Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 23650 |
| ensemblid | ENSG00000137699.17 |
| hgncid | 17274 |
| symbol | TRIM29 |
| name | tripartite motif containing 29 |
| refseq_nuc | NM_012101.4 |
| refseq_prot | NP_036233.2 |
| ensembl_nuc | ENST00000341846.10 |
| ensembl_prot | ENSP00000343129.5 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 120111286 |
| end | 120138113 |
| strand | - |
| ver | v1.2 |
| region | chr11:120111286-120138113 |
| region5000 | chr11:120106286-120143113 |
| regionname0 | TRIM29_chr11_120111286_120138113 |
| regionname5000 | TRIM29_chr11_120106286_120143113 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 588 | 365 | 95 | 68 | 141 | 14 | 45 | 107 | TRIM29_chr11_120106286_120143113 | TRIM29 | MEAAD others(583): Show |
chr11 | 120106286 | 120143113 |
| a0002 | 0/0 | 588 | 31 | 0 | 4 | 26 | 0 | 1 | 22 | TRIM29_chr11_120106286_120143113 | TRIM29 | MEAAD others(583): Show |
chr11 | 120106286 | 120143113 |
| a0003 | 0/0 | 575 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | MEAAD others(570): Show |
chr11 | 120106286 | 120143113 |
| a0004 | 0/0 | 588 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | MEAAD others(583): Show |
chr11 | 120106286 | 120143113 |
| a0005 | 0/0 | 588 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | MEAAD others(583): Show |
chr11 | 120106286 | 120143113 |
| a0006 | 0/0 | 588 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TRIM29_chr11_120106286_120143113 | TRIM29 | MEAAD others(583): Show |
chr11 | 120106286 | 120143113 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1764 | 322 | 83 | 56 | 131 | 11 | 40 | TRIM29_chr11_120106286_120143113 | TRIM29 | ATGGA others(1759): Show |
chr11 | 120106286 | 120143113 | ||
| a0001c0003 | 1/0 | 1764 | 25 | 1 | 9 | 7 | 3 | 4 | TRIM29_chr11_120106286_120143113 | TRIM29 | ATGGA others(1759): Show |
chr11 | 120106286 | 120143113 | ||
| a0001c0004 | 0/0 | 1764 | 6 | 4 | 2 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | ATGGA others(1759): Show |
chr11 | 120106286 | 120143113 | ||
| a0001c0005 | 0/0 | 1764 | 6 | 6 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | ATGGA others(1759): Show |
chr11 | 120106286 | 120143113 | ||
| a0001c0006 | 0/0 | 1764 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | ATGGA others(1759): Show |
chr11 | 120106286 | 120143113 | ||
| a0001c0007 | 0/0 | 1764 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | ATGGA others(1759): Show |
chr11 | 120106286 | 120143113 | ||
| a0001c0008 | 0/0 | 1764 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM29_chr11_120106286_120143113 | TRIM29 | ATGGA others(1759): Show |
chr11 | 120106286 | 120143113 | ||
| a0001c0010 | 0/0 | 1764 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | ATGGA others(1759): Show |
chr11 | 120106286 | 120143113 | ||
| a0001c0012 | 0/0 | 1764 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | ATGGA others(1759): Show |
chr11 | 120106286 | 120143113 | ||
| a0002c0002 | 0/0 | 1764 | 31 | 0 | 4 | 26 | 0 | 1 | TRIM29_chr11_120106286_120143113 | TRIM29 | ATGGA others(1759): Show |
chr11 | 120106286 | 120143113 | ||
| a0003c0013 | 0/0 | 1725 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | ATGGA others(1720): Show |
chr11 | 120106286 | 120143113 | ||
| a0004c0014 | 0/0 | 1764 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | ATGGA others(1759): Show |
chr11 | 120106286 | 120143113 | ||
| a0005c0009 | 0/0 | 1764 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | ATGGA others(1759): Show |
chr11 | 120106286 | 120143113 | ||
| a0006c0011 | 0/0 | 1764 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | ATGGA others(1759): Show |
chr11 | 120106286 | 120143113 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2977 | 310 | 75 | 55 | 128 | 11 | 40 | TRIM29_chr11_120106286_120143113 | TRIM29 | ACTCC others(2972): Show |
chr11 | 120106286 | 120143113 |
| a0001c0001t0003 | 0/0 | 2977 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | ACTCC others(2972): Show |
chr11 | 120106286 | 120143113 |
| a0001c0001t0004 | 0/0 | 2977 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | ACTCC others(2972): Show |
chr11 | 120106286 | 120143113 |
| a0001c0001t0005 | 0/0 | 2977 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | ACTCC others(2972): Show |
chr11 | 120106286 | 120143113 |
| a0001c0001t0007 | 0/0 | 2977 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | ACTCC others(2972): Show |
chr11 | 120106286 | 120143113 |
| a0001c0001t0008 | 0/0 | 2977 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | ACTCC others(2972): Show |
chr11 | 120106286 | 120143113 |
| a0001c0001t0009 | 0/0 | 2977 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | ACTCC others(2972): Show |
chr11 | 120106286 | 120143113 |
| a0001c0001t0010 | 0/0 | 2977 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | ACTCC others(2972): Show |
chr11 | 120106286 | 120143113 |
| a0001c0001t0012 | 0/0 | 2977 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | ACTCC others(2972): Show |
chr11 | 120106286 | 120143113 |
| a0001c0003t0001 | 1/0 | 2977 | 25 | 1 | 9 | 7 | 3 | 4 | TRIM29_chr11_120106286_120143113 | TRIM29 | ACTCC others(2972): Show |
chr11 | 120106286 | 120143113 |
| a0001c0004t0001 | 0/0 | 2977 | 5 | 3 | 2 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | ACTCC others(2972): Show |
chr11 | 120106286 | 120143113 |
| a0001c0004t0002 | 0/0 | 2977 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | ACTCC others(2972): Show |
chr11 | 120106286 | 120143113 |
| a0001c0005t0001 | 0/0 | 2977 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | ACTCC others(2972): Show |
chr11 | 120106286 | 120143113 |
| a0001c0005t0002 | 0/0 | 2977 | 5 | 5 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | ACTCC others(2972): Show |
chr11 | 120106286 | 120143113 |
| a0001c0006t0001 | 0/0 | 2977 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | ACTCC others(2972): Show |
chr11 | 120106286 | 120143113 |
| a0001c0007t0001 | 0/0 | 2977 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | ACTCC others(2972): Show |
chr11 | 120106286 | 120143113 |
| a0001c0008t0001 | 0/0 | 2977 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM29_chr11_120106286_120143113 | TRIM29 | ACTCC others(2972): Show |
chr11 | 120106286 | 120143113 |
| a0001c0010t0013 | 0/0 | 2977 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | ACTCC others(2972): Show |
chr11 | 120106286 | 120143113 |
| a0001c0012t0001 | 0/0 | 2977 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | ACTCC others(2972): Show |
chr11 | 120106286 | 120143113 |
| a0002c0002t0001 | 0/0 | 2977 | 29 | 0 | 4 | 24 | 0 | 1 | TRIM29_chr11_120106286_120143113 | TRIM29 | ACTCC others(2972): Show |
chr11 | 120106286 | 120143113 |
| a0002c0002t0006 | 0/0 | 2977 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | ACTAC others(2972): Show |
chr11 | 120106286 | 120143113 |
| a0002c0002t0011 | 0/0 | 2977 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | ACTCC others(2972): Show |
chr11 | 120106286 | 120143113 |
| a0003c0013t0001 | 0/0 | 2938 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | ACTCC others(2933): Show |
chr11 | 120106286 | 120143113 |
| a0004c0014t0001 | 0/0 | 2977 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | ACTCC others(2972): Show |
chr11 | 120106286 | 120143113 |
| a0005c0009t0001 | 0/0 | 2977 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | ACTCC others(2972): Show |
chr11 | 120106286 | 120143113 |
| a0006c0011t0001 | 0/0 | 2977 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | ACTCC others(2972): Show |
chr11 | 120106286 | 120143113 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 18 | 0 | 0 | 18 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0003 | 0/0 | 10 | 0 | 1 | 9 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0005 | 0/0 | 8 | 3 | 4 | 0 | 1 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0006 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0007 | 0/0 | 7 | 0 | 6 | 0 | 0 | 1 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0008 | 0/0 | 6 | 0 | 1 | 0 | 2 | 3 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0009 | 0/0 | 4 | 0 | 0 | 0 | 0 | 4 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0010 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0011 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0013 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0015 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0016 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0018 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0019 | 0/1 | 3 | 0 | 2 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0023 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0034 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0003g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0003g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0004g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0005g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0007g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0008g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0009g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0010g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0012g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0003t0001g0004 | 0/0 | 10 | 0 | 3 | 6 | 0 | 1 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0003t0001g0046 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0003t0001g0047 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0003t0001g0048 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0003t0001g0049 | 1/0 | 2 | 0 | 0 | 0 | 0 | 1 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0003t0001g0050 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0003t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0003t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0003t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0003t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0003t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0004t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0004t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0004t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0004t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0004t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0004t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0005t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0005t0002g0026 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0005t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0005t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0006t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0006t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0007t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0008t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0010t0013g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0012t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0002c0002t0001g0002 | 0/0 | 15 | 0 | 3 | 12 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0002c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0002c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0002c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0002c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0002c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0002c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0002c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0002c0002t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0002c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0002c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0002c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0002c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0002c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0002c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0002c0002t0006g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0002c0002t0011g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0003c0013t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0004c0014t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0005c0009t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0006c0011t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0139 | EUR | GBR | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | GBR | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0138 | EUR | GBR | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0187 | EUR | GBR | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0068 | EUR | FIN | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG00323 | hp2 | a0001 | c0003 | t0001 | g0047 | EUR | FIN | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG00408 | hp1 | a0001 | c0003 | t0001 | g0004 | EAS | CHS | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | CHS | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | CHS | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | CHS | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | CHS | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | CHS | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | CHS | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | CHS | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | CHS | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | CHS | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG00621 | hp1 | a0001 | c0003 | t0001 | g0004 | EAS | CHS | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | CHS | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG00639 | hp2 | a0001 | c0003 | t0001 | g0004 | AMR | PUR | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG00642 | hp2 | a0001 | c0010 | t0013 | g0208 | AMR | PUR | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG00673 | hp1 | a0002 | c0002 | t0001 | g0195 | EAS | CHS | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | CHS | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG00741 | hp1 | a0001 | c0003 | t0001 | g0207 | AMR | PUR | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG01069 | hp1 | a0001 | c0003 | t0001 | g0233 | AMR | PUR | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG01074 | hp2 | a0003 | c0013 | t0001 | g0256 | AMR | PUR | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG01099 | hp1 | a0001 | c0004 | t0001 | g0090 | AMR | PUR | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG01106 | hp1 | a0001 | c0003 | t0001 | g0050 | AMR | PUR | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG01109 | hp1 | a0001 | c0004 | t0001 | g0120 | AMR | PUR | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG01167 | hp1 | a0001 | c0003 | t0001 | g0050 | AMR | PUR | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG01175 | hp2 | a0004 | c0014 | t0001 | g0257 | AMR | PUR | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG01243 | hp2 | a0001 | c0001 | t0012 | g0118 | AMR | PUR | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | CLM | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | CLM | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | CLM | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | CLM | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | CLM | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG01433 | hp2 | a0001 | c0003 | t0001 | g0048 | AMR | CLM | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | CLM | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0152 | EUR | IBS | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG01515 | hp2 | a0001 | c0003 | t0001 | g0046 | EUR | IBS | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0104 | EUR | IBS | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | IBS | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG01517 | hp1 | a0001 | c0003 | t0001 | g0046 | EUR | IBS | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0238 | EUR | IBS | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | ACB | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | ACB | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG01943 | hp1 | a0002 | c0002 | t0001 | g0166 | AMR | PEL | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG01952 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PEL | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PEL | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG01981 | hp2 | a0001 | c0003 | t0001 | g0004 | AMR | PEL | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PEL | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02004 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02015 | hp1 | a0002 | c0002 | t0011 | g0245 | EAS | KHV | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | KHV | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02055 | hp1 | a0001 | c0005 | t0002 | g0253 | AFR | ACB | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | ACB | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02056 | hp2 | a0002 | c0002 | t0001 | g0241 | EAS | KHV | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | KHV | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | KHV | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | KHV | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02083 | hp1 | a0001 | c0001 | t0009 | g0251 | EAS | KHV | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | KHV | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02129 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | KHV | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | KHV | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02145 | hp2 | a0001 | c0004 | t0002 | g0122 | AFR | ACB | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02148 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | ACB | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02258 | hp1 | a0001 | c0001 | t0008 | g0175 | AFR | ACB | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | ACB | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02273 | hp1 | a0001 | c0003 | t0001 | g0004 | AMR | PEL | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | ACB | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | ACB | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | PEL | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | ACB | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02523 | hp1 | a0001 | c0003 | t0001 | g0235 | EAS | KHV | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | KHV | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02572 | hp1 | a0001 | c0001 | t0005 | g0038 | AFR | GWD | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | GWD | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0065 | SAS | PJL | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02615 | hp1 | a0001 | c0005 | t0001 | g0252 | AFR | GWD | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02615 | hp2 | a0001 | c0004 | t0001 | g0124 | AFR | GWD | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02622 | hp2 | a0001 | c0005 | t0002 | g0026 | AFR | GWD | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | GWD | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | GWD | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | GWD | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0196 | SAS | PJL | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | GWD | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | GWD | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | GWD | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | GWD | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | ESN | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02922 | hp2 | a0001 | c0005 | t0002 | g0026 | AFR | ESN | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02965 | hp1 | a0001 | c0001 | t0005 | g0038 | AFR | ESN | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | ESN | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | ESN | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | ESN | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | MSL | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | MSL | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG03130 | hp1 | a0001 | c0005 | t0002 | g0254 | AFR | ESN | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | ESN | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | ESN | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | ESN | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | ESN | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | MSL | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | MSL | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | MSL | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | MSL | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0147 | SAS | PJL | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0181 | SAS | PJL | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | MSL | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | MSL | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | MSL | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | MSL | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | PJL | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | ESN | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG03516 | hp2 | a0001 | c0004 | t0001 | g0121 | AFR | ESN | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG03540 | hp2 | a0001 | c0004 | t0001 | g0123 | AFR | GWD | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | MSL | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | MSL | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG03654 | hp1 | a0001 | c0003 | t0001 | g0049 | SAS | PJL | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG03669 | hp1 | a0001 | c0003 | t0001 | g0048 | SAS | PJL | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG03688 | hp1 | a0001 | c0003 | t0001 | g0004 | SAS | STU | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0237 | SAS | STU | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0066 | SAS | PJL | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | BEB | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | BEB | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | BEB | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG03834 | hp2 | a0001 | c0008 | t0001 | g0162 | SAS | BEB | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG03927 | hp1 | a0002 | c0002 | t0001 | g0126 | SAS | BEB | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0142 | SAS | BEB | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | BEB | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0227 | SAS | BEB | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | STU | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0204 | SAS | STU | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0216 | SAS | BEB | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | BEB | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0247 | SAS | STU | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | STU | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG04204 | hp1 | a0001 | c0003 | t0001 | g0234 | SAS | STU | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | STU | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | STU | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | STU | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | YRI | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | YRI | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | CHB | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA18906 | hp1 | a0001 | c0001 | t0007 | g0099 | AFR | YRI | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | YRI | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA18939 | hp2 | a0002 | c0002 | t0006 | g0053 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA18940 | hp1 | a0001 | c0006 | t0001 | g0184 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA18944 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA18950 | hp2 | a0002 | c0002 | t0001 | g0058 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA18956 | hp1 | a0002 | c0002 | t0001 | g0062 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA18965 | hp1 | a0002 | c0002 | t0001 | g0063 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA18967 | hp1 | a0002 | c0002 | t0001 | g0242 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA18968 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA18969 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA18971 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA18975 | hp1 | a0002 | c0002 | t0001 | g0061 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA18984 | hp1 | a0001 | c0001 | t0004 | g0029 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA18984 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA18986 | hp2 | a0001 | c0007 | t0001 | g0054 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA18988 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA18990 | hp1 | a0002 | c0002 | t0001 | g0059 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA18995 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA19009 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA19010 | hp2 | a0002 | c0002 | t0001 | g0240 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | LWK | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA19030 | hp2 | a0001 | c0001 | t0010 | g0236 | AFR | LWK | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA19043 | hp1 | a0001 | c0012 | t0001 | g0255 | AFR | LWK | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | LWK | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA19055 | hp1 | a0002 | c0002 | t0001 | g0243 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA19055 | hp2 | a0006 | c0011 | t0001 | g0190 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA19056 | hp2 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA19057 | hp2 | a0002 | c0002 | t0001 | g0244 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA19058 | hp2 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA19060 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA19064 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA19065 | hp2 | a0001 | c0001 | t0004 | g0029 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA19067 | hp2 | a0002 | c0002 | t0001 | g0155 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA19076 | hp1 | a0001 | c0006 | t0001 | g0164 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA19085 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA19088 | hp2 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA19090 | hp2 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | YRI | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | YRI | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | ASW | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0217 | AFR | ASW | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0037 | EUR | TSI | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | TSI | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | GIH | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0148 | SAS | GIH | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | CLM | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG01123 | hp2 | a0001 | c0003 | t0001 | g0232 | AMR | CLM | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | ACB | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | ACB | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02486 | hp1 | a0005 | c0009 | t0001 | g0209 | AFR | ACB | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | ACB | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0043 | AFR | ACB | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | MSL | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG03471 | hp2 | a0001 | c0005 | t0002 | g0026 | AFR | MSL | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0043 | AFR | USA | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | USA | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0206 | AFR | USA | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | USA | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA21309 | hp1 | a0001 | c0003 | t0001 | g0047 | AFR | LWK | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | LWK | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0019 | REF | REF | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| homoSapiens | grch38p0 | a0001 | c0003 | t0001 | g0049 | REF | REF | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:120115411 | T | C | 1 | a0002 | 31 | HG00673.hp1 HG01943.hp1 HG01952.hp1 others(28): Show |
missense_variant | MODERATE | c.1631A>G | p.Tyr544Cys | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 8/9 | 1713/2977 | 1631/1767 | 544/588 | chr11 | 120115411 | |||
| chr11:120125841 | T | G | 1 | a0006 | 1 | NA19055.hp2 | missense_variant | MODERATE | c.1183A>C | p.Thr395Pro | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 4/9 | 1265/2977 | 1183/1767 | 395/588 | chr11 | 120125841 | |||
| chr11:120127526 | C | T | 1 | a0005 | 1 | HG02486.hp1 | missense_variant | MODERATE | c.944G>A | p.Arg315Gln | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 3/9 | 1026/2977 | 944/1767 | 315/588 | chr11 | 120127526 | |||
| chr11:120137633 | CGAGAAAA others(32): Show |
C | 1 | a0003 | 1 | HG01074.hp2 | disruptive_inframe_deletion | MODERATE | c.360_398delCTTTGCCG others(31): Show |
p.Phe121_Ser133del | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 1/9 | 480/2977 | 360/1767 | 120/588 | chr11 | 120137633 | |||
| chr11:120137760 | G | C | 1 | a0004 | 1 | HG01175.hp2 | missense_variant | MODERATE | c.272C>G | p.Ser91Cys | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 1/9 | 354/2977 | 272/1767 | 91/588 | chr11 | 120137760 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:120118236 | G | A | 1 | a0001c0006 | 2 | NA18940.hp1 NA19076.hp1 |
synonymous_variant | LOW | c.1614C>T | p.Ser538Ser | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 7/9 | 1696/2977 | 1614/1767 | 538/588 | chr11 | 120118236 | |||
| chr11:120120610 | G | T | 1 | a0001c0010 | 1 | HG00642.hp2 | synonymous_variant | LOW | c.1491C>A | p.Thr497Thr | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 6/9 | 1573/2977 | 1491/1767 | 497/588 | chr11 | 120120610 | |||
| chr11:120125782 | G | A | 1 | a0001c0004 | 6 | HG01099.hp1 HG01109.hp1 HG02145.hp2 others(3): Show |
synonymous_variant | LOW | c.1242C>T | p.Asp414Asp | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 4/9 | 1324/2977 | 1242/1767 | 414/588 | chr11 | 120125782 | |||
| chr11:120128466 | C | T | 1 | a0001c0008 | 1 | HG03834.hp2 | synonymous_variant | LOW | c.834G>A | p.Leu278Leu | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 2/9 | 916/2977 | 834/1767 | 278/588 | chr11 | 120128466 | |||
| chr11:120128483 | A | G | 13 | a0001c0001 a0001c0004 a0001c0005 others(10): Show |
374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): Show |
synonymous_variant | LOW | c.817T>C | p.Leu273Leu | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 2/9 | 899/2977 | 817/1767 | 273/588 | chr11 | 120128483 | |||
| chr11:120137252 | C | T | 1 | a0001c0007 | 1 | NA18986.hp2 | synonymous_variant | LOW | c.780G>A | p.Val260Val | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 1/9 | 862/2977 | 780/1767 | 260/588 | chr11 | 120137252 | |||
| chr11:120137390 | G | C | 1 | a0001c0005 | 6 | HG02055.hp1 HG02615.hp1 HG02622.hp2 others(3): Show |
synonymous_variant | LOW | c.642C>G | p.Leu214Leu | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 1/9 | 724/2977 | 642/1767 | 214/588 | chr11 | 120137390 | |||
| chr11:120137570 | G | C | 1 | a0001c0012 | 1 | NA19043.hp1 | synonymous_variant | LOW | c.462C>G | p.Pro154Pro | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 1/9 | 544/2977 | 462/1767 | 154/588 | chr11 | 120137570 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:120111331 | G | A | 1 | a0001c0001t0009 | 1 | HG02083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1083C>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 9/9 | 1083 | chr11 | 120111331 | ||||||
| chr11:120111381 | A | G | 2 | a0001c0001t0003 a0001c0001t0010 |
4 | HG02559.hp1 HG06807.hp1 NA19030.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1033T>C | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 9/9 | 1033 | chr11 | 120111381 | ||||||
| chr11:120111393 | G | A | 1 | a0001c0001t0010 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1021C>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 9/9 | 1021 | chr11 | 120111393 | ||||||
| chr11:120111637 | T | C | 1 | a0002c0002t0011 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*777A>G | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 9/9 | 777 | chr11 | 120111637 | ||||||
| chr11:120111692 | C | T | 1 | a0001c0001t0005 | 2 | HG02572.hp1 HG02965.hp1 |
3_prime_UTR_variant | MODIFIER | c.*722G>A | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 9/9 | 722 | chr11 | 120111692 | ||||||
| chr11:120111795 | C | T | 1 | a0001c0001t0008 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*619G>A | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 9/9 | 619 | chr11 | 120111795 | ||||||
| chr11:120111798 | C | A | 2 | a0001c0004t0002 a0001c0005t0002 |
6 | HG02055.hp1 HG02145.hp2 HG02622.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*616G>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 9/9 | 616 | chr11 | 120111798 | ||||||
| chr11:120111997 | A | G | 1 | a0001c0001t0007 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*417T>C | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 9/9 | 417 | chr11 | 120111997 | ||||||
| chr11:120112049 | G | A | 1 | a0001c0001t0003 | 3 | HG02559.hp1 HG06807.hp1 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*365C>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 9/9 | 365 | chr11 | 120112049 | ||||||
| chr11:120112063 | G | T | 1 | a0001c0001t0003 | 3 | HG02559.hp1 HG06807.hp1 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*351C>A | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 9/9 | 351 | chr11 | 120112063 | ||||||
| chr11:120112382 | G | A | 1 | a0001c0001t0012 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*32C>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 9/9 | 32 | chr11 | 120112382 | ||||||
| chr11:120112391 | G | A | 1 | a0001c0010t0013 | 1 | HG00642.hp2 | 3_prime_UTR_variant | MODIFIER | c.*23C>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 9/9 | 23 | chr11 | 120112391 | ||||||
| chr11:120112404 | C | T | 1 | a0001c0001t0004 | 2 | NA18984.hp1 NA19065.hp2 |
3_prime_UTR_variant | MODIFIER | c.*10G>A | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 9/9 | 10 | chr11 | 120112404 | ||||||
| chr11:120138110 | G | T | 1 | a0002c0002t0006 | 1 | NA18939.hp2 | 5_prime_UTR_variant | MODIFIER | c.-79C>A | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 1/9 | 79 | chr11 | 120138110 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:120112598 | C | A | 2 | a0001c0001t0001g0210 a0005c0009t0001g0209 |
2 | HG02486.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1705-122G>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 8/8 | chr11 | 120112598 | |||||||
| chr11:120112683 | T | A | 2 | a0001c0001t0001g0144 a0001c0001t0001g0151 |
2 | HG01255.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.1705-207A>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 8/8 | chr11 | 120112683 | |||||||
| chr11:120112683 | T | C | 2 | a0001c0001t0001g0149 a0001c0001t0001g0150 |
2 | HG03195.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1705-207A>G | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 8/8 | chr11 | 120112683 | |||||||
| chr11:120113031 | C | T | 6 | a0001c0001t0001g0077 a0001c0001t0001g0182 a0001c0004t0001g0090 others(3): Show |
6 | HG00642.hp2 HG01099.hp1 HG01109.hp1 others(3): Show |
intron_variant | MODIFIER | c.1705-555G>A | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 8/8 | chr11 | 120113031 | |||||||
| chr11:120113091 | T | C | 211 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(208): Show |
327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.1705-615A>G | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 8/8 | chr11 | 120113091 | |||||||
| chr11:120113119 | A | G | 1 | a0001c0001t0001g0083 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1705-643T>C | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 8/8 | chr11 | 120113119 | |||||||
| chr11:120113123 | A | G | 214 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(211): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.1705-647T>C | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 8/8 | chr11 | 120113123 | |||||||
| chr11:120113161 | C | T | 1 | a0005c0009t0001g0209 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1705-685G>A | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 8/8 | chr11 | 120113161 | |||||||
| chr11:120113211 | C | A | 20 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0037 others(17): Show |
29 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(26): Show |
intron_variant | MODIFIER | c.1705-735G>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 8/8 | chr11 | 120113211 | |||||||
| chr11:120113232 | G | T | 3 | a0001c0001t0001g0104 a0001c0001t0001g0108 a0001c0001t0001g0131 |
3 | HG01257.hp2 HG01258.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.1705-756C>A | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 8/8 | chr11 | 120113232 | |||||||
| chr11:120113234 | A | G | 2 | a0001c0001t0001g0073 a0001c0001t0001g0074 |
2 | HG02451.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1705-758T>C | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 8/8 | chr11 | 120113234 | |||||||
| chr11:120113245 | G | A | 2 | a0001c0001t0001g0125 a0001c0001t0001g0198 |
2 | HG00558.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.1705-769C>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 8/8 | chr11 | 120113245 | |||||||
| chr11:120113333 | T | C | 1 | a0001c0001t0001g0045 | 2 | NA18964.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.1705-857A>G | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 8/8 | chr11 | 120113333 | |||||||
| chr11:120113403 | A | G | 1 | a0001c0001t0001g0067 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1705-927T>C | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 8/8 | chr11 | 120113403 | |||||||
| chr11:120113494 | A | G | 207 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(204): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.1705-1018T>C | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 8/8 | chr11 | 120113494 | |||||||
| chr11:120113587 | T | C | 1 | a0001c0001t0001g0051 | 2 | HG02132.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.1705-1111A>G | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 8/8 | chr11 | 120113587 | |||||||
| chr11:120113636 | T | A | 1 | a0001c0001t0001g0033 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1705-1160A>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 8/8 | chr11 | 120113636 | |||||||
| chr11:120113686 | G | C | 1 | a0001c0001t0001g0042 | 2 | HG02717.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1705-1210C>G | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 8/8 | chr11 | 120113686 | |||||||
| chr11:120113809 | A | G | 1 | a0001c0001t0001g0229 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1705-1333T>C | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 8/8 | chr11 | 120113809 | |||||||
| chr11:120113827 | G | C | 167 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(164): Show |
260 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(257): Show |
intron_variant | MODIFIER | c.1705-1351C>G | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 8/8 | chr11 | 120113827 | |||||||
| chr11:120113849 | G | T | 1 | a0001c0001t0001g0072 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1705-1373C>A | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 8/8 | chr11 | 120113849 | |||||||
| chr11:120113890 | G | A | 3 | a0001c0001t0001g0019 a0001c0001t0001g0105 a0001c0001t0001g0106 |
4 | HG00735.hp1 HG00738.hp1 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.1705-1414C>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 8/8 | chr11 | 120113890 | |||||||
| chr11:120113930 | C | T | 21 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0037 others(18): Show |
30 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(27): Show |
intron_variant | MODIFIER | c.1704+1408G>A | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 8/8 | chr11 | 120113930 | |||||||
| chr11:120114022 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1704+1316C>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 8/8 | chr11 | 120114022 | |||||||
| chr11:120114048 | ACAC | A | 2 | a0001c0001t0003g0043 a0001c0001t0003g0206 |
3 | HG02559.hp1 HG06807.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1704+1287_1704+128 others(7): Show |
TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 8/8 | chr11 | 120114048 | |||||||
| chr11:120114052 | A | T | 2 | a0001c0001t0003g0043 a0001c0001t0003g0206 |
3 | HG02559.hp1 HG06807.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1704+1286T>A | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 8/8 | chr11 | 120114052 | |||||||
| chr11:120114102 | G | C | 1 | a0001c0001t0001g0153 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1704+1236C>G | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 8/8 | chr11 | 120114102 | |||||||
| chr11:120114118 | G | C | 19 | a0001c0001t0003g0043 a0001c0001t0003g0206 a0002c0002t0001g0002 others(16): Show |
34 | HG00673.hp1 HG01943.hp1 HG01952.hp1 others(31): Show |
intron_variant | MODIFIER | c.1704+1220C>G | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 8/8 | chr11 | 120114118 | |||||||
| chr11:120114125 | G | A | 1 | a0001c0001t0001g0219 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1704+1213C>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 8/8 | chr11 | 120114125 | |||||||
| chr11:120114155 | C | T | 174 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(171): Show |
268 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(265): Show |
intron_variant | MODIFIER | c.1704+1183G>A | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 8/8 | chr11 | 120114155 | |||||||
| chr11:120114188 | C | A | 4 | a0001c0001t0001g0092 a0001c0001t0001g0098 a0001c0001t0001g0217 others(1): Show |
4 | HG00642.hp1 HG02109.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1704+1150G>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 8/8 | chr11 | 120114188 | |||||||
| chr11:120114226 | G | T | 1 | a0001c0001t0001g0080 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1704+1112C>A | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 8/8 | chr11 | 120114226 | |||||||
| chr11:120114303 | A | G | 13 | a0001c0001t0001g0009 a0001c0001t0001g0030 a0001c0001t0001g0035 others(10): Show |
18 | HG02056.hp1 HG02683.hp1 HG02683.hp2 others(15): Show |
intron_variant | MODIFIER | c.1704+1035T>C | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 8/8 | chr11 | 120114303 | |||||||
| chr11:120114342 | A | G | 197 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(194): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.1704+996T>C | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 8/8 | chr11 | 120114342 | |||||||
| chr11:120114397 | G | C | 4 | a0001c0001t0001g0092 a0001c0001t0001g0098 a0001c0001t0001g0217 others(1): Show |
4 | HG00642.hp1 HG02109.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1704+941C>G | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 8/8 | chr11 | 120114397 | |||||||
| chr11:120114466 | C | A | 17 | a0002c0002t0001g0002 a0002c0002t0001g0058 a0002c0002t0001g0059 others(14): Show |
31 | HG00673.hp1 HG01943.hp1 HG01952.hp1 others(28): Show |
intron_variant | MODIFIER | c.1704+872G>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 8/8 | chr11 | 120114466 | |||||||
| chr11:120114538 | A | G | 2 | a0001c0001t0001g0033 a0001c0001t0001g0103 |
3 | HG01167.hp2 HG01169.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.1704+800T>C | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 8/8 | chr11 | 120114538 | |||||||
| chr11:120114675 | A | C | 3 | a0001c0001t0001g0031 a0001c0001t0001g0096 a0001c0001t0007g0099 |
4 | HG02258.hp2 HG03486.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1704+663T>G | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 8/8 | chr11 | 120114675 | |||||||
| chr11:120114766 | C | A | 2 | a0001c0001t0001g0212 a0001c0001t0001g0213 |
2 | HG02809.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1704+572G>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 8/8 | chr11 | 120114766 | |||||||
| chr11:120114767 | C | A | 27 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0037 others(24): Show |
36 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(33): Show |
intron_variant | MODIFIER | c.1704+571G>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 8/8 | chr11 | 120114767 | |||||||
| chr11:120114791 | A | G | 17 | a0002c0002t0001g0002 a0002c0002t0001g0058 a0002c0002t0001g0059 others(14): Show |
31 | HG00673.hp1 HG01943.hp1 HG01952.hp1 others(28): Show |
intron_variant | MODIFIER | c.1704+547T>C | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 8/8 | chr11 | 120114791 | |||||||
| chr11:120114862 | A | G | 21 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0037 others(18): Show |
30 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(27): Show |
intron_variant | MODIFIER | c.1704+476T>C | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 8/8 | chr11 | 120114862 | |||||||
| chr11:120114918 | T | A | 1 | a0001c0001t0001g0093 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1704+420A>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 8/8 | chr11 | 120114918 | |||||||
| chr11:120114932 | ACTGGAGA others(3): Show |
A | 1 | a0001c0001t0001g0081 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1704+396_1704+405d others(12): Show |
TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 8/8 | chr11 | 120114932 | |||||||
| chr11:120115459 | T | C | 168 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(165): Show |
263 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(260): Show |
intron_variant | MODIFIER | c.1628-45A>G | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 7/8 | chr11 | 120115459 | |||||||
| chr11:120115467 | G | C | 25 | a0001c0001t0001g0022 a0001c0001t0001g0036 a0001c0001t0001g0077 others(22): Show |
42 | HG00621.hp2 HG00642.hp2 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.1628-53C>G | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 7/8 | chr11 | 120115467 | |||||||
| chr11:120115471 | G | T | 24 | a0001c0001t0001g0022 a0001c0001t0001g0077 a0001c0001t0001g0182 others(21): Show |
40 | HG00621.hp2 HG00642.hp2 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.1628-57C>A | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 7/8 | chr11 | 120115471 | |||||||
| chr11:120115473 | GC | G | 24 | a0001c0001t0001g0022 a0001c0001t0001g0077 a0001c0001t0001g0182 others(21): Show |
40 | HG00621.hp2 HG00642.hp2 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.1628-60delG | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 7/8 | chr11 | 120115473 | |||||||
| chr11:120115474 | C | A | 21 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0037 others(18): Show |
30 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(27): Show |
intron_variant | MODIFIER | c.1628-60G>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 7/8 | chr11 | 120115474 | |||||||
| chr11:120115474 | C | G | 1 | a0001c0001t0001g0036 | 2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1628-60G>C | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 7/8 | chr11 | 120115474 | |||||||
| chr11:120115515 | C | T | 1 | a0001c0001t0001g0036 | 2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1628-101G>A | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 7/8 | chr11 | 120115515 | |||||||
| chr11:120115534 | A | C | 17 | a0002c0002t0001g0002 a0002c0002t0001g0058 a0002c0002t0001g0059 others(14): Show |
31 | HG00673.hp1 HG01943.hp1 HG01952.hp1 others(28): Show |
intron_variant | MODIFIER | c.1628-120T>G | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 7/8 | chr11 | 120115534 | |||||||
| chr11:120115567 | A | T | 1 | a0002c0002t0001g0244 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1628-153T>A | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 7/8 | chr11 | 120115567 | |||||||
| chr11:120115581 | G | A | 1 | a0001c0001t0010g0236 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1628-167C>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 7/8 | chr11 | 120115581 | |||||||
| chr11:120115781 | C | T | 1 | a0001c0001t0001g0192 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1628-367G>A | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 7/8 | chr11 | 120115781 | |||||||
| chr11:120115986 | G | GCAGTCAG others(5): Show |
2 | a0001c0001t0003g0043 a0001c0001t0003g0206 |
3 | HG02559.hp1 HG06807.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1628-573_1628-572i others(14): Show |
TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 7/8 | chr11 | 120115986 | |||||||
| chr11:120116010 | G | A | 1 | a0001c0001t0001g0022 | 3 | HG00621.hp2 HG02040.hp1 HG02071.hp2 |
intron_variant | MODIFIER | c.1628-596C>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 7/8 | chr11 | 120116010 | |||||||
| chr11:120116019 | C | T | 1 | a0001c0001t0001g0181 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1628-605G>A | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 7/8 | chr11 | 120116019 | |||||||
| chr11:120116111 | A | AG | 4 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0003g0043 others(1): Show |
5 | HG02559.hp1 HG02809.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1628-698dupC | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 7/8 | chr11 | 120116111 | |||||||
| chr11:120116134 | C | T | 4 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0003g0043 others(1): Show |
5 | HG02559.hp1 HG02809.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1628-720G>A | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 7/8 | chr11 | 120116134 | |||||||
| chr11:120116136 | G | C | 4 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0003g0043 others(1): Show |
5 | HG02559.hp1 HG02809.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1628-722C>G | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 7/8 | chr11 | 120116136 | |||||||
| chr11:120116144 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1628-730C>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 7/8 | chr11 | 120116144 | |||||||
| chr11:120116233 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1628-819C>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 7/8 | chr11 | 120116233 | |||||||
| chr11:120116338 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1628-924G>A | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 7/8 | chr11 | 120116338 | |||||||
| chr11:120116399 | G | A | 1 | a0001c0001t0001g0183 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1628-985C>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 7/8 | chr11 | 120116399 | |||||||
| chr11:120116432 | G | A | 2 | a0001c0001t0003g0043 a0001c0001t0003g0206 |
3 | HG02559.hp1 HG06807.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1628-1018C>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 7/8 | chr11 | 120116432 | |||||||
| chr11:120116511 | C | T | 180 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(177): Show |
289 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(286): Show |
intron_variant | MODIFIER | c.1628-1097G>A | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 7/8 | chr11 | 120116511 | |||||||
| chr11:120116566 | G | T | 1 | a0002c0002t0001g0242 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1628-1152C>A | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 7/8 | chr11 | 120116566 | |||||||
| chr11:120116809 | A | G | 162 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(159): Show |
255 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(252): Show |
intron_variant | MODIFIER | c.1628-1395T>C | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 7/8 | chr11 | 120116809 | |||||||
| chr11:120116865 | G | A | 2 | a0001c0001t0001g0212 a0001c0001t0001g0213 |
2 | HG02809.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1627+1358C>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 7/8 | chr11 | 120116865 | |||||||
| chr11:120116868 | C | T | 195 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(192): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.1627+1355G>A | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 7/8 | chr11 | 120116868 | |||||||
| chr11:120117135 | G | C | 3 | a0001c0001t0001g0031 a0001c0001t0001g0096 a0001c0001t0007g0099 |
4 | HG02258.hp2 HG03486.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1627+1088C>G | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 7/8 | chr11 | 120117135 | |||||||
| chr11:120117146 | A | G | 5 | a0001c0004t0001g0090 a0001c0004t0001g0120 a0001c0004t0001g0121 others(2): Show |
5 | HG00642.hp2 HG01099.hp1 HG01109.hp1 others(2): Show |
intron_variant | MODIFIER | c.1627+1077T>C | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 7/8 | chr11 | 120117146 | |||||||
| chr11:120117316 | C | T | 1 | a0001c0001t0001g0102 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1627+907G>A | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 7/8 | chr11 | 120117316 | |||||||
| chr11:120117550 | A | C | 18 | a0001c0001t0001g0246 a0001c0001t0001g0248 a0002c0002t0001g0002 others(15): Show |
32 | HG00673.hp1 HG01943.hp1 HG01952.hp1 others(29): Show |
intron_variant | MODIFIER | c.1627+673T>G | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 7/8 | chr11 | 120117550 | |||||||
| chr11:120117630 | G | A | 2 | a0001c0001t0003g0043 a0001c0001t0003g0206 |
3 | HG02559.hp1 HG06807.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1627+593C>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 7/8 | chr11 | 120117630 | |||||||
| chr11:120117673 | G | A | 1 | a0001c0004t0001g0090 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1627+550C>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 7/8 | chr11 | 120117673 | |||||||
| chr11:120117709 | C | T | 18 | a0001c0001t0001g0246 a0001c0001t0001g0248 a0002c0002t0001g0002 others(15): Show |
32 | HG00673.hp1 HG01943.hp1 HG01952.hp1 others(29): Show |
intron_variant | MODIFIER | c.1627+514G>A | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 7/8 | chr11 | 120117709 | |||||||
| chr11:120117802 | C | A | 2 | a0001c0001t0003g0043 a0001c0001t0003g0206 |
3 | HG02559.hp1 HG06807.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1627+421G>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 7/8 | chr11 | 120117802 | |||||||
| chr11:120117830 | G | T | 1 | a0001c0001t0001g0095 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1627+393C>A | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 7/8 | chr11 | 120117830 | |||||||
| chr11:120117862 | C | T | 2 | a0001c0001t0001g0069 a0001c0001t0001g0134 |
2 | HG03710.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.1627+361G>A | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 7/8 | chr11 | 120117862 | |||||||
| chr11:120117881 | A | C | 1 | a0001c0001t0001g0101 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1627+342T>G | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 7/8 | chr11 | 120117881 | |||||||
| chr11:120117944 | T | C | 3 | a0001c0001t0001g0072 a0001c0001t0001g0212 a0001c0001t0001g0213 |
3 | HG02055.hp2 HG02809.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1627+279A>G | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 7/8 | chr11 | 120117944 | |||||||
| chr11:120118399 | C | G | 26 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0018 others(23): Show |
43 | HG00323.hp1 HG00733.hp2 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.1529-78G>C | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 6/8 | chr11 | 120118399 | |||||||
| chr11:120118415 | G | T | 28 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0018 others(25): Show |
46 | HG00323.hp1 HG00733.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.1529-94C>A | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 6/8 | chr11 | 120118415 | |||||||
| chr11:120118461 | G | A | 3 | a0001c0001t0001g0031 a0001c0001t0001g0096 a0001c0001t0007g0099 |
4 | HG02258.hp2 HG03486.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1529-140C>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 6/8 | chr11 | 120118461 | |||||||
| chr11:120118672 | G | A | 29 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0018 others(26): Show |
47 | HG00323.hp1 HG00733.hp2 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.1529-351C>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 6/8 | chr11 | 120118672 | |||||||
| chr11:120118789 | G | A | 29 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0018 others(26): Show |
47 | HG00323.hp1 HG00733.hp2 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.1529-468C>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 6/8 | chr11 | 120118789 | |||||||
| chr11:120118861 | T | C | 250 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(247): Show |
379 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(376): Show |
intron_variant | MODIFIER | c.1529-540A>G | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 6/8 | chr11 | 120118861 | |||||||
| chr11:120118864 | T | A | 54 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(51): Show |
81 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.1529-543A>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 6/8 | chr11 | 120118864 | |||||||
| chr11:120118882 | A | C | 29 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0018 others(26): Show |
47 | HG00323.hp1 HG00733.hp2 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.1529-561T>G | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 6/8 | chr11 | 120118882 | |||||||
| chr11:120118899 | C | A | 10 | a0001c0001t0001g0036 a0001c0001t0001g0088 a0001c0001t0001g0089 others(7): Show |
11 | HG01099.hp1 HG01109.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.1529-578G>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 6/8 | chr11 | 120118899 | |||||||
| chr11:120118922 | G | A | 29 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0018 others(26): Show |
47 | HG00323.hp1 HG00733.hp2 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.1529-601C>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 6/8 | chr11 | 120118922 | |||||||
| chr11:120118928 | C | T | 29 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0018 others(26): Show |
47 | HG00323.hp1 HG00733.hp2 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.1529-607G>A | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 6/8 | chr11 | 120118928 | |||||||
| chr11:120119046 | T | C | 1 | a0001c0001t0001g0021 | 3 | NA18991.hp2 NA19070.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1529-725A>G | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 6/8 | chr11 | 120119046 | |||||||
| chr11:120119055 | G | A | 15 | a0001c0001t0001g0246 a0001c0001t0001g0248 a0002c0002t0001g0002 others(12): Show |
29 | HG00673.hp1 HG01943.hp1 HG01952.hp1 others(26): Show |
intron_variant | MODIFIER | c.1529-734C>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 6/8 | chr11 | 120119055 | |||||||
| chr11:120119145 | A | G | 1 | a0001c0001t0001g0044 | 2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1529-824T>C | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 6/8 | chr11 | 120119145 | |||||||
| chr11:120119184 | A | G | 110 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(107): Show |
186 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(183): Show |
intron_variant | MODIFIER | c.1529-863T>C | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 6/8 | chr11 | 120119184 | |||||||
| chr11:120119192 | G | A | 1 | a0001c0001t0001g0085 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1529-871C>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 6/8 | chr11 | 120119192 | |||||||
| chr11:120119248 | G | T | 16 | a0001c0001t0001g0051 a0001c0001t0001g0246 a0001c0001t0001g0248 others(13): Show |
31 | HG00673.hp1 HG01943.hp1 HG01952.hp1 others(28): Show |
intron_variant | MODIFIER | c.1529-927C>A | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 6/8 | chr11 | 120119248 | |||||||
| chr11:120119253 | C | T | 15 | a0001c0001t0001g0036 a0001c0001t0001g0088 a0001c0001t0001g0089 others(12): Show |
17 | HG00642.hp1 HG01099.hp1 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.1529-932G>A | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 6/8 | chr11 | 120119253 | |||||||
| chr11:120119254 | G | A | 16 | a0001c0001t0001g0051 a0001c0001t0001g0246 a0001c0001t0001g0248 others(13): Show |
31 | HG00673.hp1 HG01943.hp1 HG01952.hp1 others(28): Show |
intron_variant | MODIFIER | c.1529-933C>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 6/8 | chr11 | 120119254 | |||||||
| chr11:120119276 | C | A | 16 | a0001c0001t0001g0051 a0001c0001t0001g0246 a0001c0001t0001g0248 others(13): Show |
31 | HG00673.hp1 HG01943.hp1 HG01952.hp1 others(28): Show |
intron_variant | MODIFIER | c.1529-955G>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 6/8 | chr11 | 120119276 | |||||||
| chr11:120119466 | G | A | 1 | a0001c0010t0013g0208 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1528+1107C>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 6/8 | chr11 | 120119466 | |||||||
| chr11:120119955 | T | G | 15 | a0001c0001t0001g0036 a0001c0001t0001g0088 a0001c0001t0001g0089 others(12): Show |
17 | HG00642.hp1 HG01099.hp1 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.1528+618A>C | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 6/8 | chr11 | 120119955 | |||||||
| chr11:120120018 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1528+555G>A | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 6/8 | chr11 | 120120018 | |||||||
| chr11:120120047 | C | G | 1 | a0001c0001t0001g0247 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1528+526G>C | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 6/8 | chr11 | 120120047 | |||||||
| chr11:120120144 | T | C | 1 | a0001c0001t0001g0191 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1528+429A>G | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 6/8 | chr11 | 120120144 | |||||||
| chr11:120120145 | C | T | 1 | a0001c0001t0001g0191 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1528+428G>A | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 6/8 | chr11 | 120120145 | |||||||
| chr11:120120146 | T | C | 1 | a0001c0001t0001g0191 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1528+427A>G | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 6/8 | chr11 | 120120146 | |||||||
| chr11:120120163 | T | C | 1 | a0001c0001t0001g0226 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1528+410A>G | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 6/8 | chr11 | 120120163 | |||||||
| chr11:120120169 | T | A | 6 | a0001c0001t0001g0042 a0001c0001t0001g0119 a0001c0001t0001g0201 others(3): Show |
7 | HG01123.hp1 HG02615.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1528+404A>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 6/8 | chr11 | 120120169 | |||||||
| chr11:120120180 | GT | G | 88 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(85): Show |
149 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.1528+392delA | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 6/8 | chr11 | 120120180 | |||||||
| chr11:120120181 | T | G | 5 | a0001c0001t0001g0158 a0001c0001t0001g0177 a0001c0001t0001g0180 others(2): Show |
5 | HG01099.hp2 HG02738.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1528+392A>C | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 6/8 | chr11 | 120120181 | |||||||
| chr11:120120188 | T | C | 1 | a0001c0001t0001g0205 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1528+385A>G | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 6/8 | chr11 | 120120188 | |||||||
| chr11:120120202 | G | C | 3 | a0001c0001t0001g0104 a0001c0001t0001g0108 a0001c0001t0001g0131 |
3 | HG01257.hp2 HG01258.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.1528+371C>G | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 6/8 | chr11 | 120120202 | |||||||
| chr11:120120265 | C | A | 1 | a0001c0001t0001g0226 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1528+308G>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 6/8 | chr11 | 120120265 | |||||||
| chr11:120120344 | T | TAC | 10 | a0001c0001t0001g0052 a0001c0001t0001g0147 a0001c0001t0001g0224 others(7): Show |
20 | HG00408.hp1 HG00597.hp1 HG00621.hp1 others(17): Show |
intron_variant | MODIFIER | c.1528+227_1528+228d others(4): Show |
TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 6/8 | chr11 | 120120344 | |||||||
| chr11:120120344 | T | TACAC | 5 | a0001c0001t0001g0065 a0001c0001t0001g0088 a0001c0001t0001g0089 others(2): Show |
6 | HG01106.hp1 HG01167.hp1 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.1528+225_1528+228d others(6): Show |
TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 6/8 | chr11 | 120120344 | |||||||
| chr11:120120344 | TAC | T | 11 | a0001c0001t0001g0077 a0001c0001t0001g0098 a0001c0001t0001g0215 others(8): Show |
13 | HG01099.hp1 HG01433.hp2 HG02056.hp2 others(10): Show |
intron_variant | MODIFIER | c.1528+227_1528+228d others(4): Show |
TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 6/8 | chr11 | 120120344 | |||||||
| chr11:120120344 | TACAC | T | 10 | a0001c0001t0001g0074 a0001c0001t0001g0227 a0001c0001t0001g0229 others(7): Show |
11 | HG00323.hp2 HG02451.hp1 HG03927.hp1 others(8): Show |
intron_variant | MODIFIER | c.1528+225_1528+228d others(6): Show |
TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 6/8 | chr11 | 120120344 | |||||||
| chr11:120120344 | TACACAC | T | 20 | a0001c0001t0001g0051 a0001c0001t0001g0073 a0001c0001t0001g0082 others(17): Show |
36 | HG00423.hp2 HG00642.hp2 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.1528+223_1528+228d others(8): Show |
TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 6/8 | chr11 | 120120344 | |||||||
| chr11:120120344 | TACACACA others(1): Show |
T | 9 | a0001c0001t0001g0036 a0001c0001t0001g0110 a0001c0001t0001g0137 others(6): Show |
10 | HG00738.hp2 HG01069.hp2 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.1528+221_1528+228d others(10): Show |
TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 6/8 | chr11 | 120120344 | |||||||
| chr11:120120344 | TACACACA others(3): Show |
T | 46 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(43): Show |
79 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(76): Show |
intron_variant | MODIFIER | c.1528+219_1528+228d others(12): Show |
TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 6/8 | chr11 | 120120344 | |||||||
| chr11:120120344 | TACACACA others(5): Show |
T | 35 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0028 others(32): Show |
45 | HG01074.hp2 HG01496.hp2 HG02055.hp2 others(42): Show |
intron_variant | MODIFIER | c.1528+217_1528+228d others(14): Show |
TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 6/8 | chr11 | 120120344 | |||||||
| chr11:120120344 | TACACACA others(7): Show |
T | 92 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(89): Show |
154 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.1528+215_1528+228d others(16): Show |
TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 6/8 | chr11 | 120120344 | |||||||
| chr11:120120344 | TACACACA others(9): Show |
T | 3 | a0001c0001t0001g0024 a0001c0001t0001g0044 a0001c0001t0001g0087 |
6 | HG02559.hp2 HG02965.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1528+213_1528+228d others(18): Show |
TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 6/8 | chr11 | 120120344 | |||||||
| chr11:120120352 | C | T | 1 | a0001c0001t0001g0226 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1528+221G>A | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 6/8 | chr11 | 120120352 | |||||||
| chr11:120120353 | ACACACAC others(6): Show |
A | 1 | a0001c0001t0001g0191 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1528+207_1528+219d others(15): Show |
TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 6/8 | chr11 | 120120353 | |||||||
| chr11:120120362 | C | A | 1 | a0001c0001t0001g0217 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1528+211G>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 6/8 | chr11 | 120120362 | |||||||
| chr11:120120392 | C | A | 1 | a0001c0001t0001g0003 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1528+181G>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 6/8 | chr11 | 120120392 | |||||||
| chr11:120120403 | G | T | 1 | a0001c0001t0001g0226 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1528+170C>A | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 6/8 | chr11 | 120120403 | |||||||
| chr11:120120458 | A | T | 93 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(90): Show |
137 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(134): Show |
intron_variant | MODIFIER | c.1528+115T>A | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 6/8 | chr11 | 120120458 | |||||||
| chr11:120120795 | A | G | 1 | a0001c0001t0001g0250 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1436-130T>C | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 5/8 | chr11 | 120120795 | |||||||
| chr11:120121057 | G | A | 2 | a0001c0001t0001g0149 a0001c0001t0001g0150 |
2 | HG03195.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1436-392C>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 5/8 | chr11 | 120121057 | |||||||
| chr11:120121370 | A | G | 1 | a0001c0001t0001g0140 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1436-705T>C | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 5/8 | chr11 | 120121370 | |||||||
| chr11:120121441 | T | C | 221 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(218): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.1436-776A>G | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 5/8 | chr11 | 120121441 | |||||||
| chr11:120121450 | A | T | 1 | a0001c0001t0001g0160 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1436-785T>A | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 5/8 | chr11 | 120121450 | |||||||
| chr11:120121544 | G | A | 3 | a0001c0001t0001g0016 a0001c0001t0001g0172 a0001c0001t0008g0175 |
6 | HG02258.hp1 HG02451.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1436-879C>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 5/8 | chr11 | 120121544 | |||||||
| chr11:120121644 | T | C | 1 | a0001c0001t0001g0068 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1436-979A>G | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 5/8 | chr11 | 120121644 | |||||||
| chr11:120121690 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1436-1025C>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 5/8 | chr11 | 120121690 | |||||||
| chr11:120121690 | G | T | 13 | a0001c0001t0001g0012 a0001c0001t0001g0067 a0001c0001t0001g0071 others(10): Show |
18 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1436-1025C>A | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 5/8 | chr11 | 120121690 | |||||||
| chr11:120121792 | G | A | 2 | a0001c0001t0001g0212 a0001c0001t0001g0213 |
2 | HG02809.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1436-1127C>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 5/8 | chr11 | 120121792 | |||||||
| chr11:120121871 | A | G | 3 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0077 |
3 | HG02451.hp1 HG02486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1435+1083T>C | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 5/8 | chr11 | 120121871 | |||||||
| chr11:120121911 | GGGCCGGC others(68): Show |
G | 1 | a0001c0001t0001g0037 | 2 | HG00639.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1435+968_1435+1042 others(78): Show |
TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 5/8 | chr11 | 120121911 | |||||||
| chr11:120121917 | G | GCTGGTTG others(12): Show |
2 | a0001c0001t0001g0073 a0001c0001t0001g0074 |
2 | HG02451.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1435+1036_1435+103 others(23): Show |
TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 5/8 | chr11 | 120121917 | |||||||
| chr11:120121919 | A | T | 2 | a0001c0001t0001g0073 a0001c0001t0001g0074 |
2 | HG02451.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1435+1035T>A | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 5/8 | chr11 | 120121919 | |||||||
| chr11:120122084 | T | G | 1 | a0001c0001t0001g0194 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1435+870A>C | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 5/8 | chr11 | 120122084 | |||||||
| chr11:120122120 | T | C | 1 | a0001c0001t0001g0037 | 2 | HG00639.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1435+834A>G | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 5/8 | chr11 | 120122120 | |||||||
| chr11:120122131 | A | AGAGTGT | 1 | a0001c0001t0001g0010 | 4 | HG01928.hp2 HG01978.hp1 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.1435+822_1435+823i others(8): Show |
TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 5/8 | chr11 | 120122131 | |||||||
| chr11:120122131 | A | AGT | 11 | a0001c0001t0001g0025 a0001c0001t0001g0073 a0001c0001t0001g0074 others(8): Show |
13 | HG00597.hp1 HG01884.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.1435+821_1435+822d others(4): Show |
TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 5/8 | chr11 | 120122131 | |||||||
| chr11:120122131 | A | AGTGT | 5 | a0001c0001t0001g0016 a0001c0001t0001g0034 a0001c0001t0001g0129 others(2): Show |
9 | HG00423.hp1 HG01192.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1435+819_1435+822d others(6): Show |
TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 5/8 | chr11 | 120122131 | |||||||
| chr11:120122131 | A | AGTGTGT | 22 | a0001c0001t0001g0005 a0001c0001t0001g0019 a0001c0001t0001g0024 others(19): Show |
33 | HG00323.hp1 HG00733.hp2 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.1435+817_1435+822d others(8): Show |
TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 5/8 | chr11 | 120122131 | |||||||
| chr11:120122131 | A | AGTGTGTG others(1): Show |
7 | a0001c0001t0001g0018 a0001c0001t0001g0033 a0001c0001t0001g0036 others(4): Show |
11 | HG00642.hp1 HG01167.hp2 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.1435+815_1435+822d others(10): Show |
TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 5/8 | chr11 | 120122131 | |||||||
| chr11:120122131 | A | AGTGTGTG others(3): Show |
4 | a0001c0003t0001g0233 a0001c0004t0001g0090 a0001c0004t0001g0123 others(1): Show |
4 | HG01069.hp1 HG01099.hp1 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.1435+813_1435+822d others(12): Show |
TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 5/8 | chr11 | 120122131 | |||||||
| chr11:120122131 | A | AGTGTGTG others(5): Show |
4 | a0001c0001t0001g0088 a0001c0001t0003g0043 a0001c0004t0001g0121 others(1): Show |
5 | HG02559.hp1 HG02615.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1435+811_1435+822d others(14): Show |
TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 5/8 | chr11 | 120122131 | |||||||
| chr11:120122131 | A | AGTGTGTG others(7): Show |
3 | a0001c0001t0001g0093 a0001c0001t0003g0206 a0001c0004t0001g0120 |
3 | HG01109.hp1 HG02976.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1435+809_1435+822d others(16): Show |
TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 5/8 | chr11 | 120122131 | |||||||
| chr11:120122131 | AGT | A | 17 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0037 others(14): Show |
26 | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.1435+821_1435+822d others(4): Show |
TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 5/8 | chr11 | 120122131 | |||||||
| chr11:120122163 | T | A | 33 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(30): Show |
60 | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.1435+791A>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 5/8 | chr11 | 120122163 | |||||||
| chr11:120122163 | T | TGA | 19 | a0001c0001t0001g0012 a0001c0001t0001g0067 a0001c0001t0001g0071 others(16): Show |
24 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.1435+789_1435+790d others(4): Show |
TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 5/8 | chr11 | 120122163 | |||||||
| chr11:120122163 | T | TGTGA | 24 | a0001c0001t0001g0015 a0001c0001t0001g0021 a0001c0001t0001g0027 others(21): Show |
34 | HG01070.hp2 HG01358.hp2 HG01496.hp1 others(31): Show |
intron_variant | MODIFIER | c.1435+790_1435+791i others(6): Show |
TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 5/8 | chr11 | 120122163 | |||||||
| chr11:120122163 | T | TGTGTGA | 68 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(65): Show |
118 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.1435+790_1435+791i others(8): Show |
TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 5/8 | chr11 | 120122163 | |||||||
| chr11:120122163 | T | TGTGTGTG others(1): Show |
23 | a0001c0001t0001g0013 a0001c0001t0001g0017 a0001c0001t0001g0023 others(20): Show |
32 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(29): Show |
intron_variant | MODIFIER | c.1435+790_1435+791i others(10): Show |
TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 5/8 | chr11 | 120122163 | |||||||
| chr11:120122163 | T | TGTGTGTG others(3): Show |
4 | a0001c0001t0001g0079 a0001c0001t0001g0139 a0001c0001t0001g0165 others(1): Show |
5 | HG00099.hp1 HG02809.hp2 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.1435+790_1435+791i others(12): Show |
TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 5/8 | chr11 | 120122163 | |||||||
| chr11:120122163 | T | TGTGTGTG others(7): Show |
1 | a0001c0001t0001g0078 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1435+790_1435+791i others(16): Show |
TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 5/8 | chr11 | 120122163 | |||||||
| chr11:120122163 | T | TGTGTGTG others(9): Show |
1 | a0001c0001t0001g0188 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1435+790_1435+791i others(18): Show |
TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 5/8 | chr11 | 120122163 | |||||||
| chr11:120122165 | A | T | 2 | a0001c0001t0001g0073 a0001c0001t0001g0074 |
2 | HG02451.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1435+789T>A | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 5/8 | chr11 | 120122165 | |||||||
| chr11:120122170 | C | T | 2 | a0001c0001t0001g0073 a0001c0001t0001g0074 |
2 | HG02451.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1435+784G>A | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 5/8 | chr11 | 120122170 | |||||||
| chr11:120122208 | C | G | 1 | a0001c0001t0001g0153 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1435+746G>C | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 5/8 | chr11 | 120122208 | |||||||
| chr11:120122317 | G | A | 1 | a0001c0006t0001g0164 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1435+637C>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 5/8 | chr11 | 120122317 | |||||||
| chr11:120122321 | C | T | 1 | a0001c0006t0001g0164 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1435+633G>A | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 5/8 | chr11 | 120122321 | |||||||
| chr11:120122326 | A | G | 1 | a0001c0006t0001g0164 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1435+628T>C | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 5/8 | chr11 | 120122326 | |||||||
| chr11:120122328 | T | G | 1 | a0001c0006t0001g0164 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1435+626A>C | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 5/8 | chr11 | 120122328 | |||||||
| chr11:120122329 | G | C | 1 | a0001c0006t0001g0164 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1435+625C>G | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 5/8 | chr11 | 120122329 | |||||||
| chr11:120122330 | C | CAGCCCTC others(6): Show |
1 | a0001c0006t0001g0164 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1435+623_1435+624i others(15): Show |
TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 5/8 | chr11 | 120122330 | |||||||
| chr11:120122333 | T | A | 1 | a0001c0006t0001g0164 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1435+621A>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 5/8 | chr11 | 120122333 | |||||||
| chr11:120122336 | T | G | 1 | a0001c0006t0001g0164 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1435+618A>C | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 5/8 | chr11 | 120122336 | |||||||
| chr11:120122346 | G | T | 1 | a0001c0006t0001g0164 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1435+608C>A | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 5/8 | chr11 | 120122346 | |||||||
| chr11:120122348 | G | A | 16 | a0001c0001t0001g0051 a0001c0001t0001g0246 a0001c0001t0001g0248 others(13): Show |
31 | HG00673.hp1 HG01943.hp1 HG01952.hp1 others(28): Show |
intron_variant | MODIFIER | c.1435+606C>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 5/8 | chr11 | 120122348 | |||||||
| chr11:120122365 | G | C | 1 | a0001c0006t0001g0164 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1435+589C>G | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 5/8 | chr11 | 120122365 | |||||||
| chr11:120122369 | C | G | 1 | a0001c0006t0001g0164 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1435+585G>C | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 5/8 | chr11 | 120122369 | |||||||
| chr11:120122371 | ACAGGGCA others(5): Show |
A | 1 | a0001c0006t0001g0164 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1435+571_1435+582d others(14): Show |
TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 5/8 | chr11 | 120122371 | |||||||
| chr11:120122384 | A | G | 1 | a0001c0006t0001g0164 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1435+570T>C | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 5/8 | chr11 | 120122384 | |||||||
| chr11:120122395 | G | T | 2 | a0001c0001t0001g0169 a0001c0001t0001g0170 |
2 | HG00408.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.1435+559C>A | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 5/8 | chr11 | 120122395 | |||||||
| chr11:120122414 | C | A | 1 | a0001c0006t0001g0164 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1435+540G>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 5/8 | chr11 | 120122414 | |||||||
| chr11:120122416 | T | G | 1 | a0001c0006t0001g0164 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1435+538A>C | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 5/8 | chr11 | 120122416 | |||||||
| chr11:120122417 | T | G | 1 | a0001c0006t0001g0164 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1435+537A>C | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 5/8 | chr11 | 120122417 | |||||||
| chr11:120122421 | G | A | 2 | a0001c0001t0001g0073 a0001c0001t0001g0074 |
2 | HG02451.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1435+533C>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 5/8 | chr11 | 120122421 | |||||||
| chr11:120122431 | G | C | 1 | a0001c0001t0001g0037 | 2 | HG00639.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1435+523C>G | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 5/8 | chr11 | 120122431 | |||||||
| chr11:120122439 | C | G | 1 | a0001c0006t0001g0164 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1435+515G>C | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 5/8 | chr11 | 120122439 | |||||||
| chr11:120122539 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1435+415C>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 5/8 | chr11 | 120122539 | |||||||
| chr11:120122542 | A | C | 3 | a0001c0001t0001g0119 a0001c0001t0001g0201 a0001c0001t0001g0203 |
3 | HG01123.hp1 HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1435+412T>G | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 5/8 | chr11 | 120122542 | |||||||
| chr11:120122615 | G | A | 1 | a0001c0001t0001g0085 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1435+339C>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 5/8 | chr11 | 120122615 | |||||||
| chr11:120122839 | G | A | 2 | a0001c0001t0001g0108 a0001c0001t0001g0131 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1435+115C>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 5/8 | chr11 | 120122839 | |||||||
| chr11:120122868 | A | G | 14 | a0001c0001t0001g0036 a0001c0001t0001g0077 a0001c0001t0001g0088 others(11): Show |
15 | HG00642.hp1 HG01099.hp1 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.1435+86T>C | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 5/8 | chr11 | 120122868 | |||||||
| chr11:120123072 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1334-17G>A | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 4/8 | chr11 | 120123072 | |||||||
| chr11:120123189 | CCT | C | 245 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(242): Show |
372 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(369): Show |
intron_variant | MODIFIER | c.1334-136_1334-135d others(4): Show |
TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 4/8 | chr11 | 120123189 | |||||||
| chr11:120123227 | G | A | 2 | a0001c0001t0001g0073 a0001c0001t0001g0074 |
2 | HG02451.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1334-172C>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 4/8 | chr11 | 120123227 | |||||||
| chr11:120123287 | G | A | 16 | a0001c0001t0001g0051 a0001c0001t0001g0246 a0001c0001t0001g0248 others(13): Show |
31 | HG00673.hp1 HG01943.hp1 HG01952.hp1 others(28): Show |
intron_variant | MODIFIER | c.1334-232C>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 4/8 | chr11 | 120123287 | |||||||
| chr11:120123300 | C | T | 5 | a0001c0001t0001g0020 a0001c0001t0001g0045 a0001c0001t0001g0220 others(2): Show |
8 | HG00609.hp2 HG02083.hp2 NA18949.hp1 others(5): Show |
intron_variant | MODIFIER | c.1334-245G>A | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 4/8 | chr11 | 120123300 | |||||||
| chr11:120123312 | C | G | 1 | a0001c0001t0001g0067 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1334-257G>C | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 4/8 | chr11 | 120123312 | |||||||
| chr11:120123443 | C | T | 1 | a0001c0001t0001g0168 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1334-388G>A | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 4/8 | chr11 | 120123443 | |||||||
| chr11:120123536 | A | G | 2 | a0001c0001t0001g0073 a0001c0001t0001g0074 |
2 | HG02451.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1334-481T>C | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 4/8 | chr11 | 120123536 | |||||||
| chr11:120123540 | T | C | 2 | a0001c0001t0001g0073 a0001c0001t0001g0074 |
2 | HG02451.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1334-485A>G | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 4/8 | chr11 | 120123540 | |||||||
| chr11:120123563 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1334-508C>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 4/8 | chr11 | 120123563 | |||||||
| chr11:120123713 | C | T | 108 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(105): Show |
154 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.1334-658G>A | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 4/8 | chr11 | 120123713 | |||||||
| chr11:120123714 | G | A | 2 | a0001c0001t0001g0073 a0001c0001t0001g0074 |
2 | HG02451.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1334-659C>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 4/8 | chr11 | 120123714 | |||||||
| chr11:120123721 | A | G | 1 | a0001c0001t0001g0158 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1334-666T>C | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 4/8 | chr11 | 120123721 | |||||||
| chr11:120123767 | G | A | 1 | a0002c0002t0001g0062 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1334-712C>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 4/8 | chr11 | 120123767 | |||||||
| chr11:120123773 | G | T | 1 | a0001c0001t0001g0217 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1334-718C>A | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 4/8 | chr11 | 120123773 | |||||||
| chr11:120124057 | G | A | 3 | a0001c0001t0001g0156 a0001c0001t0001g0187 a0004c0014t0001g0257 |
3 | HG00140.hp2 HG00733.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.1334-1002C>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 4/8 | chr11 | 120124057 | |||||||
| chr11:120124070 | A | G | 1 | a0001c0001t0001g0153 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1334-1015T>C | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 4/8 | chr11 | 120124070 | |||||||
| chr11:120124178 | C | T | 1 | a0001c0010t0013g0208 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1334-1123G>A | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 4/8 | chr11 | 120124178 | |||||||
| chr11:120124259 | T | G | 1 | a0001c0003t0001g0234 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1334-1204A>C | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 4/8 | chr11 | 120124259 | |||||||
| chr11:120124402 | C | T | 1 | a0001c0001t0001g0076 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1333+1289G>A | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 4/8 | chr11 | 120124402 | |||||||
| chr11:120124444 | A | G | 1 | a0001c0001t0001g0167 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1333+1247T>C | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 4/8 | chr11 | 120124444 | |||||||
| chr11:120124519 | C | T | 3 | a0001c0001t0001g0024 a0001c0001t0001g0044 a0001c0001t0001g0087 |
6 | HG02559.hp2 HG02965.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1333+1172G>A | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 4/8 | chr11 | 120124519 | |||||||
| chr11:120124565 | C | T | 1 | a0001c0001t0001g0028 | 2 | HG02698.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.1333+1126G>A | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 4/8 | chr11 | 120124565 | |||||||
| chr11:120124571 | A | G | 18 | a0001c0001t0001g0051 a0001c0001t0001g0188 a0001c0001t0001g0189 others(15): Show |
33 | HG00544.hp2 HG00673.hp1 HG01943.hp1 others(30): Show |
intron_variant | MODIFIER | c.1333+1120T>C | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 4/8 | chr11 | 120124571 | |||||||
| chr11:120124579 | T | C | 18 | a0001c0001t0001g0051 a0001c0001t0001g0188 a0001c0001t0001g0189 others(15): Show |
33 | HG00544.hp2 HG00673.hp1 HG01943.hp1 others(30): Show |
intron_variant | MODIFIER | c.1333+1112A>G | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 4/8 | chr11 | 120124579 | |||||||
| chr11:120124589 | G | A | 1 | a0001c0001t0001g0148 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1333+1102C>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 4/8 | chr11 | 120124589 | |||||||
| chr11:120124648 | A | G | 1 | a0001c0001t0001g0091 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1333+1043T>C | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 4/8 | chr11 | 120124648 | |||||||
| chr11:120124652 | T | C | 1 | a0001c0001t0001g0205 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1333+1039A>G | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 4/8 | chr11 | 120124652 | |||||||
| chr11:120124654 | A | C | 1 | a0006c0011t0001g0190 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1333+1037T>G | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 4/8 | chr11 | 120124654 | |||||||
| chr11:120124705 | C | T | 2 | a0002c0002t0001g0240 a0002c0002t0001g0241 |
2 | HG02056.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.1333+986G>A | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 4/8 | chr11 | 120124705 | |||||||
| chr11:120124739 | T | C | 66 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(63): Show |
107 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.1333+952A>G | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 4/8 | chr11 | 120124739 | |||||||
| chr11:120124786 | G | A | 1 | a0001c0010t0013g0208 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1333+905C>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 4/8 | chr11 | 120124786 | |||||||
| chr11:120124941 | G | A | 12 | a0001c0001t0001g0036 a0001c0001t0001g0087 a0001c0001t0001g0088 others(9): Show |
13 | HG01099.hp1 HG01109.hp1 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.1333+750C>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 4/8 | chr11 | 120124941 | |||||||
| chr11:120124943 | C | A | 4 | a0001c0005t0001g0252 a0001c0005t0002g0026 a0001c0005t0002g0253 others(1): Show |
6 | HG02055.hp1 HG02615.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1333+748G>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 4/8 | chr11 | 120124943 | |||||||
| chr11:120124960 | C | T | 14 | a0001c0001t0001g0051 a0001c0001t0001g0246 a0001c0001t0001g0247 others(11): Show |
29 | HG00673.hp1 HG01952.hp1 HG02004.hp2 others(26): Show |
intron_variant | MODIFIER | c.1333+731G>A | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 4/8 | chr11 | 120124960 | |||||||
| chr11:120125032 | G | A | 1 | a0001c0003t0001g0235 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1333+659C>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 4/8 | chr11 | 120125032 | |||||||
| chr11:120125051 | T | A | 1 | a0006c0011t0001g0190 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1333+640A>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 4/8 | chr11 | 120125051 | |||||||
| chr11:120125173 | C | T | 1 | a0001c0001t0001g0075 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1333+518G>A | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 4/8 | chr11 | 120125173 | |||||||
| chr11:120125174 | G | A | 2 | a0001c0001t0001g0210 a0005c0009t0001g0209 |
2 | HG02486.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1333+517C>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 4/8 | chr11 | 120125174 | |||||||
| chr11:120125194 | G | A | 2 | a0001c0001t0001g0210 a0005c0009t0001g0209 |
2 | HG02486.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1333+497C>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 4/8 | chr11 | 120125194 | |||||||
| chr11:120125390 | C | T | 14 | a0001c0001t0001g0051 a0001c0001t0001g0246 a0001c0001t0001g0247 others(11): Show |
29 | HG00673.hp1 HG01952.hp1 HG02004.hp2 others(26): Show |
intron_variant | MODIFIER | c.1333+301G>A | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 4/8 | chr11 | 120125390 | |||||||
| chr11:120125428 | A | G | 1 | a0001c0001t0001g0205 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1333+263T>C | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 4/8 | chr11 | 120125428 | |||||||
| chr11:120125572 | T | G | 1 | a0001c0001t0001g0191 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1333+119A>C | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 4/8 | chr11 | 120125572 | |||||||
| chr11:120125683 | G | T | 3 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0074 |
3 | HG02055.hp2 HG02451.hp1 HG02486.hp2 |
splice_region_variant&intron_variant | LOW | c.1333+8C>A | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 4/8 | chr11 | 120125683 | |||||||
| chr11:120125945 | G | A | 2 | a0001c0001t0001g0010 a0001c0001t0001g0110 |
5 | HG01928.hp2 HG01952.hp2 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.1135-56C>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 3/8 | chr11 | 120125945 | |||||||
| chr11:120125954 | C | A | 1 | a0001c0001t0001g0191 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1135-65G>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 3/8 | chr11 | 120125954 | |||||||
| chr11:120125997 | C | T | 1 | a0001c0001t0001g0216 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1135-108G>A | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 3/8 | chr11 | 120125997 | |||||||
| chr11:120126246 | ATTTC | A | 3 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0005g0038 |
4 | HG02572.hp1 HG02965.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1135-361_1135-358d others(6): Show |
TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 3/8 | chr11 | 120126246 | |||||||
| chr11:120126258 | C | CT | 22 | a0001c0001t0001g0011 a0001c0001t0001g0039 a0001c0001t0001g0051 others(19): Show |
41 | HG00140.hp1 HG00673.hp1 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.1135-370dupA | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 3/8 | chr11 | 120126258 | |||||||
| chr11:120126258 | CT | C | 56 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(53): Show |
84 | HG00323.hp1 HG00642.hp1 HG00733.hp2 others(81): Show |
intron_variant | MODIFIER | c.1135-370delA | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 3/8 | chr11 | 120126258 | |||||||
| chr11:120126396 | T | C | 1 | a0001c0001t0001g0111 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1135-507A>G | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 3/8 | chr11 | 120126396 | |||||||
| chr11:120126459 | G | A | 1 | a0001c0001t0001g0020 | 3 | HG00609.hp2 NA18982.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.1135-570C>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 3/8 | chr11 | 120126459 | |||||||
| chr11:120126579 | G | A | 3 | a0001c0001t0001g0035 a0001c0001t0001g0112 a0001c0001t0001g0113 |
4 | HG02683.hp2 HG03491.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.1135-690C>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 3/8 | chr11 | 120126579 | |||||||
| chr11:120126601 | T | C | 1 | a0001c0001t0001g0114 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1135-712A>G | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 3/8 | chr11 | 120126601 | |||||||
| chr11:120126635 | T | C | 1 | a0001c0001t0001g0152 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1134+701A>G | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 3/8 | chr11 | 120126635 | |||||||
| chr11:120126891 | T | C | 127 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(124): Show |
187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.1134+445A>G | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 3/8 | chr11 | 120126891 | |||||||
| chr11:120126962 | C | T | 1 | a0001c0001t0001g0163 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1134+374G>A | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 3/8 | chr11 | 120126962 | |||||||
| chr11:120126978 | T | C | 2 | a0001c0001t0003g0043 a0001c0001t0003g0206 |
3 | HG02559.hp1 HG06807.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1134+358A>G | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 3/8 | chr11 | 120126978 | |||||||
| chr11:120127001 | A | C | 1 | a0001c0010t0013g0208 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1134+335T>G | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 3/8 | chr11 | 120127001 | |||||||
| chr11:120127077 | A | G | 1 | a0001c0001t0001g0215 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1134+259T>C | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 3/8 | chr11 | 120127077 | |||||||
| chr11:120127269 | T | C | 1 | a0001c0001t0001g0248 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1134+67A>G | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 3/8 | chr11 | 120127269 | |||||||
| chr11:120127645 | T | C | 1 | a0001c0001t0001g0016 | 4 | HG02451.hp2 HG03130.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.901-76A>G | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 2/8 | chr11 | 120127645 | |||||||
| chr11:120128204 | C | T | 2 | a0001c0001t0001g0057 a0001c0001t0001g0128 |
2 | HG02886.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.900+196G>A | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 2/8 | chr11 | 120128204 | |||||||
| chr11:120128302 | A | T | 1 | a0001c0003t0001g0232 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.900+98T>A | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 2/8 | chr11 | 120128302 | |||||||
| chr11:120128373 | A | C | 2 | a0001c0001t0001g0210 a0005c0009t0001g0209 |
2 | HG02486.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.900+27T>G | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 2/8 | chr11 | 120128373 | |||||||
| chr11:120128567 | G | A | 14 | a0001c0001t0001g0051 a0001c0001t0001g0246 a0001c0001t0001g0247 others(11): Show |
29 | HG00673.hp1 HG01952.hp1 HG02004.hp2 others(26): Show |
intron_variant | MODIFIER | c.805-72C>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 1/8 | chr11 | 120128567 | |||||||
| chr11:120128959 | G | A | 2 | a0001c0001t0001g0210 a0005c0009t0001g0209 |
2 | HG02486.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.805-464C>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 1/8 | chr11 | 120128959 | |||||||
| chr11:120129047 | C | T | 127 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(124): Show |
187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.805-552G>A | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 1/8 | chr11 | 120129047 | |||||||
| chr11:120129068 | C | T | 1 | a0001c0001t0001g0250 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.805-573G>A | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 1/8 | chr11 | 120129068 | |||||||
| chr11:120129095 | G | A | 1 | a0001c0001t0010g0236 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.805-600C>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 1/8 | chr11 | 120129095 | |||||||
| chr11:120129105 | G | C | 1 | a0001c0001t0001g0115 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.805-610C>G | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 1/8 | chr11 | 120129105 | |||||||
| chr11:120129480 | G | A | 3 | a0001c0001t0001g0066 a0001c0001t0001g0116 a0001c0001t0001g0117 |
3 | HG02056.hp1 HG03704.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.805-985C>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 1/8 | chr11 | 120129480 | |||||||
| chr11:120129525 | C | A | 218 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(215): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.805-1030G>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 1/8 | chr11 | 120129525 | |||||||
| chr11:120129555 | T | C | 220 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(217): Show |
340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.805-1060A>G | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 1/8 | chr11 | 120129555 | |||||||
| chr11:120129651 | C | T | 14 | a0001c0001t0001g0051 a0001c0001t0001g0246 a0001c0001t0001g0247 others(11): Show |
29 | HG00673.hp1 HG01952.hp1 HG02004.hp2 others(26): Show |
intron_variant | MODIFIER | c.805-1156G>A | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 1/8 | chr11 | 120129651 | |||||||
| chr11:120129652 | G | A | 2 | a0001c0001t0001g0212 a0001c0001t0001g0213 |
2 | HG02809.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.805-1157C>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 1/8 | chr11 | 120129652 | |||||||
| chr11:120129900 | G | A | 23 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0037 others(20): Show |
33 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(30): Show |
intron_variant | MODIFIER | c.805-1405C>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 1/8 | chr11 | 120129900 | |||||||
| chr11:120129934 | C | T | 1 | a0001c0001t0001g0069 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.805-1439G>A | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 1/8 | chr11 | 120129934 | |||||||
| chr11:120130102 | C | T | 2 | a0001c0001t0001g0212 a0001c0001t0001g0213 |
2 | HG02809.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.805-1607G>A | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 1/8 | chr11 | 120130102 | |||||||
| chr11:120130164 | T | C | 220 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(217): Show |
340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.805-1669A>G | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 1/8 | chr11 | 120130164 | |||||||
| chr11:120130165 | T | G | 220 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(217): Show |
340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.805-1670A>C | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 1/8 | chr11 | 120130165 | |||||||
| chr11:120130177 | T | C | 220 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(217): Show |
340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.805-1682A>G | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 1/8 | chr11 | 120130177 | |||||||
| chr11:120130361 | C | A | 1 | a0001c0001t0001g0213 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.805-1866G>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 1/8 | chr11 | 120130361 | |||||||
| chr11:120130544 | G | A | 1 | a0001c0001t0001g0205 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.805-2049C>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 1/8 | chr11 | 120130544 | |||||||
| chr11:120130774 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.805-2279G>A | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 1/8 | chr11 | 120130774 | |||||||
| chr11:120130986 | A | G | 1 | a0001c0008t0001g0162 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.805-2491T>C | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 1/8 | chr11 | 120130986 | |||||||
| chr11:120130987 | C | T | 104 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(101): Show |
154 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(151): Show |
intron_variant | MODIFIER | c.805-2492G>A | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 1/8 | chr11 | 120130987 | |||||||
| chr11:120131231 | G | A | 2 | a0001c0001t0001g0119 a0001c0001t0012g0118 |
2 | HG01123.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.805-2736C>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 1/8 | chr11 | 120131231 | |||||||
| chr11:120131236 | T | C | 4 | a0001c0004t0001g0120 a0001c0004t0001g0121 a0001c0004t0001g0123 others(1): Show |
4 | HG01109.hp1 HG02145.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.805-2741A>G | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 1/8 | chr11 | 120131236 | |||||||
| chr11:120131362 | A | C | 1 | a0001c0001t0001g0068 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.805-2867T>G | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 1/8 | chr11 | 120131362 | |||||||
| chr11:120131381 | G | T | 1 | a0001c0001t0001g0057 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.805-2886C>A | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 1/8 | chr11 | 120131381 | |||||||
| chr11:120131586 | C | G | 1 | a0001c0001t0009g0251 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.805-3091G>C | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 1/8 | chr11 | 120131586 | |||||||
| chr11:120131761 | G | T | 1 | a0001c0001t0001g0068 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.805-3266C>A | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 1/8 | chr11 | 120131761 | |||||||
| chr11:120131910 | C | A | 1 | a0001c0001t0001g0237 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.805-3415G>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 1/8 | chr11 | 120131910 | |||||||
| chr11:120132019 | G | A | 125 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(122): Show |
185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.805-3524C>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 1/8 | chr11 | 120132019 | |||||||
| chr11:120132050 | A | T | 2 | a0001c0001t0001g0160 a0001c0001t0001g0161 |
2 | HG02040.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.805-3555T>A | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 1/8 | chr11 | 120132050 | |||||||
| chr11:120132219 | C | T | 130 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(127): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.805-3724G>A | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 1/8 | chr11 | 120132219 | |||||||
| chr11:120132266 | TCTCTCTC others(1): Show |
T | 65 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(62): Show |
108 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.805-3779_805-3772d others(10): Show |
TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 1/8 | chr11 | 120132266 | |||||||
| chr11:120132703 | G | C | 1 | a0001c0004t0001g0124 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.805-4208C>G | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 1/8 | chr11 | 120132703 | |||||||
| chr11:120132825 | C | T | 68 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(65): Show |
111 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.805-4330G>A | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 1/8 | chr11 | 120132825 | |||||||
| chr11:120132859 | C | T | 1 | a0001c0001t0001g0158 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.805-4364G>A | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 1/8 | chr11 | 120132859 | |||||||
| chr11:120132878 | T | C | 1 | a0002c0002t0006g0053 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.804+4350A>G | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 1/8 | chr11 | 120132878 | |||||||
| chr11:120133095 | C | G | 1 | a0001c0001t0001g0066 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.804+4133G>C | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 1/8 | chr11 | 120133095 | |||||||
| chr11:120133143 | G | A | 2 | a0001c0001t0001g0125 a0001c0001t0001g0198 |
2 | HG00558.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.804+4085C>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 1/8 | chr11 | 120133143 | |||||||
| chr11:120133196 | C | T | 1 | a0001c0001t0001g0157 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.804+4032G>A | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 1/8 | chr11 | 120133196 | |||||||
| chr11:120133273 | T | C | 6 | a0001c0001t0001g0060 a0002c0002t0001g0058 a0002c0002t0001g0059 others(3): Show |
6 | NA18939.hp1 NA18950.hp2 NA18956.hp1 others(3): Show |
intron_variant | MODIFIER | c.804+3955A>G | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 1/8 | chr11 | 120133273 | |||||||
| chr11:120133300 | G | A | 16 | a0001c0001t0001g0051 a0001c0001t0001g0239 a0001c0001t0001g0246 others(13): Show |
31 | HG01952.hp1 HG02004.hp2 HG02015.hp1 others(28): Show |
intron_variant | MODIFIER | c.804+3928C>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 1/8 | chr11 | 120133300 | |||||||
| chr11:120133416 | C | A | 1 | a0001c0001t0001g0199 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.804+3812G>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 1/8 | chr11 | 120133416 | |||||||
| chr11:120133418 | G | C | 2 | a0001c0001t0003g0043 a0001c0001t0003g0206 |
3 | HG02559.hp1 HG06807.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.804+3810C>G | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 1/8 | chr11 | 120133418 | |||||||
| chr11:120133560 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.804+3668G>A | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 1/8 | chr11 | 120133560 | |||||||
| chr11:120133582 | A | G | 1 | a0001c0001t0001g0064 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.804+3646T>C | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 1/8 | chr11 | 120133582 | |||||||
| chr11:120133837 | T | C | 1 | a0001c0001t0001g0200 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.804+3391A>G | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 1/8 | chr11 | 120133837 | |||||||
| chr11:120133849 | G | A | 1 | a0001c0001t0001g0200 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.804+3379C>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 1/8 | chr11 | 120133849 | |||||||
| chr11:120133899 | C | T | 1 | a0001c0001t0001g0156 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.804+3329G>A | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 1/8 | chr11 | 120133899 | |||||||
| chr11:120134174 | C | G | 6 | a0001c0001t0001g0060 a0002c0002t0001g0058 a0002c0002t0001g0059 others(3): Show |
6 | NA18939.hp1 NA18950.hp2 NA18956.hp1 others(3): Show |
intron_variant | MODIFIER | c.804+3054G>C | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 1/8 | chr11 | 120134174 | |||||||
| chr11:120134493 | C | G | 3 | a0001c0001t0001g0205 a0001c0001t0003g0043 a0001c0001t0003g0206 |
4 | HG02559.hp1 HG06807.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.804+2735G>C | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 1/8 | chr11 | 120134493 | |||||||
| chr11:120134632 | G | A | 2 | a0001c0001t0001g0212 a0001c0001t0001g0213 |
2 | HG02809.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.804+2596C>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 1/8 | chr11 | 120134632 | |||||||
| chr11:120134781 | G | C | 4 | a0001c0001t0001g0042 a0001c0001t0001g0201 a0001c0001t0001g0202 others(1): Show |
5 | HG02647.hp2 HG02717.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.804+2447C>G | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 1/8 | chr11 | 120134781 | |||||||
| chr11:120134921 | G | A | 1 | a0001c0001t0001g0203 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.804+2307C>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 1/8 | chr11 | 120134921 | |||||||
| chr11:120134925 | T | G | 122 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(119): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.804+2303A>C | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 1/8 | chr11 | 120134925 | |||||||
| chr11:120134941 | C | T | 2 | a0001c0001t0001g0212 a0001c0001t0001g0213 |
2 | HG02809.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.804+2287G>A | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 1/8 | chr11 | 120134941 | |||||||
| chr11:120134960 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.804+2268C>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 1/8 | chr11 | 120134960 | |||||||
| chr11:120135132 | C | T | 3 | a0001c0001t0001g0021 a0001c0001t0001g0154 a0002c0002t0001g0155 |
5 | HG00438.hp1 NA18991.hp2 NA19067.hp2 others(2): Show |
intron_variant | MODIFIER | c.804+2096G>A | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 1/8 | chr11 | 120135132 | |||||||
| chr11:120135438 | G | C | 15 | a0001c0001t0001g0051 a0001c0001t0001g0239 a0001c0001t0001g0246 others(12): Show |
30 | HG01952.hp1 HG02004.hp2 HG02015.hp1 others(27): Show |
intron_variant | MODIFIER | c.804+1790C>G | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 1/8 | chr11 | 120135438 | |||||||
| chr11:120135550 | C | G | 2 | a0001c0001t0001g0057 a0001c0001t0001g0128 |
2 | HG02886.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.804+1678G>C | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 1/8 | chr11 | 120135550 | |||||||
| chr11:120135575 | T | C | 1 | a0001c0001t0001g0052 | 2 | NA18993.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.804+1653A>G | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 1/8 | chr11 | 120135575 | |||||||
| chr11:120135795 | C | G | 1 | a0001c0001t0001g0056 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.804+1433G>C | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 1/8 | chr11 | 120135795 | |||||||
| chr11:120135875 | G | A | 4 | a0001c0005t0001g0252 a0001c0005t0002g0026 a0001c0005t0002g0253 others(1): Show |
6 | HG02055.hp1 HG02615.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.804+1353C>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 1/8 | chr11 | 120135875 | |||||||
| chr11:120135942 | C | A | 1 | a0001c0001t0001g0153 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.804+1286G>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 1/8 | chr11 | 120135942 | |||||||
| chr11:120135997 | A | G | 70 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(67): Show |
113 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.804+1231T>C | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 1/8 | chr11 | 120135997 | |||||||
| chr11:120136036 | C | A | 1 | a0003c0013t0001g0256 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.804+1192G>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 1/8 | chr11 | 120136036 | |||||||
| chr11:120136074 | T | C | 1 | a0001c0001t0001g0127 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.804+1154A>G | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 1/8 | chr11 | 120136074 | |||||||
| chr11:120136304 | A | T | 1 | a0001c0001t0001g0132 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.804+924T>A | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 1/8 | chr11 | 120136304 | |||||||
| chr11:120136307 | T | G | 1 | a0001c0001t0001g0132 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.804+921A>C | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 1/8 | chr11 | 120136307 | |||||||
| chr11:120136310 | T | A | 1 | a0001c0001t0001g0132 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.804+918A>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 1/8 | chr11 | 120136310 | |||||||
| chr11:120136312 | C | G | 1 | a0001c0001t0001g0132 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.804+916G>C | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 1/8 | chr11 | 120136312 | |||||||
| chr11:120136313 | A | T | 1 | a0001c0001t0001g0132 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.804+915T>A | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 1/8 | chr11 | 120136313 | |||||||
| chr11:120136314 | G | T | 1 | a0001c0001t0001g0132 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.804+914C>A | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 1/8 | chr11 | 120136314 | |||||||
| chr11:120136480 | C | T | 15 | a0001c0001t0001g0051 a0001c0001t0001g0239 a0001c0001t0001g0246 others(12): Show |
30 | HG01952.hp1 HG02004.hp2 HG02015.hp1 others(27): Show |
intron_variant | MODIFIER | c.804+748G>A | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 1/8 | chr11 | 120136480 | |||||||
| chr11:120136570 | C | A | 1 | a0001c0005t0002g0254 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.804+658G>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 1/8 | chr11 | 120136570 | |||||||
| chr11:120136789 | CA | C | 75 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(72): Show |
117 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.804+438delT | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 1/8 | chr11 | 120136789 | |||||||
| chr11:120136789 | CAA | C | 138 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(135): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.804+437_804+438del others(2): Show |
TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 1/8 | chr11 | 120136789 | |||||||
| chr11:120136798 | A | T | 15 | a0001c0001t0001g0051 a0001c0001t0001g0239 a0001c0001t0001g0246 others(12): Show |
30 | HG01952.hp1 HG02004.hp2 HG02015.hp1 others(27): Show |
intron_variant | MODIFIER | c.804+430T>A | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 1/8 | chr11 | 120136798 | |||||||
| chr11:120136812 | AGAAGAAG others(5): Show |
A | 15 | a0001c0001t0001g0051 a0001c0001t0001g0239 a0001c0001t0001g0246 others(12): Show |
30 | HG01952.hp1 HG02004.hp2 HG02015.hp1 others(27): Show |
intron_variant | MODIFIER | c.804+404_804+415del others(12): Show |
TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 1/8 | chr11 | 120136812 | |||||||
| chr11:120136987 | G | A | 1 | a0001c0001t0009g0251 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.804+241C>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 1/8 | chr11 | 120136987 | |||||||
| chr11:120137084 | G | A | 1 | a0001c0001t0001g0052 | 2 | NA18993.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.804+144C>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 1/8 | chr11 | 120137084 | |||||||
| chr11:120137181 | G | T | 98 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(95): Show |
148 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.804+47C>A | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 1/8 | chr11 | 120137181 |