Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 55521 |
| ensemblid | ENSG00000152503.10 |
| hgncid | 16280 |
| symbol | TRIM36 |
| name | tripartite motif containing 36 |
| refseq_nuc | NM_001300759.2 |
| refseq_prot | NP_001287688.1 |
| ensembl_nuc | ENST00000513154.6 |
| ensembl_prot | ENSP00000423934.1 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 115124772 |
| end | 115169908 |
| strand | - |
| ver | v1.2 |
| region | chr5:115124772-115169908 |
| region5000 | chr5:115119772-115174908 |
| regionname0 | TRIM36_chr5_115124772_115169908 |
| regionname5000 | TRIM36_chr5_115119772_115174908 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 716 | 263 | 64 | 52 | 106 | 16 | 24 | 86 | TRIM36_chr5_115119772_115174908 | TRIM36 | MEGDG others(711): Show |
chr5 | 115119772 | 115174908 |
| a0002 | 0/0 | 716 | 91 | 10 | 14 | 60 | 0 | 7 | 48 | TRIM36_chr5_115119772_115174908 | TRIM36 | MEGDG others(711): Show |
chr5 | 115119772 | 115174908 |
| a0003 | 1/0 | 716 | 41 | 17 | 3 | 19 | 1 | 0 | 13 | TRIM36_chr5_115119772_115174908 | TRIM36 | MEGDG others(711): Show |
chr5 | 115119772 | 115174908 |
| a0004 | 0/0 | 716 | 6 | 0 | 0 | 6 | 0 | 0 | 6 | TRIM36_chr5_115119772_115174908 | TRIM36 | MEGDG others(711): Show |
chr5 | 115119772 | 115174908 |
| a0005 | 0/0 | 716 | 2 | 0 | 1 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | MEGDG others(711): Show |
chr5 | 115119772 | 115174908 |
| a0006 | 0/0 | 716 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | MEGDG others(711): Show |
chr5 | 115119772 | 115174908 |
| a0007 | 0/0 | 716 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | MEGDG others(711): Show |
chr5 | 115119772 | 115174908 |
| a0008 | 0/0 | 716 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | MEGDG others(711): Show |
chr5 | 115119772 | 115174908 |
| a0009 | 0/0 | 716 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | MEGDG others(711): Show |
chr5 | 115119772 | 115174908 |
| a0010 | 0/0 | 716 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TRIM36_chr5_115119772_115174908 | TRIM36 | MEGDG others(711): Show |
chr5 | 115119772 | 115174908 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2148 | 219 | 28 | 50 | 100 | 16 | 24 | TRIM36_chr5_115119772_115174908 | TRIM36 | ATGGA others(2143): Show |
chr5 | 115119772 | 115174908 | ||
| a0001c0004 | 0/0 | 2148 | 28 | 21 | 1 | 6 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | ATGGA others(2143): Show |
chr5 | 115119772 | 115174908 | ||
| a0001c0006 | 0/0 | 2148 | 9 | 9 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | ATGGA others(2143): Show |
chr5 | 115119772 | 115174908 | ||
| a0001c0009 | 0/0 | 2148 | 4 | 4 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | ATGGA others(2143): Show |
chr5 | 115119772 | 115174908 | ||
| a0001c0010 | 0/0 | 2148 | 3 | 2 | 1 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | ATGGA others(2143): Show |
chr5 | 115119772 | 115174908 | ||
| a0002c0002 | 0/0 | 2148 | 77 | 8 | 13 | 50 | 0 | 6 | TRIM36_chr5_115119772_115174908 | TRIM36 | ATGGA others(2143): Show |
chr5 | 115119772 | 115174908 | ||
| a0002c0005 | 0/0 | 2148 | 14 | 2 | 1 | 10 | 0 | 1 | TRIM36_chr5_115119772_115174908 | TRIM36 | ATGGA others(2143): Show |
chr5 | 115119772 | 115174908 | ||
| a0003c0003 | 0/0 | 2148 | 37 | 15 | 3 | 18 | 1 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | ATGGA others(2143): Show |
chr5 | 115119772 | 115174908 | ||
| a0003c0008 | 1/0 | 2148 | 4 | 2 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | ATGGA others(2143): Show |
chr5 | 115119772 | 115174908 | ||
| a0004c0007 | 0/0 | 2148 | 6 | 0 | 0 | 6 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | ATGGA others(2143): Show |
chr5 | 115119772 | 115174908 | ||
| a0005c0011 | 0/0 | 2148 | 2 | 0 | 1 | 0 | 1 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | ATGGA others(2143): Show |
chr5 | 115119772 | 115174908 | ||
| a0006c0015 | 0/0 | 2148 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | ATGGA others(2143): Show |
chr5 | 115119772 | 115174908 | ||
| a0007c0014 | 0/0 | 2148 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | ATGGA others(2143): Show |
chr5 | 115119772 | 115174908 | ||
| a0008c0013 | 0/0 | 2148 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | ATGGA others(2143): Show |
chr5 | 115119772 | 115174908 | ||
| a0009c0016 | 0/0 | 2148 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM36_chr5_115119772_115174908 | TRIM36 | ATGGA others(2143): Show |
chr5 | 115119772 | 115174908 | ||
| a0010c0012 | 0/0 | 2148 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | ATGGA others(2143): Show |
chr5 | 115119772 | 115174908 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 4156 | 203 | 22 | 48 | 93 | 16 | 23 | TRIM36_chr5_115119772_115174908 | TRIM36 | GCAGT others(4151): Show |
chr5 | 115119772 | 115174908 |
| a0001c0001t0002 | 0/0 | 4156 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | GCAGT others(4151): Show |
chr5 | 115119772 | 115174908 |
| a0001c0001t0003 | 0/0 | 4156 | 4 | 3 | 1 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | GCAGT others(4151): Show |
chr5 | 115119772 | 115174908 |
| a0001c0001t0012 | 0/0 | 4156 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | GCAGT others(4151): Show |
chr5 | 115119772 | 115174908 |
| a0001c0001t0013 | 0/0 | 4156 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | GCAGG others(4151): Show |
chr5 | 115119772 | 115174908 |
| a0001c0001t0015 | 0/0 | 4156 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM36_chr5_115119772_115174908 | TRIM36 | GCAGT others(4151): Show |
chr5 | 115119772 | 115174908 |
| a0001c0001t0021 | 0/0 | 4156 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | GCAGT others(4151): Show |
chr5 | 115119772 | 115174908 |
| a0001c0001t0022 | 0/0 | 4156 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | GCAGT others(4151): Show |
chr5 | 115119772 | 115174908 |
| a0001c0001t0027 | 0/0 | 4156 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | GCAGT others(4151): Show |
chr5 | 115119772 | 115174908 |
| a0001c0001t0028 | 0/0 | 4156 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | GCAGT others(4151): Show |
chr5 | 115119772 | 115174908 |
| a0001c0004t0001 | 0/0 | 4156 | 7 | 7 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | GCAGT others(4151): Show |
chr5 | 115119772 | 115174908 |
| a0001c0004t0002 | 0/0 | 4156 | 5 | 0 | 0 | 5 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | GCAGT others(4151): Show |
chr5 | 115119772 | 115174908 |
| a0001c0004t0005 | 0/0 | 4151 | 5 | 5 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | GCAGT others(4146): Show |
chr5 | 115119772 | 115174908 |
| a0001c0004t0006 | 0/0 | 4156 | 4 | 4 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | GCAGT others(4151): Show |
chr5 | 115119772 | 115174908 |
| a0001c0004t0014 | 0/0 | 4156 | 2 | 1 | 1 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | GCAGT others(4151): Show |
chr5 | 115119772 | 115174908 |
| a0001c0004t0016 | 0/0 | 4151 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | GCAGT others(4146): Show |
chr5 | 115119772 | 115174908 |
| a0001c0004t0017 | 0/0 | 4156 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | GCAGT others(4151): Show |
chr5 | 115119772 | 115174908 |
| a0001c0004t0018 | 0/0 | 4151 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | GCAGT others(4146): Show |
chr5 | 115119772 | 115174908 |
| a0001c0004t0024 | 0/0 | 4156 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | GCAGT others(4151): Show |
chr5 | 115119772 | 115174908 |
| a0001c0004t0026 | 0/0 | 4156 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | GCAGT others(4151): Show |
chr5 | 115119772 | 115174908 |
| a0001c0006t0003 | 0/0 | 4156 | 9 | 9 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | GCAGT others(4151): Show |
chr5 | 115119772 | 115174908 |
| a0001c0009t0011 | 0/0 | 4156 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | GCAGT others(4151): Show |
chr5 | 115119772 | 115174908 |
| a0001c0009t0023 | 0/0 | 4156 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | GCAGT others(4151): Show |
chr5 | 115119772 | 115174908 |
| a0001c0010t0001 | 0/0 | 4156 | 3 | 2 | 1 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | GCAGT others(4151): Show |
chr5 | 115119772 | 115174908 |
| a0002c0002t0002 | 0/0 | 4156 | 69 | 3 | 13 | 49 | 0 | 4 | TRIM36_chr5_115119772_115174908 | TRIM36 | GCAGT others(4151): Show |
chr5 | 115119772 | 115174908 |
| a0002c0002t0009 | 0/0 | 4156 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | GCAGT others(4151): Show |
chr5 | 115119772 | 115174908 |
| a0002c0002t0010 | 0/0 | 4156 | 3 | 1 | 0 | 0 | 0 | 2 | TRIM36_chr5_115119772_115174908 | TRIM36 | GCAGT others(4151): Show |
chr5 | 115119772 | 115174908 |
| a0002c0002t0019 | 0/0 | 4156 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | GCAGT others(4151): Show |
chr5 | 115119772 | 115174908 |
| a0002c0002t0025 | 0/0 | 4156 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | GCAGT others(4151): Show |
chr5 | 115119772 | 115174908 |
| a0002c0005t0001 | 0/0 | 4156 | 3 | 2 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | GCAGT others(4151): Show |
chr5 | 115119772 | 115174908 |
| a0002c0005t0002 | 0/0 | 4156 | 3 | 0 | 1 | 1 | 0 | 1 | TRIM36_chr5_115119772_115174908 | TRIM36 | GCAGT others(4151): Show |
chr5 | 115119772 | 115174908 |
| a0002c0005t0004 | 0/0 | 4156 | 7 | 0 | 0 | 7 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | GCAGT others(4151): Show |
chr5 | 115119772 | 115174908 |
| a0002c0005t0020 | 0/0 | 4156 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | GCAGT others(4151): Show |
chr5 | 115119772 | 115174908 |
| a0003c0003t0001 | 0/0 | 4156 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | GCAGT others(4151): Show |
chr5 | 115119772 | 115174908 |
| a0003c0003t0003 | 0/0 | 4156 | 28 | 13 | 1 | 14 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | GCAGT others(4151): Show |
chr5 | 115119772 | 115174908 |
| a0003c0003t0007 | 0/0 | 4155 | 4 | 1 | 2 | 0 | 1 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | GCAGT others(4150): Show |
chr5 | 115119772 | 115174908 |
| a0003c0003t0008 | 0/0 | 4156 | 4 | 0 | 0 | 4 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | GCAGT others(4151): Show |
chr5 | 115119772 | 115174908 |
| a0003c0008t0003 | 1/0 | 4156 | 4 | 2 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | GCAGT others(4151): Show |
chr5 | 115119772 | 115174908 |
| a0004c0007t0003 | 0/0 | 4156 | 6 | 0 | 0 | 6 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | GCAGT others(4151): Show |
chr5 | 115119772 | 115174908 |
| a0005c0011t0001 | 0/0 | 4156 | 2 | 0 | 1 | 0 | 1 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | GCAGT others(4151): Show |
chr5 | 115119772 | 115174908 |
| a0006c0015t0001 | 0/0 | 4156 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | GCAGT others(4151): Show |
chr5 | 115119772 | 115174908 |
| a0007c0014t0001 | 0/0 | 4156 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | GCAGT others(4151): Show |
chr5 | 115119772 | 115174908 |
| a0008c0013t0002 | 0/0 | 4156 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | GCAGT others(4151): Show |
chr5 | 115119772 | 115174908 |
| a0009c0016t0001 | 0/0 | 4156 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM36_chr5_115119772_115174908 | TRIM36 | GCAGT others(4151): Show |
chr5 | 115119772 | 115174908 |
| a0010c0012t0002 | 0/0 | 4156 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | GCAGT others(4151): Show |
chr5 | 115119772 | 115174908 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 8 | 1 | 0 | 7 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0002 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0003 | 0/0 | 6 | 0 | 4 | 0 | 1 | 1 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0005 | 0/0 | 5 | 1 | 2 | 0 | 0 | 2 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0013 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0304 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0003g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0003g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0003g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0012g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0012g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0013g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0015g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0021g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0022g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0027g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0001t0028g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0004t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0004t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0004t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0004t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0004t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0004t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0004t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0004t0002g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0004t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0004t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0004t0005g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0004t0005g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0004t0005g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0004t0005g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0004t0005g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0004t0006g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0004t0006g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0004t0006g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0004t0006g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0004t0014g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0004t0014g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0004t0016g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0004t0017g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0004t0018g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0004t0024g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0004t0026g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0006t0003g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0006t0003g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0006t0003g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0006t0003g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0006t0003g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0006t0003g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0006t0003g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0006t0003g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0006t0003g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0009t0011g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0009t0011g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0009t0023g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0010t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0010t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0001c0010t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0002c0002t0002g0008 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0002c0002t0002g0009 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0002c0002t0002g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0002c0002t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0002c0002t0002g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0002c0002t0002g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0002c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0002c0002t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0002c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0002c0002t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0002c0002t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0002c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0002c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0002c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0002c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0002c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0002c0002t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0002c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0002c0002t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0002c0002t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0002c0002t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0002c0002t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0002c0002t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0002c0002t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0002c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0002c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0002c0002t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0002c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0002c0002t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0002c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0002c0002t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0002c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0002c0002t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0002c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0002c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0002c0002t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0002c0002t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0002c0002t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0002c0002t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0002c0002t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0002c0002t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0002c0002t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0002c0002t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0002c0002t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0002c0002t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0002c0002t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0002c0002t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0002c0002t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0002c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0002c0002t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0002c0002t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0002c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0002c0002t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0002c0002t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0002c0002t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0002c0002t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0002c0002t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0002c0002t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0002c0002t0002g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0002c0002t0002g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0002c0002t0009g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0002c0002t0009g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0002c0002t0010g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0002c0002t0010g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0002c0002t0010g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0002c0002t0019g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0002c0002t0025g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0002c0005t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0002c0005t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0002c0005t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0002c0005t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0002c0005t0002g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0002c0005t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0002c0005t0004g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0002c0005t0004g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0002c0005t0004g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0002c0005t0004g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0002c0005t0004g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0002c0005t0020g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0003c0003t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0003c0003t0003g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0003c0003t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0003c0003t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0003c0003t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0003c0003t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0003c0003t0003g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0003c0003t0003g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0003c0003t0003g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0003c0003t0003g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0003c0003t0003g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0003c0003t0003g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0003c0003t0003g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0003c0003t0003g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0003c0003t0003g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0003c0003t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0003c0003t0003g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0003c0003t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0003c0003t0003g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0003c0003t0003g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0003c0003t0003g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0003c0003t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0003c0003t0003g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0003c0003t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0003c0003t0003g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0003c0003t0003g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0003c0003t0003g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0003c0003t0003g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0003c0003t0007g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0003c0003t0007g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0003c0003t0007g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0003c0003t0008g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0003c0003t0008g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0003c0003t0008g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0003c0003t0008g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0003c0008t0003g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0003c0008t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0003c0008t0003g0152 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0004c0007t0003g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0004c0007t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0004c0007t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0004c0007t0003g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0004c0007t0003g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0005c0011t0001g0340 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0005c0011t0001g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0006c0015t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0007c0014t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0008c0013t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0009c0016t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| a0010c0012t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0005 | c0011 | t0001 | g0340 | EUR | GBR | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | GBR | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0278 | EUR | GBR | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0098 | EUR | GBR | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG00280 | hp1 | a0003 | c0003 | t0007 | g0261 | EUR | FIN | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0137 | EUR | FIN | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0303 | EUR | FIN | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0144 | EUR | FIN | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | CHS | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG00423 | hp2 | a0002 | c0002 | t0002 | g0210 | EAS | CHS | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG00558 | hp1 | a0002 | c0002 | t0002 | g0010 | EAS | CHS | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG00558 | hp2 | a0002 | c0002 | t0002 | g0188 | EAS | CHS | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG00597 | hp1 | a0002 | c0002 | t0002 | g0212 | EAS | CHS | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0327 | EAS | CHS | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | CHS | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | CHS | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG00639 | hp1 | a0001 | c0001 | t0022 | g0125 | AMR | PUR | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG00673 | hp1 | a0003 | c0003 | t0003 | g0239 | EAS | CHS | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | CHS | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG00733 | hp1 | a0003 | c0003 | t0003 | g0262 | AMR | PUR | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG00735 | hp1 | a0005 | c0011 | t0001 | g0341 | AMR | PUR | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0335 | AMR | PUR | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG00741 | hp1 | a0002 | c0002 | t0002 | g0209 | AMR | PUR | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG01069 | hp2 | a0002 | c0002 | t0002 | g0206 | AMR | PUR | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0272 | AMR | PUR | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG01071 | hp1 | a0002 | c0002 | t0002 | g0008 | AMR | PUR | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0277 | AMR | PUR | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG01074 | hp1 | a0001 | c0004 | t0014 | g0347 | AMR | PUR | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0246 | AMR | PUR | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG01099 | hp1 | a0002 | c0002 | t0002 | g0208 | AMR | PUR | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG01106 | hp1 | a0003 | c0003 | t0007 | g0027 | AMR | PUR | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG01167 | hp1 | a0002 | c0002 | t0002 | g0189 | AMR | PUR | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | PUR | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0084 | AMR | PUR | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0294 | AMR | PUR | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG01243 | hp2 | a0001 | c0010 | t0001 | g0079 | AMR | PUR | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | CLM | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG01261 | hp2 | a0002 | c0005 | t0002 | g0225 | AMR | CLM | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | CLM | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG01358 | hp1 | a0003 | c0003 | t0007 | g0027 | AMR | CLM | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0332 | AMR | CLM | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | CLM | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0301 | AMR | CLM | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG01433 | hp1 | a0002 | c0002 | t0002 | g0198 | AMR | CLM | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0298 | AMR | CLM | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG01496 | hp1 | a0002 | c0002 | t0002 | g0066 | AMR | CLM | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | CLM | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0110 | EUR | IBS | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0329 | EUR | IBS | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0292 | EUR | IBS | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0156 | EUR | IBS | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0330 | EUR | IBS | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0153 | EUR | IBS | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0076 | AFR | ACB | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0264 | AFR | ACB | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG01891 | hp1 | a0002 | c0002 | t0002 | g0069 | AFR | ACB | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0093 | AFR | ACB | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG01928 | hp1 | a0002 | c0002 | t0002 | g0213 | AMR | PEL | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PEL | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG01934 | hp2 | a0002 | c0002 | t0002 | g0288 | AMR | PEL | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0302 | AMR | PEL | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PEL | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | PEL | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG01975 | hp2 | a0002 | c0002 | t0002 | g0009 | AMR | PEL | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PEL | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PEL | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PEL | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG01981 | hp2 | a0002 | c0002 | t0002 | g0207 | AMR | PEL | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG02015 | hp2 | a0002 | c0005 | t0001 | g0289 | EAS | KHV | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG02027 | hp1 | a0002 | c0002 | t0002 | g0205 | EAS | KHV | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG02040 | hp1 | a0003 | c0003 | t0003 | g0028 | EAS | KHV | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG02055 | hp2 | a0001 | c0006 | t0003 | g0242 | AFR | ACB | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG02056 | hp1 | a0006 | c0015 | t0001 | g0275 | EAS | KHV | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG02056 | hp2 | a0003 | c0003 | t0003 | g0258 | EAS | KHV | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG02071 | hp2 | a0002 | c0002 | t0002 | g0228 | EAS | KHV | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG02074 | hp1 | a0002 | c0002 | t0002 | g0216 | EAS | KHV | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG02074 | hp2 | a0003 | c0003 | t0003 | g0256 | EAS | KHV | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | KHV | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG02080 | hp2 | a0002 | c0002 | t0002 | g0009 | EAS | KHV | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | KHV | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG02083 | hp2 | a0002 | c0002 | t0002 | g0009 | EAS | KHV | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG02129 | hp1 | a0002 | c0002 | t0002 | g0186 | EAS | KHV | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG02132 | hp1 | a0002 | c0002 | t0002 | g0203 | EAS | KHV | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | KHV | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | KHV | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG02145 | hp1 | a0003 | c0003 | t0003 | g0036 | AFR | ACB | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0336 | AFR | ACB | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | CDX | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG02155 | hp2 | a0001 | c0004 | t0026 | g0074 | EAS | CDX | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG02257 | hp1 | a0001 | c0001 | t0028 | g0345 | AFR | ACB | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG02257 | hp2 | a0001 | c0004 | t0001 | g0169 | AFR | ACB | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG02258 | hp1 | a0007 | c0014 | t0001 | g0131 | AFR | ACB | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG02258 | hp2 | a0001 | c0004 | t0017 | g0035 | AFR | ACB | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG02273 | hp1 | a0002 | c0002 | t0002 | g0008 | AMR | PEL | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PEL | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG02280 | hp1 | a0001 | c0004 | t0005 | g0326 | AFR | ACB | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG02280 | hp2 | a0003 | c0003 | t0003 | g0178 | AFR | ACB | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG02293 | hp1 | a0002 | c0002 | t0002 | g0008 | AMR | PEL | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PEL | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PEL | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG02451 | hp1 | a0001 | c0010 | t0001 | g0078 | AFR | ACB | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG02451 | hp2 | a0001 | c0004 | t0005 | g0323 | AFR | ACB | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG02523 | hp1 | a0003 | c0003 | t0003 | g0245 | EAS | KHV | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG02523 | hp2 | a0008 | c0013 | t0002 | g0200 | EAS | KHV | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG02572 | hp1 | a0003 | c0003 | t0001 | g0040 | AFR | GWD | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG02572 | hp2 | a0001 | c0009 | t0011 | g0016 | AFR | GWD | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG02615 | hp1 | a0001 | c0006 | t0003 | g0241 | AFR | GWD | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0265 | AFR | GWD | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG02622 | hp1 | a0001 | c0009 | t0023 | g0033 | AFR | GWD | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG02622 | hp2 | a0001 | c0004 | t0001 | g0063 | AFR | GWD | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG02647 | hp1 | a0003 | c0003 | t0003 | g0039 | AFR | GWD | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG02647 | hp2 | a0003 | c0008 | t0003 | g0022 | AFR | GWD | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG02717 | hp1 | a0001 | c0004 | t0024 | g0310 | AFR | GWD | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG02717 | hp2 | a0001 | c0004 | t0006 | g0268 | AFR | GWD | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG02723 | hp2 | a0002 | c0002 | t0010 | g0171 | AFR | GWD | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG02735 | hp2 | a0002 | c0002 | t0002 | g0194 | SAS | PJL | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0092 | AFR | GWD | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG02818 | hp2 | a0001 | c0006 | t0003 | g0307 | AFR | GWD | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG02886 | hp2 | a0003 | c0003 | t0003 | g0172 | AFR | GWD | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG02895 | hp1 | a0001 | c0001 | t0013 | g0014 | AFR | GWD | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG02895 | hp2 | a0003 | c0003 | t0003 | g0038 | AFR | GWD | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG02896 | hp1 | a0001 | c0004 | t0006 | g0054 | AFR | GWD | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG02897 | hp2 | a0001 | c0001 | t0013 | g0014 | AFR | GWD | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG02922 | hp1 | a0001 | c0006 | t0003 | g0311 | AFR | ESN | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG02922 | hp2 | a0002 | c0002 | t0002 | g0316 | AFR | ESN | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG02965 | hp1 | a0002 | c0005 | t0001 | g0055 | AFR | ESN | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG02965 | hp2 | a0003 | c0008 | t0003 | g0022 | AFR | ESN | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG02970 | hp1 | a0001 | c0004 | t0006 | g0042 | AFR | ESN | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG02970 | hp2 | a0003 | c0003 | t0003 | g0177 | AFR | ESN | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG02976 | hp1 | a0003 | c0003 | t0003 | g0174 | AFR | ESN | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG02976 | hp2 | a0001 | c0004 | t0001 | g0056 | AFR | ESN | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG03041 | hp2 | a0002 | c0005 | t0001 | g0053 | AFR | GWD | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG03098 | hp1 | a0001 | c0004 | t0005 | g0325 | AFR | MSL | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG03098 | hp2 | a0001 | c0006 | t0003 | g0313 | AFR | MSL | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG03130 | hp1 | a0001 | c0006 | t0003 | g0312 | AFR | ESN | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG03130 | hp2 | a0001 | c0004 | t0018 | g0308 | AFR | ESN | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG03139 | hp1 | a0003 | c0003 | t0003 | g0173 | AFR | ESN | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | ESN | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG03209 | hp1 | a0003 | c0003 | t0003 | g0052 | AFR | MSL | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG03209 | hp2 | a0003 | c0003 | t0003 | g0175 | AFR | MSL | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG03225 | hp1 | a0003 | c0003 | t0003 | g0061 | AFR | MSL | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG03225 | hp2 | a0001 | c0004 | t0005 | g0322 | AFR | MSL | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG03239 | hp1 | a0002 | c0002 | t0002 | g0201 | SAS | PJL | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0328 | SAS | PJL | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG03453 | hp1 | a0002 | c0002 | t0002 | g0068 | AFR | MSL | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG03453 | hp2 | a0002 | c0002 | t0009 | g0015 | AFR | MSL | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG03486 | hp1 | a0001 | c0004 | t0001 | g0168 | AFR | MSL | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG03486 | hp2 | a0001 | c0004 | t0005 | g0321 | AFR | MSL | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0160 | SAS | PJL | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG03516 | hp1 | a0001 | c0004 | t0001 | g0057 | AFR | ESN | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | ESN | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG03540 | hp1 | a0001 | c0004 | t0016 | g0324 | AFR | GWD | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0270 | AFR | GWD | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG03579 | hp1 | a0001 | c0006 | t0003 | g0315 | AFR | MSL | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG03579 | hp2 | a0003 | c0003 | t0003 | g0176 | AFR | MSL | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG03654 | hp1 | a0002 | c0002 | t0010 | g0333 | SAS | PJL | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0305 | SAS | PJL | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0339 | SAS | PJL | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG03688 | hp1 | a0001 | c0001 | t0015 | g0276 | SAS | STU | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0159 | SAS | STU | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG03704 | hp2 | a0002 | c0002 | t0002 | g0086 | SAS | PJL | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0337 | SAS | PJL | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG03831 | hp1 | a0002 | c0002 | t0002 | g0211 | SAS | BEB | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG03831 | hp2 | a0009 | c0016 | t0001 | g0141 | SAS | BEB | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0338 | SAS | BEB | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG03927 | hp2 | a0002 | c0005 | t0002 | g0219 | SAS | BEB | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | STU | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0158 | SAS | STU | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG04184 | hp1 | a0002 | c0002 | t0010 | g0334 | SAS | BEB | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0285 | SAS | BEB | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0148 | SAS | STU | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0282 | SAS | STU | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA18612 | hp1 | a0001 | c0001 | t0021 | g0089 | EAS | CHB | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA18747 | hp2 | a0003 | c0003 | t0003 | g0250 | EAS | CHB | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA18906 | hp1 | a0001 | c0004 | t0006 | g0041 | AFR | YRI | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA18906 | hp2 | a0001 | c0006 | t0003 | g0240 | AFR | YRI | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA18939 | hp1 | a0002 | c0005 | t0002 | g0193 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA18941 | hp1 | a0002 | c0002 | t0002 | g0237 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA18942 | hp2 | a0002 | c0002 | t0002 | g0223 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA18943 | hp1 | a0004 | c0007 | t0003 | g0082 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA18943 | hp2 | a0002 | c0002 | t0002 | g0190 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA18944 | hp1 | a0001 | c0004 | t0002 | g0007 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA18944 | hp2 | a0002 | c0002 | t0002 | g0067 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA18945 | hp2 | a0001 | c0001 | t0012 | g0031 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA18946 | hp2 | a0002 | c0002 | t0002 | g0195 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA18947 | hp1 | a0003 | c0008 | t0003 | g0115 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA18949 | hp1 | a0003 | c0003 | t0003 | g0244 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0342 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA18950 | hp2 | a0002 | c0002 | t0002 | g0236 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA18957 | hp2 | a0003 | c0003 | t0003 | g0343 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA18963 | hp1 | a0001 | c0001 | t0012 | g0031 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA18963 | hp2 | a0002 | c0002 | t0002 | g0202 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA18964 | hp1 | a0002 | c0002 | t0002 | g0075 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA18965 | hp1 | a0002 | c0002 | t0002 | g0226 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA18966 | hp2 | a0002 | c0002 | t0002 | g0215 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA18967 | hp2 | a0003 | c0003 | t0008 | g0251 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA18969 | hp2 | a0001 | c0004 | t0002 | g0007 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA18970 | hp1 | a0003 | c0003 | t0003 | g0254 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA18971 | hp2 | a0002 | c0002 | t0002 | g0197 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA18972 | hp1 | a0002 | c0002 | t0002 | g0218 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA18973 | hp2 | a0001 | c0001 | t0012 | g0306 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA18979 | hp1 | a0004 | c0007 | t0003 | g0253 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA18979 | hp2 | a0002 | c0002 | t0002 | g0181 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA18980 | hp1 | a0002 | c0002 | t0002 | g0224 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA18983 | hp1 | a0001 | c0001 | t0027 | g0344 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA18983 | hp2 | a0001 | c0004 | t0002 | g0234 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA18984 | hp1 | a0001 | c0004 | t0002 | g0007 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA18985 | hp1 | a0002 | c0002 | t0002 | g0179 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA18985 | hp2 | a0002 | c0005 | t0004 | g0071 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA18987 | hp2 | a0004 | c0007 | t0003 | g0026 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA18988 | hp1 | a0002 | c0002 | t0002 | g0238 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA18992 | hp1 | a0002 | c0002 | t0002 | g0024 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA18994 | hp2 | a0002 | c0002 | t0002 | g0191 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA19000 | hp1 | a0003 | c0003 | t0003 | g0263 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA19000 | hp2 | a0002 | c0002 | t0002 | g0025 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA19001 | hp1 | a0010 | c0012 | t0002 | g0196 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA19001 | hp2 | a0002 | c0005 | t0004 | g0293 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA19002 | hp2 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA19003 | hp1 | a0004 | c0007 | t0003 | g0248 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA19005 | hp2 | a0003 | c0003 | t0008 | g0257 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA19006 | hp1 | a0002 | c0002 | t0002 | g0023 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA19007 | hp1 | a0002 | c0005 | t0004 | g0006 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA19009 | hp2 | a0002 | c0002 | t0025 | g0070 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA19010 | hp1 | a0004 | c0007 | t0003 | g0247 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA19011 | hp2 | a0002 | c0002 | t0002 | g0062 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA19030 | hp1 | a0001 | c0004 | t0001 | g0170 | AFR | LWK | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | LWK | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA19043 | hp1 | a0001 | c0004 | t0014 | g0346 | AFR | LWK | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA19043 | hp2 | a0001 | c0009 | t0011 | g0051 | AFR | LWK | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA19057 | hp1 | a0003 | c0003 | t0008 | g0249 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA19060 | hp2 | a0002 | c0002 | t0002 | g0184 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA19062 | hp1 | a0002 | c0002 | t0002 | g0235 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA19062 | hp2 | a0003 | c0003 | t0003 | g0243 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA19064 | hp1 | a0002 | c0002 | t0002 | g0227 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA19064 | hp2 | a0003 | c0003 | t0003 | g0259 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA19065 | hp1 | a0002 | c0002 | t0002 | g0024 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA19065 | hp2 | a0002 | c0005 | t0004 | g0073 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA19067 | hp1 | a0002 | c0002 | t0002 | g0192 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA19067 | hp2 | a0003 | c0003 | t0003 | g0255 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA19068 | hp1 | a0002 | c0002 | t0002 | g0199 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA19070 | hp1 | a0002 | c0005 | t0020 | g0072 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA19070 | hp2 | a0003 | c0003 | t0008 | g0252 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA19075 | hp2 | a0002 | c0002 | t0002 | g0087 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA19077 | hp1 | a0002 | c0005 | t0004 | g0233 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA19077 | hp2 | a0002 | c0002 | t0002 | g0023 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA19079 | hp1 | a0003 | c0003 | t0003 | g0028 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA19079 | hp2 | a0002 | c0002 | t0002 | g0204 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA19082 | hp1 | a0002 | c0005 | t0004 | g0006 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA19083 | hp1 | a0002 | c0005 | t0004 | g0006 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA19083 | hp2 | a0002 | c0002 | t0002 | g0217 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA19084 | hp2 | a0002 | c0002 | t0002 | g0025 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA19085 | hp1 | a0002 | c0002 | t0002 | g0180 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA19085 | hp2 | a0001 | c0004 | t0002 | g0187 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA19086 | hp1 | a0002 | c0002 | t0002 | g0185 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA19087 | hp1 | a0002 | c0002 | t0002 | g0214 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA19090 | hp1 | a0002 | c0002 | t0002 | g0222 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | YRI | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA19240 | hp2 | a0001 | c0009 | t0011 | g0016 | AFR | YRI | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA20129 | hp1 | a0001 | c0004 | t0001 | g0034 | AFR | ASW | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ASW | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0291 | EUR | TSI | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0019 | EUR | TSI | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0136 | EUR | TSI | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0297 | EUR | TSI | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0300 | AMR | CLM | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | CLM | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | ACB | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0320 | AFR | ACB | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0309 | AFR | ACB | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG02559 | hp1 | a0003 | c0003 | t0003 | g0037 | AFR | ACB | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG02559 | hp2 | a0002 | c0002 | t0009 | g0059 | AFR | ACB | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG03471 | hp1 | a0001 | c0010 | t0001 | g0077 | AFR | MSL | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG03471 | hp2 | a0001 | c0006 | t0003 | g0314 | AFR | MSL | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | USA | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| HG06807 | hp2 | a0003 | c0003 | t0007 | g0260 | AFR | USA | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA18955 | hp1 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA18955 | hp2 | a0004 | c0007 | t0003 | g0026 | EAS | JPT | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA20300 | hp1 | a0002 | c0002 | t0019 | g0049 | AFR | USA | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | USA | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0319 | AFR | LWK | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| NA21309 | hp2 | a0002 | c0002 | t0009 | g0015 | AFR | LWK | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0304 | REF | REF | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| homoSapiens | grch38p0 | a0003 | c0008 | t0003 | g0152 | REF | REF | TRIM36_chr5_115119772_115174908 | TRIM36 | chr5 | 115119772 | 115174908 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:115126517 | G | C | 1 | a0004 | 6 | NA18943.hp1 NA18955.hp2 NA18979.hp1 others(3): Show |
missense_variant | MODERATE | c.2137C>G | p.Gln713Glu | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 10/10 | 2411/4156 | 2137/2151 | 713/716 | chr5 | 115126517 | |||
| chr5:115126658 | C | T | 8 | a0001 a0002 a0005 others(5): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
missense_variant | MODERATE | c.1996G>A | p.Asp666Asn | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 10/10 | 2270/4156 | 1996/2151 | 666/716 | chr5 | 115126658 | |||
| chr5:115126781 | T | G | 1 | a0006 | 1 | HG02056.hp1 | missense_variant | MODERATE | c.1873A>C | p.Thr625Pro | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 10/10 | 2147/4156 | 1873/2151 | 625/716 | chr5 | 115126781 | |||
| chr5:115134027 | T | C | 3 | a0002 a0008 a0010 |
93 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(90): Show |
missense_variant | MODERATE | c.1331A>G | p.Asn444Ser | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 8/10 | 1605/4156 | 1331/2151 | 444/716 | chr5 | 115134027 | |||
| chr5:115134139 | C | T | 1 | a0005 | 2 | HG00099.hp1 HG00735.hp1 |
missense_variant | MODERATE | c.1219G>A | p.Val407Met | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 8/10 | 1493/4156 | 1219/2151 | 407/716 | chr5 | 115134139 | |||
| chr5:115137568 | G | C | 1 | a0009 | 1 | HG03831.hp2 | missense_variant | MODERATE | c.880C>G | p.Leu294Val | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 6/10 | 1154/4156 | 880/2151 | 294/716 | chr5 | 115137568 | |||
| chr5:115141365 | A | T | 1 | a0007 | 1 | HG02258.hp1 | missense_variant | MODERATE | c.745T>A | p.Ser249Thr | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 5/10 | 1019/4156 | 745/2151 | 249/716 | chr5 | 115141365 | |||
| chr5:115144627 | T | C | 1 | a0008 | 1 | HG02523.hp2 | missense_variant | MODERATE | c.706A>G | p.Thr236Ala | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 4/10 | 980/4156 | 706/2151 | 236/716 | chr5 | 115144627 | |||
| chr5:115144656 | C | T | 1 | a0010 | 1 | NA19001.hp1 | missense_variant | MODERATE | c.677G>A | p.Gly226Asp | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 4/10 | 951/4156 | 677/2151 | 226/716 | chr5 | 115144656 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:115144616 | A | G | 1 | a0001c0006 | 9 | HG02055.hp2 HG02615.hp1 HG02818.hp2 others(6): Show |
synonymous_variant | LOW | c.717T>C | p.Ser239Ser | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 4/10 | 991/4156 | 717/2151 | 239/716 | chr5 | 115144616 | |||
| chr5:115144667 | C | T | 8 | a0001c0004 a0001c0006 a0001c0009 others(5): Show |
163 | HG00280.hp1 HG00423.hp2 HG00558.hp1 others(160): Show |
synonymous_variant | LOW | c.666G>A | p.Leu222Leu | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 4/10 | 940/4156 | 666/2151 | 222/716 | chr5 | 115144667 | |||
| chr5:115147150 | T | C | 1 | a0001c0009 | 4 | HG02572.hp2 HG02622.hp1 NA19043.hp2 others(1): Show |
synonymous_variant | LOW | c.507A>G | p.Glu169Glu | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 3/10 | 781/4156 | 507/2151 | 169/716 | chr5 | 115147150 | |||
| chr5:115163666 | A | G | 1 | a0001c0010 | 3 | HG01243.hp2 HG02451.hp1 HG03471.hp1 |
synonymous_variant | LOW | c.114T>C | p.His38His | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/10 | 388/4156 | 114/2151 | 38/716 | chr5 | 115163666 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:115124842 | T | C | 10 | a0001c0001t0002 a0001c0004t0002 a0001c0004t0026 others(7): Show |
91 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*1661A>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 10/10 | 1661 | chr5 | 115124842 | ||||||
| chr5:115124883 | C | G | 30 | a0001c0001t0001 a0001c0001t0012 a0001c0001t0013 others(27): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
3_prime_UTR_variant | MODIFIER | c.*1620G>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 10/10 | 1620 | chr5 | 115124883 | ||||||
| chr5:115124925 | A | C | 1 | a0001c0004t0024 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1578T>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 10/10 | 1578 | chr5 | 115124925 | ||||||
| chr5:115125027 | TG | T | 1 | a0003c0003t0007 | 4 | HG00280.hp1 HG01106.hp1 HG01358.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1475delC | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 10/10 | 1475 | chr5 | 115125027 | ||||||
| chr5:115125029 | C | G | 1 | a0002c0002t0009 | 3 | HG02559.hp2 HG03453.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1474G>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 10/10 | 1474 | chr5 | 115125029 | ||||||
| chr5:115125051 | A | G | 3 | a0001c0004t0006 a0001c0004t0017 a0001c0009t0023 |
6 | HG02258.hp2 HG02622.hp1 HG02717.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1452T>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 10/10 | 1452 | chr5 | 115125051 | ||||||
| chr5:115125063 | T | C | 6 | a0001c0004t0005 a0001c0004t0014 a0001c0004t0016 others(3): Show |
13 | HG01074.hp1 HG02280.hp1 HG02451.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1440A>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 10/10 | 1440 | chr5 | 115125063 | ||||||
| chr5:115125175 | C | G | 1 | a0002c0002t0009 | 3 | HG02559.hp2 HG03453.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1328G>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 10/10 | 1328 | chr5 | 115125175 | ||||||
| chr5:115125272 | A | G | 1 | a0002c0005t0020 | 1 | NA19070.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1231T>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 10/10 | 1231 | chr5 | 115125272 | ||||||
| chr5:115125330 | G | A | 1 | a0003c0003t0008 | 4 | NA18967.hp2 NA19005.hp2 NA19057.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1173C>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 10/10 | 1173 | chr5 | 115125330 | ||||||
| chr5:115125436 | G | T | 1 | a0002c0002t0019 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1067C>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 10/10 | 1067 | chr5 | 115125436 | ||||||
| chr5:115125468 | G | T | 1 | a0001c0004t0014 | 2 | HG01074.hp1 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1035C>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 10/10 | 1035 | chr5 | 115125468 | ||||||
| chr5:115125473 | A | G | 1 | a0001c0004t0016 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1030T>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 10/10 | 1030 | chr5 | 115125473 | ||||||
| chr5:115125502 | TTATAA | T | 3 | a0001c0004t0005 a0001c0004t0016 a0001c0004t0018 |
7 | HG02280.hp1 HG02451.hp2 HG03098.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*996_*1000delTTATA | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 10/10 | 996 | chr5 | 115125502 | ||||||
| chr5:115125522 | C | T | 1 | a0001c0004t0017 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*981G>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 10/10 | 981 | chr5 | 115125522 | ||||||
| chr5:115125620 | G | A | 1 | a0001c0001t0021 | 1 | NA18612.hp1 | 3_prime_UTR_variant | MODIFIER | c.*883C>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 10/10 | 883 | chr5 | 115125620 | ||||||
| chr5:115125651 | T | C | 1 | a0001c0001t0022 | 1 | HG00639.hp1 | 3_prime_UTR_variant | MODIFIER | c.*852A>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 10/10 | 852 | chr5 | 115125651 | ||||||
| chr5:115125693 | C | T | 2 | a0001c0004t0006 a0001c0004t0017 |
5 | HG02258.hp2 HG02717.hp2 HG02896.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*810G>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 10/10 | 810 | chr5 | 115125693 | ||||||
| chr5:115125915 | T | A | 3 | a0001c0004t0024 a0001c0009t0011 a0001c0009t0023 |
5 | HG02572.hp2 HG02622.hp1 HG02717.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*588A>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 10/10 | 588 | chr5 | 115125915 | ||||||
| chr5:115125955 | T | C | 1 | a0001c0001t0012 | 3 | NA18945.hp2 NA18963.hp1 NA18973.hp2 |
3_prime_UTR_variant | MODIFIER | c.*548A>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 10/10 | 548 | chr5 | 115125955 | ||||||
| chr5:115126037 | T | C | 1 | a0002c0002t0025 | 1 | NA19009.hp2 | 3_prime_UTR_variant | MODIFIER | c.*466A>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 10/10 | 466 | chr5 | 115126037 | ||||||
| chr5:115126100 | A | G | 2 | a0001c0004t0005 a0001c0004t0016 |
6 | HG02280.hp1 HG02451.hp2 HG03098.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*403T>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 10/10 | 403 | chr5 | 115126100 | ||||||
| chr5:115126176 | C | G | 1 | a0001c0001t0015 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*327G>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 10/10 | 327 | chr5 | 115126176 | ||||||
| chr5:115126389 | T | C | 1 | a0001c0004t0026 | 1 | HG02155.hp2 | 3_prime_UTR_variant | MODIFIER | c.*114A>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 10/10 | 114 | chr5 | 115126389 | ||||||
| chr5:115169767 | T | C | 1 | a0001c0001t0027 | 1 | NA18983.hp1 | 5_prime_UTR_variant | MODIFIER | c.-133A>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 1/10 | 133 | chr5 | 115169767 | ||||||
| chr5:115169794 | G | C | 1 | a0001c0001t0028 | 1 | HG02257.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-160C>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 1/10 | chr5 | 115169794 | |||||||
| chr5:115169855 | T | C | 1 | a0001c0004t0014 | 2 | HG01074.hp1 NA19043.hp1 |
5_prime_UTR_variant | MODIFIER | c.-221A>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 1/10 | 221 | chr5 | 115169855 | ||||||
| chr5:115169904 | A | C | 1 | a0001c0001t0013 | 2 | HG02895.hp1 HG02897.hp2 |
5_prime_UTR_variant | MODIFIER | c.-270T>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 1/10 | 270 | chr5 | 115169904 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:115126892 | A | C | 339 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(336): Show |
400 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(397): Show |
intron_variant | MODIFIER | c.1797-35T>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 9/9 | chr5 | 115126892 | |||||||
| chr5:115126895 | A | C | 6 | a0001c0004t0005g0321 a0001c0004t0005g0322 a0001c0004t0005g0323 others(3): Show |
6 | HG02280.hp1 HG02451.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1797-38T>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 9/9 | chr5 | 115126895 | |||||||
| chr5:115126933 | T | C | 155 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0013 others(152): Show |
176 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(173): Show |
intron_variant | MODIFIER | c.1797-76A>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 9/9 | chr5 | 115126933 | |||||||
| chr5:115126971 | G | A | 1 | a0001c0001t0001g0232 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1797-114C>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 9/9 | chr5 | 115126971 | |||||||
| chr5:115127043 | C | T | 1 | a0001c0004t0024g0310 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1797-186G>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 9/9 | chr5 | 115127043 | |||||||
| chr5:115127044 | C | T | 27 | a0003c0003t0003g0028 a0003c0003t0003g0239 a0003c0003t0003g0243 others(24): Show |
30 | HG00280.hp1 HG00673.hp1 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.1797-187G>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 9/9 | chr5 | 115127044 | |||||||
| chr5:115127286 | T | C | 302 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(299): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.1797-429A>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 9/9 | chr5 | 115127286 | |||||||
| chr5:115127287 | G | A | 46 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0011 others(43): Show |
66 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.1797-430C>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 9/9 | chr5 | 115127287 | |||||||
| chr5:115127298 | T | C | 1 | a0001c0001t0001g0331 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1797-441A>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 9/9 | chr5 | 115127298 | |||||||
| chr5:115127430 | G | A | 1 | a0001c0001t0001g0319 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1797-573C>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 9/9 | chr5 | 115127430 | |||||||
| chr5:115127480 | G | A | 2 | a0002c0002t0009g0015 a0002c0002t0009g0059 |
3 | HG02559.hp2 HG03453.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1797-623C>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 9/9 | chr5 | 115127480 | |||||||
| chr5:115127487 | G | A | 11 | a0001c0004t0014g0346 a0001c0004t0014g0347 a0001c0006t0003g0240 others(8): Show |
11 | HG01074.hp1 HG02055.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.1797-630C>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 9/9 | chr5 | 115127487 | |||||||
| chr5:115127506 | G | A | 1 | a0001c0004t0001g0170 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1797-649C>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 9/9 | chr5 | 115127506 | |||||||
| chr5:115127559 | T | C | 2 | a0001c0001t0001g0272 a0001c0001t0001g0277 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1797-702A>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 9/9 | chr5 | 115127559 | |||||||
| chr5:115127648 | T | C | 1 | a0001c0001t0001g0081 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1797-791A>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 9/9 | chr5 | 115127648 | |||||||
| chr5:115127661 | G | A | 1 | a0003c0003t0003g0172 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1797-804C>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 9/9 | chr5 | 115127661 | |||||||
| chr5:115127912 | T | C | 1 | a0001c0001t0001g0139 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1797-1055A>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 9/9 | chr5 | 115127912 | |||||||
| chr5:115128043 | A | T | 1 | a0001c0001t0001g0269 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1797-1186T>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 9/9 | chr5 | 115128043 | |||||||
| chr5:115128061 | A | C | 1 | a0001c0004t0018g0308 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1797-1204T>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 9/9 | chr5 | 115128061 | |||||||
| chr5:115128089 | T | TGG | 117 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0017 others(114): Show |
133 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.1797-1234_1797-123 others(6): Show |
TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 9/9 | chr5 | 115128089 | |||||||
| chr5:115128089 | T | TGGG | 31 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0080 others(28): Show |
36 | HG00609.hp1 HG00639.hp1 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.1797-1235_1797-123 others(7): Show |
TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 9/9 | chr5 | 115128089 | |||||||
| chr5:115128153 | G | A | 1 | a0001c0001t0001g0046 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1797-1296C>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 9/9 | chr5 | 115128153 | |||||||
| chr5:115128237 | C | T | 33 | a0001c0004t0005g0321 a0001c0004t0005g0322 a0001c0004t0005g0323 others(30): Show |
36 | HG00280.hp1 HG00673.hp1 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.1797-1380G>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 9/9 | chr5 | 115128237 | |||||||
| chr5:115128318 | G | GA | 7 | a0002c0002t0002g0024 a0002c0002t0002g0180 a0002c0002t0002g0189 others(4): Show |
8 | HG01167.hp1 HG01433.hp1 HG01981.hp2 others(5): Show |
intron_variant | MODIFIER | c.1797-1462dupT | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 9/9 | chr5 | 115128318 | |||||||
| chr5:115128320 | G | A | 70 | a0001c0004t0002g0007 a0001c0004t0002g0187 a0001c0004t0002g0234 others(67): Show |
81 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.1797-1463C>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 9/9 | chr5 | 115128320 | |||||||
| chr5:115128327 | C | A | 1 | a0001c0004t0024g0310 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1797-1470G>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 9/9 | chr5 | 115128327 | |||||||
| chr5:115128369 | CA | C | 341 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(338): Show |
402 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(399): Show |
intron_variant | MODIFIER | c.1797-1513delT | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 9/9 | chr5 | 115128369 | |||||||
| chr5:115128386 | G | C | 2 | a0002c0005t0002g0219 a0002c0005t0002g0225 |
2 | HG01261.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1797-1529C>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 9/9 | chr5 | 115128386 | |||||||
| chr5:115128467 | T | C | 2 | a0001c0004t0006g0042 a0001c0009t0023g0033 |
2 | HG02622.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1797-1610A>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 9/9 | chr5 | 115128467 | |||||||
| chr5:115128515 | G | C | 16 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(13): Show |
18 | HG00323.hp2 HG00642.hp1 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.1797-1658C>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 9/9 | chr5 | 115128515 | |||||||
| chr5:115128608 | C | T | 67 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(64): Show |
91 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.1797-1751G>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 9/9 | chr5 | 115128608 | |||||||
| chr5:115128684 | G | A | 2 | a0001c0001t0001g0264 a0002c0002t0002g0203 |
2 | HG01884.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.1797-1827C>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 9/9 | chr5 | 115128684 | |||||||
| chr5:115128700 | T | C | 189 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0013 others(186): Show |
214 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.1797-1843A>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 9/9 | chr5 | 115128700 | |||||||
| chr5:115128721 | C | T | 1 | a0001c0001t0001g0342 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1797-1864G>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 9/9 | chr5 | 115128721 | |||||||
| chr5:115128758 | C | CAAAAAA | 13 | a0001c0004t0001g0034 a0001c0004t0001g0168 a0001c0004t0006g0041 others(10): Show |
13 | HG01074.hp1 HG02055.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.1796+1828_1796+183 others(10): Show |
TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 9/9 | chr5 | 115128758 | |||||||
| chr5:115128758 | C | CAAAAAAA others(3): Show |
5 | a0001c0001t0001g0124 a0001c0001t0001g0166 a0001c0001t0001g0231 others(2): Show |
5 | HG00639.hp1 HG01891.hp2 HG02040.hp2 others(2): Show |
intron_variant | MODIFIER | c.1796+1824_1796+183 others(14): Show |
TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 9/9 | chr5 | 115128758 | |||||||
| chr5:115128758 | C | CAAAAAAA others(4): Show |
7 | a0001c0001t0001g0119 a0001c0001t0001g0127 a0001c0001t0001g0144 others(4): Show |
7 | HG00323.hp2 HG00735.hp2 HG00738.hp1 others(4): Show |
intron_variant | MODIFIER | c.1796+1823_1796+183 others(15): Show |
TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 9/9 | chr5 | 115128758 | |||||||
| chr5:115128758 | C | CAAAAAAA others(5): Show |
7 | a0001c0001t0001g0135 a0001c0001t0001g0143 a0001c0001t0001g0145 others(4): Show |
7 | HG00738.hp2 HG01074.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1796+1822_1796+183 others(16): Show |
TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 9/9 | chr5 | 115128758 | |||||||
| chr5:115128758 | C | CAAAAAAA others(6): Show |
1 | a0001c0001t0001g0147 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1796+1821_1796+183 others(17): Show |
TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 9/9 | chr5 | 115128758 | |||||||
| chr5:115128758 | C | CAAAAAAA others(7): Show |
2 | a0001c0001t0001g0291 a0001c0010t0001g0079 |
2 | HG01243.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1796+1820_1796+183 others(18): Show |
TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 9/9 | chr5 | 115128758 | |||||||
| chr5:115128758 | C | CAAAAAAA others(8): Show |
2 | a0001c0001t0001g0118 a0001c0001t0001g0153 |
2 | HG01517.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.1796+1819_1796+183 others(19): Show |
TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 9/9 | chr5 | 115128758 | |||||||
| chr5:115128758 | C | CAAAAAAA others(9): Show |
7 | a0001c0001t0001g0121 a0001c0001t0001g0129 a0001c0001t0001g0136 others(4): Show |
7 | HG00673.hp2 HG01358.hp2 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.1796+1818_1796+183 others(20): Show |
TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 9/9 | chr5 | 115128758 | |||||||
| chr5:115128758 | C | CAAAAAAA others(10): Show |
9 | a0001c0001t0001g0128 a0001c0001t0001g0132 a0001c0001t0001g0133 others(6): Show |
9 | HG00280.hp2 HG00423.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.1796+1817_1796+183 others(21): Show |
TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 9/9 | chr5 | 115128758 | |||||||
| chr5:115128758 | C | CAAAAAAA others(11): Show |
2 | a0001c0001t0001g0139 a0001c0001t0001g0157 |
2 | HG01192.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.1796+1816_1796+183 others(22): Show |
TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 9/9 | chr5 | 115128758 | |||||||
| chr5:115128758 | C | CAAAAAAA others(13): Show |
6 | a0001c0001t0001g0091 a0001c0001t0001g0107 a0001c0001t0001g0108 others(3): Show |
6 | HG01070.hp1 HG01515.hp1 HG03492.hp2 others(3): Show |
intron_variant | MODIFIER | c.1796+1814_1796+183 others(24): Show |
TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 9/9 | chr5 | 115128758 | |||||||
| chr5:115128758 | C | CAAAAAAA others(14): Show |
10 | a0001c0001t0001g0017 a0001c0001t0001g0105 a0001c0001t0001g0109 others(7): Show |
11 | HG01069.hp1 HG02015.hp1 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.1796+1813_1796+183 others(25): Show |
TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 9/9 | chr5 | 115128758 | |||||||
| chr5:115128758 | C | CAAAAAAA others(15): Show |
4 | a0001c0001t0001g0112 a0001c0001t0001g0150 a0001c0001t0001g0160 others(1): Show |
4 | HG00733.hp2 HG01981.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.1796+1812_1796+183 others(26): Show |
TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 9/9 | chr5 | 115128758 | |||||||
| chr5:115128758 | C | CAAAAAAA others(16): Show |
2 | a0001c0001t0001g0158 a0002c0002t0010g0333 |
2 | HG03654.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1796+1811_1796+183 others(27): Show |
TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 9/9 | chr5 | 115128758 | |||||||
| chr5:115128758 | C | CAAAAAAA others(17): Show |
2 | a0001c0001t0001g0230 a0005c0011t0001g0340 |
2 | HG00099.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.1796+1810_1796+183 others(28): Show |
TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 9/9 | chr5 | 115128758 | |||||||
| chr5:115128758 | C | CAAAAAAA others(19): Show |
1 | a0005c0011t0001g0341 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1796+1808_1796+183 others(30): Show |
TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 9/9 | chr5 | 115128758 | |||||||
| chr5:115128758 | CA | C | 75 | a0001c0001t0001g0050 a0001c0001t0001g0058 a0001c0001t0001g0117 others(72): Show |
87 | HG00558.hp1 HG00558.hp2 HG01069.hp2 others(84): Show |
intron_variant | MODIFIER | c.1796+1833delT | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 9/9 | chr5 | 115128758 | |||||||
| chr5:115128758 | CAA | C | 41 | a0001c0009t0011g0016 a0001c0009t0011g0051 a0002c0002t0002g0214 others(38): Show |
47 | HG00280.hp1 HG00673.hp1 HG00733.hp1 others(44): Show |
intron_variant | MODIFIER | c.1796+1832_1796+183 others(6): Show |
TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 9/9 | chr5 | 115128758 | |||||||
| chr5:115128758 | CAAA | C | 4 | a0001c0001t0001g0012 a0001c0001t0001g0281 a0001c0001t0001g0298 others(1): Show |
6 | HG01361.hp2 HG01433.hp2 NA18956.hp2 others(3): Show |
intron_variant | MODIFIER | c.1796+1831_1796+183 others(7): Show |
TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 9/9 | chr5 | 115128758 | |||||||
| chr5:115128758 | CAAAA | C | 60 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(57): Show |
82 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.1796+1830_1796+183 others(8): Show |
TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 9/9 | chr5 | 115128758 | |||||||
| chr5:115128758 | CAAAAAAA | C | 6 | a0001c0001t0001g0060 a0001c0001t0001g0080 a0001c0001t0001g0088 others(3): Show |
6 | HG00140.hp2 HG01952.hp1 HG02083.hp1 others(3): Show |
intron_variant | MODIFIER | c.1796+1827_1796+183 others(11): Show |
TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 9/9 | chr5 | 115128758 | |||||||
| chr5:115128758 | CAAAAAAA others(1): Show |
C | 13 | a0001c0001t0001g0004 a0001c0001t0001g0019 a0001c0001t0001g0020 others(10): Show |
19 | HG00609.hp1 HG00642.hp2 HG01123.hp2 others(16): Show |
intron_variant | MODIFIER | c.1796+1826_1796+183 others(12): Show |
TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 9/9 | chr5 | 115128758 | |||||||
| chr5:115128758 | CAAAAAAA others(4): Show |
C | 3 | a0001c0001t0001g0101 a0001c0001t0001g0103 a0001c0001t0001g0161 |
3 | NA18966.hp1 NA18980.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1796+1823_1796+183 others(15): Show |
TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 9/9 | chr5 | 115128758 | |||||||
| chr5:115128758 | CAAAAAAA others(5): Show |
C | 15 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0094 others(12): Show |
22 | HG02015.hp2 HG02027.hp2 HG02080.hp1 others(19): Show |
intron_variant | MODIFIER | c.1796+1822_1796+183 others(16): Show |
TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 9/9 | chr5 | 115128758 | |||||||
| chr5:115128796 | T | A | 1 | a0001c0004t0018g0308 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1796+1796A>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 9/9 | chr5 | 115128796 | |||||||
| chr5:115128854 | C | G | 1 | a0001c0001t0001g0112 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1796+1738G>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 9/9 | chr5 | 115128854 | |||||||
| chr5:115129023 | G | A | 1 | a0001c0004t0024g0310 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1796+1569C>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 9/9 | chr5 | 115129023 | |||||||
| chr5:115129045 | C | T | 1 | a0002c0002t0002g0067 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1796+1547G>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 9/9 | chr5 | 115129045 | |||||||
| chr5:115129415 | G | A | 2 | a0001c0009t0011g0016 a0001c0009t0011g0051 |
3 | HG02572.hp2 NA19043.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1796+1177C>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 9/9 | chr5 | 115129415 | |||||||
| chr5:115129426 | T | C | 1 | a0001c0004t0001g0063 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1796+1166A>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 9/9 | chr5 | 115129426 | |||||||
| chr5:115129483 | G | A | 1 | a0001c0001t0001g0095 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1796+1109C>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 9/9 | chr5 | 115129483 | |||||||
| chr5:115129486 | A | G | 1 | a0001c0001t0001g0044 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1796+1106T>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 9/9 | chr5 | 115129486 | |||||||
| chr5:115129499 | G | A | 27 | a0003c0003t0003g0028 a0003c0003t0003g0239 a0003c0003t0003g0243 others(24): Show |
30 | HG00280.hp1 HG00673.hp1 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.1796+1093C>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 9/9 | chr5 | 115129499 | |||||||
| chr5:115129510 | A | G | 4 | a0001c0001t0001g0018 a0001c0001t0001g0094 a0001c0001t0001g0095 others(1): Show |
5 | NA18952.hp1 NA18956.hp1 NA18967.hp1 others(2): Show |
intron_variant | MODIFIER | c.1796+1082T>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 9/9 | chr5 | 115129510 | |||||||
| chr5:115129582 | A | G | 3 | a0002c0002t0009g0015 a0002c0002t0009g0059 a0002c0002t0019g0049 |
4 | HG02559.hp2 HG03453.hp2 NA20300.hp1 others(1): Show |
intron_variant | MODIFIER | c.1796+1010T>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 9/9 | chr5 | 115129582 | |||||||
| chr5:115129666 | T | C | 1 | a0001c0001t0001g0278 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1796+926A>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 9/9 | chr5 | 115129666 | |||||||
| chr5:115129821 | C | A | 1 | a0001c0004t0006g0054 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1796+771G>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 9/9 | chr5 | 115129821 | |||||||
| chr5:115130006 | G | A | 338 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(335): Show |
399 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(396): Show |
intron_variant | MODIFIER | c.1796+586C>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 9/9 | chr5 | 115130006 | |||||||
| chr5:115130013 | T | C | 3 | a0001c0006t0003g0240 a0001c0006t0003g0241 a0001c0006t0003g0242 |
3 | HG02055.hp2 HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1796+579A>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 9/9 | chr5 | 115130013 | |||||||
| chr5:115130059 | G | T | 2 | a0001c0004t0001g0056 a0001c0004t0001g0057 |
2 | HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1796+533C>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 9/9 | chr5 | 115130059 | |||||||
| chr5:115130157 | T | C | 6 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(3): Show |
6 | HG02055.hp1 HG02723.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1796+435A>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 9/9 | chr5 | 115130157 | |||||||
| chr5:115130290 | G | A | 6 | a0001c0004t0005g0321 a0001c0004t0005g0322 a0001c0004t0005g0323 others(3): Show |
6 | HG02280.hp1 HG02451.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1796+302C>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 9/9 | chr5 | 115130290 | |||||||
| chr5:115130448 | C | T | 145 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(142): Show |
179 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.1796+144G>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 9/9 | chr5 | 115130448 | |||||||
| chr5:115130581 | C | T | 1 | a0002c0002t0002g0086 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1796+11G>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 9/9 | chr5 | 115130581 | |||||||
| chr5:115131128 | A | AG | 2 | a0001c0001t0001g0021 a0001c0001t0001g0309 |
3 | HG02486.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1499-240_1499-239i others(3): Show |
TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 8/9 | chr5 | 115131128 | |||||||
| chr5:115131130 | G | A | 2 | a0001c0001t0001g0021 a0001c0001t0001g0309 |
3 | HG02486.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1499-241C>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 8/9 | chr5 | 115131130 | |||||||
| chr5:115131237 | A | G | 1 | a0001c0001t0001g0297 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1499-348T>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 8/9 | chr5 | 115131237 | |||||||
| chr5:115131238 | A | C | 1 | a0001c0001t0013g0014 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1499-349T>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 8/9 | chr5 | 115131238 | |||||||
| chr5:115131372 | T | G | 1 | a0001c0001t0001g0137 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1499-483A>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 8/9 | chr5 | 115131372 | |||||||
| chr5:115131413 | G | C | 1 | a0001c0004t0024g0310 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1499-524C>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 8/9 | chr5 | 115131413 | |||||||
| chr5:115131610 | A | T | 79 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(76): Show |
104 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.1499-721T>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 8/9 | chr5 | 115131610 | |||||||
| chr5:115131702 | C | T | 2 | a0003c0003t0003g0052 a0003c0008t0003g0022 |
3 | HG02647.hp2 HG02965.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1499-813G>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 8/9 | chr5 | 115131702 | |||||||
| chr5:115131998 | T | C | 3 | a0001c0009t0011g0016 a0001c0009t0011g0051 a0001c0009t0023g0033 |
4 | HG02572.hp2 HG02622.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1499-1109A>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 8/9 | chr5 | 115131998 | |||||||
| chr5:115132016 | A | G | 1 | a0001c0001t0001g0280 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1499-1127T>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 8/9 | chr5 | 115132016 | |||||||
| chr5:115132184 | A | ATG | 175 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0013 others(172): Show |
201 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.1499-1297_1499-129 others(6): Show |
TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 8/9 | chr5 | 115132184 | |||||||
| chr5:115132184 | A | ATGTG | 9 | a0001c0001t0001g0100 a0001c0001t0001g0149 a0001c0004t0001g0034 others(6): Show |
10 | HG01257.hp2 HG02027.hp2 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1499-1299_1499-129 others(8): Show |
TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 8/9 | chr5 | 115132184 | |||||||
| chr5:115132206 | A | G | 337 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(334): Show |
398 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(395): Show |
intron_variant | MODIFIER | c.1499-1317T>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 8/9 | chr5 | 115132206 | |||||||
| chr5:115132208 | A | G | 183 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(180): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.1499-1319T>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 8/9 | chr5 | 115132208 | |||||||
| chr5:115132271 | C | A | 1 | a0001c0001t0001g0319 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1499-1382G>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 8/9 | chr5 | 115132271 | |||||||
| chr5:115132272 | G | A | 1 | a0001c0001t0001g0319 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1499-1383C>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 8/9 | chr5 | 115132272 | |||||||
| chr5:115132276 | A | G | 1 | a0002c0005t0004g0293 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1499-1387T>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 8/9 | chr5 | 115132276 | |||||||
| chr5:115132369 | C | G | 29 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(26): Show |
43 | HG01358.hp2 HG02056.hp1 HG02071.hp1 others(40): Show |
intron_variant | MODIFIER | c.1499-1480G>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 8/9 | chr5 | 115132369 | |||||||
| chr5:115132491 | C | T | 3 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 |
3 | HG01192.hp1 HG02109.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.1498+1369G>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 8/9 | chr5 | 115132491 | |||||||
| chr5:115132550 | GA | G | 147 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0013 others(144): Show |
171 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.1498+1309delT | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 8/9 | chr5 | 115132550 | |||||||
| chr5:115132617 | T | C | 1 | a0001c0001t0001g0102 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1498+1243A>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 8/9 | chr5 | 115132617 | |||||||
| chr5:115132651 | T | C | 1 | a0004c0007t0003g0253 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1498+1209A>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 8/9 | chr5 | 115132651 | |||||||
| chr5:115133086 | G | A | 2 | a0001c0004t0001g0056 a0001c0004t0001g0057 |
2 | HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1498+774C>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 8/9 | chr5 | 115133086 | |||||||
| chr5:115133182 | A | G | 1 | a0001c0001t0013g0014 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1498+678T>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 8/9 | chr5 | 115133182 | |||||||
| chr5:115133326 | A | C | 154 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0013 others(151): Show |
176 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(173): Show |
intron_variant | MODIFIER | c.1498+534T>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 8/9 | chr5 | 115133326 | |||||||
| chr5:115133328 | T | G | 1 | a0002c0002t0010g0171 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1498+532A>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 8/9 | chr5 | 115133328 | |||||||
| chr5:115133341 | C | G | 1 | a0001c0001t0013g0014 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1498+519G>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 8/9 | chr5 | 115133341 | |||||||
| chr5:115134154 | G | A | 74 | a0001c0004t0026g0074 a0002c0002t0002g0008 a0002c0002t0002g0009 others(71): Show |
85 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(82): Show |
splice_region_variant&intron_variant | LOW | c.1211-7C>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 7/9 | chr5 | 115134154 | |||||||
| chr5:115134280 | A | G | 130 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0013 others(127): Show |
150 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.1211-133T>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 7/9 | chr5 | 115134280 | |||||||
| chr5:115134316 | T | G | 132 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0013 others(129): Show |
152 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.1211-169A>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 7/9 | chr5 | 115134316 | |||||||
| chr5:115134428 | C | G | 2 | a0002c0002t0010g0333 a0002c0002t0010g0334 |
2 | HG03654.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.1211-281G>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 7/9 | chr5 | 115134428 | |||||||
| chr5:115134546 | A | AT | 32 | a0001c0001t0001g0095 a0001c0004t0024g0310 a0003c0003t0003g0028 others(29): Show |
36 | HG00280.hp1 HG00673.hp1 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.1211-400dupA | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 7/9 | chr5 | 115134546 | |||||||
| chr5:115134546 | AT | A | 120 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0013 others(117): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.1211-400delA | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 7/9 | chr5 | 115134546 | |||||||
| chr5:115134547 | T | A | 1 | a0002c0002t0002g0209 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1211-400A>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 7/9 | chr5 | 115134547 | |||||||
| chr5:115134567 | G | C | 1 | a0001c0001t0001g0327 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1211-420C>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 7/9 | chr5 | 115134567 | |||||||
| chr5:115134598 | T | C | 1 | a0001c0001t0001g0267 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1211-451A>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 7/9 | chr5 | 115134598 | |||||||
| chr5:115134653 | G | A | 1 | a0003c0003t0003g0245 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1211-506C>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 7/9 | chr5 | 115134653 | |||||||
| chr5:115134655 | C | T | 5 | a0003c0003t0001g0040 a0003c0003t0003g0036 a0003c0003t0003g0037 others(2): Show |
5 | HG02145.hp1 HG02559.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1211-508G>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 7/9 | chr5 | 115134655 | |||||||
| chr5:115134890 | C | T | 1 | a0007c0014t0001g0131 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1211-743G>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 7/9 | chr5 | 115134890 | |||||||
| chr5:115134950 | A | G | 2 | a0001c0001t0001g0335 a0001c0001t0001g0339 |
2 | HG00738.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.1211-803T>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 7/9 | chr5 | 115134950 | |||||||
| chr5:115135206 | C | T | 1 | a0001c0001t0001g0291 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1211-1059G>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 7/9 | chr5 | 115135206 | |||||||
| chr5:115135270 | A | T | 3 | a0001c0004t0005g0325 a0002c0002t0010g0333 a0002c0002t0010g0334 |
3 | HG03098.hp1 HG03654.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.1211-1123T>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 7/9 | chr5 | 115135270 | |||||||
| chr5:115135281 | C | CTTCTTTT others(3): Show |
1 | a0001c0001t0001g0284 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1211-1135_1211-113 others(14): Show |
TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 7/9 | chr5 | 115135281 | |||||||
| chr5:115135300 | C | G | 1 | a0007c0014t0001g0131 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1211-1153G>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 7/9 | chr5 | 115135300 | |||||||
| chr5:115135373 | G | A | 78 | a0001c0004t0026g0074 a0002c0002t0002g0008 a0002c0002t0002g0009 others(75): Show |
90 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.1211-1226C>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 7/9 | chr5 | 115135373 | |||||||
| chr5:115135412 | C | A | 115 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0013 others(112): Show |
134 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.1211-1265G>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 7/9 | chr5 | 115135412 | |||||||
| chr5:115135433 | G | A | 78 | a0001c0004t0026g0074 a0002c0002t0002g0008 a0002c0002t0002g0009 others(75): Show |
90 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.1211-1286C>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 7/9 | chr5 | 115135433 | |||||||
| chr5:115135443 | T | C | 160 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(157): Show |
197 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.1211-1296A>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 7/9 | chr5 | 115135443 | |||||||
| chr5:115135451 | T | C | 1 | a0003c0003t0008g0251 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1211-1304A>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 7/9 | chr5 | 115135451 | |||||||
| chr5:115135479 | T | TA | 82 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(79): Show |
107 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.1211-1333dupT | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 7/9 | chr5 | 115135479 | |||||||
| chr5:115135524 | T | C | 38 | a0001c0001t0001g0095 a0001c0004t0024g0310 a0003c0003t0001g0040 others(35): Show |
42 | HG00280.hp1 HG00673.hp1 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.1211-1377A>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 7/9 | chr5 | 115135524 | |||||||
| chr5:115135612 | C | T | 1 | a0001c0004t0018g0308 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1210+1388G>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 7/9 | chr5 | 115135612 | |||||||
| chr5:115135757 | A | C | 2 | a0001c0004t0001g0168 a0001c0004t0001g0169 |
2 | HG02257.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1210+1243T>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 7/9 | chr5 | 115135757 | |||||||
| chr5:115135831 | T | A | 1 | a0001c0004t0001g0170 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1210+1169A>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 7/9 | chr5 | 115135831 | |||||||
| chr5:115135959 | G | C | 339 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(336): Show |
400 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(397): Show |
intron_variant | MODIFIER | c.1210+1041C>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 7/9 | chr5 | 115135959 | |||||||
| chr5:115135989 | T | A | 1 | a0002c0002t0002g0316 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1210+1011A>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 7/9 | chr5 | 115135989 | |||||||
| chr5:115136100 | C | A | 35 | a0001c0001t0001g0095 a0003c0003t0001g0040 a0003c0003t0003g0028 others(32): Show |
38 | HG00280.hp1 HG00673.hp1 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.1210+900G>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 7/9 | chr5 | 115136100 | |||||||
| chr5:115136169 | C | T | 1 | a0001c0001t0001g0030 | 2 | NA18948.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.1210+831G>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 7/9 | chr5 | 115136169 | |||||||
| chr5:115136215 | T | C | 1 | a0002c0002t0010g0171 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1210+785A>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 7/9 | chr5 | 115136215 | |||||||
| chr5:115136305 | C | CACAA | 339 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(336): Show |
400 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(397): Show |
intron_variant | MODIFIER | c.1210+694_1210+695i others(6): Show |
TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 7/9 | chr5 | 115136305 | |||||||
| chr5:115136614 | AGGAAAAA others(3): Show |
A | 1 | a0002c0002t0002g0195 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1210+376_1210+385d others(12): Show |
TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 7/9 | chr5 | 115136614 | |||||||
| chr5:115136624 | T | A | 1 | a0002c0002t0002g0214 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1210+376A>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 7/9 | chr5 | 115136624 | |||||||
| chr5:115136792 | A | T | 1 | a0001c0001t0001g0080 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1210+208T>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 7/9 | chr5 | 115136792 | |||||||
| chr5:115136883 | G | C | 2 | a0001c0004t0014g0346 a0001c0004t0014g0347 |
2 | HG01074.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1210+117C>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 7/9 | chr5 | 115136883 | |||||||
| chr5:115137291 | A | G | 2 | a0002c0002t0010g0171 a0002c0002t0019g0049 |
2 | HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1085+72T>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 6/9 | chr5 | 115137291 | |||||||
| chr5:115137296 | G | C | 1 | a0001c0001t0013g0014 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1085+67C>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 6/9 | chr5 | 115137296 | |||||||
| chr5:115137298 | G | A | 1 | a0002c0002t0002g0226 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1085+65C>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 6/9 | chr5 | 115137298 | |||||||
| chr5:115137339 | A | C | 1 | a0002c0002t0002g0203 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1085+24T>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 6/9 | chr5 | 115137339 | |||||||
| chr5:115137847 | C | T | 339 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(336): Show |
400 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(397): Show |
intron_variant | MODIFIER | c.832-231G>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 5/9 | chr5 | 115137847 | |||||||
| chr5:115138043 | T | C | 7 | a0003c0003t0001g0040 a0003c0003t0003g0036 a0003c0003t0003g0037 others(4): Show |
7 | HG02145.hp1 HG02559.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.832-427A>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 5/9 | chr5 | 115138043 | |||||||
| chr5:115138102 | T | C | 1 | a0001c0001t0001g0320 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.832-486A>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 5/9 | chr5 | 115138102 | |||||||
| chr5:115138200 | G | A | 215 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(212): Show |
258 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.832-584C>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 5/9 | chr5 | 115138200 | |||||||
| chr5:115138250 | C | T | 6 | a0003c0003t0003g0173 a0003c0003t0003g0174 a0003c0003t0003g0175 others(3): Show |
6 | HG02280.hp2 HG02970.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.832-634G>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 5/9 | chr5 | 115138250 | |||||||
| chr5:115138256 | C | T | 1 | a0002c0002t0002g0185 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.832-640G>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 5/9 | chr5 | 115138256 | |||||||
| chr5:115138345 | C | G | 2 | a0001c0004t0014g0346 a0001c0004t0014g0347 |
2 | HG01074.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.832-729G>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 5/9 | chr5 | 115138345 | |||||||
| chr5:115138350 | C | T | 1 | a0001c0004t0005g0322 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.832-734G>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 5/9 | chr5 | 115138350 | |||||||
| chr5:115138530 | T | C | 1 | a0001c0004t0024g0310 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.832-914A>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 5/9 | chr5 | 115138530 | |||||||
| chr5:115138570 | GA | G | 28 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(25): Show |
42 | HG02056.hp1 HG02071.hp1 HG02132.hp2 others(39): Show |
intron_variant | MODIFIER | c.832-955delT | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 5/9 | chr5 | 115138570 | |||||||
| chr5:115138573 | A | T | 1 | a0003c0003t0008g0251 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.832-957T>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 5/9 | chr5 | 115138573 | |||||||
| chr5:115138745 | G | C | 3 | a0003c0003t0001g0040 a0003c0003t0003g0037 a0003c0003t0003g0039 |
3 | HG02559.hp1 HG02572.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.832-1129C>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 5/9 | chr5 | 115138745 | |||||||
| chr5:115138847 | G | A | 2 | a0001c0001t0001g0302 a0001c0001t0001g0305 |
2 | HG01943.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.832-1231C>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 5/9 | chr5 | 115138847 | |||||||
| chr5:115138855 | G | A | 1 | a0001c0001t0013g0014 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.832-1239C>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 5/9 | chr5 | 115138855 | |||||||
| chr5:115138860 | G | T | 3 | a0001c0001t0001g0021 a0001c0001t0001g0309 a0003c0008t0003g0022 |
5 | HG02486.hp2 HG02647.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.832-1244C>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 5/9 | chr5 | 115138860 | |||||||
| chr5:115138885 | G | A | 1 | a0002c0002t0019g0049 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.832-1269C>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 5/9 | chr5 | 115138885 | |||||||
| chr5:115138961 | G | A | 1 | a0003c0003t0003g0175 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.832-1345C>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 5/9 | chr5 | 115138961 | |||||||
| chr5:115139012 | G | A | 2 | a0001c0004t0001g0056 a0001c0004t0001g0057 |
2 | HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.832-1396C>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 5/9 | chr5 | 115139012 | |||||||
| chr5:115139232 | T | C | 75 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(72): Show |
101 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.832-1616A>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 5/9 | chr5 | 115139232 | |||||||
| chr5:115139246 | G | A | 2 | a0002c0002t0002g0023 a0002c0002t0002g0181 |
3 | NA18979.hp2 NA19006.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.832-1630C>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 5/9 | chr5 | 115139246 | |||||||
| chr5:115139277 | G | T | 1 | a0001c0004t0024g0310 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.832-1661C>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 5/9 | chr5 | 115139277 | |||||||
| chr5:115139312 | C | A | 340 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(337): Show |
401 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(398): Show |
intron_variant | MODIFIER | c.832-1696G>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 5/9 | chr5 | 115139312 | |||||||
| chr5:115139373 | G | A | 2 | a0001c0001t0001g0153 a0001c0001t0001g0156 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.832-1757C>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 5/9 | chr5 | 115139373 | |||||||
| chr5:115139464 | G | C | 68 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(65): Show |
92 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.831+1815C>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 5/9 | chr5 | 115139464 | |||||||
| chr5:115139483 | T | C | 188 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(185): Show |
230 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.831+1796A>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 5/9 | chr5 | 115139483 | |||||||
| chr5:115139519 | G | T | 5 | a0002c0002t0002g0008 a0002c0002t0002g0202 a0002c0002t0002g0206 others(2): Show |
7 | HG01069.hp2 HG01071.hp1 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.831+1760C>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 5/9 | chr5 | 115139519 | |||||||
| chr5:115139530 | T | C | 12 | a0001c0004t0001g0063 a0001c0004t0014g0346 a0001c0004t0014g0347 others(9): Show |
12 | HG01074.hp1 HG02055.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.831+1749A>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 5/9 | chr5 | 115139530 | |||||||
| chr5:115139601 | C | A | 1 | a0003c0003t0003g0173 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.831+1678G>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 5/9 | chr5 | 115139601 | |||||||
| chr5:115139693 | T | A | 3 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0099 |
3 | HG00140.hp2 HG01123.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.831+1586A>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 5/9 | chr5 | 115139693 | |||||||
| chr5:115139730 | T | C | 6 | a0001c0001t0001g0107 a0001c0001t0001g0110 a0001c0001t0001g0111 others(3): Show |
6 | HG00741.hp2 HG01069.hp1 HG01070.hp1 others(3): Show |
intron_variant | MODIFIER | c.831+1549A>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 5/9 | chr5 | 115139730 | |||||||
| chr5:115139768 | T | C | 1 | a0003c0003t0003g0052 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.831+1511A>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 5/9 | chr5 | 115139768 | |||||||
| chr5:115139835 | C | A | 1 | a0001c0001t0001g0090 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.831+1444G>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 5/9 | chr5 | 115139835 | |||||||
| chr5:115140002 | A | G | 79 | a0001c0001t0002g0064 a0001c0001t0002g0065 a0001c0004t0002g0007 others(76): Show |
92 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.831+1277T>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 5/9 | chr5 | 115140002 | |||||||
| chr5:115140077 | T | C | 35 | a0001c0001t0001g0095 a0003c0003t0001g0040 a0003c0003t0003g0028 others(32): Show |
38 | HG00280.hp1 HG00673.hp1 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.831+1202A>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 5/9 | chr5 | 115140077 | |||||||
| chr5:115140202 | G | A | 2 | a0001c0001t0002g0064 a0001c0001t0002g0065 |
2 | HG02080.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.831+1077C>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 5/9 | chr5 | 115140202 | |||||||
| chr5:115140213 | T | G | 2 | a0002c0005t0001g0053 a0002c0005t0001g0055 |
2 | HG02965.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.831+1066A>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 5/9 | chr5 | 115140213 | |||||||
| chr5:115140372 | C | T | 4 | a0002c0002t0009g0015 a0002c0002t0009g0059 a0002c0002t0010g0171 others(1): Show |
5 | HG02559.hp2 HG02723.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.831+907G>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 5/9 | chr5 | 115140372 | |||||||
| chr5:115140689 | G | T | 221 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(218): Show |
263 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.831+590C>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 5/9 | chr5 | 115140689 | |||||||
| chr5:115140773 | T | C | 3 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 |
3 | HG01192.hp1 HG02109.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.831+506A>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 5/9 | chr5 | 115140773 | |||||||
| chr5:115140860 | A | G | 14 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0094 others(11): Show |
21 | HG02027.hp2 HG02080.hp1 HG02155.hp1 others(18): Show |
intron_variant | MODIFIER | c.831+419T>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 5/9 | chr5 | 115140860 | |||||||
| chr5:115141072 | A | G | 3 | a0002c0002t0002g0194 a0002c0002t0002g0201 a0002c0002t0002g0211 |
3 | HG02735.hp2 HG03239.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.831+207T>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 5/9 | chr5 | 115141072 | |||||||
| chr5:115141113 | T | A | 3 | a0001c0001t0001g0021 a0001c0001t0001g0309 a0003c0008t0003g0022 |
5 | HG02486.hp2 HG02647.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.831+166A>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 5/9 | chr5 | 115141113 | |||||||
| chr5:115141604 | G | A | 3 | a0002c0002t0009g0015 a0002c0002t0009g0059 a0002c0002t0019g0049 |
4 | HG02559.hp2 HG03453.hp2 NA20300.hp1 others(1): Show |
intron_variant | MODIFIER | c.736-230C>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 4/9 | chr5 | 115141604 | |||||||
| chr5:115141646 | C | T | 205 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(202): Show |
244 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.736-272G>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 4/9 | chr5 | 115141646 | |||||||
| chr5:115141774 | G | A | 1 | a0001c0001t0003g0084 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.736-400C>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 4/9 | chr5 | 115141774 | |||||||
| chr5:115141783 | C | A | 2 | a0001c0004t0001g0168 a0001c0004t0001g0169 |
2 | HG02257.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.736-409G>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 4/9 | chr5 | 115141783 | |||||||
| chr5:115141831 | T | C | 1 | a0003c0003t0003g0175 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.736-457A>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 4/9 | chr5 | 115141831 | |||||||
| chr5:115141836 | T | C | 2 | a0002c0005t0001g0053 a0002c0005t0001g0055 |
2 | HG02965.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.736-462A>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 4/9 | chr5 | 115141836 | |||||||
| chr5:115141887 | T | A | 3 | a0001c0001t0001g0182 a0001c0001t0001g0279 a0001c0001t0001g0318 |
3 | NA18959.hp2 NA18999.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.736-513A>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 4/9 | chr5 | 115141887 | |||||||
| chr5:115141957 | T | C | 77 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(74): Show |
101 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.736-583A>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 4/9 | chr5 | 115141957 | |||||||
| chr5:115142051 | C | T | 1 | a0003c0003t0007g0261 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.736-677G>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 4/9 | chr5 | 115142051 | |||||||
| chr5:115142129 | T | C | 2 | a0002c0005t0001g0053 a0002c0005t0001g0055 |
2 | HG02965.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.736-755A>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 4/9 | chr5 | 115142129 | |||||||
| chr5:115142188 | A | G | 2 | a0001c0004t0001g0170 a0001c0004t0018g0308 |
2 | HG03130.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.736-814T>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 4/9 | chr5 | 115142188 | |||||||
| chr5:115142196 | C | A | 1 | a0001c0004t0024g0310 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.736-822G>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 4/9 | chr5 | 115142196 | |||||||
| chr5:115142245 | C | G | 2 | a0001c0009t0011g0016 a0001c0009t0011g0051 |
3 | HG02572.hp2 NA19043.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.736-871G>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 4/9 | chr5 | 115142245 | |||||||
| chr5:115142345 | C | G | 8 | a0001c0001t0001g0106 a0002c0002t0010g0171 a0003c0003t0003g0173 others(5): Show |
8 | HG02280.hp2 HG02723.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.736-971G>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 4/9 | chr5 | 115142345 | |||||||
| chr5:115142440 | T | G | 1 | a0001c0001t0001g0299 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.736-1066A>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 4/9 | chr5 | 115142440 | |||||||
| chr5:115142557 | A | T | 1 | a0005c0011t0001g0341 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.736-1183T>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 4/9 | chr5 | 115142557 | |||||||
| chr5:115142703 | A | G | 2 | a0002c0005t0001g0053 a0002c0005t0001g0055 |
2 | HG02965.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.736-1329T>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 4/9 | chr5 | 115142703 | |||||||
| chr5:115142744 | C | G | 7 | a0002c0002t0010g0171 a0003c0003t0003g0173 a0003c0003t0003g0174 others(4): Show |
7 | HG02280.hp2 HG02723.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.736-1370G>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 4/9 | chr5 | 115142744 | |||||||
| chr5:115143080 | A | T | 3 | a0001c0004t0005g0325 a0002c0002t0010g0333 a0002c0002t0010g0334 |
3 | HG03098.hp1 HG03654.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.735+1518T>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 4/9 | chr5 | 115143080 | |||||||
| chr5:115143087 | T | C | 12 | a0001c0004t0001g0063 a0001c0004t0014g0346 a0001c0004t0014g0347 others(9): Show |
12 | HG01074.hp1 HG02055.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.735+1511A>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 4/9 | chr5 | 115143087 | |||||||
| chr5:115143155 | G | C | 6 | a0003c0003t0003g0173 a0003c0003t0003g0174 a0003c0003t0003g0175 others(3): Show |
6 | HG02280.hp2 HG02970.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.735+1443C>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 4/9 | chr5 | 115143155 | |||||||
| chr5:115143196 | A | C | 36 | a0001c0001t0001g0095 a0001c0004t0024g0310 a0003c0003t0001g0040 others(33): Show |
39 | HG00280.hp1 HG00673.hp1 HG00733.hp1 others(36): Show |
intron_variant | MODIFIER | c.735+1402T>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 4/9 | chr5 | 115143196 | |||||||
| chr5:115143222 | C | CA | 25 | a0001c0001t0001g0020 a0001c0001t0001g0060 a0001c0001t0001g0120 others(22): Show |
26 | HG00423.hp1 HG00738.hp1 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.735+1375dupT | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 4/9 | chr5 | 115143222 | |||||||
| chr5:115143222 | C | CAA | 5 | a0001c0001t0001g0119 a0001c0001t0001g0127 a0001c0006t0003g0242 others(2): Show |
6 | HG00735.hp2 HG01081.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.735+1374_735+1375d others(4): Show |
TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 4/9 | chr5 | 115143222 | |||||||
| chr5:115143222 | CA | C | 119 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(116): Show |
138 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.735+1375delT | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 4/9 | chr5 | 115143222 | |||||||
| chr5:115143222 | CAA | C | 83 | a0001c0001t0001g0013 a0001c0001t0001g0021 a0001c0001t0001g0050 others(80): Show |
95 | HG00323.hp2 HG00423.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.735+1374_735+1375d others(4): Show |
TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 4/9 | chr5 | 115143222 | |||||||
| chr5:115143222 | CAAA | C | 10 | a0002c0002t0009g0015 a0002c0002t0010g0171 a0002c0005t0001g0053 others(7): Show |
11 | HG02280.hp2 HG02723.hp2 HG02965.hp1 others(8): Show |
intron_variant | MODIFIER | c.735+1373_735+1375d others(5): Show |
TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 4/9 | chr5 | 115143222 | |||||||
| chr5:115143222 | CAAAAAAA others(1): Show |
C | 38 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0011 others(35): Show |
58 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.735+1368_735+1375d others(10): Show |
TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 4/9 | chr5 | 115143222 | |||||||
| chr5:115143224 | A | G | 1 | a0001c0001t0013g0014 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.735+1374T>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 4/9 | chr5 | 115143224 | |||||||
| chr5:115143236 | A | C | 1 | a0001c0001t0001g0157 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.735+1362T>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 4/9 | chr5 | 115143236 | |||||||
| chr5:115143254 | T | C | 8 | a0001c0004t0005g0321 a0001c0004t0005g0322 a0001c0004t0005g0323 others(5): Show |
8 | HG02280.hp1 HG02451.hp2 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.735+1344A>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 4/9 | chr5 | 115143254 | |||||||
| chr5:115143318 | T | C | 6 | a0002c0005t0004g0006 a0002c0005t0004g0071 a0002c0005t0004g0073 others(3): Show |
8 | NA18985.hp2 NA19001.hp2 NA19007.hp1 others(5): Show |
intron_variant | MODIFIER | c.735+1280A>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 4/9 | chr5 | 115143318 | |||||||
| chr5:115143348 | C | T | 1 | a0001c0001t0001g0297 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.735+1250G>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 4/9 | chr5 | 115143348 | |||||||
| chr5:115143383 | C | T | 208 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(205): Show |
247 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.735+1215G>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 4/9 | chr5 | 115143383 | |||||||
| chr5:115143498 | A | G | 1 | a0003c0003t0003g0172 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.735+1100T>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 4/9 | chr5 | 115143498 | |||||||
| chr5:115143633 | AAAAGTTT others(14): Show |
A | 7 | a0002c0002t0010g0171 a0003c0003t0003g0173 a0003c0003t0003g0174 others(4): Show |
7 | HG02280.hp2 HG02723.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.735+944_735+964del others(21): Show |
TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 4/9 | chr5 | 115143633 | |||||||
| chr5:115143773 | G | A | 221 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(218): Show |
261 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.735+825C>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 4/9 | chr5 | 115143773 | |||||||
| chr5:115143801 | G | A | 2 | a0003c0003t0007g0260 a0003c0003t0007g0261 |
2 | HG00280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.735+797C>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 4/9 | chr5 | 115143801 | |||||||
| chr5:115143845 | A | C | 1 | a0002c0002t0002g0066 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.735+753T>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 4/9 | chr5 | 115143845 | |||||||
| chr5:115143869 | G | T | 1 | a0001c0004t0018g0308 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.735+729C>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 4/9 | chr5 | 115143869 | |||||||
| chr5:115143916 | G | T | 71 | a0001c0001t0002g0064 a0001c0001t0002g0065 a0001c0004t0002g0007 others(68): Show |
82 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.735+682C>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 4/9 | chr5 | 115143916 | |||||||
| chr5:115143931 | C | T | 8 | a0001c0004t0005g0321 a0001c0004t0005g0322 a0001c0004t0005g0323 others(5): Show |
8 | HG02280.hp1 HG02451.hp2 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.735+667G>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 4/9 | chr5 | 115143931 | |||||||
| chr5:115143934 | G | A | 1 | a0001c0001t0001g0295 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.735+664C>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 4/9 | chr5 | 115143934 | |||||||
| chr5:115143973 | G | C | 13 | a0001c0004t0001g0034 a0001c0004t0001g0056 a0001c0004t0001g0057 others(10): Show |
14 | HG02257.hp2 HG02258.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.735+625C>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 4/9 | chr5 | 115143973 | |||||||
| chr5:115144020 | G | A | 1 | a0001c0001t0001g0332 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.735+578C>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 4/9 | chr5 | 115144020 | |||||||
| chr5:115144037 | A | AT | 13 | a0001c0004t0001g0034 a0001c0004t0001g0056 a0001c0004t0001g0057 others(10): Show |
14 | HG02257.hp2 HG02258.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.735+560dupA | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 4/9 | chr5 | 115144037 | |||||||
| chr5:115144037 | A | ATT | 208 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(205): Show |
248 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.735+559_735+560dup others(2): Show |
TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 4/9 | chr5 | 115144037 | |||||||
| chr5:115144287 | T | C | 1 | a0001c0001t0001g0088 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.735+311A>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 4/9 | chr5 | 115144287 | |||||||
| chr5:115144561 | C | T | 9 | a0002c0002t0002g0024 a0002c0002t0002g0180 a0002c0002t0002g0189 others(6): Show |
10 | HG01167.hp1 HG01433.hp1 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.735+37G>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 4/9 | chr5 | 115144561 | |||||||
| chr5:115144830 | A | G | 2 | a0001c0006t0003g0311 a0001c0006t0003g0312 |
2 | HG02922.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.589-86T>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 3/9 | chr5 | 115144830 | |||||||
| chr5:115144955 | G | A | 5 | a0001c0004t0001g0034 a0001c0004t0006g0041 a0001c0004t0006g0042 others(2): Show |
5 | HG02258.hp2 HG02717.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.589-211C>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 3/9 | chr5 | 115144955 | |||||||
| chr5:115144975 | T | C | 2 | a0001c0006t0003g0313 a0001c0006t0003g0314 |
2 | HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.589-231A>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 3/9 | chr5 | 115144975 | |||||||
| chr5:115145060 | G | C | 1 | a0001c0004t0018g0308 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.589-316C>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 3/9 | chr5 | 115145060 | |||||||
| chr5:115145118 | A | G | 13 | a0001c0004t0001g0034 a0001c0004t0001g0056 a0001c0004t0001g0057 others(10): Show |
14 | HG02257.hp2 HG02258.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.589-374T>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 3/9 | chr5 | 115145118 | |||||||
| chr5:115145278 | A | C | 2 | a0001c0004t0001g0056 a0001c0004t0001g0057 |
2 | HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.589-534T>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 3/9 | chr5 | 115145278 | |||||||
| chr5:115145306 | C | G | 219 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(216): Show |
260 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.589-562G>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 3/9 | chr5 | 115145306 | |||||||
| chr5:115145424 | T | C | 36 | a0001c0004t0005g0325 a0003c0003t0001g0040 a0003c0003t0003g0028 others(33): Show |
39 | HG00280.hp1 HG00673.hp1 HG00733.hp1 others(36): Show |
intron_variant | MODIFIER | c.589-680A>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 3/9 | chr5 | 115145424 | |||||||
| chr5:115145533 | T | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(127): Show |
157 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.589-789A>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 3/9 | chr5 | 115145533 | |||||||
| chr5:115145533 | T | TTATTTAT others(5): Show |
12 | a0001c0004t0001g0056 a0001c0004t0001g0057 a0001c0004t0001g0168 others(9): Show |
13 | HG02257.hp2 HG02258.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.589-790_589-789ins others(12): Show |
TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 3/9 | chr5 | 115145533 | |||||||
| chr5:115145533 | T | TTATTTAT others(9): Show |
1 | a0001c0004t0001g0034 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.589-790_589-789ins others(16): Show |
TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 3/9 | chr5 | 115145533 | |||||||
| chr5:115145547 | G | A | 7 | a0002c0002t0010g0171 a0003c0003t0003g0173 a0003c0003t0003g0174 others(4): Show |
7 | HG02280.hp2 HG02723.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.589-803C>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 3/9 | chr5 | 115145547 | |||||||
| chr5:115145622 | G | A | 67 | a0001c0004t0002g0007 a0001c0004t0002g0187 a0001c0004t0002g0234 others(64): Show |
78 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.589-878C>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 3/9 | chr5 | 115145622 | |||||||
| chr5:115145671 | C | T | 6 | a0001c0001t0001g0142 a0001c0001t0001g0144 a0001c0001t0001g0145 others(3): Show |
6 | HG00323.hp2 HG00642.hp1 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.589-927G>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 3/9 | chr5 | 115145671 | |||||||
| chr5:115145738 | A | T | 1 | a0003c0003t0003g0250 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.589-994T>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 3/9 | chr5 | 115145738 | |||||||
| chr5:115145850 | A | G | 1 | a0001c0004t0001g0063 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.589-1106T>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 3/9 | chr5 | 115145850 | |||||||
| chr5:115145964 | A | G | 13 | a0001c0004t0001g0034 a0001c0004t0001g0056 a0001c0004t0001g0057 others(10): Show |
14 | HG02257.hp2 HG02258.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.588+1105T>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 3/9 | chr5 | 115145964 | |||||||
| chr5:115146095 | T | A | 4 | a0001c0004t0002g0007 a0001c0004t0002g0187 a0001c0004t0002g0234 others(1): Show |
6 | HG00558.hp2 NA18944.hp1 NA18969.hp2 others(3): Show |
intron_variant | MODIFIER | c.588+974A>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 3/9 | chr5 | 115146095 | |||||||
| chr5:115146378 | A | G | 3 | a0001c0009t0011g0016 a0001c0009t0011g0051 a0001c0009t0023g0033 |
4 | HG02572.hp2 HG02622.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.588+691T>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 3/9 | chr5 | 115146378 | |||||||
| chr5:115146444 | G | T | 13 | a0001c0004t0001g0034 a0001c0004t0001g0056 a0001c0004t0001g0057 others(10): Show |
14 | HG02257.hp2 HG02258.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.588+625C>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 3/9 | chr5 | 115146444 | |||||||
| chr5:115146636 | A | G | 1 | a0001c0004t0018g0308 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.588+433T>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 3/9 | chr5 | 115146636 | |||||||
| chr5:115146643 | T | A | 1 | a0003c0003t0003g0174 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.588+426A>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 3/9 | chr5 | 115146643 | |||||||
| chr5:115146898 | C | G | 71 | a0001c0004t0002g0007 a0001c0004t0002g0187 a0001c0004t0002g0234 others(68): Show |
82 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.588+171G>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 3/9 | chr5 | 115146898 | |||||||
| chr5:115147405 | A | G | 1 | a0002c0002t0002g0316 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.263-11T>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115147405 | |||||||
| chr5:115147487 | A | G | 2 | a0002c0005t0001g0053 a0002c0005t0001g0055 |
2 | HG02965.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.263-93T>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115147487 | |||||||
| chr5:115147564 | T | A | 1 | a0001c0004t0017g0035 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.263-170A>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115147564 | |||||||
| chr5:115147628 | C | T | 1 | a0002c0002t0002g0316 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.263-234G>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115147628 | |||||||
| chr5:115147703 | C | G | 226 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(223): Show |
268 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.263-309G>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115147703 | |||||||
| chr5:115147856 | C | T | 1 | a0001c0001t0001g0128 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.263-462G>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115147856 | |||||||
| chr5:115147964 | A | G | 1 | a0001c0001t0013g0014 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.263-570T>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115147964 | |||||||
| chr5:115147979 | A | C | 1 | a0001c0001t0013g0014 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.263-585T>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115147979 | |||||||
| chr5:115148006 | A | G | 1 | a0002c0005t0020g0072 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.263-612T>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115148006 | |||||||
| chr5:115148017 | C | T | 2 | a0001c0004t0014g0346 a0001c0004t0014g0347 |
2 | HG01074.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.263-623G>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115148017 | |||||||
| chr5:115148063 | T | C | 1 | a0003c0003t0003g0255 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.263-669A>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115148063 | |||||||
| chr5:115148067 | T | C | 107 | a0001c0001t0001g0118 a0001c0001t0001g0121 a0001c0001t0001g0128 others(104): Show |
121 | HG00423.hp1 HG00423.hp2 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.263-673A>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115148067 | |||||||
| chr5:115148086 | G | C | 1 | a0002c0005t0020g0072 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.263-692C>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115148086 | |||||||
| chr5:115148315 | C | T | 13 | a0001c0004t0001g0034 a0001c0004t0001g0056 a0001c0004t0001g0057 others(10): Show |
14 | HG02257.hp2 HG02258.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.263-921G>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115148315 | |||||||
| chr5:115148339 | T | C | 230 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(227): Show |
272 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.263-945A>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115148339 | |||||||
| chr5:115148415 | C | CT | 82 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(79): Show |
106 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.263-1022dupA | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115148415 | |||||||
| chr5:115148415 | C | CTT | 54 | a0001c0001t0001g0273 a0001c0001t0001g0281 a0001c0001t0001g0284 others(51): Show |
57 | HG00280.hp1 HG00597.hp2 HG00673.hp1 others(54): Show |
intron_variant | MODIFIER | c.263-1023_263-1022d others(4): Show |
TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115148415 | |||||||
| chr5:115148415 | C | CTTT | 70 | a0001c0001t0002g0064 a0001c0001t0002g0065 a0001c0004t0001g0168 others(67): Show |
82 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.263-1024_263-1022d others(5): Show |
TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115148415 | |||||||
| chr5:115148415 | C | CTTTT | 11 | a0002c0002t0002g0024 a0002c0002t0002g0181 a0002c0002t0002g0197 others(8): Show |
12 | HG00741.hp1 HG01433.hp1 HG02074.hp1 others(9): Show |
intron_variant | MODIFIER | c.263-1025_263-1022d others(6): Show |
TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115148415 | |||||||
| chr5:115148415 | CTTTTTTT others(6): Show |
C | 28 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(25): Show |
36 | HG00140.hp2 HG00642.hp2 HG00741.hp2 others(33): Show |
intron_variant | MODIFIER | c.263-1034_263-1022d others(15): Show |
TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115148415 | |||||||
| chr5:115148449 | T | C | 35 | a0003c0003t0001g0040 a0003c0003t0003g0028 a0003c0003t0003g0036 others(32): Show |
38 | HG00280.hp1 HG00673.hp1 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.263-1055A>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115148449 | |||||||
| chr5:115148740 | G | C | 1 | a0002c0002t0002g0208 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.263-1346C>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115148740 | |||||||
| chr5:115148811 | T | A | 1 | a0001c0001t0001g0320 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.263-1417A>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115148811 | |||||||
| chr5:115148895 | A | G | 5 | a0001c0004t0005g0321 a0001c0004t0005g0322 a0001c0004t0005g0323 others(2): Show |
5 | HG02280.hp1 HG02451.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.263-1501T>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115148895 | |||||||
| chr5:115149027 | C | T | 1 | a0001c0004t0006g0054 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.263-1633G>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115149027 | |||||||
| chr5:115149104 | T | C | 1 | a0002c0002t0002g0208 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.263-1710A>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115149104 | |||||||
| chr5:115149123 | A | C | 78 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(75): Show |
102 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.263-1729T>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115149123 | |||||||
| chr5:115149169 | A | G | 224 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(221): Show |
265 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.263-1775T>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115149169 | |||||||
| chr5:115149289 | G | C | 1 | a0002c0005t0020g0072 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.263-1895C>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115149289 | |||||||
| chr5:115149307 | T | G | 1 | a0001c0001t0002g0064 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.263-1913A>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115149307 | |||||||
| chr5:115149317 | G | T | 3 | a0001c0001t0001g0011 a0001c0001t0001g0271 a0001c0001t0001g0286 |
5 | NA18941.hp2 NA18984.hp2 NA18986.hp2 others(2): Show |
intron_variant | MODIFIER | c.263-1923C>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115149317 | |||||||
| chr5:115149364 | C | T | 13 | a0001c0004t0001g0034 a0001c0004t0001g0056 a0001c0004t0001g0057 others(10): Show |
14 | HG02257.hp2 HG02258.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.263-1970G>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115149364 | |||||||
| chr5:115149418 | A | G | 68 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(65): Show |
92 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.263-2024T>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115149418 | |||||||
| chr5:115149429 | G | A | 1 | a0001c0001t0001g0281 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.263-2035C>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115149429 | |||||||
| chr5:115149431 | T | TA | 77 | a0001c0001t0002g0064 a0001c0001t0002g0065 a0001c0004t0002g0007 others(74): Show |
90 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.263-2038dupT | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115149431 | |||||||
| chr5:115149544 | C | A | 2 | a0001c0006t0003g0307 a0001c0006t0003g0315 |
2 | HG02818.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.263-2150G>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115149544 | |||||||
| chr5:115149569 | G | GA | 106 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(103): Show |
136 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.263-2176dupT | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115149569 | |||||||
| chr5:115149569 | G | GAA | 22 | a0001c0001t0001g0032 a0001c0001t0001g0048 a0001c0001t0001g0264 others(19): Show |
24 | HG00323.hp1 HG01175.hp1 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.263-2177_263-2176d others(4): Show |
TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115149569 | |||||||
| chr5:115149569 | G | GAAA | 12 | a0001c0001t0002g0064 a0001c0004t0026g0074 a0002c0002t0002g0066 others(9): Show |
12 | HG00673.hp1 HG01496.hp1 HG02074.hp2 others(9): Show |
intron_variant | MODIFIER | c.263-2178_263-2176d others(5): Show |
TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115149569 | |||||||
| chr5:115149569 | G | GAAAA | 50 | a0001c0001t0002g0065 a0001c0004t0002g0187 a0001c0004t0006g0041 others(47): Show |
58 | HG00558.hp1 HG01069.hp2 HG01071.hp1 others(55): Show |
intron_variant | MODIFIER | c.263-2179_263-2176d others(6): Show |
TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115149569 | |||||||
| chr5:115149569 | G | GAAAAA | 28 | a0001c0004t0002g0007 a0001c0004t0002g0234 a0001c0004t0006g0268 others(25): Show |
33 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(30): Show |
intron_variant | MODIFIER | c.263-2180_263-2176d others(7): Show |
TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115149569 | |||||||
| chr5:115149569 | G | GAAAAAA | 9 | a0001c0004t0001g0034 a0001c0006t0003g0307 a0001c0006t0003g0314 others(6): Show |
9 | HG01891.hp1 HG02818.hp2 HG03471.hp2 others(6): Show |
intron_variant | MODIFIER | c.263-2181_263-2176d others(8): Show |
TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115149569 | |||||||
| chr5:115149569 | GA | G | 15 | a0001c0001t0001g0090 a0001c0001t0001g0094 a0001c0001t0001g0107 others(12): Show |
15 | HG00099.hp1 HG00733.hp2 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.263-2176delT | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115149569 | |||||||
| chr5:115149642 | T | TA | 7 | a0001c0001t0001g0148 a0001c0001t0001g0272 a0001c0001t0001g0317 others(4): Show |
9 | HG01070.hp2 HG02559.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.263-2249dupT | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115149642 | |||||||
| chr5:115149642 | T | TAA | 157 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(154): Show |
194 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.263-2250_263-2249d others(4): Show |
TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115149642 | |||||||
| chr5:115149642 | T | TAAA | 55 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0004t0001g0034 others(52): Show |
58 | HG00280.hp1 HG00673.hp1 HG00733.hp1 others(55): Show |
intron_variant | MODIFIER | c.263-2251_263-2249d others(5): Show |
TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115149642 | |||||||
| chr5:115149642 | T | TAAAAA | 6 | a0001c0004t0005g0322 a0001c0004t0005g0323 a0001c0004t0005g0325 others(3): Show |
6 | HG02280.hp1 HG02451.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.263-2253_263-2249d others(7): Show |
TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115149642 | |||||||
| chr5:115149642 | TA | T | 36 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0018 others(33): Show |
45 | HG00140.hp2 HG00642.hp2 HG00741.hp2 others(42): Show |
intron_variant | MODIFIER | c.263-2249delT | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115149642 | |||||||
| chr5:115149789 | C | T | 1 | a0001c0001t0001g0265 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.263-2395G>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115149789 | |||||||
| chr5:115149820 | G | A | 1 | a0001c0001t0001g0335 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.263-2426C>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115149820 | |||||||
| chr5:115149830 | C | G | 92 | a0001c0001t0002g0064 a0001c0001t0002g0065 a0001c0004t0002g0007 others(89): Show |
106 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.263-2436G>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115149830 | |||||||
| chr5:115149844 | C | T | 11 | a0001c0004t0001g0170 a0001c0004t0005g0321 a0001c0004t0005g0322 others(8): Show |
11 | HG02280.hp1 HG02451.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.263-2450G>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115149844 | |||||||
| chr5:115149884 | G | A | 2 | a0002c0002t0002g0068 a0002c0002t0002g0069 |
2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.263-2490C>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115149884 | |||||||
| chr5:115149934 | A | AT | 11 | a0001c0004t0001g0034 a0001c0004t0001g0056 a0001c0004t0001g0057 others(8): Show |
11 | HG02257.hp2 HG02258.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.263-2541dupA | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115149934 | |||||||
| chr5:115150061 | A | G | 2 | a0002c0002t0010g0171 a0003c0003t0003g0176 |
2 | HG02723.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.263-2667T>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115150061 | |||||||
| chr5:115150192 | T | G | 2 | a0001c0001t0001g0284 a0001c0001t0001g0285 |
2 | HG04184.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.263-2798A>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115150192 | |||||||
| chr5:115150287 | T | C | 1 | a0001c0004t0001g0170 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.263-2893A>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115150287 | |||||||
| chr5:115150323 | T | C | 2 | a0002c0005t0002g0219 a0002c0005t0002g0225 |
2 | HG01261.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.263-2929A>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115150323 | |||||||
| chr5:115150331 | A | G | 2 | a0001c0004t0001g0056 a0001c0004t0001g0057 |
2 | HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.263-2937T>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115150331 | |||||||
| chr5:115150529 | G | A | 2 | a0001c0001t0001g0166 a0001c0001t0001g0167 |
2 | HG01934.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.263-3135C>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115150529 | |||||||
| chr5:115150533 | G | T | 4 | a0001c0004t0002g0007 a0001c0004t0002g0187 a0001c0004t0002g0234 others(1): Show |
6 | HG00558.hp2 NA18944.hp1 NA18969.hp2 others(3): Show |
intron_variant | MODIFIER | c.263-3139C>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115150533 | |||||||
| chr5:115150688 | C | T | 3 | a0002c0002t0002g0010 a0002c0002t0002g0223 a0002c0002t0002g0224 |
5 | HG00558.hp1 NA18942.hp2 NA18955.hp1 others(2): Show |
intron_variant | MODIFIER | c.263-3294G>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115150688 | |||||||
| chr5:115150694 | A | C | 13 | a0001c0004t0001g0034 a0001c0004t0001g0056 a0001c0004t0001g0057 others(10): Show |
14 | HG02257.hp2 HG02258.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.263-3300T>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115150694 | |||||||
| chr5:115150749 | C | A | 9 | a0001c0001t0001g0002 a0001c0001t0001g0100 a0001c0001t0001g0101 others(6): Show |
15 | HG02027.hp2 NA18612.hp1 NA18747.hp1 others(12): Show |
intron_variant | MODIFIER | c.263-3355G>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115150749 | |||||||
| chr5:115150796 | G | A | 1 | a0001c0001t0001g0159 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.263-3402C>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115150796 | |||||||
| chr5:115150853 | G | A | 3 | a0001c0001t0001g0021 a0001c0001t0001g0309 a0003c0008t0003g0022 |
5 | HG02486.hp2 HG02647.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.263-3459C>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115150853 | |||||||
| chr5:115151036 | C | G | 209 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(206): Show |
250 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.263-3642G>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115151036 | |||||||
| chr5:115151107 | G | A | 6 | a0001c0001t0001g0142 a0001c0001t0001g0144 a0001c0001t0001g0145 others(3): Show |
6 | HG00323.hp2 HG00642.hp1 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.263-3713C>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115151107 | |||||||
| chr5:115151158 | T | A | 30 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(27): Show |
38 | HG00140.hp2 HG00642.hp2 HG00741.hp2 others(35): Show |
intron_variant | MODIFIER | c.263-3764A>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115151158 | |||||||
| chr5:115151229 | G | C | 1 | a0001c0004t0016g0324 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.263-3835C>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115151229 | |||||||
| chr5:115151254 | G | A | 2 | a0002c0002t0002g0068 a0002c0002t0002g0069 |
2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.263-3860C>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115151254 | |||||||
| chr5:115151270 | G | A | 1 | a0002c0005t0004g0073 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.263-3876C>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115151270 | |||||||
| chr5:115151359 | G | A | 1 | a0001c0001t0001g0105 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.263-3965C>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115151359 | |||||||
| chr5:115151493 | C | G | 1 | a0001c0004t0005g0325 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.263-4099G>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115151493 | |||||||
| chr5:115151857 | G | A | 2 | a0001c0004t0001g0168 a0001c0004t0001g0169 |
2 | HG02257.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.263-4463C>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115151857 | |||||||
| chr5:115151919 | G | A | 6 | a0001c0004t0005g0321 a0001c0004t0005g0322 a0001c0004t0005g0323 others(3): Show |
6 | HG02280.hp1 HG02451.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.263-4525C>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115151919 | |||||||
| chr5:115152092 | A | T | 2 | a0001c0009t0011g0016 a0001c0009t0011g0051 |
3 | HG02572.hp2 NA19043.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.263-4698T>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115152092 | |||||||
| chr5:115152133 | G | T | 6 | a0001c0004t0005g0321 a0001c0004t0005g0322 a0001c0004t0005g0323 others(3): Show |
6 | HG02280.hp1 HG02451.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.263-4739C>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115152133 | |||||||
| chr5:115152160 | T | C | 2 | a0002c0005t0001g0053 a0002c0005t0001g0055 |
2 | HG02965.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.263-4766A>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115152160 | |||||||
| chr5:115152238 | T | G | 1 | a0001c0001t0001g0106 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.263-4844A>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115152238 | |||||||
| chr5:115152262 | A | C | 1 | a0001c0004t0024g0310 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.263-4868T>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115152262 | |||||||
| chr5:115152280 | C | T | 6 | a0003c0003t0003g0173 a0003c0003t0003g0174 a0003c0003t0003g0175 others(3): Show |
6 | HG02280.hp2 HG02970.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.263-4886G>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115152280 | |||||||
| chr5:115152302 | A | G | 3 | a0001c0009t0011g0016 a0001c0009t0011g0051 a0001c0009t0023g0033 |
4 | HG02572.hp2 HG02622.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.263-4908T>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115152302 | |||||||
| chr5:115152374 | G | A | 2 | a0001c0004t0014g0346 a0001c0004t0014g0347 |
2 | HG01074.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.263-4980C>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115152374 | |||||||
| chr5:115152587 | A | T | 1 | a0001c0001t0001g0132 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.263-5193T>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115152587 | |||||||
| chr5:115152771 | C | T | 212 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(209): Show |
255 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.263-5377G>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115152771 | |||||||
| chr5:115152893 | C | T | 2 | a0003c0003t0008g0249 a0003c0003t0008g0257 |
2 | NA19005.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.263-5499G>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115152893 | |||||||
| chr5:115153099 | T | C | 2 | a0001c0004t0001g0056 a0001c0004t0001g0057 |
2 | HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.263-5705A>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115153099 | |||||||
| chr5:115153203 | T | C | 1 | a0001c0004t0001g0034 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.263-5809A>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115153203 | |||||||
| chr5:115153282 | A | G | 3 | a0001c0001t0001g0011 a0001c0001t0001g0271 a0001c0001t0001g0286 |
5 | NA18941.hp2 NA18984.hp2 NA18986.hp2 others(2): Show |
intron_variant | MODIFIER | c.263-5888T>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115153282 | |||||||
| chr5:115153339 | C | CAATCCTA others(2): Show |
89 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(86): Show |
117 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.263-5954_263-5946d others(11): Show |
TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115153339 | |||||||
| chr5:115153355 | T | C | 36 | a0001c0004t0006g0054 a0001c0004t0024g0310 a0003c0003t0001g0040 others(33): Show |
39 | HG00280.hp1 HG00673.hp1 HG00733.hp1 others(36): Show |
intron_variant | MODIFIER | c.263-5961A>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115153355 | |||||||
| chr5:115153481 | A | G | 1 | a0001c0001t0001g0118 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.263-6087T>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115153481 | |||||||
| chr5:115153514 | T | C | 1 | a0001c0004t0017g0035 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.263-6120A>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115153514 | |||||||
| chr5:115153541 | T | C | 1 | a0002c0002t0002g0227 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.263-6147A>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115153541 | |||||||
| chr5:115153737 | C | T | 1 | a0002c0002t0002g0066 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.263-6343G>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115153737 | |||||||
| chr5:115153774 | G | A | 3 | a0002c0002t0009g0015 a0002c0002t0009g0059 a0002c0002t0019g0049 |
4 | HG02559.hp2 HG03453.hp2 NA20300.hp1 others(1): Show |
intron_variant | MODIFIER | c.263-6380C>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115153774 | |||||||
| chr5:115153947 | A | G | 1 | a0001c0001t0001g0142 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.263-6553T>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115153947 | |||||||
| chr5:115154089 | C | CA | 85 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(82): Show |
111 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.263-6696dupT | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115154089 | |||||||
| chr5:115154089 | CA | C | 6 | a0003c0003t0003g0173 a0003c0003t0003g0174 a0003c0003t0003g0175 others(3): Show |
6 | HG02280.hp2 HG02970.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.263-6696delT | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115154089 | |||||||
| chr5:115154136 | C | A | 1 | a0001c0004t0005g0325 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.263-6742G>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115154136 | |||||||
| chr5:115154185 | C | CGAA | 78 | a0001c0001t0002g0064 a0001c0001t0002g0065 a0001c0004t0002g0007 others(75): Show |
91 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.263-6792_263-6791i others(5): Show |
TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115154185 | |||||||
| chr5:115154188 | T | TTCACA | 78 | a0001c0001t0002g0064 a0001c0001t0002g0065 a0001c0004t0002g0007 others(75): Show |
91 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.263-6795_263-6794i others(7): Show |
TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115154188 | |||||||
| chr5:115154189 | G | A | 78 | a0001c0001t0002g0064 a0001c0001t0002g0065 a0001c0004t0002g0007 others(75): Show |
91 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.263-6795C>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115154189 | |||||||
| chr5:115154194 | G | C | 1 | a0001c0004t0006g0054 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.263-6800C>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115154194 | |||||||
| chr5:115154207 | A | G | 3 | a0001c0009t0011g0016 a0001c0009t0011g0051 a0001c0009t0023g0033 |
4 | HG02572.hp2 HG02622.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.263-6813T>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115154207 | |||||||
| chr5:115154216 | C | T | 3 | a0001c0009t0011g0016 a0001c0009t0011g0051 a0001c0009t0023g0033 |
4 | HG02572.hp2 HG02622.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.263-6822G>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115154216 | |||||||
| chr5:115154317 | G | T | 2 | a0001c0004t0001g0056 a0001c0004t0001g0057 |
2 | HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.263-6923C>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115154317 | |||||||
| chr5:115154417 | A | C | 2 | a0002c0005t0001g0053 a0002c0005t0001g0055 |
2 | HG02965.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.263-7023T>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115154417 | |||||||
| chr5:115154505 | C | T | 80 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(77): Show |
106 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.263-7111G>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115154505 | |||||||
| chr5:115154559 | T | C | 2 | a0001c0004t0006g0041 a0001c0004t0006g0268 |
2 | HG02717.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.263-7165A>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115154559 | |||||||
| chr5:115154622 | A | T | 264 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(261): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.263-7228T>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115154622 | |||||||
| chr5:115154722 | C | T | 2 | a0001c0004t0014g0346 a0001c0004t0014g0347 |
2 | HG01074.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.263-7328G>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115154722 | |||||||
| chr5:115154801 | T | C | 16 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(13): Show |
18 | HG00323.hp2 HG00642.hp1 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.263-7407A>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115154801 | |||||||
| chr5:115154811 | G | A | 22 | a0003c0003t0003g0028 a0003c0003t0003g0239 a0003c0003t0003g0243 others(19): Show |
24 | HG00673.hp1 HG02040.hp1 HG02056.hp2 others(21): Show |
intron_variant | MODIFIER | c.263-7417C>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115154811 | |||||||
| chr5:115155026 | C | CA | 8 | a0001c0001t0001g0149 a0002c0002t0010g0171 a0003c0003t0003g0173 others(5): Show |
8 | HG01257.hp2 HG02280.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.263-7633dupT | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115155026 | |||||||
| chr5:115155048 | G | C | 76 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(73): Show |
100 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.263-7654C>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115155048 | |||||||
| chr5:115155192 | AAAAT | A | 69 | a0001c0004t0002g0007 a0001c0004t0002g0187 a0001c0004t0002g0234 others(66): Show |
80 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.263-7802_263-7799d others(6): Show |
TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115155192 | |||||||
| chr5:115155327 | A | G | 1 | a0001c0004t0018g0308 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.263-7933T>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115155327 | |||||||
| chr5:115155333 | G | C | 2 | a0003c0003t0007g0260 a0003c0003t0007g0261 |
2 | HG00280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.263-7939C>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115155333 | |||||||
| chr5:115155345 | G | A | 2 | a0001c0004t0001g0170 a0001c0004t0018g0308 |
2 | HG03130.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.263-7951C>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115155345 | |||||||
| chr5:115155372 | T | C | 77 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(74): Show |
101 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.263-7978A>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115155372 | |||||||
| chr5:115155498 | G | A | 1 | a0002c0002t0002g0087 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.262+8020C>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115155498 | |||||||
| chr5:115155507 | A | T | 1 | a0001c0001t0001g0106 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.262+8011T>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115155507 | |||||||
| chr5:115155614 | T | A | 1 | a0001c0004t0018g0308 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.262+7904A>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115155614 | |||||||
| chr5:115155615 | C | T | 5 | a0001c0004t0001g0034 a0001c0004t0006g0041 a0001c0004t0006g0042 others(2): Show |
5 | HG02258.hp2 HG02717.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.262+7903G>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115155615 | |||||||
| chr5:115155641 | A | C | 4 | a0001c0001t0001g0081 a0001c0001t0001g0264 a0001c0001t0001g0269 others(1): Show |
4 | HG01175.hp1 HG01884.hp2 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.262+7877T>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115155641 | |||||||
| chr5:115155781 | C | T | 1 | a0001c0001t0001g0342 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.262+7737G>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115155781 | |||||||
| chr5:115155820 | T | C | 1 | a0002c0002t0002g0222 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.262+7698A>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115155820 | |||||||
| chr5:115155825 | C | A | 3 | a0002c0002t0002g0010 a0002c0002t0002g0223 a0002c0002t0002g0224 |
5 | HG00558.hp1 NA18942.hp2 NA18955.hp1 others(2): Show |
intron_variant | MODIFIER | c.262+7693G>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115155825 | |||||||
| chr5:115155881 | A | G | 3 | a0002c0002t0002g0190 a0002c0002t0002g0191 a0002c0002t0002g0192 |
3 | NA18943.hp2 NA18994.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.262+7637T>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115155881 | |||||||
| chr5:115155928 | C | T | 1 | a0003c0003t0003g0173 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.262+7590G>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115155928 | |||||||
| chr5:115155980 | A | T | 1 | a0001c0001t0002g0064 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.262+7538T>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115155980 | |||||||
| chr5:115156061 | C | CA | 6 | a0001c0001t0001g0106 a0001c0001t0001g0286 a0001c0006t0003g0241 others(3): Show |
6 | HG02056.hp2 HG02615.hp1 NA19005.hp2 others(3): Show |
intron_variant | MODIFIER | c.262+7456dupT | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115156061 | |||||||
| chr5:115156160 | T | C | 1 | a0001c0001t0003g0076 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.262+7358A>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115156160 | |||||||
| chr5:115156215 | T | C | 2 | a0002c0005t0001g0053 a0002c0005t0001g0055 |
2 | HG02965.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.262+7303A>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115156215 | |||||||
| chr5:115156300 | TA | T | 7 | a0001c0001t0001g0029 a0001c0001t0021g0089 a0002c0002t0002g0189 others(4): Show |
9 | HG00639.hp2 HG01167.hp1 HG01346.hp1 others(6): Show |
intron_variant | MODIFIER | c.262+7217delT | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115156300 | |||||||
| chr5:115156430 | T | C | 1 | a0001c0004t0024g0310 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.262+7088A>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115156430 | |||||||
| chr5:115156526 | A | G | 93 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0002g0064 others(90): Show |
106 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.262+6992T>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115156526 | |||||||
| chr5:115156584 | G | C | 43 | a0001c0004t0006g0054 a0002c0002t0009g0015 a0002c0002t0009g0059 others(40): Show |
47 | HG00280.hp1 HG00673.hp1 HG00733.hp1 others(44): Show |
intron_variant | MODIFIER | c.262+6934C>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115156584 | |||||||
| chr5:115156781 | C | A | 1 | a0003c0003t0003g0259 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.262+6737G>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115156781 | |||||||
| chr5:115157017 | A | G | 1 | a0001c0001t0001g0336 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.262+6501T>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115157017 | |||||||
| chr5:115157146 | T | TA | 21 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(18): Show |
21 | HG00733.hp2 HG00741.hp2 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.262+6371dupT | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115157146 | |||||||
| chr5:115157211 | G | T | 1 | a0003c0003t0007g0260 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.262+6307C>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115157211 | |||||||
| chr5:115157220 | G | A | 1 | a0001c0001t0013g0014 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.262+6298C>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115157220 | |||||||
| chr5:115157338 | G | T | 4 | a0001c0004t0002g0007 a0001c0004t0002g0187 a0001c0004t0002g0234 others(1): Show |
6 | HG00558.hp2 NA18944.hp1 NA18969.hp2 others(3): Show |
intron_variant | MODIFIER | c.262+6180C>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115157338 | |||||||
| chr5:115157388 | C | A | 2 | a0002c0002t0002g0068 a0002c0002t0002g0069 |
2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.262+6130G>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115157388 | |||||||
| chr5:115157564 | C | A | 1 | a0001c0001t0001g0130 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.262+5954G>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115157564 | |||||||
| chr5:115157609 | T | A | 7 | a0002c0002t0002g0025 a0002c0002t0002g0062 a0002c0002t0002g0184 others(4): Show |
8 | HG02071.hp2 NA18965.hp1 NA19000.hp2 others(5): Show |
intron_variant | MODIFIER | c.262+5909A>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115157609 | |||||||
| chr5:115157618 | C | T | 211 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(208): Show |
252 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.262+5900G>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115157618 | |||||||
| chr5:115157766 | C | T | 6 | a0003c0003t0001g0040 a0003c0003t0003g0036 a0003c0003t0003g0037 others(3): Show |
6 | HG02145.hp1 HG02559.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.262+5752G>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115157766 | |||||||
| chr5:115157826 | G | C | 1 | a0002c0002t0002g0186 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.262+5692C>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115157826 | |||||||
| chr5:115157841 | T | C | 1 | a0002c0002t0002g0227 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.262+5677A>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115157841 | |||||||
| chr5:115157942 | A | G | 2 | a0002c0005t0001g0053 a0002c0005t0001g0055 |
2 | HG02965.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.262+5576T>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115157942 | |||||||
| chr5:115158125 | T | A | 1 | a0002c0002t0002g0228 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.262+5393A>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115158125 | |||||||
| chr5:115158128 | T | A | 1 | a0001c0001t0001g0287 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.262+5390A>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115158128 | |||||||
| chr5:115158134 | T | TAAAA | 221 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(218): Show |
264 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.262+5383_262+5384i others(6): Show |
TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115158134 | |||||||
| chr5:115158134 | T | TAAAG | 8 | a0001c0004t0005g0321 a0001c0004t0005g0322 a0001c0004t0005g0323 others(5): Show |
8 | HG02280.hp1 HG02451.hp2 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.262+5383_262+5384i others(6): Show |
TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115158134 | |||||||
| chr5:115158212 | CTG | C | 24 | a0003c0003t0003g0028 a0003c0003t0003g0239 a0003c0003t0003g0243 others(21): Show |
26 | HG00280.hp1 HG00673.hp1 HG00733.hp1 others(23): Show |
intron_variant | MODIFIER | c.262+5304_262+5305d others(4): Show |
TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115158212 | |||||||
| chr5:115158295 | T | C | 2 | a0001c0001t0001g0116 a0001c0001t0001g0117 |
2 | NA18975.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.262+5223A>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115158295 | |||||||
| chr5:115158318 | A | C | 8 | a0001c0004t0005g0321 a0001c0004t0005g0322 a0001c0004t0005g0323 others(5): Show |
8 | HG02280.hp1 HG02451.hp2 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.262+5200T>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115158318 | |||||||
| chr5:115158345 | A | T | 317 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(314): Show |
373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.262+5173T>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115158345 | |||||||
| chr5:115158398 | G | T | 1 | a0002c0002t0002g0186 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.262+5120C>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115158398 | |||||||
| chr5:115158488 | C | A | 1 | a0007c0014t0001g0131 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.262+5030G>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115158488 | |||||||
| chr5:115158491 | G | A | 2 | a0003c0003t0007g0260 a0003c0003t0007g0261 |
2 | HG00280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.262+5027C>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115158491 | |||||||
| chr5:115158657 | A | G | 2 | a0001c0009t0011g0016 a0001c0009t0011g0051 |
3 | HG02572.hp2 NA19043.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.262+4861T>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115158657 | |||||||
| chr5:115158695 | A | G | 1 | a0002c0002t0002g0185 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.262+4823T>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115158695 | |||||||
| chr5:115158739 | C | T | 1 | a0001c0001t0001g0088 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.262+4779G>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115158739 | |||||||
| chr5:115159164 | G | T | 1 | a0001c0001t0003g0076 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.262+4354C>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115159164 | |||||||
| chr5:115159226 | A | C | 1 | a0001c0001t0001g0232 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.262+4292T>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115159226 | |||||||
| chr5:115159247 | T | C | 1 | a0001c0001t0001g0157 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.262+4271A>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115159247 | |||||||
| chr5:115159375 | G | A | 1 | a0002c0005t0001g0055 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.262+4143C>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115159375 | |||||||
| chr5:115159586 | T | C | 1 | a0002c0002t0002g0316 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.262+3932A>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115159586 | |||||||
| chr5:115159611 | C | T | 2 | a0002c0002t0009g0015 a0002c0002t0009g0059 |
3 | HG02559.hp2 HG03453.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.262+3907G>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115159611 | |||||||
| chr5:115159685 | C | T | 1 | a0001c0004t0005g0321 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.262+3833G>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115159685 | |||||||
| chr5:115159771 | A | C | 8 | a0001c0004t0005g0321 a0001c0004t0005g0322 a0001c0004t0005g0323 others(5): Show |
8 | HG02280.hp1 HG02451.hp2 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.262+3747T>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115159771 | |||||||
| chr5:115159854 | C | T | 1 | a0003c0003t0003g0061 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.262+3664G>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115159854 | |||||||
| chr5:115159863 | T | C | 26 | a0003c0003t0003g0028 a0003c0003t0003g0239 a0003c0003t0003g0243 others(23): Show |
29 | HG00280.hp1 HG00673.hp1 HG00733.hp1 others(26): Show |
intron_variant | MODIFIER | c.262+3655A>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115159863 | |||||||
| chr5:115160087 | A | G | 1 | a0001c0001t0001g0335 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.262+3431T>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115160087 | |||||||
| chr5:115160275 | G | A | 1 | a0001c0001t0001g0050 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.262+3243C>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115160275 | |||||||
| chr5:115160439 | A | C | 1 | a0001c0001t0001g0043 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.262+3079T>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115160439 | |||||||
| chr5:115160477 | T | C | 1 | a0003c0003t0003g0262 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.262+3041A>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115160477 | |||||||
| chr5:115160493 | G | A | 2 | a0005c0011t0001g0340 a0005c0011t0001g0341 |
2 | HG00099.hp1 HG00735.hp1 |
intron_variant | MODIFIER | c.262+3025C>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115160493 | |||||||
| chr5:115160515 | C | T | 1 | a0001c0001t0001g0269 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.262+3003G>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115160515 | |||||||
| chr5:115160516 | G | A | 1 | a0001c0004t0005g0326 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.262+3002C>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115160516 | |||||||
| chr5:115160663 | C | T | 73 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(70): Show |
98 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.262+2855G>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115160663 | |||||||
| chr5:115160684 | T | A | 6 | a0001c0004t0005g0321 a0001c0004t0005g0322 a0001c0004t0005g0323 others(3): Show |
6 | HG02280.hp1 HG02451.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.262+2834A>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115160684 | |||||||
| chr5:115160706 | G | A | 73 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(70): Show |
98 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.262+2812C>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115160706 | |||||||
| chr5:115160710 | G | A | 6 | a0001c0004t0001g0034 a0001c0004t0006g0041 a0001c0004t0006g0042 others(3): Show |
6 | HG02258.hp2 HG02622.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.262+2808C>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115160710 | |||||||
| chr5:115160728 | C | G | 1 | a0001c0004t0017g0035 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.262+2790G>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115160728 | |||||||
| chr5:115160731 | C | T | 1 | a0001c0001t0001g0294 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.262+2787G>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115160731 | |||||||
| chr5:115160743 | G | A | 3 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 |
3 | HG03491.hp2 HG03688.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.262+2775C>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115160743 | |||||||
| chr5:115160845 | G | C | 1 | a0001c0001t0003g0076 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.262+2673C>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115160845 | |||||||
| chr5:115160923 | C | CA | 4 | a0002c0002t0009g0015 a0002c0002t0009g0059 a0002c0002t0010g0171 others(1): Show |
5 | HG02559.hp2 HG02723.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.262+2594dupT | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115160923 | |||||||
| chr5:115161076 | G | A | 86 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0004t0001g0170 others(83): Show |
97 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(94): Show |
intron_variant | MODIFIER | c.262+2442C>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115161076 | |||||||
| chr5:115161195 | T | TA | 79 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(76): Show |
104 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.262+2322dupT | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115161195 | |||||||
| chr5:115161426 | C | T | 1 | a0002c0002t0002g0184 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.262+2092G>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115161426 | |||||||
| chr5:115161431 | C | A | 2 | a0001c0004t0006g0041 a0001c0004t0006g0268 |
2 | HG02717.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.262+2087G>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115161431 | |||||||
| chr5:115161485 | A | G | 77 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(74): Show |
102 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.262+2033T>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115161485 | |||||||
| chr5:115161552 | T | C | 4 | a0002c0002t0009g0015 a0002c0002t0009g0059 a0002c0002t0010g0171 others(1): Show |
5 | HG02559.hp2 HG02723.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.262+1966A>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115161552 | |||||||
| chr5:115161651 | G | A | 4 | a0002c0002t0009g0015 a0002c0002t0009g0059 a0002c0002t0010g0171 others(1): Show |
5 | HG02559.hp2 HG02723.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.262+1867C>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115161651 | |||||||
| chr5:115161764 | GGGCTGAT | G | 2 | a0001c0009t0011g0016 a0001c0009t0011g0051 |
3 | HG02572.hp2 NA19043.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.262+1747_262+1753d others(9): Show |
TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115161764 | |||||||
| chr5:115161851 | GGA | G | 72 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0013 others(69): Show |
88 | HG00140.hp2 HG00423.hp1 HG00609.hp1 others(85): Show |
intron_variant | MODIFIER | c.262+1665_262+1666d others(4): Show |
TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115161851 | |||||||
| chr5:115161866 | T | C | 1 | a0001c0004t0017g0035 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.262+1652A>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115161866 | |||||||
| chr5:115161978 | T | A | 3 | a0001c0001t0001g0058 a0001c0004t0001g0056 a0001c0004t0001g0057 |
3 | HG02976.hp2 HG03516.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.262+1540A>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115161978 | |||||||
| chr5:115162011 | C | T | 209 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(206): Show |
249 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.262+1507G>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115162011 | |||||||
| chr5:115162047 | T | C | 1 | a0001c0004t0024g0310 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.262+1471A>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115162047 | |||||||
| chr5:115162115 | A | G | 2 | a0001c0004t0006g0041 a0001c0004t0006g0268 |
2 | HG02717.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.262+1403T>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115162115 | |||||||
| chr5:115162148 | T | G | 1 | a0001c0004t0002g0234 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.262+1370A>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115162148 | |||||||
| chr5:115162203 | G | C | 1 | a0001c0004t0014g0347 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.262+1315C>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115162203 | |||||||
| chr5:115162207 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.262+1311G>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115162207 | |||||||
| chr5:115162234 | T | C | 5 | a0001c0001t0001g0302 a0001c0001t0001g0303 a0001c0001t0001g0305 others(2): Show |
5 | HG00323.hp1 HG01515.hp2 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.262+1284A>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115162234 | |||||||
| chr5:115162275 | G | T | 123 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(120): Show |
154 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.262+1243C>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115162275 | |||||||
| chr5:115162339 | C | G | 1 | a0001c0004t0001g0170 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.262+1179G>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115162339 | |||||||
| chr5:115162392 | A | G | 2 | a0002c0002t0002g0023 a0002c0002t0002g0181 |
3 | NA18979.hp2 NA19006.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.262+1126T>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115162392 | |||||||
| chr5:115162419 | A | G | 34 | a0003c0003t0001g0040 a0003c0003t0003g0028 a0003c0003t0003g0036 others(31): Show |
37 | HG00280.hp1 HG00673.hp1 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.262+1099T>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115162419 | |||||||
| chr5:115162450 | A | G | 67 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(64): Show |
91 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.262+1068T>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115162450 | |||||||
| chr5:115162691 | T | C | 3 | a0001c0010t0001g0077 a0001c0010t0001g0078 a0001c0010t0001g0079 |
3 | HG01243.hp2 HG02451.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.262+827A>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115162691 | |||||||
| chr5:115162712 | T | G | 6 | a0001c0004t0005g0321 a0001c0004t0005g0322 a0001c0004t0005g0323 others(3): Show |
6 | HG02280.hp1 HG02451.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.262+806A>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115162712 | |||||||
| chr5:115162819 | G | A | 2 | a0001c0001t0001g0161 a0001c0001t0001g0162 |
2 | NA18980.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.262+699C>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115162819 | |||||||
| chr5:115162825 | C | T | 3 | a0001c0001t0001g0058 a0001c0004t0001g0056 a0001c0004t0001g0057 |
3 | HG02976.hp2 HG03516.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.262+693G>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115162825 | |||||||
| chr5:115162887 | T | C | 1 | a0001c0001t0003g0076 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.262+631A>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115162887 | |||||||
| chr5:115162959 | C | CT | 12 | a0001c0001t0001g0309 a0001c0004t0001g0063 a0001c0004t0024g0310 others(9): Show |
12 | HG02486.hp2 HG02615.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.262+558dupA | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115162959 | |||||||
| chr5:115162959 | CT | C | 21 | a0001c0001t0001g0005 a0001c0001t0001g0163 a0001c0001t0001g0294 others(18): Show |
25 | HG00323.hp1 HG00597.hp2 HG01123.hp1 others(22): Show |
intron_variant | MODIFIER | c.262+558delA | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115162959 | |||||||
| chr5:115163011 | G | A | 2 | a0001c0004t0014g0346 a0001c0004t0014g0347 |
2 | HG01074.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.262+507C>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115163011 | |||||||
| chr5:115163018 | C | T | 1 | a0001c0004t0018g0308 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.262+500G>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115163018 | |||||||
| chr5:115163020 | C | T | 2 | a0001c0001t0001g0080 a0003c0003t0003g0245 |
2 | HG02523.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.262+498G>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115163020 | |||||||
| chr5:115163107 | G | A | 95 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(92): Show |
122 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.262+411C>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115163107 | |||||||
| chr5:115163107 | G | C | 1 | a0001c0009t0023g0033 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.262+411C>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115163107 | |||||||
| chr5:115163163 | G | C | 1 | a0001c0001t0012g0306 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.262+355C>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115163163 | |||||||
| chr5:115163378 | T | C | 2 | a0001c0009t0011g0016 a0001c0009t0023g0033 |
3 | HG02572.hp2 HG02622.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.262+140A>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 2/9 | chr5 | 115163378 | |||||||
| chr5:115164007 | C | A | 12 | a0001c0001t0001g0309 a0001c0004t0024g0310 a0001c0006t0003g0240 others(9): Show |
12 | HG02055.hp2 HG02486.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.28-255G>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 1/9 | chr5 | 115164007 | |||||||
| chr5:115164055 | C | G | 9 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(6): Show |
9 | HG02055.hp1 HG02723.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.28-303G>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 1/9 | chr5 | 115164055 | |||||||
| chr5:115164203 | T | G | 1 | a0001c0001t0001g0164 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.28-451A>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 1/9 | chr5 | 115164203 | |||||||
| chr5:115164224 | A | T | 13 | a0001c0004t0001g0034 a0001c0004t0006g0041 a0001c0004t0006g0042 others(10): Show |
13 | HG02145.hp1 HG02258.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.28-472T>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 1/9 | chr5 | 115164224 | |||||||
| chr5:115164526 | G | C | 2 | a0001c0001t0001g0021 a0003c0008t0003g0022 |
4 | HG02647.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.28-774C>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 1/9 | chr5 | 115164526 | |||||||
| chr5:115164536 | A | T | 2 | a0001c0001t0001g0264 a0001c0001t0001g0265 |
2 | HG01884.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.28-784T>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 1/9 | chr5 | 115164536 | |||||||
| chr5:115164665 | A | G | 3 | a0001c0001t0013g0014 a0001c0004t0001g0170 a0003c0003t0003g0061 |
4 | HG02895.hp1 HG02897.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.28-913T>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 1/9 | chr5 | 115164665 | |||||||
| chr5:115164831 | A | G | 153 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(150): Show |
187 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.28-1079T>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 1/9 | chr5 | 115164831 | |||||||
| chr5:115165040 | A | C | 237 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(234): Show |
284 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.28-1288T>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 1/9 | chr5 | 115165040 | |||||||
| chr5:115165060 | C | T | 1 | a0002c0002t0002g0180 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.28-1308G>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 1/9 | chr5 | 115165060 | |||||||
| chr5:115165142 | C | T | 25 | a0001c0001t0001g0246 a0003c0003t0003g0028 a0003c0003t0003g0243 others(22): Show |
28 | HG00280.hp1 HG00733.hp1 HG01081.hp2 others(25): Show |
intron_variant | MODIFIER | c.28-1390G>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 1/9 | chr5 | 115165142 | |||||||
| chr5:115165340 | G | A | 8 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(5): Show |
8 | HG02055.hp1 HG02723.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.28-1588C>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 1/9 | chr5 | 115165340 | |||||||
| chr5:115165414 | G | A | 1 | a0001c0009t0011g0051 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.28-1662C>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 1/9 | chr5 | 115165414 | |||||||
| chr5:115165501 | G | A | 3 | a0001c0001t0001g0058 a0001c0004t0001g0056 a0001c0004t0001g0057 |
3 | HG02976.hp2 HG03516.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.28-1749C>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 1/9 | chr5 | 115165501 | |||||||
| chr5:115165626 | G | A | 1 | a0003c0003t0003g0052 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.28-1874C>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 1/9 | chr5 | 115165626 | |||||||
| chr5:115165641 | C | T | 1 | a0001c0006t0003g0307 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.28-1889G>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 1/9 | chr5 | 115165641 | |||||||
| chr5:115165650 | C | T | 85 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(82): Show |
112 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.28-1898G>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 1/9 | chr5 | 115165650 | |||||||
| chr5:115165726 | C | A | 1 | a0001c0004t0014g0347 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.28-1974G>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 1/9 | chr5 | 115165726 | |||||||
| chr5:115165904 | G | A | 2 | a0001c0001t0001g0317 a0001c0001t0001g0318 |
2 | NA18959.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.28-2152C>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 1/9 | chr5 | 115165904 | |||||||
| chr5:115165997 | G | A | 1 | a0001c0001t0001g0165 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.28-2245C>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 1/9 | chr5 | 115165997 | |||||||
| chr5:115166169 | T | C | 2 | a0001c0001t0001g0166 a0001c0001t0001g0167 |
2 | HG01934.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.28-2417A>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 1/9 | chr5 | 115166169 | |||||||
| chr5:115166230 | A | G | 1 | a0001c0004t0001g0063 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.28-2478T>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 1/9 | chr5 | 115166230 | |||||||
| chr5:115166371 | G | T | 101 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(98): Show |
130 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.28-2619C>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 1/9 | chr5 | 115166371 | |||||||
| chr5:115166439 | G | A | 1 | a0001c0001t0001g0327 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.28-2687C>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 1/9 | chr5 | 115166439 | |||||||
| chr5:115166450 | C | G | 1 | a0002c0005t0001g0055 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.28-2698G>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 1/9 | chr5 | 115166450 | |||||||
| chr5:115166452 | G | A | 1 | a0001c0001t0001g0328 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.28-2700C>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 1/9 | chr5 | 115166452 | |||||||
| chr5:115166527 | T | G | 1 | a0002c0005t0001g0055 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.28-2775A>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 1/9 | chr5 | 115166527 | |||||||
| chr5:115166649 | T | C | 19 | a0001c0001t0001g0058 a0001c0004t0001g0034 a0001c0004t0001g0056 others(16): Show |
19 | HG01074.hp1 HG02145.hp1 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.28-2897A>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 1/9 | chr5 | 115166649 | |||||||
| chr5:115166680 | T | C | 2 | a0001c0001t0001g0329 a0001c0001t0001g0330 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.27+2928A>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 1/9 | chr5 | 115166680 | |||||||
| chr5:115166688 | G | A | 2 | a0001c0004t0001g0168 a0001c0004t0001g0169 |
2 | HG02257.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.27+2920C>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 1/9 | chr5 | 115166688 | |||||||
| chr5:115166806 | A | G | 3 | a0001c0001t0001g0058 a0001c0004t0001g0056 a0001c0004t0001g0057 |
3 | HG02976.hp2 HG03516.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.27+2802T>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 1/9 | chr5 | 115166806 | |||||||
| chr5:115166870 | C | T | 1 | a0001c0009t0023g0033 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.27+2738G>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 1/9 | chr5 | 115166870 | |||||||
| chr5:115166890 | C | T | 1 | a0003c0003t0003g0244 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.27+2718G>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 1/9 | chr5 | 115166890 | |||||||
| chr5:115166908 | G | T | 1 | a0003c0003t0003g0243 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.27+2700C>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 1/9 | chr5 | 115166908 | |||||||
| chr5:115166961 | C | T | 2 | a0001c0004t0014g0346 a0001c0004t0014g0347 |
2 | HG01074.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.27+2647G>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 1/9 | chr5 | 115166961 | |||||||
| chr5:115166966 | G | A | 3 | a0001c0001t0001g0058 a0001c0004t0001g0056 a0001c0004t0001g0057 |
3 | HG02976.hp2 HG03516.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.27+2642C>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 1/9 | chr5 | 115166966 | |||||||
| chr5:115167171 | G | A | 1 | a0001c0009t0011g0051 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.27+2437C>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 1/9 | chr5 | 115167171 | |||||||
| chr5:115167205 | T | A | 1 | a0001c0001t0001g0331 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.27+2403A>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 1/9 | chr5 | 115167205 | |||||||
| chr5:115167254 | C | G | 1 | a0002c0002t0002g0179 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.27+2354G>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 1/9 | chr5 | 115167254 | |||||||
| chr5:115167271 | T | C | 153 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(150): Show |
187 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.27+2337A>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 1/9 | chr5 | 115167271 | |||||||
| chr5:115167468 | C | T | 1 | a0003c0003t0003g0061 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.27+2140G>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 1/9 | chr5 | 115167468 | |||||||
| chr5:115167580 | C | T | 1 | a0002c0002t0002g0062 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.27+2028G>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 1/9 | chr5 | 115167580 | |||||||
| chr5:115167684 | T | A | 1 | a0001c0001t0001g0332 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.27+1924A>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 1/9 | chr5 | 115167684 | |||||||
| chr5:115167767 | C | G | 8 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(5): Show |
8 | HG02055.hp1 HG02723.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.27+1841G>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 1/9 | chr5 | 115167767 | |||||||
| chr5:115167801 | C | T | 1 | a0003c0003t0003g0061 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.27+1807G>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 1/9 | chr5 | 115167801 | |||||||
| chr5:115167803 | C | A | 1 | a0001c0001t0001g0058 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.27+1805G>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 1/9 | chr5 | 115167803 | |||||||
| chr5:115167874 | T | C | 3 | a0001c0001t0001g0058 a0001c0004t0001g0056 a0001c0004t0001g0057 |
3 | HG02976.hp2 HG03516.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.27+1734A>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 1/9 | chr5 | 115167874 | |||||||
| chr5:115167896 | T | C | 113 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(110): Show |
144 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.27+1712A>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 1/9 | chr5 | 115167896 | |||||||
| chr5:115167904 | C | G | 1 | a0003c0003t0003g0052 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.27+1704G>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 1/9 | chr5 | 115167904 | |||||||
| chr5:115167952 | G | A | 128 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(125): Show |
159 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.27+1656C>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 1/9 | chr5 | 115167952 | |||||||
| chr5:115168054 | G | A | 2 | a0003c0003t0003g0177 a0003c0003t0003g0178 |
2 | HG02280.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.27+1554C>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 1/9 | chr5 | 115168054 | |||||||
| chr5:115168061 | G | A | 68 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0220 others(65): Show |
79 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.27+1547C>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 1/9 | chr5 | 115168061 | |||||||
| chr5:115168078 | C | T | 1 | a0001c0001t0001g0060 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.27+1530G>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 1/9 | chr5 | 115168078 | |||||||
| chr5:115168082 | C | T | 3 | a0001c0006t0003g0240 a0001c0006t0003g0241 a0001c0006t0003g0242 |
3 | HG02055.hp2 HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.27+1526G>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 1/9 | chr5 | 115168082 | |||||||
| chr5:115168156 | A | G | 8 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(5): Show |
8 | HG02055.hp1 HG02723.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.27+1452T>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 1/9 | chr5 | 115168156 | |||||||
| chr5:115168161 | A | G | 1 | a0001c0009t0011g0051 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.27+1447T>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 1/9 | chr5 | 115168161 | |||||||
| chr5:115168250 | C | G | 138 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(135): Show |
169 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.27+1358G>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 1/9 | chr5 | 115168250 | |||||||
| chr5:115168881 | A | G | 1 | a0001c0009t0011g0051 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.27+727T>C | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 1/9 | chr5 | 115168881 | |||||||
| chr5:115168892 | T | C | 109 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(106): Show |
138 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.27+716A>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 1/9 | chr5 | 115168892 | |||||||
| chr5:115168905 | G | A | 7 | a0001c0004t0006g0041 a0001c0004t0006g0042 a0003c0003t0001g0040 others(4): Show |
7 | HG02145.hp1 HG02559.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.27+703C>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 1/9 | chr5 | 115168905 | |||||||
| chr5:115169122 | G | T | 1 | a0001c0001t0028g0345 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.27+486C>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 1/9 | chr5 | 115169122 | |||||||
| chr5:115169127 | C | T | 10 | a0001c0004t0001g0034 a0001c0004t0006g0041 a0001c0004t0006g0042 others(7): Show |
10 | HG02145.hp1 HG02258.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.27+481G>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 1/9 | chr5 | 115169127 | |||||||
| chr5:115169150 | G | T | 8 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(5): Show |
8 | HG02055.hp1 HG02723.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.27+458C>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 1/9 | chr5 | 115169150 | |||||||
| chr5:115169158 | G | A | 7 | a0001c0001t0001g0335 a0001c0001t0001g0336 a0001c0001t0001g0337 others(4): Show |
7 | HG00099.hp1 HG00735.hp1 HG00738.hp2 others(4): Show |
intron_variant | MODIFIER | c.27+450C>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 1/9 | chr5 | 115169158 | |||||||
| chr5:115169250 | C | T | 10 | a0001c0004t0001g0034 a0001c0004t0006g0041 a0001c0004t0006g0042 others(7): Show |
10 | HG02145.hp1 HG02258.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.27+358G>A | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 1/9 | chr5 | 115169250 | |||||||
| chr5:115169394 | C | A | 2 | a0001c0004t0014g0346 a0001c0004t0014g0347 |
2 | HG01074.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.27+214G>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 1/9 | chr5 | 115169394 | |||||||
| chr5:115169411 | G | A | 1 | a0001c0001t0001g0342 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.27+197C>T | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 1/9 | chr5 | 115169411 | |||||||
| chr5:115169526 | G | C | 1 | a0003c0003t0003g0343 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.27+82C>G | TRIM36 | ENSG00000152503.10 | transcript | ENST00000513154.6 | protein_coding | 1/9 | chr5 | 115169526 |