | chr1 | 33147188 | |||
| chr1:33159844 | G | A | 1 | a0003 | 2 | NA18960.hp1 NA19090.hp1 |
missense_variant | MODERATE | c.605C>T | p.Ala202Val | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 3/5 | 1216/3817 | 605/1428 | 202/475 | chr1 | 33159844 | |||
| chr1:33181158 | G | A | 1 | a0004 | 1 | NA19091.hp2 | missense_variant | MODERATE | c.275C>T | p.Pro92Leu | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/5 | 886/3817 | 275/1428 | 92/475 | chr1 | 33181158 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:33147414 | G | A | 1 | a0001c0008 | 1 | HG03710.hp2 | synonymous_variant | LOW | c.1191C>T | p.Tyr397Tyr | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 5/5 | 1802/3817 | 1191/1428 | 397/475 | chr1 | 33147414 | |||
| chr1:33147453 | G | A | 1 | a0001c0009 | 1 | NA19004.hp1 | synonymous_variant | LOW | c.1152C>T | p.Arg384Arg | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 5/5 | 1763/3817 | 1152/1428 | 384/475 | chr1 | 33147453 | |||
| chr1:33147585 | C | G | 1 | a0001c0006 | 1 | HG02922.hp2 | synonymous_variant | LOW | c.1020G>C | p.Val340Val | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 5/5 | 1631/3817 | 1020/1428 | 340/475 | chr1 | 33147585 | |||
| chr1:33147672 | C | T | 1 | a0001c0007 | 1 | NA18522.hp1 | synonymous_variant | LOW | c.933G>A | p.Ser311Ser | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 5/5 | 1544/3817 | 933/1428 | 311/475 | chr1 | 33147672 | |||
| chr1:33158302 | G | A | 1 | a0001c0011 | 1 | HG03540.hp1 | synonymous_variant | LOW | c.828C>T | p.Gly276Gly | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/5 | 1439/3817 | 828/1428 | 276/475 | chr1 | 33158302 | |||
| chr1:33159747 | C | T | 2 | a0001c0004 a0001c0006 |
7 | HG02109.hp1 HG02109.hp2 HG02818.hp2 others(4): Show |
synonymous_variant | LOW | c.702G>A | p.Glu234Glu | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 3/5 | 1313/3817 | 702/1428 | 234/475 | chr1 | 33159747 | |||
| chr1:33159822 | G | A | 1 | a0001c0012 | 1 | HG06807.hp2 | synonymous_variant | LOW | c.627C>T | p.Thr209Thr | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 3/5 | 1238/3817 | 627/1428 | 209/475 | chr1 | 33159822 | |||
| chr1:33159834 | G | C | 1 | a0001c0013 | 1 | HG00408.hp2 | synonymous_variant | LOW | c.615C>G | p.Ala205Ala | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 3/5 | 1226/3817 | 615/1428 | 205/475 | chr1 | 33159834 | |||
| chr1:33159903 | G | A | 1 | a0001c0014 | 1 | NA19043.hp1 | synonymous_variant | LOW | c.546C>T | p.Phe182Phe | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 3/5 | 1157/3817 | 546/1428 | 182/475 | chr1 | 33159903 | |||
| chr1:33181349 | A | G | 8 | a0001c0001 a0001c0004 a0001c0006 others(5): Show |
236 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(233): Show |
synonymous_variant | LOW | c.84T>C | p.His28His | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/5 | 695/3817 | 84/1428 | 28/475 | chr1 | 33181349 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:33145432 | T | C | 1 | a0001c0001t0005 | 4 | NA18948.hp1 NA18967.hp1 NA18988.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1745A>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 5/5 | 1745 | chr1 | 33145432 | ||||||
| chr1:33145583 | G | A | 2 | a0002c0003t0004 a0002c0003t0013 |
8 | HG01891.hp2 HG03130.hp1 HG03195.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1594C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 5/5 | 1594 | chr1 | 33145583 | ||||||
| chr1:33145749 | G | A | 3 | a0001c0001t0008 a0001c0002t0009 a0001c0002t0010 |
6 | HG02451.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1428C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 5/5 | 1428 | chr1 | 33145749 | ||||||
| chr1:33145853 | T | C | 1 | a0001c0001t0012 | 1 | NA18747.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1324A>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 5/5 | 1324 | chr1 | 33145853 | ||||||
| chr1:33146289 | C | T | 14 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0006 others(11): Show |
201 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(198): Show |
3_prime_UTR_variant | MODIFIER | c.*888G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 5/5 | 888 | chr1 | 33146289 | ||||||
| chr1:33146386 | G | A | 1 | a0001c0002t0009 | 2 | HG02451.hp1 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*791C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 5/5 | 791 | chr1 | 33146386 | ||||||
| chr1:33146597 | A | G | 2 | a0001c0001t0007 a0001c0004t0007 |
2 | HG02109.hp1 HG02559.hp1 |
3_prime_UTR_variant | MODIFIER | c.*580T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 5/5 | 580 | chr1 | 33146597 | ||||||
| chr1:33146599 | C | T | 1 | a0001c0001t0006 | 2 | NA19079.hp1 NA19081.hp1 |
3_prime_UTR_variant | MODIFIER | c.*578G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 5/5 | 578 | chr1 | 33146599 | ||||||
| chr1:33146619 | T | C | 1 | a0002c0003t0013 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*558A>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 5/5 | 558 | chr1 | 33146619 | ||||||
| chr1:33146863 | G | A | 1 | a0001c0012t0015 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*314C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 5/5 | 314 | chr1 | 33146863 | ||||||
| chr1:33146907 | G | A | 4 | a0001c0001t0002 a0001c0002t0002 a0001c0013t0002 others(1): Show |
63 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*270C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 5/5 | 270 | chr1 | 33146907 | ||||||
| chr1:33146985 | C | T | 1 | a0001c0001t0011 | 1 | HG00544.hp2 | 3_prime_UTR_variant | MODIFIER | c.*192G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 5/5 | 192 | chr1 | 33146985 | ||||||
| chr1:33181533 | G | A | 1 | a0001c0007t0014 | 1 | NA18522.hp1 | 5_prime_UTR_variant | MODIFIER | c.-101C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/5 | 101 | chr1 | 33181533 | ||||||
| chr1:33181787 | C | T | 1 | a0001c0002t0016 | 1 | HG01884.hp1 | 5_prime_UTR_variant | MODIFIER | c.-355G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/5 | 355 | chr1 | 33181787 | ||||||
| chr1:33181894 | G | A | 1 | a0001c0012t0015 | 1 | HG06807.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-462C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/5 | chr1 | 33181894 | |||||||
| chr1:33181949 | C | A | 4 | a0001c0002t0010 a0001c0002t0016 a0001c0002t0017 others(1): Show |
5 | HG01109.hp2 HG01884.hp1 HG02622.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-517G>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/5 | 517 | chr1 | 33181949 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:33147883 | C | T | 1 | a0001c0001t0001g0052 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.878-156G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33147883 | |||||||
| chr1:33148149 | A | G | 1 | a0001c0001t0003g0163 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.878-422T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33148149 | |||||||
| chr1:33148180 | G | A | 1 | a0004c0010t0001g0178 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.878-453C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33148180 | |||||||
| chr1:33148561 | T | C | 50 | a0001c0001t0002g0100 a0001c0001t0002g0175 a0001c0001t0002g0176 others(47): Show |
88 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.878-834A>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33148561 | |||||||
| chr1:33148767 | T | C | 5 | a0001c0001t0008g0016 a0001c0002t0009g0180 a0001c0002t0009g0181 others(2): Show |
6 | HG02451.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.878-1040A>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33148767 | |||||||
| chr1:33148781 | A | T | 1 | a0001c0004t0007g0156 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.878-1054T>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33148781 | |||||||
| chr1:33148887 | A | T | 4 | a0001c0004t0003g0010 a0001c0004t0003g0072 a0001c0004t0003g0073 others(1): Show |
6 | HG02109.hp2 HG02818.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.878-1160T>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33148887 | |||||||
| chr1:33149064 | A | T | 165 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(162): Show |
229 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(226): Show |
intron_variant | MODIFIER | c.878-1337T>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33149064 | |||||||
| chr1:33149110 | G | T | 3 | a0001c0001t0008g0016 a0001c0002t0010g0231 a0001c0002t0010g0232 |
4 | HG02896.hp1 HG02897.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.878-1383C>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33149110 | |||||||
| chr1:33149161 | T | G | 1 | a0001c0001t0001g0049 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.878-1434A>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33149161 | |||||||
| chr1:33149199 | C | A | 165 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(162): Show |
229 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(226): Show |
intron_variant | MODIFIER | c.878-1472G>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33149199 | |||||||
| chr1:33149403 | C | T | 7 | a0002c0003t0003g0216 a0002c0003t0003g0217 a0002c0003t0003g0222 others(4): Show |
12 | HG01891.hp2 HG02486.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.878-1676G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33149403 | |||||||
| chr1:33149405 | C | T | 5 | a0001c0002t0003g0212 a0001c0004t0003g0010 a0001c0004t0003g0072 others(2): Show |
7 | HG01884.hp2 HG02109.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.878-1678G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33149405 | |||||||
| chr1:33149457 | T | TA | 30 | a0001c0001t0002g0100 a0001c0001t0002g0175 a0001c0001t0002g0176 others(27): Show |
63 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.878-1731_878-1730i others(3): Show |
TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33149457 | |||||||
| chr1:33149458 | T | A | 33 | a0001c0001t0001g0146 a0001c0001t0002g0100 a0001c0001t0002g0175 others(30): Show |
66 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.878-1731A>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33149458 | |||||||
| chr1:33149458 | T | TA | 17 | a0001c0001t0003g0036 a0001c0001t0003g0037 a0001c0001t0003g0038 others(14): Show |
22 | HG00597.hp1 HG00673.hp1 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.878-1732dupT | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33149458 | |||||||
| chr1:33149636 | A | G | 31 | a0001c0001t0002g0100 a0001c0001t0002g0175 a0001c0001t0002g0176 others(28): Show |
64 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.878-1909T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33149636 | |||||||
| chr1:33149697 | C | G | 20 | a0001c0001t0003g0064 a0001c0001t0003g0065 a0001c0001t0003g0066 others(17): Show |
26 | HG00639.hp1 HG01243.hp1 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.878-1970G>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33149697 | |||||||
| chr1:33149792 | G | C | 1 | a0001c0001t0001g0139 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.878-2065C>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33149792 | |||||||
| chr1:33149994 | C | T | 1 | a0001c0001t0002g0175 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.878-2267G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33149994 | |||||||
| chr1:33150007 | G | C | 5 | a0001c0001t0001g0020 a0001c0001t0001g0117 a0001c0001t0001g0148 others(2): Show |
6 | HG00544.hp2 HG02145.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.878-2280C>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33150007 | |||||||
| chr1:33150015 | C | T | 1 | a0001c0001t0001g0055 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.878-2288G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33150015 | |||||||
| chr1:33150186 | G | C | 1 | a0001c0002t0003g0212 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.878-2459C>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33150186 | |||||||
| chr1:33150275 | A | G | 31 | a0001c0001t0002g0100 a0001c0001t0002g0175 a0001c0001t0002g0176 others(28): Show |
64 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.878-2548T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33150275 | |||||||
| chr1:33150292 | TCTCCCTA | T | 5 | a0002c0003t0003g0222 a0002c0003t0003g0224 a0002c0003t0004g0005 others(2): Show |
10 | HG01891.hp2 HG02486.hp2 HG03130.hp1 others(7): Show |
intron_variant | MODIFIER | c.878-2572_878-2566d others(9): Show |
TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33150292 | |||||||
| chr1:33150612 | C | T | 1 | a0001c0001t0001g0053 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.878-2885G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33150612 | |||||||
| chr1:33150648 | G | A | 1 | a0001c0001t0003g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.878-2921C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33150648 | |||||||
| chr1:33150649 | G | T | 1 | a0001c0002t0002g0201 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.878-2922C>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33150649 | |||||||
| chr1:33150707 | G | A | 1 | a0001c0004t0007g0156 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.878-2980C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33150707 | |||||||
| chr1:33150709 | C | G | 48 | a0001c0001t0002g0100 a0001c0001t0002g0175 a0001c0001t0002g0176 others(45): Show |
86 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.878-2982G>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33150709 | |||||||
| chr1:33150722 | G | A | 2 | a0001c0001t0001g0015 a0001c0001t0001g0048 |
3 | HG02280.hp2 HG02451.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.878-2995C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33150722 | |||||||
| chr1:33150864 | T | C | 223 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(220): Show |
330 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(327): Show |
intron_variant | MODIFIER | c.878-3137A>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33150864 | |||||||
| chr1:33151013 | C | T | 1 | a0001c0001t0001g0028 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.878-3286G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33151013 | |||||||
| chr1:33151108 | G | A | 1 | a0001c0002t0009g0180 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.878-3381C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33151108 | |||||||
| chr1:33151150 | G | C | 49 | a0001c0001t0002g0100 a0001c0001t0002g0175 a0001c0001t0002g0176 others(46): Show |
87 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.878-3423C>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33151150 | |||||||
| chr1:33151185 | T | C | 1 | a0001c0002t0003g0192 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.878-3458A>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33151185 | |||||||
| chr1:33151321 | C | T | 1 | a0001c0012t0015g0227 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.878-3594G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33151321 | |||||||
| chr1:33151356 | C | T | 2 | a0001c0001t0001g0084 a0001c0001t0001g0088 |
2 | HG00099.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.878-3629G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33151356 | |||||||
| chr1:33151366 | T | C | 7 | a0001c0001t0001g0011 a0001c0001t0001g0027 a0001c0001t0001g0080 others(4): Show |
10 | HG00741.hp1 HG01081.hp1 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.878-3639A>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33151366 | |||||||
| chr1:33151542 | T | C | 1 | a0001c0002t0009g0180 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.878-3815A>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33151542 | |||||||
| chr1:33151657 | G | A | 29 | a0001c0001t0002g0100 a0001c0001t0002g0175 a0001c0001t0002g0176 others(26): Show |
62 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.878-3930C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33151657 | |||||||
| chr1:33151709 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.878-3982G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33151709 | |||||||
| chr1:33151747 | A | G | 20 | a0001c0001t0003g0064 a0001c0001t0003g0065 a0001c0001t0003g0066 others(17): Show |
26 | HG00639.hp1 HG01243.hp1 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.878-4020T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33151747 | |||||||
| chr1:33151799 | A | T | 1 | a0001c0004t0007g0156 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.878-4072T>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33151799 | |||||||
| chr1:33151809 | C | T | 195 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(192): Show |
292 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(289): Show |
intron_variant | MODIFIER | c.878-4082G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33151809 | |||||||
| chr1:33151860 | C | T | 1 | a0001c0002t0002g0200 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.878-4133G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33151860 | |||||||
| chr1:33151978 | T | C | 10 | a0001c0001t0003g0064 a0001c0001t0003g0065 a0001c0001t0003g0066 others(7): Show |
14 | HG02080.hp2 HG03710.hp1 NA18945.hp2 others(11): Show |
intron_variant | MODIFIER | c.878-4251A>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33151978 | |||||||
| chr1:33152303 | C | T | 1 | a0001c0001t0001g0026 | 2 | NA18983.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.878-4576G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33152303 | |||||||
| chr1:33152337 | A | C | 7 | a0002c0003t0003g0216 a0002c0003t0003g0217 a0002c0003t0003g0222 others(4): Show |
12 | HG01891.hp2 HG02486.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.878-4610T>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33152337 | |||||||
| chr1:33152422 | C | T | 2 | a0001c0001t0006g0140 a0001c0001t0006g0152 |
2 | NA19079.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.878-4695G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33152422 | |||||||
| chr1:33152425 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.878-4698G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33152425 | |||||||
| chr1:33152431 | G | T | 3 | a0001c0004t0003g0072 a0001c0004t0003g0073 a0001c0006t0003g0174 |
3 | HG02922.hp1 HG02922.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.878-4704C>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33152431 | |||||||
| chr1:33152466 | C | T | 1 | a0001c0004t0007g0156 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.878-4739G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33152466 | |||||||
| chr1:33152482 | G | A | 7 | a0002c0003t0003g0216 a0002c0003t0003g0217 a0002c0003t0003g0222 others(4): Show |
12 | HG01891.hp2 HG02486.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.878-4755C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33152482 | |||||||
| chr1:33152506 | G | A | 1 | a0001c0001t0001g0012 | 3 | HG02071.hp1 NA18957.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.878-4779C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33152506 | |||||||
| chr1:33152573 | G | GA | 21 | a0001c0001t0001g0058 a0001c0001t0001g0083 a0001c0001t0001g0105 others(18): Show |
25 | HG00597.hp1 HG00673.hp1 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.878-4847dupT | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33152573 | |||||||
| chr1:33152573 | GA | G | 38 | a0001c0001t0001g0035 a0001c0001t0001g0048 a0001c0001t0001g0097 others(35): Show |
73 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.878-4847delT | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33152573 | |||||||
| chr1:33152812 | C | T | 36 | a0001c0001t0002g0100 a0001c0001t0002g0175 a0001c0001t0002g0176 others(33): Show |
70 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.878-5085G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33152812 | |||||||
| chr1:33152869 | G | C | 1 | a0001c0002t0003g0193 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.878-5142C>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33152869 | |||||||
| chr1:33152899 | C | T | 5 | a0001c0002t0003g0212 a0001c0004t0003g0010 a0001c0004t0003g0072 others(2): Show |
7 | HG01884.hp2 HG02109.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.878-5172G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33152899 | |||||||
| chr1:33153015 | A | G | 4 | a0001c0001t0001g0014 a0001c0001t0001g0128 a0001c0001t0001g0129 others(1): Show |
6 | HG01891.hp1 HG01934.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.877+5238T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33153015 | |||||||
| chr1:33153038 | G | C | 146 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(143): Show |
204 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.877+5215C>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33153038 | |||||||
| chr1:33153297 | C | T | 6 | a0001c0001t0001g0018 a0001c0001t0001g0042 a0001c0001t0001g0060 others(3): Show |
8 | HG00639.hp2 HG01070.hp1 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.877+4956G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33153297 | |||||||
| chr1:33153561 | A | G | 1 | a0001c0002t0002g0199 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.877+4692T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33153561 | |||||||
| chr1:33154134 | A | G | 1 | a0001c0001t0001g0108 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.877+4119T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33154134 | |||||||
| chr1:33154259 | A | G | 228 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(225): Show |
336 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(333): Show |
intron_variant | MODIFIER | c.877+3994T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33154259 | |||||||
| chr1:33154508 | T | G | 1 | a0001c0001t0001g0135 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.877+3745A>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33154508 | |||||||
| chr1:33154603 | C | G | 1 | a0001c0001t0001g0118 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.877+3650G>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33154603 | |||||||
| chr1:33154603 | C | T | 4 | a0001c0004t0003g0010 a0001c0004t0003g0072 a0001c0004t0003g0073 others(1): Show |
6 | HG02109.hp2 HG02818.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.877+3650G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33154603 | |||||||
| chr1:33154609 | C | A | 2 | a0001c0001t0001g0177 a0001c0001t0011g0147 |
2 | HG00544.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.877+3644G>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33154609 | |||||||
| chr1:33154965 | T | C | 52 | a0001c0001t0002g0100 a0001c0001t0002g0175 a0001c0001t0002g0176 others(49): Show |
92 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.877+3288A>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33154965 | |||||||
| chr1:33155041 | C | T | 1 | a0001c0001t0007g0068 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.877+3212G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33155041 | |||||||
| chr1:33155078 | G | A | 29 | a0001c0001t0002g0100 a0001c0001t0002g0175 a0001c0001t0002g0176 others(26): Show |
62 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.877+3175C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33155078 | |||||||
| chr1:33155098 | G | T | 1 | a0001c0001t0001g0141 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.877+3155C>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33155098 | |||||||
| chr1:33155102 | C | T | 8 | a0001c0001t0001g0020 a0001c0001t0001g0117 a0001c0001t0001g0148 others(5): Show |
9 | HG00544.hp2 HG01884.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.877+3151G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33155102 | |||||||
| chr1:33155135 | G | A | 1 | a0002c0003t0003g0222 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.877+3118C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33155135 | |||||||
| chr1:33155314 | C | T | 1 | a0001c0001t0007g0068 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.877+2939G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33155314 | |||||||
| chr1:33155356 | C | A | 2 | a0001c0002t0010g0231 a0001c0002t0010g0232 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.877+2897G>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33155356 | |||||||
| chr1:33155366 | C | T | 10 | a0001c0001t0001g0020 a0001c0001t0001g0067 a0001c0001t0001g0069 others(7): Show |
11 | HG00544.hp2 HG02145.hp2 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.877+2887G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33155366 | |||||||
| chr1:33155408 | T | C | 2 | a0001c0002t0009g0180 a0001c0002t0009g0181 |
2 | HG02451.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.877+2845A>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33155408 | |||||||
| chr1:33155530 | A | C | 1 | a0001c0001t0001g0154 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.877+2723T>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33155530 | |||||||
| chr1:33155547 | G | A | 1 | a0001c0001t0001g0169 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.877+2706C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33155547 | |||||||
| chr1:33155569 | G | A | 2 | a0001c0001t0003g0149 a0001c0002t0003g0218 |
2 | HG02055.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.877+2684C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33155569 | |||||||
| chr1:33155782 | T | C | 29 | a0001c0001t0002g0100 a0001c0001t0002g0175 a0001c0001t0002g0176 others(26): Show |
62 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.877+2471A>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33155782 | |||||||
| chr1:33156063 | G | T | 1 | a0001c0004t0007g0156 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.877+2190C>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33156063 | |||||||
| chr1:33156085 | C | T | 29 | a0001c0001t0002g0100 a0001c0001t0002g0175 a0001c0001t0002g0176 others(26): Show |
62 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.877+2168G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33156085 | |||||||
| chr1:33156142 | A | G | 228 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(225): Show |
336 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(333): Show |
intron_variant | MODIFIER | c.877+2111T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33156142 | |||||||
| chr1:33156236 | A | G | 1 | a0001c0002t0002g0190 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.877+2017T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33156236 | |||||||
| chr1:33156283 | T | G | 1 | a0002c0003t0003g0217 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.877+1970A>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33156283 | |||||||
| chr1:33156472 | G | C | 1 | a0001c0001t0001g0063 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.877+1781C>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33156472 | |||||||
| chr1:33156476 | T | C | 223 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(220): Show |
330 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(327): Show |
intron_variant | MODIFIER | c.877+1777A>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33156476 | |||||||
| chr1:33156493 | C | T | 2 | a0001c0001t0003g0149 a0001c0002t0003g0218 |
2 | HG02055.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.877+1760G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33156493 | |||||||
| chr1:33156523 | T | G | 1 | a0001c0001t0001g0131 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.877+1730A>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33156523 | |||||||
| chr1:33156681 | T | C | 29 | a0001c0001t0002g0100 a0001c0001t0002g0175 a0001c0001t0002g0176 others(26): Show |
62 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.877+1572A>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33156681 | |||||||
| chr1:33156756 | T | C | 1 | a0001c0001t0001g0121 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.877+1497A>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33156756 | |||||||
| chr1:33156876 | C | T | 2 | a0001c0002t0009g0180 a0001c0002t0009g0181 |
2 | HG02451.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.877+1377G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33156876 | |||||||
| chr1:33157018 | C | G | 3 | a0001c0001t0001g0033 a0001c0001t0001g0134 a0001c0001t0012g0136 |
4 | HG00609.hp2 HG02129.hp2 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.877+1235G>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33157018 | |||||||
| chr1:33157038 | C | T | 8 | a0001c0001t0001g0018 a0001c0001t0001g0042 a0001c0001t0001g0059 others(5): Show |
10 | HG00639.hp2 HG01070.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.877+1215G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33157038 | |||||||
| chr1:33157105 | G | A | 29 | a0001c0001t0002g0100 a0001c0001t0002g0175 a0001c0001t0002g0176 others(26): Show |
62 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.877+1148C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33157105 | |||||||
| chr1:33157127 | C | T | 2 | a0001c0002t0002g0044 a0001c0013t0002g0205 |
3 | HG00408.hp2 HG02071.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.877+1126G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33157127 | |||||||
| chr1:33157428 | C | T | 1 | a0001c0014t0002g0182 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.877+825G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33157428 | |||||||
| chr1:33157491 | C | G | 2 | a0001c0002t0010g0231 a0001c0002t0010g0232 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.877+762G>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33157491 | |||||||
| chr1:33157544 | T | G | 2 | a0001c0002t0009g0180 a0001c0002t0009g0181 |
2 | HG02451.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.877+709A>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33157544 | |||||||
| chr1:33157545 | C | T | 2 | a0001c0002t0009g0180 a0001c0002t0009g0181 |
2 | HG02451.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.877+708G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33157545 | |||||||
| chr1:33157554 | A | G | 5 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0002t0001g0179 others(2): Show |
5 | HG01884.hp1 HG02572.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.877+699T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33157554 | |||||||
| chr1:33157555 | T | A | 2 | a0001c0002t0009g0180 a0001c0002t0009g0181 |
2 | HG02451.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.877+698A>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33157555 | |||||||
| chr1:33157775 | G | A | 6 | a0001c0001t0003g0126 a0001c0001t0003g0157 a0001c0001t0003g0159 others(3): Show |
6 | HG01109.hp2 HG02809.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.877+478C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33157775 | |||||||
| chr1:33157833 | T | G | 1 | a0001c0001t0001g0051 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.877+420A>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33157833 | |||||||
| chr1:33157882 | G | A | 11 | a0001c0001t0003g0036 a0001c0001t0003g0037 a0001c0001t0003g0038 others(8): Show |
15 | HG00597.hp1 HG00673.hp1 NA18948.hp2 others(12): Show |
intron_variant | MODIFIER | c.877+371C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33157882 | |||||||
| chr1:33157904 | A | T | 4 | a0001c0004t0003g0010 a0001c0004t0003g0072 a0001c0004t0003g0073 others(1): Show |
6 | HG02109.hp2 HG02818.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.877+349T>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33157904 | |||||||
| chr1:33157909 | A | G | 19 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0013 others(16): Show |
32 | HG00423.hp2 HG00438.hp2 HG00597.hp2 others(29): Show |
intron_variant | MODIFIER | c.877+344T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33157909 | |||||||
| chr1:33157976 | C | T | 2 | a0001c0001t0002g0175 a0001c0001t0002g0176 |
2 | HG02083.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.877+277G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33157976 | |||||||
| chr1:33158047 | G | A | 1 | a0001c0012t0015g0227 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.877+206C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33158047 | |||||||
| chr1:33158047 | G | C | 1 | a0002c0003t0003g0222 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.877+206C>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33158047 | |||||||
| chr1:33158421 | A | G | 2 | a0001c0001t0001g0082 a0001c0002t0003g0194 |
2 | NA18988.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.762-53T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 3/4 | chr1 | 33158421 | |||||||
| chr1:33158428 | G | C | 2 | a0001c0001t0003g0149 a0001c0002t0003g0218 |
2 | HG02055.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.762-60C>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 3/4 | chr1 | 33158428 | |||||||
| chr1:33158434 | C | T | 1 | a0002c0003t0003g0224 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.762-66G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 3/4 | chr1 | 33158434 | |||||||
| chr1:33158441 | A | T | 1 | a0001c0001t0001g0090 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.762-73T>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 3/4 | chr1 | 33158441 | |||||||
| chr1:33158443 | C | T | 1 | a0001c0002t0003g0045 | 2 | HG02723.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.762-75G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 3/4 | chr1 | 33158443 | |||||||
| chr1:33158846 | C | CT | 7 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0107 others(4): Show |
7 | HG00741.hp1 HG00741.hp2 HG01109.hp1 others(4): Show |
intron_variant | MODIFIER | c.762-479dupA | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 3/4 | chr1 | 33158846 | |||||||
| chr1:33158997 | C | T | 1 | a0001c0001t0007g0068 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.762-629G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 3/4 | chr1 | 33158997 | |||||||
| chr1:33159093 | C | G | 2 | a0001c0001t0001g0031 a0001c0001t0001g0091 |
3 | HG03239.hp2 HG04184.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.761+595G>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 3/4 | chr1 | 33159093 | |||||||
| chr1:33159097 | G | A | 7 | a0002c0003t0003g0216 a0002c0003t0003g0217 a0002c0003t0003g0222 others(4): Show |
12 | HG01891.hp2 HG02486.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.761+591C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 3/4 | chr1 | 33159097 | |||||||
| chr1:33159099 | C | T | 29 | a0001c0001t0002g0100 a0001c0001t0002g0175 a0001c0001t0002g0176 others(26): Show |
62 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.761+589G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 3/4 | chr1 | 33159099 | |||||||
| chr1:33159122 | G | T | 1 | a0001c0002t0002g0198 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.761+566C>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 3/4 | chr1 | 33159122 | |||||||
| chr1:33159144 | A | G | 146 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(143): Show |
204 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.761+544T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 3/4 | chr1 | 33159144 | |||||||
| chr1:33159247 | G | C | 2 | a0001c0002t0002g0203 a0001c0002t0002g0204 |
2 | NA18960.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.761+441C>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 3/4 | chr1 | 33159247 | |||||||
| chr1:33159456 | G | A | 1 | a0001c0002t0003g0195 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.761+232C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 3/4 | chr1 | 33159456 | |||||||
| chr1:33159569 | A | C | 1 | a0001c0001t0001g0106 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.761+119T>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 3/4 | chr1 | 33159569 | |||||||
| chr1:33159674 | C | T | 2 | a0001c0002t0002g0190 a0001c0002t0002g0197 |
2 | HG01074.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.761+14G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 3/4 | chr1 | 33159674 | |||||||
| chr1:33159675 | G | A | 2 | a0001c0001t0003g0159 a0001c0001t0003g0162 |
2 | NA19058.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.761+13C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 3/4 | chr1 | 33159675 | |||||||
| chr1:33160059 | C | G | 1 | a0001c0012t0015g0227 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.505-115G>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33160059 | |||||||
| chr1:33160408 | A | G | 2 | a0001c0001t0001g0090 a0001c0001t0001g0094 |
2 | NA18962.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.505-464T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33160408 | |||||||
| chr1:33160413 | T | A | 2 | a0001c0001t0001g0049 a0001c0001t0001g0050 |
2 | HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.505-469A>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33160413 | |||||||
| chr1:33160493 | C | T | 1 | a0001c0001t0001g0034 | 2 | HG00408.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.505-549G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33160493 | |||||||
| chr1:33160518 | C | T | 5 | a0001c0001t0001g0022 a0001c0001t0001g0078 a0001c0001t0001g0093 others(2): Show |
6 | HG00438.hp2 HG02040.hp2 HG02074.hp1 others(3): Show |
intron_variant | MODIFIER | c.505-574G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33160518 | |||||||
| chr1:33160553 | C | T | 55 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(52): Show |
89 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.505-609G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33160553 | |||||||
| chr1:33160597 | G | A | 5 | a0001c0001t0008g0016 a0001c0002t0009g0180 a0001c0002t0009g0181 others(2): Show |
6 | HG02451.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.505-653C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33160597 | |||||||
| chr1:33160636 | G | C | 36 | a0001c0001t0002g0100 a0001c0001t0002g0175 a0001c0001t0002g0176 others(33): Show |
71 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.505-692C>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33160636 | |||||||
| chr1:33160683 | G | A | 146 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(143): Show |
204 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.505-739C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33160683 | |||||||
| chr1:33160684 | C | T | 1 | a0001c0006t0003g0174 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.505-740G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33160684 | |||||||
| chr1:33160690 | C | G | 1 | a0001c0002t0003g0045 | 2 | HG02723.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.505-746G>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33160690 | |||||||
| chr1:33160974 | A | G | 2 | a0001c0002t0009g0180 a0001c0002t0009g0181 |
2 | HG02451.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.505-1030T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33160974 | |||||||
| chr1:33161003 | C | T | 17 | a0001c0001t0003g0064 a0001c0001t0003g0065 a0001c0001t0003g0066 others(14): Show |
23 | HG01884.hp2 HG02080.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.505-1059G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33161003 | |||||||
| chr1:33161080 | T | C | 1 | a0001c0001t0001g0101 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.505-1136A>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33161080 | |||||||
| chr1:33161162 | C | T | 11 | a0001c0001t0003g0036 a0001c0001t0003g0037 a0001c0001t0003g0038 others(8): Show |
15 | HG00597.hp1 HG00673.hp1 NA18948.hp2 others(12): Show |
intron_variant | MODIFIER | c.505-1218G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33161162 | |||||||
| chr1:33161212 | G | A | 5 | a0001c0001t0001g0079 a0001c0001t0003g0126 a0001c0001t0003g0159 others(2): Show |
5 | HG02886.hp2 HG03704.hp1 HG03927.hp1 others(2): Show |
intron_variant | MODIFIER | c.505-1268C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33161212 | |||||||
| chr1:33161232 | G | A | 2 | a0001c0001t0001g0132 a0001c0001t0001g0133 |
2 | HG01123.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.505-1288C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33161232 | |||||||
| chr1:33161342 | A | G | 1 | a0001c0001t0001g0172 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.505-1398T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33161342 | |||||||
| chr1:33161421 | G | A | 1 | a0001c0012t0015g0227 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.505-1477C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33161421 | |||||||
| chr1:33161592 | G | A | 5 | a0001c0004t0003g0010 a0001c0004t0003g0072 a0001c0004t0003g0073 others(2): Show |
7 | HG02109.hp1 HG02109.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.505-1648C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33161592 | |||||||
| chr1:33161648 | C | T | 142 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(139): Show |
199 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.505-1704G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33161648 | |||||||
| chr1:33161656 | C | T | 3 | a0001c0001t0001g0025 a0001c0001t0001g0032 a0001c0001t0001g0089 |
5 | HG00621.hp1 HG02165.hp1 NA18965.hp1 others(2): Show |
intron_variant | MODIFIER | c.505-1712G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33161656 | |||||||
| chr1:33161697 | G | A | 2 | a0001c0002t0009g0180 a0001c0002t0009g0181 |
2 | HG02451.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.505-1753C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33161697 | |||||||
| chr1:33161723 | C | A | 5 | a0001c0004t0003g0010 a0001c0004t0003g0072 a0001c0004t0003g0073 others(2): Show |
7 | HG02109.hp1 HG02109.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.505-1779G>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33161723 | |||||||
| chr1:33161810 | C | G | 29 | a0001c0001t0002g0100 a0001c0001t0002g0175 a0001c0001t0002g0176 others(26): Show |
62 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.505-1866G>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33161810 | |||||||
| chr1:33161823 | T | C | 148 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(145): Show |
206 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(203): Show |
intron_variant | MODIFIER | c.505-1879A>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33161823 | |||||||
| chr1:33161916 | C | T | 3 | a0001c0001t0008g0016 a0001c0002t0010g0231 a0001c0002t0010g0232 |
4 | HG02896.hp1 HG02897.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.505-1972G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33161916 | |||||||
| chr1:33161930 | C | T | 2 | a0001c0001t0006g0140 a0001c0001t0006g0152 |
2 | NA19079.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.505-1986G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33161930 | |||||||
| chr1:33162056 | C | T | 5 | a0001c0001t0001g0019 a0001c0001t0001g0055 a0001c0001t0001g0056 others(2): Show |
6 | HG01069.hp1 HG02055.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.505-2112G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33162056 | |||||||
| chr1:33162197 | A | G | 211 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(208): Show |
314 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(311): Show |
intron_variant | MODIFIER | c.505-2253T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33162197 | |||||||
| chr1:33162317 | C | A | 1 | a0001c0002t0009g0181 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.505-2373G>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33162317 | |||||||
| chr1:33162426 | T | G | 12 | a0001c0001t0003g0036 a0001c0001t0003g0037 a0001c0001t0003g0038 others(9): Show |
16 | HG00597.hp1 HG00673.hp1 NA18948.hp2 others(13): Show |
intron_variant | MODIFIER | c.505-2482A>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33162426 | |||||||
| chr1:33162563 | C | T | 1 | a0001c0002t0003g0045 | 2 | HG02723.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.505-2619G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33162563 | |||||||
| chr1:33162674 | G | A | 2 | a0001c0002t0010g0231 a0001c0002t0010g0232 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.505-2730C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33162674 | |||||||
| chr1:33162740 | A | G | 150 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(147): Show |
209 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(206): Show |
intron_variant | MODIFIER | c.504+2731T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33162740 | |||||||
| chr1:33162934 | T | C | 1 | a0001c0002t0003g0045 | 2 | HG02723.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.504+2537A>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33162934 | |||||||
| chr1:33163094 | A | AC | 10 | a0001c0001t0003g0064 a0001c0001t0003g0065 a0001c0001t0003g0066 others(7): Show |
14 | HG02080.hp2 HG03710.hp1 NA18945.hp2 others(11): Show |
intron_variant | MODIFIER | c.504+2376_504+2377i others(3): Show |
TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33163094 | |||||||
| chr1:33163095 | G | A | 10 | a0001c0001t0003g0064 a0001c0001t0003g0065 a0001c0001t0003g0066 others(7): Show |
14 | HG02080.hp2 HG03710.hp1 NA18945.hp2 others(11): Show |
intron_variant | MODIFIER | c.504+2376C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33163095 | |||||||
| chr1:33163101 | C | T | 1 | a0001c0002t0003g0045 | 2 | HG02723.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.504+2370G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33163101 | |||||||
| chr1:33163323 | G | A | 1 | a0001c0001t0001g0144 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.504+2148C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33163323 | |||||||
| chr1:33163327 | C | G | 1 | a0002c0003t0003g0216 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.504+2144G>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33163327 | |||||||
| chr1:33163340 | A | AT | 7 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(4): Show |
7 | HG04184.hp1 HG04199.hp2 NA18989.hp1 others(4): Show |
intron_variant | MODIFIER | c.504+2130dupA | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33163340 | |||||||
| chr1:33163340 | AT | A | 7 | a0002c0003t0003g0216 a0002c0003t0003g0217 a0002c0003t0003g0222 others(4): Show |
12 | HG01891.hp2 HG02486.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.504+2130delA | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33163340 | |||||||
| chr1:33163361 | C | A | 1 | a0001c0001t0001g0070 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.504+2110G>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33163361 | |||||||
| chr1:33163361 | C | CT | 17 | a0001c0001t0003g0064 a0001c0001t0003g0065 a0001c0001t0003g0066 others(14): Show |
22 | HG00639.hp1 HG01243.hp1 HG02080.hp2 others(19): Show |
intron_variant | MODIFIER | c.504+2109dupA | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33163361 | |||||||
| chr1:33163411 | G | A | 1 | a0001c0001t0001g0135 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.504+2060C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33163411 | |||||||
| chr1:33163435 | A | G | 1 | a0001c0001t0001g0135 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.504+2036T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33163435 | |||||||
| chr1:33163640 | T | C | 224 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(221): Show |
331 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(328): Show |
intron_variant | MODIFIER | c.504+1831A>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33163640 | |||||||
| chr1:33163687 | G | A | 1 | a0001c0001t0001g0133 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.504+1784C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33163687 | |||||||
| chr1:33163697 | C | T | 1 | a0002c0003t0003g0222 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.504+1774G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33163697 | |||||||
| chr1:33164039 | A | T | 12 | a0001c0001t0003g0036 a0001c0001t0003g0037 a0001c0001t0003g0038 others(9): Show |
16 | HG00597.hp1 HG00673.hp1 NA18948.hp2 others(13): Show |
intron_variant | MODIFIER | c.504+1432T>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33164039 | |||||||
| chr1:33164067 | T | C | 29 | a0001c0001t0002g0100 a0001c0001t0002g0175 a0001c0001t0002g0176 others(26): Show |
62 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.504+1404A>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33164067 | |||||||
| chr1:33164068 | C | A | 29 | a0001c0001t0002g0100 a0001c0001t0002g0175 a0001c0001t0002g0176 others(26): Show |
62 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.504+1403G>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33164068 | |||||||
| chr1:33164319 | G | C | 1 | a0001c0012t0015g0227 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.504+1152C>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33164319 | |||||||
| chr1:33164382 | A | G | 1 | a0001c0002t0002g0187 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.504+1089T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33164382 | |||||||
| chr1:33164418 | A | T | 1 | a0001c0001t0002g0100 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.504+1053T>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33164418 | |||||||
| chr1:33164553 | A | G | 5 | a0001c0004t0003g0010 a0001c0004t0003g0072 a0001c0004t0003g0073 others(2): Show |
7 | HG02109.hp1 HG02109.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.504+918T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33164553 | |||||||
| chr1:33164585 | C | CTGTT | 3 | a0001c0002t0002g0190 a0001c0002t0002g0196 a0001c0012t0015g0227 |
3 | HG01346.hp2 HG06807.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.504+882_504+885dup others(4): Show |
TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33164585 | |||||||
| chr1:33164613 | C | T | 1 | a0001c0001t0007g0068 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.504+858G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33164613 | |||||||
| chr1:33164651 | C | T | 1 | a0001c0001t0001g0088 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.504+820G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33164651 | |||||||
| chr1:33164695 | A | G | 2 | a0001c0001t0003g0126 a0001c0001t0003g0159 |
2 | HG03704.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.504+776T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33164695 | |||||||
| chr1:33164766 | T | TATTCATT others(1): Show |
4 | a0001c0004t0003g0010 a0001c0004t0003g0072 a0001c0004t0003g0073 others(1): Show |
6 | HG02109.hp2 HG02818.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.504+697_504+704dup others(8): Show |
TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33164766 | |||||||
| chr1:33164766 | T | TATTCATT others(5): Show |
1 | a0001c0006t0003g0174 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.504+693_504+704dup others(12): Show |
TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33164766 | |||||||
| chr1:33164766 | TATTCATT others(5): Show |
T | 1 | a0001c0001t0001g0135 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.504+693_504+704del others(12): Show |
TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33164766 | |||||||
| chr1:33164790 | C | T | 1 | a0001c0001t0007g0068 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.504+681G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33164790 | |||||||
| chr1:33164807 | A | G | 12 | a0001c0001t0003g0036 a0001c0001t0003g0037 a0001c0001t0003g0038 others(9): Show |
16 | HG00597.hp1 HG00673.hp1 NA18948.hp2 others(13): Show |
intron_variant | MODIFIER | c.504+664T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33164807 | |||||||
| chr1:33164939 | C | T | 2 | a0001c0001t0001g0118 a0001c0001t0001g0124 |
2 | NA19007.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.504+532G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33164939 | |||||||
| chr1:33164955 | AT | A | 188 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(185): Show |
283 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(280): Show |
intron_variant | MODIFIER | c.504+515delA | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33164955 | |||||||
| chr1:33165045 | G | T | 2 | a0001c0004t0003g0072 a0001c0004t0003g0073 |
2 | HG02922.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.504+426C>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33165045 | |||||||
| chr1:33165148 | C | T | 2 | a0001c0001t0001g0021 a0001c0001t0001g0086 |
3 | HG01070.hp2 HG01071.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.504+323G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33165148 | |||||||
| chr1:33165176 | C | T | 1 | a0001c0001t0005g0170 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.504+295G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33165176 | |||||||
| chr1:33165333 | T | TAGAA | 12 | a0001c0001t0003g0036 a0001c0001t0003g0037 a0001c0001t0003g0038 others(9): Show |
16 | HG00597.hp1 HG00673.hp1 NA18948.hp2 others(13): Show |
intron_variant | MODIFIER | c.504+137_504+138ins others(4): Show |
TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33165333 | |||||||
| chr1:33165403 | T | C | 12 | a0001c0001t0003g0036 a0001c0001t0003g0037 a0001c0001t0003g0038 others(9): Show |
16 | HG00597.hp1 HG00673.hp1 NA18948.hp2 others(13): Show |
intron_variant | MODIFIER | c.504+68A>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33165403 | |||||||
| chr1:33165443 | C | T | 3 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0002t0001g0179 |
3 | HG02572.hp1 HG02630.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.504+28G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33165443 | |||||||
| chr1:33165459 | G | A | 1 | a0001c0012t0015g0227 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.504+12C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33165459 | |||||||
| chr1:33165468 | C | A | 31 | a0001c0001t0001g0135 a0001c0001t0002g0100 a0001c0001t0002g0175 others(28): Show |
64 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(61): Show |
splice_region_variant&intron_variant | LOW | c.504+3G>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33165468 | |||||||
| chr1:33165643 | G | A | 1 | a0001c0007t0014g0226 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.409-77C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33165643 | |||||||
| chr1:33165659 | G | A | 1 | a0001c0001t0001g0049 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.409-93C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33165659 | |||||||
| chr1:33165724 | G | A | 1 | a0001c0001t0007g0068 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.409-158C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33165724 | |||||||
| chr1:33165755 | C | T | 2 | a0001c0001t0001g0006 a0001c0001t0003g0087 |
6 | HG00438.hp1 HG00609.hp1 HG00621.hp2 others(3): Show |
intron_variant | MODIFIER | c.409-189G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33165755 | |||||||
| chr1:33165874 | C | T | 2 | a0001c0001t0001g0021 a0001c0001t0001g0086 |
3 | HG01070.hp2 HG01071.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.409-308G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33165874 | |||||||
| chr1:33165952 | G | A | 2 | a0001c0001t0006g0140 a0001c0001t0006g0152 |
2 | NA19079.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.409-386C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33165952 | |||||||
| chr1:33166006 | C | T | 5 | a0001c0001t0003g0126 a0001c0001t0003g0149 a0001c0001t0003g0159 others(2): Show |
5 | HG02055.hp1 HG02818.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.409-440G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33166006 | |||||||
| chr1:33166160 | A | G | 177 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(174): Show |
247 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(244): Show |
intron_variant | MODIFIER | c.409-594T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33166160 | |||||||
| chr1:33166189 | G | A | 1 | a0001c0001t0001g0101 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.409-623C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33166189 | |||||||
| chr1:33166215 | G | A | 7 | a0002c0003t0003g0216 a0002c0003t0003g0217 a0002c0003t0003g0222 others(4): Show |
12 | HG01891.hp2 HG02486.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.409-649C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33166215 | |||||||
| chr1:33166304 | G | T | 1 | a0001c0001t0003g0164 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.409-738C>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33166304 | |||||||
| chr1:33166595 | A | C | 1 | a0001c0004t0007g0156 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.409-1029T>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33166595 | |||||||
| chr1:33166898 | G | A | 7 | a0002c0003t0003g0216 a0002c0003t0003g0217 a0002c0003t0003g0222 others(4): Show |
12 | HG01891.hp2 HG02486.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.409-1332C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33166898 | |||||||
| chr1:33166919 | A | C | 1 | a0001c0001t0001g0031 | 2 | HG03239.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.409-1353T>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33166919 | |||||||
| chr1:33166987 | C | T | 1 | a0001c0001t0001g0023 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.409-1421G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33166987 | |||||||
| chr1:33167524 | A | G | 48 | a0001c0001t0001g0021 a0001c0001t0001g0067 a0001c0001t0001g0069 others(45): Show |
86 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.409-1958T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33167524 | |||||||
| chr1:33167603 | A | G | 1 | a0001c0001t0003g0065 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.409-2037T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33167603 | |||||||
| chr1:33167875 | T | C | 11 | a0001c0001t0001g0021 a0001c0001t0001g0067 a0001c0001t0001g0069 others(8): Show |
12 | HG01070.hp2 HG01071.hp2 HG02080.hp2 others(9): Show |
intron_variant | MODIFIER | c.409-2309A>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33167875 | |||||||
| chr1:33167922 | G | A | 2 | a0001c0001t0003g0159 a0001c0001t0003g0160 |
2 | HG02886.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.409-2356C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33167922 | |||||||
| chr1:33168081 | A | G | 1 | a0001c0001t0001g0151 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.409-2515T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33168081 | |||||||
| chr1:33168387 | C | CT | 148 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(145): Show |
208 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.409-2822dupA | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33168387 | |||||||
| chr1:33168393 | T | C | 12 | a0001c0001t0003g0036 a0001c0001t0003g0037 a0001c0001t0003g0038 others(9): Show |
16 | HG00597.hp1 HG00673.hp1 NA18948.hp2 others(13): Show |
intron_variant | MODIFIER | c.409-2827A>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33168393 | |||||||
| chr1:33168458 | C | T | 216 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(213): Show |
320 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(317): Show |
intron_variant | MODIFIER | c.409-2892G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33168458 | |||||||
| chr1:33168707 | T | C | 3 | a0001c0002t0010g0231 a0001c0002t0010g0232 a0001c0002t0018g0230 |
3 | HG01109.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.409-3141A>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33168707 | |||||||
| chr1:33168975 | A | T | 1 | a0001c0001t0001g0104 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.409-3409T>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33168975 | |||||||
| chr1:33169017 | TC | T | 168 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(165): Show |
234 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(231): Show |
intron_variant | MODIFIER | c.409-3452delG | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33169017 | |||||||
| chr1:33169138 | C | T | 168 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(165): Show |
234 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(231): Show |
intron_variant | MODIFIER | c.409-3572G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33169138 | |||||||
| chr1:33169162 | C | G | 5 | a0001c0001t0007g0068 a0001c0004t0003g0010 a0001c0004t0003g0072 others(2): Show |
7 | HG02109.hp2 HG02559.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.409-3596G>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33169162 | |||||||
| chr1:33169205 | C | T | 1 | a0001c0001t0001g0069 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.409-3639G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33169205 | |||||||
| chr1:33169236 | C | T | 14 | a0001c0001t0001g0021 a0001c0001t0001g0067 a0001c0001t0001g0069 others(11): Show |
15 | HG01070.hp2 HG01071.hp2 HG02080.hp2 others(12): Show |
intron_variant | MODIFIER | c.409-3670G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33169236 | |||||||
| chr1:33169260 | T | G | 228 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(225): Show |
336 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(333): Show |
intron_variant | MODIFIER | c.409-3694A>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33169260 | |||||||
| chr1:33169261 | G | T | 1 | a0001c0001t0001g0085 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.409-3695C>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33169261 | |||||||
| chr1:33169423 | G | A | 14 | a0001c0001t0001g0021 a0001c0001t0001g0067 a0001c0001t0001g0069 others(11): Show |
15 | HG01070.hp2 HG01071.hp2 HG02080.hp2 others(12): Show |
intron_variant | MODIFIER | c.409-3857C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33169423 | |||||||
| chr1:33169424 | G | A | 14 | a0001c0001t0001g0021 a0001c0001t0001g0067 a0001c0001t0001g0069 others(11): Show |
15 | HG01070.hp2 HG01071.hp2 HG02080.hp2 others(12): Show |
intron_variant | MODIFIER | c.409-3858C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33169424 | |||||||
| chr1:33169530 | C | T | 1 | a0001c0002t0002g0190 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.409-3964G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33169530 | |||||||
| chr1:33169582 | G | A | 12 | a0001c0001t0003g0036 a0001c0001t0003g0037 a0001c0001t0003g0038 others(9): Show |
16 | HG00597.hp1 HG00673.hp1 NA18948.hp2 others(13): Show |
intron_variant | MODIFIER | c.409-4016C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33169582 | |||||||
| chr1:33169602 | G | A | 9 | a0001c0002t0001g0179 a0001c0002t0003g0045 a0002c0003t0003g0216 others(6): Show |
15 | HG01891.hp2 HG02486.hp2 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.409-4036C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33169602 | |||||||
| chr1:33169778 | C | T | 12 | a0001c0001t0003g0036 a0001c0001t0003g0037 a0001c0001t0003g0038 others(9): Show |
16 | HG00597.hp1 HG00673.hp1 NA18948.hp2 others(13): Show |
intron_variant | MODIFIER | c.409-4212G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33169778 | |||||||
| chr1:33169783 | A | G | 48 | a0001c0001t0001g0021 a0001c0001t0001g0067 a0001c0001t0001g0069 others(45): Show |
86 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.409-4217T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33169783 | |||||||
| chr1:33170104 | T | C | 4 | a0001c0001t0003g0064 a0001c0001t0003g0065 a0001c0001t0003g0066 others(1): Show |
4 | HG02080.hp2 HG03710.hp1 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.409-4538A>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33170104 | |||||||
| chr1:33170158 | C | T | 9 | a0001c0002t0001g0179 a0001c0002t0003g0045 a0002c0003t0003g0216 others(6): Show |
15 | HG01891.hp2 HG02486.hp2 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.409-4592G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33170158 | |||||||
| chr1:33170187 | A | G | 216 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(213): Show |
320 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(317): Show |
intron_variant | MODIFIER | c.409-4621T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33170187 | |||||||
| chr1:33170283 | C | T | 1 | a0001c0001t0001g0151 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.409-4717G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33170283 | |||||||
| chr1:33170321 | TA | T | 219 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(216): Show |
323 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(320): Show |
intron_variant | MODIFIER | c.409-4756delT | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33170321 | |||||||
| chr1:33170425 | T | C | 1 | a0001c0001t0001g0151 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.409-4859A>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33170425 | |||||||
| chr1:33170476 | C | T | 1 | a0001c0001t0001g0135 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.409-4910G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33170476 | |||||||
| chr1:33170793 | T | C | 1 | a0001c0014t0002g0182 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.409-5227A>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33170793 | |||||||
| chr1:33170927 | T | C | 8 | a0001c0001t0007g0068 a0001c0002t0010g0231 a0001c0002t0010g0232 others(5): Show |
10 | HG01109.hp2 HG02109.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.409-5361A>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33170927 | |||||||
| chr1:33171056 | G | A | 135 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(132): Show |
192 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(189): Show |
intron_variant | MODIFIER | c.409-5490C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33171056 | |||||||
| chr1:33171136 | C | T | 1 | a0001c0002t0002g0189 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.409-5570G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33171136 | |||||||
| chr1:33171309 | T | G | 1 | a0001c0002t0003g0207 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.409-5743A>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33171309 | |||||||
| chr1:33171575 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.409-6009G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33171575 | |||||||
| chr1:33171632 | G | T | 216 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(213): Show |
320 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(317): Show |
intron_variant | MODIFIER | c.409-6066C>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33171632 | |||||||
| chr1:33172333 | G | A | 12 | a0001c0001t0003g0036 a0001c0001t0003g0037 a0001c0001t0003g0038 others(9): Show |
16 | HG00597.hp1 HG00673.hp1 NA18948.hp2 others(13): Show |
intron_variant | MODIFIER | c.409-6767C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33172333 | |||||||
| chr1:33172378 | C | T | 12 | a0001c0001t0003g0036 a0001c0001t0003g0037 a0001c0001t0003g0038 others(9): Show |
16 | HG00597.hp1 HG00673.hp1 NA18948.hp2 others(13): Show |
intron_variant | MODIFIER | c.409-6812G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33172378 | |||||||
| chr1:33172556 | G | A | 5 | a0001c0001t0007g0068 a0001c0004t0003g0010 a0001c0004t0003g0072 others(2): Show |
7 | HG02109.hp2 HG02559.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.409-6990C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33172556 | |||||||
| chr1:33172559 | C | A | 228 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(225): Show |
336 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(333): Show |
intron_variant | MODIFIER | c.409-6993G>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33172559 | |||||||
| chr1:33172602 | G | A | 4 | a0001c0002t0003g0215 a0001c0002t0003g0218 a0001c0002t0003g0219 others(1): Show |
4 | HG02818.hp1 HG03471.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.409-7036C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33172602 | |||||||
| chr1:33172824 | C | T | 34 | a0001c0001t0002g0175 a0001c0001t0002g0176 a0001c0002t0002g0001 others(31): Show |
71 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.409-7258G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33172824 | |||||||
| chr1:33172888 | C | T | 5 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(2): Show |
5 | HG01243.hp2 HG02572.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.409-7322G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33172888 | |||||||
| chr1:33172982 | A | T | 1 | a0001c0012t0015g0227 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.409-7416T>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33172982 | |||||||
| chr1:33173059 | A | C | 1 | a0001c0002t0002g0188 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.409-7493T>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33173059 | |||||||
| chr1:33173092 | C | G | 1 | a0001c0001t0001g0080 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.409-7526G>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33173092 | |||||||
| chr1:33173135 | C | T | 216 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(213): Show |
320 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(317): Show |
intron_variant | MODIFIER | c.409-7569G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33173135 | |||||||
| chr1:33173191 | C | T | 3 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0150 |
3 | HG02559.hp2 HG02965.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.409-7625G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33173191 | |||||||
| chr1:33173192 | C | T | 1 | a0001c0002t0003g0218 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.409-7626G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33173192 | |||||||
| chr1:33173596 | C | G | 1 | a0001c0004t0003g0010 | 3 | HG02109.hp2 HG02818.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.408+7429G>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33173596 | |||||||
| chr1:33173678 | CT | C | 215 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(212): Show |
318 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(315): Show |
intron_variant | MODIFIER | c.408+7346delA | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33173678 | |||||||
| chr1:33173754 | A | G | 3 | a0001c0001t0001g0060 a0001c0001t0001g0062 a0001c0001t0001g0063 |
3 | HG01243.hp2 HG02572.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.408+7271T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33173754 | |||||||
| chr1:33173918 | C | T | 12 | a0001c0001t0003g0036 a0001c0001t0003g0037 a0001c0001t0003g0038 others(9): Show |
16 | HG00597.hp1 HG00673.hp1 NA18948.hp2 others(13): Show |
intron_variant | MODIFIER | c.408+7107G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33173918 | |||||||
| chr1:33174089 | A | G | 3 | a0001c0002t0001g0210 a0001c0002t0001g0211 a0001c0002t0003g0212 |
3 | HG01069.hp2 HG01071.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.408+6936T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174089 | |||||||
| chr1:33174371 | A | G | 1 | a0002c0003t0003g0222 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.408+6654T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174371 | |||||||
| chr1:33174404 | G | A | 2 | a0001c0001t0006g0140 a0001c0001t0006g0152 |
2 | NA19079.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.408+6621C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174404 | |||||||
| chr1:33174558 | A | C | 1 | a0001c0002t0003g0212 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.408+6467T>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174558 | |||||||
| chr1:33174607 | A | C | 12 | a0001c0001t0003g0036 a0001c0001t0003g0037 a0001c0001t0003g0038 others(9): Show |
16 | HG00597.hp1 HG00673.hp1 NA18948.hp2 others(13): Show |
intron_variant | MODIFIER | c.408+6418T>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174607 | |||||||
| chr1:33174893 | ATG | A | 3 | a0001c0001t0001g0121 a0001c0001t0001g0127 a0001c0014t0002g0182 |
3 | HG00733.hp1 HG03942.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.408+6130_408+6131d others(4): Show |
TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174893 | |||||||
| chr1:33174897 | GTGTGTGT others(35): Show |
G | 1 | a0001c0001t0003g0160 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.408+6086_408+6127d others(44): Show |
TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174897 | |||||||
| chr1:33174903 | G | GTA | 13 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0003g0036 others(10): Show |
15 | HG00597.hp1 HG00673.hp1 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.408+6121_408+6122i others(4): Show |
TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174903 | |||||||
| chr1:33174903 | GTGTATAT others(43): Show |
G | 1 | a0001c0001t0001g0020 | 2 | HG02809.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.408+6072_408+6121d others(52): Show |
TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174903 | |||||||
| chr1:33174903 | GTGTATAT others(53): Show |
G | 1 | a0001c0001t0007g0068 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.408+6062_408+6121d others(62): Show |
TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174903 | |||||||
| chr1:33174905 | G | A | 216 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(213): Show |
321 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(318): Show |
intron_variant | MODIFIER | c.408+6120C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174905 | |||||||
| chr1:33174905 | G | GTA | 4 | a0001c0001t0003g0037 a0001c0001t0003g0039 a0001c0001t0003g0166 others(1): Show |
5 | NA18953.hp1 NA18974.hp1 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.408+6118_408+6119d others(4): Show |
TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174905 | |||||||
| chr1:33174920 | C | T | 6 | a0001c0002t0001g0210 a0001c0002t0001g0211 a0001c0002t0003g0212 others(3): Show |
6 | HG01069.hp2 HG01071.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.408+6105G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174920 | |||||||
| chr1:33174939 | A | ATG | 4 | a0001c0001t0003g0159 a0001c0004t0003g0072 a0001c0004t0003g0073 others(1): Show |
4 | HG02922.hp1 HG03139.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.408+6084_408+6085d others(4): Show |
TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174939 | |||||||
| chr1:33174939 | A | ATGTG | 1 | a0001c0004t0003g0010 | 3 | HG02109.hp2 HG02818.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.408+6082_408+6085d others(6): Show |
TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174939 | |||||||
| chr1:33174940 | T | C | 1 | a0001c0001t0001g0172 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.408+6085A>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174940 | |||||||
| chr1:33174945 | G | GTATATAT others(3): Show |
5 | a0001c0001t0003g0036 a0001c0001t0003g0037 a0001c0001t0003g0039 others(2): Show |
8 | NA18948.hp2 NA18953.hp1 NA18954.hp1 others(5): Show |
intron_variant | MODIFIER | c.408+6070_408+6079d others(12): Show |
TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174945 | |||||||
| chr1:33174945 | G | GTATATAT others(5): Show |
4 | a0001c0001t0003g0038 a0001c0001t0003g0162 a0001c0001t0003g0167 others(1): Show |
5 | HG00673.hp1 NA19057.hp1 NA19058.hp1 others(2): Show |
intron_variant | MODIFIER | c.408+6068_408+6079d others(14): Show |
TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174945 | |||||||
| chr1:33174945 | G | GTATATAT others(7): Show |
1 | a0001c0001t0003g0163 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.408+6066_408+6079d others(16): Show |
TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174945 | |||||||
| chr1:33174945 | GTA | G | 27 | a0001c0002t0002g0001 a0001c0002t0002g0044 a0001c0002t0002g0184 others(24): Show |
59 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.408+6078_408+6079d others(4): Show |
TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174945 | |||||||
| chr1:33174945 | GTATA | G | 6 | a0001c0002t0002g0043 a0001c0002t0002g0183 a0001c0002t0002g0187 others(3): Show |
7 | HG02451.hp1 HG03490.hp1 HG03669.hp1 others(4): Show |
intron_variant | MODIFIER | c.408+6076_408+6079d others(6): Show |
TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174945 | |||||||
| chr1:33174945 | GTATATA | G | 3 | a0001c0001t0001g0018 a0001c0001t0001g0050 a0001c0001t0001g0129 |
4 | HG02976.hp2 HG03098.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.408+6074_408+6079d others(8): Show |
TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174945 | |||||||
| chr1:33174945 | GTATATAT others(1): Show |
G | 136 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(133): Show |
192 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(189): Show |
intron_variant | MODIFIER | c.408+6072_408+6079d others(10): Show |
TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174945 | |||||||
| chr1:33174945 | GTATATAT others(3): Show |
G | 1 | a0001c0001t0001g0060 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.408+6070_408+6079d others(12): Show |
TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174945 | |||||||
| chr1:33174947 | A | G | 16 | a0001c0001t0001g0021 a0001c0001t0001g0067 a0001c0001t0001g0069 others(13): Show |
21 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.408+6078T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174947 | |||||||
| chr1:33174958 | TATATATA others(9): Show |
T | 1 | a0001c0002t0003g0213 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.408+6051_408+6066d others(18): Show |
TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174958 | |||||||
| chr1:33174962 | T | C | 4 | a0001c0002t0003g0215 a0001c0002t0003g0218 a0001c0002t0003g0219 others(1): Show |
4 | HG02818.hp1 HG03471.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.408+6063A>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174962 | |||||||
| chr1:33174962 | TATATATA others(1): Show |
T | 6 | a0001c0002t0001g0210 a0001c0002t0001g0211 a0001c0002t0003g0212 others(3): Show |
6 | HG01069.hp2 HG01071.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.408+6055_408+6062d others(10): Show |
TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174962 | |||||||
| chr1:33174964 | TATATAC | T | 7 | a0001c0002t0001g0179 a0001c0002t0003g0045 a0002c0003t0003g0217 others(4): Show |
13 | HG01891.hp2 HG02630.hp1 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.408+6055_408+6060d others(8): Show |
TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174964 | |||||||
| chr1:33174968 | T | C | 34 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0153 others(31): Show |
74 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.408+6057A>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174968 | |||||||
| chr1:33174968 | TAC | T | 3 | a0001c0002t0010g0231 a0001c0002t0010g0232 a0001c0002t0018g0230 |
3 | HG01109.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.408+6055_408+6056d others(4): Show |
TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174968 | |||||||
| chr1:33174970 | C | T | 34 | a0001c0001t0001g0021 a0001c0001t0001g0067 a0001c0001t0001g0069 others(31): Show |
41 | HG00597.hp1 HG00673.hp1 HG01070.hp2 others(38): Show |
intron_variant | MODIFIER | c.408+6055G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174970 | |||||||
| chr1:33174971 | A | G | 4 | a0001c0002t0003g0214 a0001c0002t0003g0218 a0001c0002t0003g0219 others(1): Show |
4 | HG01243.hp1 HG02818.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.408+6054T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174971 | |||||||
| chr1:33174974 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.408+6051G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174974 | |||||||
| chr1:33174976 | T | C | 5 | a0001c0002t0003g0214 a0001c0002t0003g0215 a0001c0002t0003g0218 others(2): Show |
5 | HG01243.hp1 HG02818.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.408+6049A>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174976 | |||||||
| chr1:33174978 | T | C | 4 | a0001c0002t0003g0214 a0001c0002t0003g0218 a0001c0002t0003g0219 others(1): Show |
4 | HG01243.hp1 HG02818.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.408+6047A>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174978 | |||||||
| chr1:33174979 | A | G | 1 | a0001c0002t0003g0215 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.408+6046T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174979 | |||||||
| chr1:33174980 | C | T | 1 | a0001c0002t0003g0215 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.408+6045G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174980 | |||||||
| chr1:33174981 | A | C | 1 | a0001c0001t0001g0023 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.408+6044T>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174981 | |||||||
| chr1:33174983 | A | G | 4 | a0001c0002t0003g0214 a0001c0002t0003g0218 a0001c0002t0003g0219 others(1): Show |
4 | HG01243.hp1 HG02818.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.408+6042T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174983 | |||||||
| chr1:33174983 | A | T | 1 | a0001c0002t0003g0215 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.408+6042T>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174983 | |||||||
| chr1:33174987 | A | T | 4 | a0001c0002t0003g0214 a0001c0002t0003g0218 a0001c0002t0003g0219 others(1): Show |
4 | HG01243.hp1 HG02818.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.408+6038T>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174987 | |||||||
| chr1:33174989 | G | A | 3 | a0001c0002t0003g0218 a0001c0002t0003g0219 a0001c0011t0001g0220 |
3 | HG02818.hp1 HG03540.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.408+6036C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174989 | |||||||
| chr1:33174990 | C | T | 4 | a0001c0002t0003g0215 a0001c0002t0003g0218 a0001c0002t0003g0219 others(1): Show |
4 | HG02818.hp1 HG03471.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.408+6035G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174990 | |||||||
| chr1:33174992 | C | T | 4 | a0001c0002t0003g0215 a0001c0002t0003g0218 a0001c0002t0003g0219 others(1): Show |
4 | HG02818.hp1 HG03471.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.408+6033G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174992 | |||||||
| chr1:33174993 | A | G | 3 | a0001c0002t0003g0218 a0001c0002t0003g0219 a0001c0011t0001g0220 |
3 | HG02818.hp1 HG03540.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.408+6032T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174993 | |||||||
| chr1:33174994 | C | T | 4 | a0001c0002t0003g0215 a0001c0002t0003g0218 a0001c0002t0003g0219 others(1): Show |
4 | HG02818.hp1 HG03471.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.408+6031G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174994 | |||||||
| chr1:33174995 | A | G | 1 | a0001c0002t0003g0215 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.408+6030T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174995 | |||||||
| chr1:33174996 | C | T | 5 | a0001c0002t0003g0214 a0001c0002t0003g0215 a0001c0002t0003g0218 others(2): Show |
5 | HG01243.hp1 HG02818.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.408+6029G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174996 | |||||||
| chr1:33174998 | C | T | 5 | a0001c0002t0003g0214 a0001c0002t0003g0215 a0001c0002t0003g0218 others(2): Show |
5 | HG01243.hp1 HG02818.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.408+6027G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174998 | |||||||
| chr1:33174999 | A | G | 4 | a0001c0002t0003g0214 a0001c0002t0003g0218 a0001c0002t0003g0219 others(1): Show |
4 | HG01243.hp1 HG02818.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.408+6026T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174999 | |||||||
| chr1:33175001 | G | A | 4 | a0001c0002t0003g0214 a0001c0002t0003g0218 a0001c0002t0003g0219 others(1): Show |
4 | HG01243.hp1 HG02818.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.408+6024C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33175001 | |||||||
| chr1:33175001 | G | GTATATGT others(7): Show |
1 | a0001c0001t0001g0113 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.408+6023_408+6024i others(16): Show |
TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33175001 | |||||||
| chr1:33175001 | G | GTATGTAT others(5): Show |
4 | a0001c0001t0001g0059 a0001c0001t0001g0103 a0001c0001t0001g0153 others(1): Show |
4 | HG01109.hp2 HG02015.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.408+6012_408+6023d others(14): Show |
TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33175001 | |||||||
| chr1:33175001 | G | GTATGTAT others(11): Show |
8 | a0001c0001t0001g0014 a0001c0001t0001g0060 a0001c0001t0001g0061 others(5): Show |
10 | HG01891.hp1 HG01934.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.408+6006_408+6023d others(20): Show |
TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33175001 | |||||||
| chr1:33175001 | G | GTATGTAT others(17): Show |
8 | a0001c0001t0001g0018 a0001c0001t0001g0042 a0001c0001t0001g0062 others(5): Show |
10 | HG00639.hp2 HG01070.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.408+6000_408+6023d others(26): Show |
TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33175001 | |||||||
| chr1:33175001 | G | GTATGTAT others(29): Show |
1 | a0001c0002t0009g0180 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.408+6023_408+6024i others(38): Show |
TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33175001 | |||||||
| chr1:33175001 | G | GTATTTA | 22 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0015 others(19): Show |
33 | HG00438.hp1 HG00609.hp1 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.408+6023_408+6024i others(8): Show |
TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33175001 | |||||||
| chr1:33175001 | G | GTATTTAT others(5): Show |
57 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0020 others(54): Show |
81 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.408+6023_408+6024i others(14): Show |
TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33175001 | |||||||
| chr1:33175001 | G | GTATTTAT others(11): Show |
36 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(33): Show |
57 | HG00438.hp2 HG00544.hp2 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.408+6023_408+6024i others(20): Show |
TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33175001 | |||||||
| chr1:33175001 | G | GTATTTAT others(17): Show |
30 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0031 others(27): Show |
37 | HG00099.hp2 HG00609.hp2 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.408+6023_408+6024i others(26): Show |
TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33175001 | |||||||
| chr1:33175001 | G | GTATTTAT others(23): Show |
10 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0131 others(7): Show |
12 | HG00673.hp1 HG01123.hp1 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.408+6023_408+6024i others(32): Show |
TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33175001 | |||||||
| chr1:33175001 | G | GTATTTAT others(29): Show |
4 | a0001c0001t0001g0112 a0001c0001t0001g0135 a0001c0001t0001g0137 others(1): Show |
4 | HG02257.hp1 NA18747.hp2 NA19086.hp2 others(1): Show |
intron_variant | MODIFIER | c.408+6023_408+6024i others(38): Show |
TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33175001 | |||||||
| chr1:33175005 | G | T | 9 | a0001c0001t0001g0067 a0001c0001t0001g0079 a0001c0001t0001g0114 others(6): Show |
11 | HG02109.hp2 HG02559.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.408+6020C>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33175005 | |||||||
| chr1:33175019 | ATATGTAT others(5): Show |
A | 1 | a0001c0002t0003g0212 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.408+5994_408+6005d others(14): Show |
TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33175019 | |||||||
| chr1:33175031 | T | A | 188 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(185): Show |
259 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(256): Show |
intron_variant | MODIFIER | c.408+5994A>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33175031 | |||||||
| chr1:33175031 | T | G | 1 | a0001c0001t0001g0135 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.408+5994A>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33175031 | |||||||
| chr1:33175049 | A | ATATGTAT others(9): Show |
2 | a0001c0001t0001g0114 a0001c0001t0001g0115 |
2 | HG02735.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.408+5975_408+5976i others(18): Show |
TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33175049 | |||||||
| chr1:33175051 | T | A | 2 | a0001c0001t0001g0114 a0001c0001t0001g0115 |
2 | HG02735.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.408+5974A>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33175051 | |||||||
| chr1:33175102 | T | C | 190 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(187): Show |
261 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(258): Show |
intron_variant | MODIFIER | c.408+5923A>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33175102 | |||||||
| chr1:33175141 | C | T | 2 | a0001c0001t0001g0022 a0001c0001t0001g0078 |
3 | HG00438.hp2 HG02040.hp2 HG02074.hp1 |
intron_variant | MODIFIER | c.408+5884G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33175141 | |||||||
| chr1:33175206 | AT | A | 53 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0034 others(50): Show |
63 | HG00408.hp1 HG00544.hp2 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.408+5818delA | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33175206 | |||||||
| chr1:33175232 | AGAGATGG | A | 3 | a0001c0002t0001g0210 a0001c0002t0001g0211 a0001c0002t0003g0212 |
3 | HG01069.hp2 HG01071.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.408+5786_408+5792d others(9): Show |
TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33175232 | |||||||
| chr1:33175284 | C | T | 1 | a0001c0001t0003g0066 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.408+5741G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33175284 | |||||||
| chr1:33175655 | C | T | 80 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(77): Show |
127 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.408+5370G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33175655 | |||||||
| chr1:33175682 | G | T | 1 | a0001c0001t0001g0077 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.408+5343C>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33175682 | |||||||
| chr1:33175795 | C | T | 2 | a0001c0001t0001g0075 a0001c0001t0001g0076 |
2 | HG01175.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.408+5230G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33175795 | |||||||
| chr1:33176233 | C | T | 1 | a0001c0002t0002g0186 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.408+4792G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33176233 | |||||||
| chr1:33176331 | A | G | 225 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(222): Show |
333 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(330): Show |
intron_variant | MODIFIER | c.408+4694T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33176331 | |||||||
| chr1:33176346 | C | T | 2 | a0001c0002t0003g0213 a0001c0002t0003g0214 |
2 | HG00639.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.408+4679G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33176346 | |||||||
| chr1:33176533 | G | C | 12 | a0001c0001t0003g0036 a0001c0001t0003g0037 a0001c0001t0003g0038 others(9): Show |
16 | HG00597.hp1 HG00673.hp1 NA18948.hp2 others(13): Show |
intron_variant | MODIFIER | c.408+4492C>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33176533 | |||||||
| chr1:33176551 | C | T | 171 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(168): Show |
236 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(233): Show |
intron_variant | MODIFIER | c.408+4474G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33176551 | |||||||
| chr1:33176711 | G | A | 190 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(187): Show |
261 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(258): Show |
intron_variant | MODIFIER | c.408+4314C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33176711 | |||||||
| chr1:33176762 | C | T | 2 | a0001c0001t0001g0015 a0001c0001t0001g0048 |
3 | HG02280.hp2 HG02451.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.408+4263G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33176762 | |||||||
| chr1:33176816 | A | G | 2 | a0001c0001t0003g0159 a0001c0001t0003g0160 |
2 | HG02886.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.408+4209T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33176816 | |||||||
| chr1:33176822 | T | C | 1 | a0001c0001t0001g0153 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.408+4203A>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33176822 | |||||||
| chr1:33176989 | A | G | 3 | a0001c0002t0010g0231 a0001c0002t0010g0232 a0001c0002t0018g0230 |
3 | HG01109.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.408+4036T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33176989 | |||||||
| chr1:33177039 | GCACACAC others(7): Show |
G | 1 | a0001c0001t0003g0168 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.408+3972_408+3985d others(16): Show |
TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33177039 | |||||||
| chr1:33177050 | C | CAT | 160 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(157): Show |
224 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(221): Show |
intron_variant | MODIFIER | c.408+3974_408+3975i others(4): Show |
TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33177050 | |||||||
| chr1:33177051 | G | A | 29 | a0001c0001t0001g0021 a0001c0001t0001g0067 a0001c0001t0001g0069 others(26): Show |
36 | HG00597.hp1 HG00673.hp1 HG01070.hp2 others(33): Show |
intron_variant | MODIFIER | c.408+3974C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33177051 | |||||||
| chr1:33177052 | C | T | 29 | a0001c0001t0001g0021 a0001c0001t0001g0067 a0001c0001t0001g0069 others(26): Show |
36 | HG00597.hp1 HG00673.hp1 HG01070.hp2 others(33): Show |
intron_variant | MODIFIER | c.408+3973G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33177052 | |||||||
| chr1:33177053 | A | G | 29 | a0001c0001t0001g0021 a0001c0001t0001g0067 a0001c0001t0001g0069 others(26): Show |
36 | HG00597.hp1 HG00673.hp1 HG01070.hp2 others(33): Show |
intron_variant | MODIFIER | c.408+3972T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33177053 | |||||||
| chr1:33177055 | A | G | 18 | a0001c0001t0001g0021 a0001c0001t0001g0067 a0001c0001t0001g0069 others(15): Show |
21 | HG01070.hp2 HG01071.hp2 HG02080.hp2 others(18): Show |
intron_variant | MODIFIER | c.408+3970T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33177055 | |||||||
| chr1:33177067 | GCACA | G | 168 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(165): Show |
233 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(230): Show |
intron_variant | MODIFIER | c.408+3954_408+3957d others(6): Show |
TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33177067 | |||||||
| chr1:33177090 | A | C | 171 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(168): Show |
236 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(233): Show |
intron_variant | MODIFIER | c.408+3935T>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33177090 | |||||||
| chr1:33177103 | GCACACAC others(21): Show |
G | 2 | a0001c0001t0003g0064 a0001c0001t0003g0065 |
2 | NA19000.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.408+3894_408+3921d others(30): Show |
TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33177103 | |||||||
| chr1:33177136 | C | T | 141 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(138): Show |
199 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.408+3889G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33177136 | |||||||
| chr1:33177187 | C | T | 18 | a0001c0001t0001g0021 a0001c0001t0001g0067 a0001c0001t0001g0069 others(15): Show |
21 | HG01070.hp2 HG01071.hp2 HG02080.hp2 others(18): Show |
intron_variant | MODIFIER | c.408+3838G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33177187 | |||||||
| chr1:33177313 | A | G | 5 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(2): Show |
5 | HG01243.hp2 HG02572.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.408+3712T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33177313 | |||||||
| chr1:33177348 | A | T | 3 | a0001c0002t0010g0231 a0001c0002t0010g0232 a0001c0002t0018g0230 |
3 | HG01109.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.408+3677T>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33177348 | |||||||
| chr1:33177440 | G | A | 2 | a0001c0001t0003g0157 a0001c0004t0007g0156 |
2 | HG02109.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.408+3585C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33177440 | |||||||
| chr1:33177760 | A | G | 171 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(168): Show |
236 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(233): Show |
intron_variant | MODIFIER | c.408+3265T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33177760 | |||||||
| chr1:33177796 | G | A | 1 | a0001c0001t0001g0158 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.408+3229C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33177796 | |||||||
| chr1:33178064 | G | A | 2 | a0001c0001t0003g0159 a0001c0001t0003g0160 |
2 | HG02886.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.408+2961C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33178064 | |||||||
| chr1:33178150 | C | T | 1 | a0001c0001t0001g0020 | 2 | HG02809.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.408+2875G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33178150 | |||||||
| chr1:33178198 | C | T | 5 | a0001c0001t0001g0019 a0001c0001t0001g0055 a0001c0001t0001g0056 others(2): Show |
6 | HG01069.hp1 HG02055.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.408+2827G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33178198 | |||||||
| chr1:33178215 | T | C | 12 | a0001c0001t0003g0036 a0001c0001t0003g0037 a0001c0001t0003g0038 others(9): Show |
16 | HG00597.hp1 HG00673.hp1 NA18948.hp2 others(13): Show |
intron_variant | MODIFIER | c.408+2810A>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33178215 | |||||||
| chr1:33178382 | C | T | 32 | a0001c0002t0002g0001 a0001c0002t0002g0008 a0001c0002t0002g0043 others(29): Show |
69 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.408+2643G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33178382 | |||||||
| chr1:33178717 | A | G | 3 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 |
3 | NA18962.hp2 NA19062.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.408+2308T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33178717 | |||||||
| chr1:33178751 | A | G | 171 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(168): Show |
236 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(233): Show |
intron_variant | MODIFIER | c.408+2274T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33178751 | |||||||
| chr1:33178758 | C | T | 1 | a0001c0002t0002g0185 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.408+2267G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33178758 | |||||||
| chr1:33178764 | A | G | 2 | a0001c0002t0009g0180 a0001c0002t0009g0181 |
2 | HG02451.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.408+2261T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33178764 | |||||||
| chr1:33178992 | G | A | 12 | a0001c0001t0003g0036 a0001c0001t0003g0037 a0001c0001t0003g0038 others(9): Show |
16 | HG00597.hp1 HG00673.hp1 NA18948.hp2 others(13): Show |
intron_variant | MODIFIER | c.408+2033C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33178992 | |||||||
| chr1:33179043 | G | T | 171 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(168): Show |
236 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(233): Show |
intron_variant | MODIFIER | c.408+1982C>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33179043 | |||||||
| chr1:33179197 | A | G | 225 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(222): Show |
333 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(330): Show |
intron_variant | MODIFIER | c.408+1828T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33179197 | |||||||
| chr1:33179198 | A | C | 225 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(222): Show |
333 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(330): Show |
intron_variant | MODIFIER | c.408+1827T>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33179198 | |||||||
| chr1:33179231 | G | A | 5 | a0002c0003t0003g0222 a0002c0003t0003g0224 a0002c0003t0004g0005 others(2): Show |
10 | HG01891.hp2 HG02486.hp2 HG03130.hp1 others(7): Show |
intron_variant | MODIFIER | c.408+1794C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33179231 | |||||||
| chr1:33179572 | G | A | 3 | a0001c0002t0009g0180 a0001c0002t0009g0181 a0001c0014t0002g0182 |
3 | HG02451.hp1 NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.408+1453C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33179572 | |||||||
| chr1:33179688 | G | C | 6 | a0001c0001t0001g0040 a0001c0001t0001g0169 a0001c0001t0001g0172 others(3): Show |
8 | NA18941.hp2 NA18948.hp1 NA18967.hp1 others(5): Show |
intron_variant | MODIFIER | c.408+1337C>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33179688 | |||||||
| chr1:33179888 | A | G | 3 | a0001c0002t0001g0210 a0001c0002t0001g0211 a0001c0002t0003g0212 |
3 | HG01069.hp2 HG01071.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.408+1137T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33179888 | |||||||
| chr1:33179915 | GT | G | 33 | a0001c0002t0002g0001 a0001c0002t0002g0008 a0001c0002t0002g0043 others(30): Show |
70 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.408+1109delA | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33179915 | |||||||
| chr1:33179916 | T | G | 2 | a0001c0002t0002g0183 a0001c0002t0002g0184 |
2 | HG03834.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.408+1109A>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33179916 | |||||||
| chr1:33180051 | T | C | 3 | a0001c0002t0010g0231 a0001c0002t0010g0232 a0001c0002t0018g0230 |
3 | HG01109.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.408+974A>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33180051 | |||||||
| chr1:33180060 | GCT | G | 190 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(187): Show |
261 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(258): Show |
intron_variant | MODIFIER | c.408+963_408+964del others(2): Show |
TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33180060 | |||||||
| chr1:33180064 | A | C | 190 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(187): Show |
261 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(258): Show |
intron_variant | MODIFIER | c.408+961T>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33180064 | |||||||
| chr1:33180065 | A | T | 190 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(187): Show |
261 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(258): Show |
intron_variant | MODIFIER | c.408+960T>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33180065 | |||||||
| chr1:33180117 | C | T | 1 | a0001c0001t0001g0018 | 2 | HG02976.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.408+908G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33180117 | |||||||
| chr1:33180209 | A | G | 2 | a0001c0001t0001g0017 a0001c0001t0001g0051 |
3 | HG01255.hp1 HG02145.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.408+816T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33180209 | |||||||
| chr1:33180370 | C | T | 171 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(168): Show |
236 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(233): Show |
intron_variant | MODIFIER | c.408+655G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33180370 | |||||||
| chr1:33180498 | C | T | 2 | a0001c0002t0003g0213 a0001c0002t0003g0214 |
2 | HG00639.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.408+527G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33180498 | |||||||
| chr1:33180544 | G | A | 174 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(171): Show |
239 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(236): Show |
intron_variant | MODIFIER | c.408+481C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33180544 | |||||||
| chr1:33180589 | C | G | 1 | a0001c0001t0002g0175 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.408+436G>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33180589 | |||||||
| chr1:33180648 | T | C | 16 | a0001c0002t0001g0179 a0001c0002t0003g0045 a0001c0002t0003g0213 others(13): Show |
22 | HG00639.hp1 HG01243.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.408+377A>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33180648 | |||||||
| chr1:33180651 | C | T | 32 | a0001c0002t0002g0001 a0001c0002t0002g0008 a0001c0002t0002g0043 others(29): Show |
69 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.408+374G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33180651 | |||||||
| chr1:33180751 | T | A | 1 | a0001c0001t0001g0173 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.408+274A>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33180751 | |||||||
| chr1:33180760 | C | G | 1 | a0001c0002t0009g0180 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.408+265G>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33180760 | |||||||
| chr1:33180773 | G | C | 1 | a0001c0006t0003g0174 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.408+252C>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33180773 | |||||||
| chr1:33180818 | A | AGGCCCCG others(23): Show |
3 | a0001c0002t0009g0180 a0001c0002t0009g0181 a0001c0014t0002g0182 |
3 | HG02451.hp1 NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.408+177_408+206dup others(30): Show |
TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33180818 | |||||||
| chr1:33180836 | C | A | 3 | a0001c0001t0001g0177 a0001c0001t0002g0175 a0001c0001t0002g0176 |
3 | HG02083.hp2 NA18967.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.408+189G>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33180836 | |||||||
| chr1:33180896 | T | C | 190 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(187): Show |
261 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(258): Show |
intron_variant | MODIFIER | c.408+129A>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33180896 | |||||||
| chr1:33180899 | C | A | 1 | a0001c0001t0001g0042 | 2 | HG00639.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.408+126G>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33180899 | |||||||
| chr1:33180906 | C | T | 5 | a0001c0001t0001g0015 a0001c0001t0001g0048 a0001c0001t0001g0049 others(2): Show |
7 | HG02280.hp2 HG02451.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.408+119G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33180906 | |||||||
| chr1:33180953 | T | C | 1 | a0001c0002t0002g0225 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.408+72A>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33180953 | |||||||
| chr1:33180967 | G | T | 1 | a0001c0002t0001g0179 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.408+58C>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33180967 | |||||||
| chr1:33181013 | C | G | 2 | a0001c0001t0001g0046 a0001c0001t0001g0047 |
2 | NA18946.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.408+12G>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33181013 |