Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| 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 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and 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 | copy fasta | chr11 | 120106286 | 120143113 |
| a0002 | 0/0 | 588 | 31 | 0 | 4 | 26 | 0 | 1 | 22 | TRIM29_chr11_120106286_120143113 | TRIM29 | copy fasta | chr11 | 120106286 | 120143113 |
| a0003 | 0/0 | 588 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | copy fasta | chr11 | 120106286 | 120143113 |
| a0004 | 0/0 | 575 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | copy fasta | chr11 | 120106286 | 120143113 |
| a0005 | 0/0 | 588 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | copy fasta | chr11 | 120106286 | 120143113 |
| a0006 | 0/0 | 588 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TRIM29_chr11_120106286_120143113 | TRIM29 | copy fasta | chr11 | 120106286 | 120143113 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 1767 | 322 | 83 | 56 | 131 | 11 | 40 | TRIM29_chr11_120106286_120143113 | TRIM29 | copy fasta | chr11 | 120106286 | 120143113 |
| c0002 | 0/0 | 1767 | 31 | 0 | 4 | 26 | 0 | 1 | TRIM29_chr11_120106286_120143113 | TRIM29 | copy fasta | chr11 | 120106286 | 120143113 |
| c0003 | 1/0 | 1767 | 25 | 1 | 9 | 7 | 3 | 4 | TRIM29_chr11_120106286_120143113 | TRIM29 | copy fasta | chr11 | 120106286 | 120143113 |
| c0004 | 0/0 | 1767 | 6 | 4 | 2 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | copy fasta | chr11 | 120106286 | 120143113 |
| c0005 | 0/0 | 1767 | 6 | 6 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | copy fasta | chr11 | 120106286 | 120143113 |
| c0006 | 0/0 | 1767 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | copy fasta | chr11 | 120106286 | 120143113 |
| c0007 | 0/0 | 1767 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | copy fasta | chr11 | 120106286 | 120143113 |
| c0008 | 0/0 | 1767 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM29_chr11_120106286_120143113 | TRIM29 | copy fasta | chr11 | 120106286 | 120143113 |
| c0009 | 0/0 | 1767 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | copy fasta | chr11 | 120106286 | 120143113 |
| c0010 | 0/0 | 1767 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | copy fasta | chr11 | 120106286 | 120143113 |
| c0011 | 0/0 | 1767 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | copy fasta | chr11 | 120106286 | 120143113 |
| c0012 | 0/0 | 1767 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | copy fasta | chr11 | 120106286 | 120143113 |
| c0013 | 0/0 | 1728 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | copy fasta | chr11 | 120106286 | 120143113 |
| c0014 | 0/0 | 1767 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | copy fasta | chr11 | 120106286 | 120143113 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 1211 | 379 | 82 | 72 | 163 | 14 | 46 | TRIM29_chr11_120106286_120143113 | TRIM29 | copy fasta | chr11 | 120106286 | 120143113 |
| t0002 | 0/0 | 1211 | 6 | 6 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | copy fasta | chr11 | 120106286 | 120143113 |
| t0003 | 0/0 | 1211 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | copy fasta | chr11 | 120106286 | 120143113 |
| t0004 | 0/0 | 1211 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | copy fasta | chr11 | 120106286 | 120143113 |
| t0005 | 0/0 | 1211 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | copy fasta | chr11 | 120106286 | 120143113 |
| t0006 | 0/0 | 1211 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | copy fasta | chr11 | 120106286 | 120143113 |
| t0007 | 0/0 | 1211 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | copy fasta | chr11 | 120106286 | 120143113 |
| t0008 | 0/0 | 1211 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | copy fasta | chr11 | 120106286 | 120143113 |
| t0009 | 0/0 | 1211 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | copy fasta | chr11 | 120106286 | 120143113 |
| t0010 | 0/0 | 1211 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | copy fasta | chr11 | 120106286 | 120143113 |
| t0011 | 0/0 | 1211 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | copy fasta | chr11 | 120106286 | 120143113 |
| t0012 | 0/0 | 1211 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | copy fasta | chr11 | 120106286 | 120143113 |
| t0013 | 0/0 | 1211 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | copy fasta | chr11 | 120106286 | 120143113 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 18 | 0 | 0 | 18 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0002 | 0/0 | 15 | 0 | 3 | 12 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0003 | 0/0 | 10 | 0 | 3 | 6 | 0 | 1 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0004 | 0/0 | 9 | 0 | 1 | 8 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0005 | 0/0 | 8 | 3 | 4 | 0 | 1 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0006 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0007 | 0/0 | 7 | 0 | 6 | 0 | 0 | 1 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0008 | 0/0 | 6 | 0 | 1 | 0 | 2 | 3 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0009 | 0/0 | 4 | 0 | 0 | 0 | 0 | 4 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0010 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0011 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0013 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0015 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0016 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0018 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0019 | 0/1 | 3 | 0 | 2 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0023 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0026 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0030 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0034 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0035 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0037 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0046 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0047 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0048 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0049 | 1/0 | 2 | 0 | 0 | 0 | 0 | 1 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0050 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1767 | 322 | 83 | 56 | 131 | 11 | 40 | TRIM29_chr11_120106286_120143113 | TRIM29 | copy fasta | chr11 | 120106286 | 120143113 |
| a0001c0003 | 1/0 | 1767 | 25 | 1 | 9 | 7 | 3 | 4 | TRIM29_chr11_120106286_120143113 | TRIM29 | copy fasta | chr11 | 120106286 | 120143113 |
| a0001c0004 | 0/0 | 1767 | 6 | 4 | 2 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | copy fasta | chr11 | 120106286 | 120143113 |
| a0001c0005 | 0/0 | 1767 | 6 | 6 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | copy fasta | chr11 | 120106286 | 120143113 |
| a0001c0006 | 0/0 | 1767 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | copy fasta | chr11 | 120106286 | 120143113 |
| a0001c0007 | 0/0 | 1767 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | copy fasta | chr11 | 120106286 | 120143113 |
| a0001c0008 | 0/0 | 1767 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM29_chr11_120106286_120143113 | TRIM29 | copy fasta | chr11 | 120106286 | 120143113 |
| a0001c0010 | 0/0 | 1767 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | copy fasta | chr11 | 120106286 | 120143113 |
| a0001c0012 | 0/0 | 1767 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | copy fasta | chr11 | 120106286 | 120143113 |
| a0002c0002 | 0/0 | 1767 | 31 | 0 | 4 | 26 | 0 | 1 | TRIM29_chr11_120106286_120143113 | TRIM29 | copy fasta | chr11 | 120106286 | 120143113 |
| a0003c0014 | 0/0 | 1767 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | copy fasta | chr11 | 120106286 | 120143113 |
| a0004c0013 | 0/0 | 1728 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | copy fasta | chr11 | 120106286 | 120143113 |
| a0005c0009 | 0/0 | 1767 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | copy fasta | chr11 | 120106286 | 120143113 |
| a0006c0011 | 0/0 | 1767 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | copy fasta | 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 | copy fasta | chr11 | 120106286 | 120143113 |
| a0001c0001t0003 | 0/0 | 2977 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | copy fasta | chr11 | 120106286 | 120143113 |
| a0001c0001t0004 | 0/0 | 2977 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | copy fasta | chr11 | 120106286 | 120143113 |
| a0001c0001t0005 | 0/0 | 2977 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | copy fasta | chr11 | 120106286 | 120143113 |
| a0001c0001t0007 | 0/0 | 2977 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | copy fasta | chr11 | 120106286 | 120143113 |
| a0001c0001t0008 | 0/0 | 2977 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | copy fasta | chr11 | 120106286 | 120143113 |
| a0001c0001t0009 | 0/0 | 2977 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | copy fasta | chr11 | 120106286 | 120143113 |
| a0001c0001t0010 | 0/0 | 2977 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | copy fasta | chr11 | 120106286 | 120143113 |
| a0001c0001t0012 | 0/0 | 2977 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | copy fasta | chr11 | 120106286 | 120143113 |
| a0001c0003t0001 | 1/0 | 2977 | 25 | 1 | 9 | 7 | 3 | 4 | TRIM29_chr11_120106286_120143113 | TRIM29 | copy fasta | chr11 | 120106286 | 120143113 |
| a0001c0004t0001 | 0/0 | 2977 | 5 | 3 | 2 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | copy fasta | chr11 | 120106286 | 120143113 |
| a0001c0004t0002 | 0/0 | 2977 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | copy fasta | chr11 | 120106286 | 120143113 |
| a0001c0005t0001 | 0/0 | 2977 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | copy fasta | chr11 | 120106286 | 120143113 |
| a0001c0005t0002 | 0/0 | 2977 | 5 | 5 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | copy fasta | chr11 | 120106286 | 120143113 |
| a0001c0006t0001 | 0/0 | 2977 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | copy fasta | chr11 | 120106286 | 120143113 |
| a0001c0007t0001 | 0/0 | 2977 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | copy fasta | chr11 | 120106286 | 120143113 |
| a0001c0008t0001 | 0/0 | 2977 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM29_chr11_120106286_120143113 | TRIM29 | copy fasta | chr11 | 120106286 | 120143113 |
| a0001c0010t0013 | 0/0 | 2977 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | copy fasta | chr11 | 120106286 | 120143113 |
| a0001c0012t0001 | 0/0 | 2977 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | copy fasta | chr11 | 120106286 | 120143113 |
| a0002c0002t0001 | 0/0 | 2977 | 29 | 0 | 4 | 24 | 0 | 1 | TRIM29_chr11_120106286_120143113 | TRIM29 | copy fasta | chr11 | 120106286 | 120143113 |
| a0002c0002t0006 | 0/0 | 2977 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | copy fasta | chr11 | 120106286 | 120143113 |
| a0002c0002t0011 | 0/0 | 2977 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | copy fasta | chr11 | 120106286 | 120143113 |
| a0003c0014t0001 | 0/0 | 2977 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | copy fasta | chr11 | 120106286 | 120143113 |
| a0004c0013t0001 | 0/0 | 2938 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | copy fasta | chr11 | 120106286 | 120143113 |
| a0005c0009t0001 | 0/0 | 2977 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | copy fasta | chr11 | 120106286 | 120143113 |
| a0006c0011t0001 | 0/0 | 2977 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | copy fasta | chr11 | 120106286 | 120143113 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and 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 |
| a0001c0001t0001g0004 | 0/0 | 9 | 0 | 1 | 8 | 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 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | 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 | 0 | 1 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 0 | 0 | 0 | 0 | 1 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 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 | 1 | 0 | 0 | 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 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 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 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0190 | 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 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0206 | 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 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0251 | 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 |
| a0001c0001t0003g0207 | 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 |
| a0001c0001t0007g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0008g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0009g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0010g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0001t0012g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0003t0001g0003 | 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 |
| a0001c0003t0001g0208 | 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 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0003t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0003t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0004t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0004t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0004t0001g0122 | 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 |
| a0001c0004t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0004t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0005t0001g0253 | 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 |
| a0001c0005t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0005t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0006t0001g0165 | 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 |
| a0001c0008t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0010t0013g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0001c0012t0001g0256 | 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 |
| a0002c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0002c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0002c0002t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0002c0002t0001g0196 | 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 |
| a0002c0002t0001g0245 | 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 |
| a0002c0002t0011g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0003c0014t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0004c0013t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0005c0009t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| a0006c0011t0001g0191 | 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 | g0140 | 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 | g0139 | EUR | GBR | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0188 | 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 | g0003 | EAS | CHS | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | CHS | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0130 | 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 | g0155 | 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 | g0190 | EAS | CHS | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0199 | 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 | g0225 | EAS | CHS | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0004 | 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 | g0003 | 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 | g0003 | AMR | PUR | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG00642 | hp2 | a0001 | c0010 | t0013 | g0209 | AMR | PUR | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG00673 | hp1 | a0002 | c0002 | t0001 | g0196 | EAS | CHS | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | CHS | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0157 | 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 | g0137 | AMR | PUR | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG00741 | hp1 | a0001 | c0003 | t0001 | g0208 | 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 | g0234 | AMR | PUR | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0144 | 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 | g0098 | AMR | PUR | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG01074 | hp2 | a0004 | c0013 | t0001 | g0257 | 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 | g0091 | AMR | PUR | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0159 | 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 | g0121 | 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 | a0003 | c0014 | t0001 | g0258 | 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 | g0141 | AMR | PUR | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG01243 | hp2 | a0001 | c0001 | t0012 | g0119 | 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 | g0145 | AMR | CLM | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0152 | 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 | g0147 | AMR | CLM | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0132 | 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 | g0109 | 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 | g0106 | AMR | CLM | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0153 | 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 | g0105 | 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 | g0239 | EUR | IBS | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | ACB | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0108 | 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 | g0167 | 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 | g0111 | 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 | g0131 | 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 | g0003 | 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 | g0169 | 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 | g0246 | 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 | g0161 | EAS | KHV | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02055 | hp1 | a0001 | c0005 | t0002 | g0254 | 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 | g0118 | EAS | KHV | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02056 | hp2 | a0002 | c0002 | t0001 | g0242 | EAS | KHV | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0126 | 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 | g0189 | EAS | KHV | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | KHV | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02083 | hp1 | a0001 | c0001 | t0009 | g0252 | EAS | KHV | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0223 | 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 | g0216 | 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 | g0123 | 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 | g0101 | AFR | ACB | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02258 | hp1 | a0001 | c0001 | t0008 | g0176 | AFR | ACB | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | ACB | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02273 | hp1 | a0001 | c0003 | t0001 | g0003 | AMR | PEL | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0004 | 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 | g0201 | AFR | ACB | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0229 | 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 | g0236 | EAS | KHV | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0231 | 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 | g0175 | AFR | GWD | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0128 | 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 | g0253 | AFR | GWD | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02615 | hp2 | a0001 | c0004 | t0001 | g0125 | 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 | g0095 | 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 | g0203 | 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 | g0154 | 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 | g0211 | 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 | g0104 | 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 | g0198 | SAS | PJL | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | GWD | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0174 | 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 | g0115 | AFR | GWD | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0213 | 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 | g0094 | 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 | g0212 | 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 | g0255 | 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 | g0172 | AFR | ESN | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | ESN | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | ESN | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0202 | 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 | g0220 | AFR | MSL | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | MSL | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | MSL | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0148 | 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 | g0110 | 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 | g0113 | 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 | g0122 | 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 | g0124 | AFR | GWD | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0099 | 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 | g0003 | SAS | STU | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0238 | 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 | g0102 | SAS | PJL | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0135 | 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 | g0117 | 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 | g0163 | SAS | BEB | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG03927 | hp1 | a0002 | c0002 | t0001 | g0127 | SAS | BEB | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0143 | 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 | g0228 | SAS | BEB | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | STU | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0205 | SAS | STU | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0217 | 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 | g0248 | 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 | g0235 | SAS | STU | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0114 | 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 | g0150 | 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 | g0100 | AFR | YRI | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0206 | 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 | g0133 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0004 | 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 | g0249 | 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 | g0158 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0222 | 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 | g0085 | 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 | g0180 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0251 | 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 | g0230 | 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 | g0243 | 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 | g0171 | 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 | g0195 | 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 | g0192 | 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 | g0162 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0226 | 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 | g0004 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0185 | 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 | g0134 | 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 | g0194 | 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 | g0227 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0004 | 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 | g0240 | 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 | g0187 | 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 | g0084 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0232 | 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 | g0004 | 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 | g0004 | 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 | g0241 | 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 | g0237 | AFR | LWK | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA19043 | hp1 | a0001 | c0012 | t0001 | g0256 | AFR | LWK | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0088 | 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 | g0244 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA19055 | hp2 | a0006 | c0011 | t0001 | g0191 | 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 | g0003 | 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 | g0245 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA19058 | hp2 | a0001 | c0003 | t0001 | g0003 | 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 | g0004 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0221 | 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 | g0168 | 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 | g0156 | 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 | g0116 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA19076 | hp1 | a0001 | c0006 | t0001 | g0165 | 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 | g0186 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0087 | 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 | g0003 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA19090 | hp2 | a0001 | c0003 | t0001 | g0003 | 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 | g0247 | EAS | JPT | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | YRI | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0204 | 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 | g0218 | 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 | g0103 | SAS | GIH | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0149 | SAS | GIH | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | CLM | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG01123 | hp2 | a0001 | c0003 | t0001 | g0233 | 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 | g0219 | AFR | ACB | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| HG02486 | hp1 | a0005 | c0009 | t0001 | g0210 | 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 | g0207 | 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 | g0200 | AFR | LWK | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0019 | REF | REF | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| homoSapiens_grch38 | hp1 | a0001 | c0003 | t0001 | g0049 | REF | REF | TRIM29_chr11_120106286_120143113 | TRIM29 | chr11 | 120106286 | 120143113 |
| 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 | a0004 | 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 | a0003 | 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 |
| 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 | a0001c0001a0001c0004a0001c0005others(10): Show | 375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): 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 |
| 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 | a0001c0001t0003a0001c0001t0010 | 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 | a0001c0004t0002a0001c0005t0002 | 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 |
| 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 | a0001c0001t0001g0211a0005c0009t0001g0210 | 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 | a0001c0001t0001g0145a0001c0001t0001g0152 | 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 | a0001c0001t0001g0150a0001c0001t0001g0151 | 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 | a0001c0001t0001g0077a0001c0001t0001g0182a0001c0004t0001g0091others(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 | 212 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(209): Show | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): 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 | 215 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(212): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): 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 | a0005c0009t0001g0210 | 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 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0037others(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 | a0001c0001t0001g0105a0001c0001t0001g0109a0001c0001t0001g0132 | 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 | a0001c0001t0001g0073a0001c0001t0001g0074 | 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 | a0001c0001t0001g0126a0001c0001t0001g0199 | 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 | 208 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(205): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): 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 | a0001c0001t0001g0230 | 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 | 168 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(165): Show | 261 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(258): 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 | a0001c0001t0001g0019a0001c0001t0001g0106a0001c0001t0001g0107 | 5 | HG00735.hp1 HG00738.hp1 HG01496.hp2 others(2): 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 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0037others(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 | a0001c0001t0003g0043a0001c0001t0003g0207 | 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 | a0001c0001t0003g0043a0001c0001t0003g0207 | 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 | a0001c0001t0001g0154 | 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 | a0001c0001t0003g0043a0001c0001t0003g0207a0002c0002t0001g0002others(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 | a0001c0001t0001g0220 | 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 | 175 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(172): Show | 269 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(266): 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 | a0001c0001t0001g0093a0001c0001t0001g0099a0001c0001t0001g0218others(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 | a0001c0001t0001g0009a0001c0001t0001g0030a0001c0001t0001g0035others(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 | 198 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(195): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): 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 | a0001c0001t0001g0093a0001c0001t0001g0099a0001c0001t0001g0218others(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 | a0002c0002t0001g0002a0002c0002t0001g0058a0002c0002t0001g0059others(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 | a0001c0001t0001g0033a0001c0001t0001g0104 | 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 | a0001c0001t0001g0031a0001c0001t0001g0097a0001c0001t0007g0100 | 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 | a0001c0001t0001g0213a0001c0001t0001g0214 | 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 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0037others(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 | a0002c0002t0001g0002a0002c0002t0001g0058a0002c0002t0001g0059others(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 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0037others(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 | a0001c0001t0001g0094 | 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 | 169 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(166): Show | 264 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(261): 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 | a0001c0001t0001g0022a0001c0001t0001g0036a0001c0001t0001g0077others(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 | a0001c0001t0001g0022a0001c0001t0001g0077a0001c0001t0001g0182others(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 | a0001c0001t0001g0022a0001c0001t0001g0077a0001c0001t0001g0182others(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 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0037others(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 | a0002c0002t0001g0002a0002c0002t0001g0058a0002c0002t0001g0059others(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 | a0002c0002t0001g0245 | 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 | a0001c0001t0010g0237 | 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 | a0001c0001t0001g0193 | 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 | a0001c0001t0003g0043a0001c0001t0003g0207 | 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 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0003g0043others(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 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0003g0043others(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 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0003g0043others(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 | a0001c0001t0001g0090 | 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 | a0001c0001t0001g0143 | 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 | a0001c0001t0001g0095 | 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 | a0001c0001t0003g0043a0001c0001t0003g0207 | 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 | 181 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(178): Show | 290 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(287): 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 | a0002c0002t0001g0243 | 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 | 163 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(160): Show | 256 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(253): 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 | a0001c0001t0001g0213a0001c0001t0001g0214 | 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 | 196 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(193): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): 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 | a0001c0001t0001g0031a0001c0001t0001g0097a0001c0001t0007g0100 | 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 | a0001c0004t0001g0091a0001c0004t0001g0121a0001c0004t0001g0122others(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 | a0001c0001t0001g0103 | 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 | a0001c0001t0001g0247a0001c0001t0001g0249a0002c0002t0001g0002others(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 | a0001c0001t0003g0043a0001c0001t0003g0207 | 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 | a0001c0004t0001g0091 | 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 | a0001c0001t0001g0247a0001c0001t0001g0249a0002c0002t0001g0002others(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 | a0001c0001t0003g0043a0001c0001t0003g0207 | 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 | a0001c0001t0001g0096 | 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 | a0001c0001t0001g0069a0001c0001t0001g0135 | 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 | a0001c0001t0001g0102 | 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 | a0001c0001t0001g0072a0001c0001t0001g0213a0001c0001t0001g0214 | 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 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0018others(23): Show | 44 | HG00323.hp1 HG00733.hp2 HG00735.hp1 others(41): 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 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0018others(25): Show | 47 | HG00323.hp1 HG00733.hp2 HG00735.hp1 others(44): 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 | a0001c0001t0001g0031a0001c0001t0001g0097a0001c0001t0007g0100 | 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 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0018others(26): Show | 48 | HG00323.hp1 HG00733.hp2 HG00735.hp1 others(45): 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 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0018others(26): Show | 48 | HG00323.hp1 HG00733.hp2 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.1529-468C>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 6/8 | chr11 | 120118789 | ||||||
| chr11:120118861
|
T | C | 251 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(248): Show | 380 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(377): Show |
intron_variant | MODIFIER | c.1529-540A>G | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 6/8 | chr11 | 120118861 | ||||||
| chr11:120118864
|
T | A | 55 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(52): 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 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0018others(26): Show | 48 | HG00323.hp1 HG00733.hp2 HG00735.hp1 others(45): 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 | a0001c0001t0001g0036a0001c0001t0001g0089a0001c0001t0001g0090others(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 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0018others(26): Show | 48 | HG00323.hp1 HG00733.hp2 HG00735.hp1 others(45): 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 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0018others(26): Show | 48 | HG00323.hp1 HG00733.hp2 HG00735.hp1 others(45): 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 | a0001c0001t0001g0247a0001c0001t0001g0249a0002c0002t0001g0002others(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 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(107): Show | 187 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(184): 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 | a0001c0001t0001g0086 | 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 | a0001c0001t0001g0051a0001c0001t0001g0247a0001c0001t0001g0249others(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 | a0001c0001t0001g0036a0001c0001t0001g0089a0001c0001t0001g0090others(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 | a0001c0001t0001g0051a0001c0001t0001g0247a0001c0001t0001g0249others(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 | a0001c0001t0001g0051a0001c0001t0001g0247a0001c0001t0001g0249others(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 | a0001c0010t0013g0209 | 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 | a0001c0001t0001g0036a0001c0001t0001g0089a0001c0001t0001g0090others(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 | a0001c0001t0001g0090 | 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 | a0001c0001t0001g0248 | 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 | a0001c0001t0001g0192 | 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 | a0001c0001t0001g0192 | 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 | a0001c0001t0001g0192 | 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 | a0001c0001t0001g0227 | 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 | a0001c0001t0001g0042a0001c0001t0001g0120a0001c0001t0001g0202others(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 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(85): Show | 150 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.1528+392delA | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 6/8 | chr11 | 120120180 | ||||||
| chr11:120120181
|
T | G | 5 | a0001c0001t0001g0159a0001c0001t0001g0179a0001c0001t0001g0185others(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 | a0001c0001t0001g0206 | 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 | a0001c0001t0001g0105a0001c0001t0001g0109a0001c0001t0001g0132 | 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 | a0001c0001t0001g0227 | 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 | a0001c0001t0001g0052a0001c0001t0001g0148a0001c0001t0001g0225others(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 | a0001c0001t0001g0065a0001c0001t0001g0089a0001c0001t0001g0090others(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 | a0001c0001t0001g0077a0001c0001t0001g0099a0001c0001t0001g0216others(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 | a0001c0001t0001g0074a0001c0001t0001g0228a0001c0001t0001g0230others(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 | a0001c0001t0001g0051a0001c0001t0001g0073a0001c0001t0001g0082others(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 | a0001c0001t0001g0036a0001c0001t0001g0111a0001c0001t0001g0138others(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 | 47 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(44): 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 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0028others(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 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(89): Show | 155 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(152): 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 | a0001c0001t0001g0024a0001c0001t0001g0044a0001c0001t0001g0088 | 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 | a0001c0001t0001g0227 | 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 | a0001c0001t0001g0192 | 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 | a0001c0001t0001g0218 | 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 | a0001c0001t0001g0084 | 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 | a0001c0001t0001g0227 | 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 | 94 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(91): 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 | a0001c0001t0001g0251 | 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 | a0001c0001t0001g0150a0001c0001t0001g0151 | 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 | a0001c0001t0001g0141 | 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 | 222 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(219): Show | 344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): 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 | a0001c0001t0001g0161 | 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 | a0001c0001t0001g0016a0001c0001t0001g0173a0001c0001t0008g0176 | 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 | a0001c0001t0001g0107 | 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 | a0001c0001t0001g0012a0001c0001t0001g0067a0001c0001t0001g0071others(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 | a0001c0001t0001g0213a0001c0001t0001g0214 | 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 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0077 | 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 | a0001c0001t0001g0073a0001c0001t0001g0074 | 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 | a0001c0001t0001g0073a0001c0001t0001g0074 | 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 | a0001c0001t0001g0195 | 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 | a0001c0001t0001g0025a0001c0001t0001g0073a0001c0001t0001g0074others(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 | a0001c0001t0001g0016a0001c0001t0001g0034a0001c0001t0001g0130others(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 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0024others(19): Show | 34 | HG00323.hp1 HG00733.hp2 HG00735.hp1 others(31): 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 | a0001c0001t0001g0018a0001c0001t0001g0033a0001c0001t0001g0036others(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 | a0001c0003t0001g0234a0001c0004t0001g0091a0001c0004t0001g0124others(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 | a0001c0001t0001g0089a0001c0001t0003g0043a0001c0004t0001g0122others(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 | a0001c0001t0001g0094a0001c0001t0003g0207a0001c0004t0001g0121 | 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 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0037others(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 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(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 | a0001c0001t0001g0012a0001c0001t0001g0067a0001c0001t0001g0071others(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 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0027others(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 | 69 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(66): 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 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0023others(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 | a0001c0001t0001g0079a0001c0001t0001g0140a0001c0001t0001g0166others(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 | a0001c0001t0001g0189 | 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 | a0001c0001t0001g0073a0001c0001t0001g0074 | 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 | a0001c0001t0001g0073a0001c0001t0001g0074 | 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 | a0001c0001t0001g0154 | 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 | a0001c0006t0001g0165 | 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 | a0001c0006t0001g0165 | 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 | a0001c0006t0001g0165 | 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 | a0001c0006t0001g0165 | 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 | a0001c0006t0001g0165 | 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 | a0001c0006t0001g0165 | 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 | a0001c0006t0001g0165 | 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 | a0001c0006t0001g0165 | 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 | a0001c0006t0001g0165 | 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 | a0001c0001t0001g0051a0001c0001t0001g0247a0001c0001t0001g0249others(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 | a0001c0006t0001g0165 | 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 | a0001c0006t0001g0165 | 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 | a0001c0006t0001g0165 | 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 | a0001c0006t0001g0165 | 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 | a0001c0001t0001g0170a0001c0001t0001g0171 | 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 | a0001c0006t0001g0165 | 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 | a0001c0006t0001g0165 | 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 | a0001c0006t0001g0165 | 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 | a0001c0001t0001g0073a0001c0001t0001g0074 | 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 | a0001c0006t0001g0165 | 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 | a0001c0001t0001g0147 | 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 | a0001c0001t0001g0120a0001c0001t0001g0202a0001c0001t0001g0204 | 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 | a0001c0001t0001g0086 | 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 | a0001c0001t0001g0109a0001c0001t0001g0132 | 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 | a0001c0001t0001g0036a0001c0001t0001g0077a0001c0001t0001g0089others(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 | a0001c0001t0001g0137 | 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 | 246 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(243): Show | 373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): 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 | a0001c0001t0001g0073a0001c0001t0001g0074 | 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 | a0001c0001t0001g0051a0001c0001t0001g0247a0001c0001t0001g0249others(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 | a0001c0001t0001g0020a0001c0001t0001g0045a0001c0001t0001g0221others(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 | a0001c0001t0001g0169 | 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 | a0001c0001t0001g0073a0001c0001t0001g0074 | 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 | a0001c0001t0001g0073a0001c0001t0001g0074 | 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 | a0001c0001t0001g0154 | 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 | 109 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(106): 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 | a0001c0001t0001g0073a0001c0001t0001g0074 | 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 | a0001c0001t0001g0159 | 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 | a0001c0001t0001g0218 | 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 | a0001c0001t0001g0157a0001c0001t0001g0188a0003c0014t0001g0258 | 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 | a0001c0001t0001g0154 | 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 | a0001c0010t0013g0209 | 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 | a0001c0003t0001g0235 | 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 | a0001c0001t0001g0168 | 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 | a0001c0001t0001g0024a0001c0001t0001g0044a0001c0001t0001g0088 | 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 | a0001c0001t0001g0051a0001c0001t0001g0189a0001c0001t0001g0190others(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 | a0001c0001t0001g0051a0001c0001t0001g0189a0001c0001t0001g0190others(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 | a0001c0001t0001g0149 | 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 | a0001c0001t0001g0092 | 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 | a0001c0001t0001g0206 | 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 | a0006c0011t0001g0191 | 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 | a0002c0002t0001g0241a0002c0002t0001g0242 | 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 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(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 | a0001c0010t0013g0209 | 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 | a0001c0001t0001g0036a0001c0001t0001g0088a0001c0001t0001g0089others(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 | a0001c0005t0001g0253a0001c0005t0002g0026a0001c0005t0002g0254others(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 | a0001c0001t0001g0051a0001c0001t0001g0247a0001c0001t0001g0248others(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 | a0001c0003t0001g0236 | 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 | a0006c0011t0001g0191 | 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 | a0001c0001t0001g0211a0005c0009t0001g0210 | 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 | a0001c0001t0001g0211a0005c0009t0001g0210 | 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 | a0001c0001t0001g0051a0001c0001t0001g0247a0001c0001t0001g0248others(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 | a0001c0001t0001g0206 | 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 | a0001c0001t0001g0192 | 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 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074 | 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 | a0001c0001t0001g0010a0001c0001t0001g0111 | 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 | a0001c0001t0001g0192 | 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 | a0001c0001t0001g0217 | 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 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0005g0038 | 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 | a0001c0001t0001g0011a0001c0001t0001g0039a0001c0001t0001g0051others(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 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(53): Show | 85 | HG00323.hp1 HG00642.hp1 HG00733.hp2 others(82): Show |
intron_variant | MODIFIER | c.1135-370delA | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 3/8 | chr11 | 120126258 | ||||||
| chr11:120126396
|
T | C | 1 | a0001c0001t0001g0112 | 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 | a0001c0001t0001g0035a0001c0001t0001g0113a0001c0001t0001g0114 | 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 | a0001c0001t0001g0115 | 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 | a0001c0001t0001g0153 | 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 | 128 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(125): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): 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 | a0001c0001t0001g0164 | 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 | a0001c0001t0003g0043a0001c0001t0003g0207 | 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 | a0001c0010t0013g0209 | 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 | a0001c0001t0001g0216 | 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 | a0001c0001t0001g0249 | 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 | a0001c0001t0001g0057a0001c0001t0001g0129 | 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 | a0001c0003t0001g0233 | 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 | a0001c0001t0001g0211a0005c0009t0001g0210 | 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 | a0001c0001t0001g0051a0001c0001t0001g0247a0001c0001t0001g0248others(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 | a0001c0001t0001g0211a0005c0009t0001g0210 | 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 | 128 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(125): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): 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 | a0001c0001t0001g0251 | 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 | a0001c0001t0010g0237 | 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 | a0001c0001t0001g0116 | 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 | a0001c0001t0001g0066a0001c0001t0001g0117a0001c0001t0001g0118 | 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 | 219 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(216): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.805-1030G>T | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 1/8 | chr11 | 120129525 | ||||||
| chr11:120129555
|
T | C | 221 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(218): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): 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 | a0001c0001t0001g0051a0001c0001t0001g0247a0001c0001t0001g0248others(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 | a0001c0001t0001g0213a0001c0001t0001g0214 | 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 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0037others(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 | a0001c0001t0001g0213a0001c0001t0001g0214 | 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 | 221 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(218): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.805-1669A>G | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 1/8 | chr11 | 120130164 | ||||||
| chr11:120130165
|
T | G | 221 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(218): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.805-1670A>C | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 1/8 | chr11 | 120130165 | ||||||
| chr11:120130177
|
T | C | 221 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(218): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): 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 | a0001c0001t0001g0214 | 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 | a0001c0001t0001g0206 | 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 | a0001c0001t0001g0131 | 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 | a0001c0008t0001g0163 | 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 | 105 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(102): Show | 155 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(152): 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 | a0001c0001t0001g0120a0001c0001t0012g0119 | 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 | a0001c0004t0001g0121a0001c0004t0001g0122a0001c0004t0001g0124others(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 | a0001c0001t0009g0252 | 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 | a0001c0001t0001g0238 | 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 | 126 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(123): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): 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 | a0001c0001t0001g0161a0001c0001t0001g0162 | 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 | 131 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): 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 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(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 | a0001c0004t0001g0125 | 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 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(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 | a0001c0001t0001g0159 | 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 | a0001c0001t0001g0126a0001c0001t0001g0199 | 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 | a0001c0001t0001g0158 | 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 | a0001c0001t0001g0060a0002c0002t0001g0058a0002c0002t0001g0059others(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 | a0001c0001t0001g0051a0001c0001t0001g0240a0001c0001t0001g0247others(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 | a0001c0001t0001g0200 | 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 | a0001c0001t0003g0043a0001c0001t0003g0207 | 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 | a0001c0001t0001g0201 | 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 | a0001c0001t0001g0201 | 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 | a0001c0001t0001g0157 | 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 | a0001c0001t0001g0060a0002c0002t0001g0058a0002c0002t0001g0059others(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 | a0001c0001t0001g0206a0001c0001t0003g0043a0001c0001t0003g0207 | 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 | a0001c0001t0001g0213a0001c0001t0001g0214 | 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 | a0001c0001t0001g0042a0001c0001t0001g0202a0001c0001t0001g0203others(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 | a0001c0001t0001g0204 | 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 | 123 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(120): Show | 182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): 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 | a0001c0001t0001g0213a0001c0001t0001g0214 | 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 | a0001c0001t0001g0154 | 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 | a0001c0001t0001g0021a0001c0001t0001g0155a0002c0002t0001g0156 | 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 | a0001c0001t0001g0051a0001c0001t0001g0240a0001c0001t0001g0247others(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 | a0001c0001t0001g0057a0001c0001t0001g0129 | 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 | a0001c0005t0001g0253a0001c0005t0002g0026a0001c0005t0002g0254others(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 | a0001c0001t0001g0154 | 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 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(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 | a0004c0013t0001g0257 | 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 | a0001c0001t0001g0128 | 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 | a0001c0001t0001g0133 | 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 | a0001c0001t0001g0133 | 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 | a0001c0001t0001g0133 | 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 | a0001c0001t0001g0133 | 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 | a0001c0001t0001g0133 | 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 | a0001c0001t0001g0133 | 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 | a0001c0001t0001g0051a0001c0001t0001g0240a0001c0001t0001g0247others(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 | a0001c0005t0002g0255 | 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 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(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 | 139 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(136): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): 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 | a0001c0001t0001g0051a0001c0001t0001g0240a0001c0001t0001g0247others(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 | a0001c0001t0001g0051a0001c0001t0001g0240a0001c0001t0001g0247others(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 | a0001c0001t0009g0252 | 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 | 99 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(96): Show | 149 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.804+47C>A | TRIM29 | ENSG00000137699.17 | transcript | ENST00000341846.10 | protein_coding | 1/8 | chr11 | 120137181 |