| geneid | 131405 |
|---|---|
| ensemblid | ENSG00000206557.6 |
| hgncid | 32669 |
| symbol | TRIM71 |
| name | tripartite motif containing 71 |
| refseq_nuc | NM_001039111.3 |
| refseq_prot | NP_001034200.1 |
| ensembl_nuc | ENST00000383763.6 |
| ensembl_prot | ENSP00000373272.3 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 32817997 |
| end | 32897824 |
| strand | + |
| ver | v1.2 |
| region | chr3:32817997-32897824 |
| region5000 | chr3:32812997-32902824 |
| regionname0 | TRIM71_chr3_32817997_32897824 |
| regionname5000 | TRIM71_chr3_32812997_32902824 |
| 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 | 868 | 325 | 92 | 50 | 131 | 16 | 34 | 95 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| a0002 | 0/0 | 868 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| a0003 | 0/0 | 868 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| 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 | 2607 | 234 | 62 | 38 | 89 | 15 | 29 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| c0002 | 0/0 | 2607 | 69 | 11 | 11 | 42 | 0 | 5 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| c0003 | 0/0 | 2607 | 16 | 15 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| c0004 | 1/0 | 2607 | 4 | 3 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| c0005 | 0/0 | 2607 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| c0006 | 0/0 | 2607 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| c0007 | 0/0 | 2607 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| c0008 | 0/0 | 2607 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| 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 | 0/0 | 6100 | 75 | 11 | 16 | 25 | 7 | 16 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| t0002 | 0/0 | 6098 | 74 | 26 | 9 | 35 | 0 | 4 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| t0003 | 0/1 | 6093 | 23 | 4 | 8 | 3 | 3 | 4 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| t0004 | 0/0 | 6096 | 17 | 0 | 0 | 16 | 1 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| t0005 | 0/0 | 6098 | 16 | 15 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| t0006 | 0/0 | 6100 | 13 | 0 | 0 | 13 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| t0007 | 0/0 | 6098 | 11 | 10 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| t0008 | 0/0 | 6096 | 11 | 0 | 0 | 11 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| t0009 | 0/0 | 6098 | 8 | 1 | 3 | 0 | 2 | 2 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| t0010 | 0/0 | 6102 | 4 | 2 | 2 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| t0011 | 1/0 | 6098 | 4 | 3 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| t0012 | 0/0 | 6093 | 4 | 2 | 1 | 0 | 1 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| t0013 | 0/0 | 6098 | 4 | 0 | 0 | 4 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| t0014 | 0/0 | 6102 | 3 | 0 | 3 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| t0015 | 0/0 | 6100 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| t0016 | 0/0 | 6098 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| t0017 | 0/0 | 6100 | 3 | 0 | 0 | 2 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| t0018 | 0/0 | 6102 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| t0019 | 0/0 | 6101 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| t0020 | 0/0 | 6096 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| t0021 | 0/0 | 6100 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| t0022 | 0/0 | 6100 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| t0023 | 0/0 | 6098 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| t0024 | 0/0 | 6098 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| t0025 | 0/0 | 6096 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| t0026 | 0/0 | 6093 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| t0027 | 0/0 | 6100 | 2 | 0 | 0 | 1 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| t0028 | 0/0 | 6102 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| t0029 | 0/0 | 6093 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| t0030 | 0/0 | 6100 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| t0031 | 0/0 | 6100 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| t0032 | 0/0 | 6100 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| t0033 | 0/0 | 6101 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| t0034 | 0/0 | 6100 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| t0035 | 0/0 | 6100 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| t0036 | 0/0 | 6100 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| t0037 | 0/0 | 6100 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| t0038 | 0/0 | 6100 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| t0039 | 0/0 | 6101 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| t0040 | 0/0 | 6100 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| t0041 | 0/0 | 6096 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| t0042 | 0/0 | 6100 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| t0043 | 0/0 | 6100 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| t0044 | 0/0 | 6100 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| t0045 | 0/0 | 6098 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| t0046 | 0/0 | 6098 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| t0047 | 0/0 | 6098 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| t0048 | 0/0 | 6093 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| t0049 | 0/0 | 6093 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| t0050 | 0/0 | 6093 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| t0051 | 0/0 | 6098 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| t0052 | 0/0 | 6094 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| t0053 | 0/0 | 6101 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| t0054 | 0/0 | 6100 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| t0055 | 0/0 | 6096 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| t0056 | 0/0 | 6096 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| t0057 | 0/0 | 6097 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| t0058 | 0/0 | 6094 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| t0059 | 0/0 | 6100 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| 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 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0146 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0306 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| 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 | 2607 | 234 | 62 | 38 | 89 | 15 | 29 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| a0001c0002 | 0/0 | 2607 | 69 | 11 | 11 | 42 | 0 | 5 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| a0001c0003 | 0/0 | 2607 | 16 | 15 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| a0001c0004 | 1/0 | 2607 | 4 | 3 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| a0001c0007 | 0/0 | 2607 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| a0001c0008 | 0/0 | 2607 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| a0002c0005 | 0/0 | 2607 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| a0003c0006 | 0/0 | 2607 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 8706 | 72 | 10 | 16 | 23 | 7 | 16 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| a0001c0001t0002 | 0/0 | 8704 | 17 | 16 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| a0001c0001t0003 | 0/1 | 8699 | 23 | 4 | 8 | 3 | 3 | 4 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| a0001c0001t0004 | 0/0 | 8702 | 17 | 0 | 0 | 16 | 1 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| a0001c0001t0006 | 0/0 | 8706 | 13 | 0 | 0 | 13 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| a0001c0001t0007 | 0/0 | 8704 | 10 | 9 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| a0001c0001t0008 | 0/0 | 8702 | 11 | 0 | 0 | 11 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| a0001c0001t0009 | 0/0 | 8704 | 8 | 1 | 3 | 0 | 2 | 2 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| a0001c0001t0010 | 0/0 | 8708 | 4 | 2 | 2 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| a0001c0001t0012 | 0/0 | 8699 | 3 | 2 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| a0001c0001t0014 | 0/0 | 8708 | 3 | 0 | 3 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| a0001c0001t0015 | 0/0 | 8706 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| a0001c0001t0016 | 0/0 | 8704 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| a0001c0001t0017 | 0/0 | 8706 | 3 | 0 | 0 | 2 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| a0001c0001t0018 | 0/0 | 8708 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| a0001c0001t0019 | 0/0 | 8707 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| a0001c0001t0020 | 0/0 | 8702 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| a0001c0001t0021 | 0/0 | 8706 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| a0001c0001t0022 | 0/0 | 8706 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| a0001c0001t0026 | 0/0 | 8699 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| a0001c0001t0027 | 0/0 | 8706 | 2 | 0 | 0 | 1 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| a0001c0001t0028 | 0/0 | 8708 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| a0001c0001t0029 | 0/0 | 8699 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| a0001c0001t0030 | 0/0 | 8706 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| a0001c0001t0031 | 0/0 | 8706 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| a0001c0001t0032 | 0/0 | 8706 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| a0001c0001t0033 | 0/0 | 8707 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| a0001c0001t0034 | 0/0 | 8706 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| a0001c0001t0035 | 0/0 | 8706 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| a0001c0001t0036 | 0/0 | 8706 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| a0001c0001t0037 | 0/0 | 8706 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| a0001c0001t0038 | 0/0 | 8706 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| a0001c0001t0039 | 0/0 | 8707 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| a0001c0001t0040 | 0/0 | 8706 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| a0001c0001t0041 | 0/0 | 8702 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| a0001c0001t0042 | 0/0 | 8706 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| a0001c0001t0043 | 0/0 | 8706 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| a0001c0001t0044 | 0/0 | 8706 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| a0001c0001t0045 | 0/0 | 8704 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| a0001c0001t0048 | 0/0 | 8699 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| a0001c0001t0049 | 0/0 | 8699 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| a0001c0001t0050 | 0/0 | 8699 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| a0001c0001t0051 | 0/0 | 8704 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| a0001c0001t0052 | 0/0 | 8700 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| a0001c0001t0053 | 0/0 | 8707 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| a0001c0001t0054 | 0/0 | 8706 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| a0001c0001t0055 | 0/0 | 8702 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| a0001c0001t0056 | 0/0 | 8702 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| a0001c0001t0057 | 0/0 | 8703 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| a0001c0001t0058 | 0/0 | 8700 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| a0001c0001t0059 | 0/0 | 8706 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| a0001c0002t0001 | 0/0 | 8706 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| a0001c0002t0002 | 0/0 | 8704 | 56 | 10 | 8 | 34 | 0 | 4 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| a0001c0002t0013 | 0/0 | 8704 | 4 | 0 | 0 | 4 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| a0001c0002t0023 | 0/0 | 8704 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| a0001c0002t0024 | 0/0 | 8704 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| a0001c0002t0025 | 0/0 | 8702 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| a0001c0002t0046 | 0/0 | 8704 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| a0001c0002t0047 | 0/0 | 8704 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| a0001c0003t0005 | 0/0 | 8704 | 16 | 15 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| a0001c0004t0011 | 1/0 | 8704 | 4 | 3 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| a0001c0007t0012 | 0/0 | 8699 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| a0001c0008t0007 | 0/0 | 8704 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| a0002c0005t0001 | 0/0 | 8706 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| a0003c0006t0002 | 0/0 | 8704 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | copy fasta | chr3 | 32812997 | 32902824 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0002g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0002g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0002g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0002g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0002g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0002g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0002g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0003g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0003g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0003g0146 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0003g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0003g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0003g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0003g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0003g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0004g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0004g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0004g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0004g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0004g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0004g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0004g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0004g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0004g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0004g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0004g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0004g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0004g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0004g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0004g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0004g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0004g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0006g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0006g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0006g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0006g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0006g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0006g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0006g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0006g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0006g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0006g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0006g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0006g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0006g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0007g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0007g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0007g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0007g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0007g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0007g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0007g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0007g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0007g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0008g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0008g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0008g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0008g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0008g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0008g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0008g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0008g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0008g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0008g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0008g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0009g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0009g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0009g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0009g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0009g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0009g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0009g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0009g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0010g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0010g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0010g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0010g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0012g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0012g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0012g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0014g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0014g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0014g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0015g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0015g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0015g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0016g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0016g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0017g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0017g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0017g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0018g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0018g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0019g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0019g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0020g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0020g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0021g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0021g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0022g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0022g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0026g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0026g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0027g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0027g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0028g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0029g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0030g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0031g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0032g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0033g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0034g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0035g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0036g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0037g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0038g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0039g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0040g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0041g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0042g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0043g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0044g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0045g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0048g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0049g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0050g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0051g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0052g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0053g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0054g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0055g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0056g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0057g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0058g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0001t0059g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0002t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0002t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0002t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0002t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0002t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0002t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0002t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0002t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0002t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0002t0002g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0002t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0002t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0002t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0002t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0002t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0002t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0002t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0002t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0002t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0002t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0002t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0002t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0002t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0002t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0002t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0002t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0002t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0002t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0002t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0002t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0002t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0002t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0002t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0002t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0002t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0002t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0002t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0002t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0002t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0002t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0002t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0002t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0002t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0002t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0002t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0002t0002g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0002t0013g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0002t0013g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0002t0013g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0002t0013g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0002t0023g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0002t0023g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0002t0024g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0002t0024g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0002t0025g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0002t0025g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0002t0046g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0002t0047g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0003t0005g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0003t0005g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0003t0005g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0003t0005g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0003t0005g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0003t0005g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0003t0005g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0003t0005g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0003t0005g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0003t0005g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0003t0005g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0003t0005g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0003t0005g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0003t0005g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0003t0005g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0003t0005g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0004t0011g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0004t0011g0306 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0004t0011g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0004t0011g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0007t0012g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0001c0008t0007g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0002c0005t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0002c0005t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| a0003c0006t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0193 | EUR | GBR | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0104 | EUR | GBR | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG00140 | hp1 | a0001 | c0001 | t0009 | g0164 | EUR | GBR | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG00140 | hp2 | a0001 | c0001 | t0034 | g0254 | EUR | GBR | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0140 | EUR | FIN | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG00280 | hp2 | a0001 | c0001 | t0004 | g0218 | EUR | FIN | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG00323 | hp1 | a0001 | c0007 | t0012 | g0137 | EUR | FIN | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG00323 | hp2 | a0001 | c0001 | t0028 | g0222 | EUR | FIN | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG00423 | hp2 | a0001 | c0002 | t0002 | g0154 | EAS | CHS | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG00438 | hp1 | a0002 | c0005 | t0001 | g0157 | EAS | CHS | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG00438 | hp2 | a0001 | c0001 | t0004 | g0046 | EAS | CHS | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG00544 | hp1 | a0001 | c0002 | t0025 | g0210 | EAS | CHS | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG00544 | hp2 | a0001 | c0001 | t0027 | g0279 | EAS | CHS | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG00558 | hp1 | a0001 | c0002 | t0002 | g0027 | EAS | CHS | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | CHS | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG00597 | hp1 | a0001 | c0001 | t0004 | g0145 | EAS | CHS | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG00597 | hp2 | a0001 | c0002 | t0002 | g0158 | EAS | CHS | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG00609 | hp1 | a0001 | c0002 | t0002 | g0090 | EAS | CHS | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG00609 | hp2 | a0001 | c0002 | t0002 | g0207 | EAS | CHS | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG00621 | hp1 | a0002 | c0005 | t0001 | g0005 | EAS | CHS | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG00621 | hp2 | a0001 | c0002 | t0002 | g0160 | EAS | CHS | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG00639 | hp1 | a0001 | c0001 | t0007 | g0069 | AMR | PUR | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG00639 | hp2 | a0001 | c0002 | t0002 | g0135 | AMR | PUR | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0253 | AMR | PUR | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0192 | AMR | PUR | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG01069 | hp1 | a0001 | c0001 | t0009 | g0228 | AMR | PUR | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0240 | AMR | PUR | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0251 | AMR | PUR | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG01081 | hp2 | a0001 | c0001 | t0003 | g0191 | AMR | PUR | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0243 | AMR | PUR | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG01106 | hp2 | a0001 | c0002 | t0002 | g0051 | AMR | PUR | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG01109 | hp1 | a0001 | c0002 | t0002 | g0111 | AMR | PUR | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG01109 | hp2 | a0001 | c0002 | t0002 | g0022 | AMR | PUR | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG01167 | hp1 | a0001 | c0001 | t0009 | g0242 | AMR | PUR | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG01167 | hp2 | a0001 | c0001 | t0012 | g0153 | AMR | PUR | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG01175 | hp2 | a0001 | c0001 | t0014 | g0282 | AMR | PUR | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG01192 | hp1 | a0001 | c0002 | t0002 | g0255 | AMR | PUR | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG01192 | hp2 | a0001 | c0002 | t0002 | g0170 | AMR | PUR | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG01243 | hp1 | a0001 | c0001 | t0010 | g0237 | AMR | PUR | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG01243 | hp2 | a0001 | c0001 | t0030 | g0325 | AMR | PUR | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG01255 | hp1 | a0001 | c0001 | t0059 | g0129 | AMR | CLM | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG01255 | hp2 | a0001 | c0001 | t0010 | g0238 | AMR | CLM | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0298 | AMR | CLM | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG01256 | hp2 | a0001 | c0001 | t0014 | g0248 | AMR | CLM | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG01258 | hp1 | a0001 | c0001 | t0014 | g0252 | AMR | CLM | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG01258 | hp2 | a0001 | c0001 | t0031 | g0151 | AMR | CLM | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0079 | AMR | CLM | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | CLM | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | CLM | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG01358 | hp2 | a0001 | c0002 | t0024 | g0139 | AMR | CLM | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | CLM | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0226 | AMR | CLM | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG01516 | hp1 | a0001 | c0001 | t0003 | g0194 | EUR | IBS | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0055 | EUR | IBS | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG01517 | hp1 | a0001 | c0001 | t0009 | g0167 | EUR | IBS | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0050 | EUR | IBS | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG01884 | hp1 | a0001 | c0004 | t0011 | g0312 | AFR | ACB | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG01884 | hp2 | a0001 | c0008 | t0007 | g0023 | AFR | ACB | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG01891 | hp1 | a0001 | c0001 | t0010 | g0239 | AFR | ACB | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG01891 | hp2 | a0001 | c0003 | t0005 | g0301 | AFR | ACB | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | PEL | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG01934 | hp2 | a0001 | c0003 | t0005 | g0025 | AMR | PEL | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG01952 | hp1 | a0001 | c0002 | t0002 | g0091 | AMR | PEL | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG01952 | hp2 | a0001 | c0002 | t0024 | g0208 | AMR | PEL | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG01978 | hp1 | a0001 | c0002 | t0046 | g0065 | AMR | PEL | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PEL | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0247 | AMR | PEL | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | PEL | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG01993 | hp1 | a0001 | c0002 | t0002 | g0131 | AMR | PEL | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG01993 | hp2 | a0001 | c0001 | t0003 | g0187 | AMR | PEL | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG02015 | hp1 | a0001 | c0001 | t0006 | g0150 | EAS | KHV | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG02015 | hp2 | a0001 | c0001 | t0021 | g0045 | EAS | KHV | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG02027 | hp1 | a0001 | c0002 | t0002 | g0290 | EAS | KHV | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG02027 | hp2 | a0001 | c0002 | t0002 | g0206 | EAS | KHV | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | KHV | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG02040 | hp2 | a0001 | c0001 | t0004 | g0038 | EAS | KHV | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0203 | AFR | ACB | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0114 | AFR | ACB | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG02056 | hp1 | a0001 | c0001 | t0033 | g0149 | EAS | KHV | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG02056 | hp2 | a0001 | c0001 | t0019 | g0326 | EAS | KHV | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG02074 | hp1 | a0001 | c0002 | t0002 | g0138 | EAS | KHV | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG02074 | hp2 | a0001 | c0001 | t0008 | g0268 | EAS | KHV | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | KHV | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG02080 | hp2 | a0001 | c0001 | t0008 | g0276 | EAS | KHV | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | KHV | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG02129 | hp2 | a0001 | c0002 | t0002 | g0092 | EAS | KHV | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG02132 | hp1 | a0001 | c0001 | t0008 | g0277 | EAS | KHV | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG02132 | hp2 | a0001 | c0001 | t0006 | g0134 | EAS | KHV | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0074 | AFR | ACB | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0056 | AFR | ACB | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG02148 | hp1 | a0001 | c0001 | t0003 | g0105 | AMR | PEL | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PEL | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG02155 | hp1 | a0001 | c0002 | t0002 | g0147 | EAS | CDX | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG02155 | hp2 | a0001 | c0002 | t0013 | g0258 | EAS | CDX | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG02165 | hp1 | a0001 | c0001 | t0006 | g0010 | EAS | CDX | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG02165 | hp2 | a0001 | c0001 | t0021 | g0172 | EAS | CDX | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG02257 | hp1 | a0001 | c0001 | t0007 | g0314 | AFR | ACB | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG02257 | hp2 | a0001 | c0002 | t0002 | g0015 | AFR | ACB | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG02258 | hp1 | a0001 | c0002 | t0001 | g0236 | AFR | ACB | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG02258 | hp2 | a0001 | c0001 | t0015 | g0072 | AFR | ACB | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0305 | AFR | ACB | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG02451 | hp2 | a0001 | c0001 | t0007 | g0123 | AFR | ACB | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG02523 | hp1 | a0001 | c0001 | t0006 | g0165 | EAS | KHV | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG02523 | hp2 | a0001 | c0001 | t0006 | g0029 | EAS | KHV | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG02572 | hp1 | a0001 | c0003 | t0005 | g0013 | AFR | GWD | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG02572 | hp2 | a0001 | c0002 | t0002 | g0019 | AFR | GWD | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0189 | SAS | PJL | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG02615 | hp1 | a0001 | c0001 | t0012 | g0063 | AFR | GWD | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG02615 | hp2 | a0001 | c0001 | t0007 | g0311 | AFR | GWD | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG02622 | hp1 | a0001 | c0003 | t0005 | g0300 | AFR | GWD | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG02630 | hp1 | a0001 | c0003 | t0005 | g0117 | AFR | GWD | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG02630 | hp2 | a0001 | c0002 | t0002 | g0021 | AFR | GWD | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG02647 | hp1 | a0001 | c0003 | t0005 | g0284 | AFR | GWD | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG02647 | hp2 | a0001 | c0001 | t0045 | g0071 | AFR | GWD | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0148 | SAS | PJL | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG02683 | hp2 | a0001 | c0002 | t0047 | g0101 | SAS | PJL | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG02698 | hp1 | a0001 | c0002 | t0002 | g0186 | SAS | PJL | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG02698 | hp2 | a0001 | c0002 | t0002 | g0106 | SAS | PJL | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0320 | AFR | GWD | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG02717 | hp2 | a0001 | c0003 | t0005 | g0323 | AFR | GWD | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG02723 | hp1 | a0001 | c0001 | t0026 | g0321 | AFR | GWD | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0319 | AFR | GWD | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG02735 | hp1 | a0001 | c0001 | t0017 | g0280 | SAS | PJL | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG02735 | hp2 | a0001 | c0001 | t0009 | g0115 | SAS | PJL | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0216 | SAS | PJL | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG02809 | hp1 | a0001 | c0003 | t0005 | g0068 | AFR | GWD | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG02809 | hp2 | a0001 | c0003 | t0005 | g0302 | AFR | GWD | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG02818 | hp1 | a0001 | c0001 | t0007 | g0313 | AFR | GWD | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG02818 | hp2 | a0001 | c0001 | t0037 | g0322 | AFR | GWD | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG02886 | hp1 | a0001 | c0002 | t0002 | g0324 | AFR | GWD | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0316 | AFR | GWD | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0304 | AFR | GWD | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG02896 | hp2 | a0001 | c0003 | t0005 | g0285 | AFR | GWD | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG02965 | hp1 | a0001 | c0003 | t0005 | g0084 | AFR | ESN | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG02965 | hp2 | a0001 | c0001 | t0016 | g0080 | AFR | ESN | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0234 | AFR | ESN | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG02970 | hp2 | a0001 | c0002 | t0002 | g0018 | AFR | ESN | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG02976 | hp1 | a0001 | c0001 | t0007 | g0121 | AFR | ESN | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG02976 | hp2 | a0001 | c0001 | t0036 | g0303 | AFR | ESN | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | PJL | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | GWD | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG03041 | hp2 | a0001 | c0001 | t0038 | g0318 | AFR | GWD | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0067 | AFR | MSL | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG03098 | hp2 | a0001 | c0001 | t0007 | g0286 | AFR | MSL | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG03130 | hp1 | a0001 | c0002 | t0002 | g0016 | AFR | ESN | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG03130 | hp2 | a0001 | c0004 | t0011 | g0245 | AFR | ESN | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG03139 | hp1 | a0001 | c0001 | t0016 | g0001 | AFR | ESN | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ESN | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG03195 | hp1 | a0001 | c0002 | t0002 | g0020 | AFR | ESN | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG03195 | hp2 | a0001 | c0001 | t0012 | g0008 | AFR | ESN | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG03209 | hp1 | a0001 | c0001 | t0007 | g0002 | AFR | MSL | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG03209 | hp2 | a0001 | c0001 | t0026 | g0066 | AFR | MSL | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG03225 | hp1 | a0001 | c0001 | t0007 | g0098 | AFR | MSL | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG03239 | hp2 | a0001 | c0001 | t0009 | g0089 | SAS | PJL | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0168 | AFR | MSL | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG03453 | hp2 | a0001 | c0002 | t0002 | g0017 | AFR | MSL | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG03486 | hp1 | a0001 | c0001 | t0010 | g0244 | AFR | MSL | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG03486 | hp2 | a0001 | c0001 | t0007 | g0002 | AFR | MSL | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG03491 | hp2 | a0001 | c0001 | t0042 | g0107 | SAS | PJL | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG03492 | hp2 | a0001 | c0001 | t0049 | g0130 | SAS | PJL | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0315 | AFR | ESN | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0078 | AFR | ESN | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG03540 | hp2 | a0001 | c0003 | t0005 | g0122 | AFR | GWD | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG03579 | hp1 | a0001 | c0003 | t0005 | g0308 | AFR | MSL | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG03579 | hp2 | a0001 | c0001 | t0016 | g0001 | AFR | MSL | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG03669 | hp1 | a0001 | c0001 | t0003 | g0093 | SAS | PJL | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG03669 | hp2 | a0001 | c0001 | t0035 | g0082 | SAS | PJL | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0250 | SAS | STU | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG03688 | hp2 | a0001 | c0001 | t0050 | g0094 | SAS | STU | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG03710 | hp1 | a0001 | c0002 | t0002 | g0058 | SAS | PJL | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0212 | SAS | PJL | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG03834 | hp1 | a0001 | c0001 | t0040 | g0256 | SAS | BEB | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG03834 | hp2 | a0001 | c0001 | t0003 | g0219 | SAS | BEB | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG03927 | hp1 | a0001 | c0002 | t0002 | g0059 | SAS | BEB | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | STU | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0163 | SAS | STU | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG04228 | hp1 | a0001 | c0001 | t0027 | g0261 | SAS | STU | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | STU | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0083 | AFR | YRI | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0317 | AFR | YRI | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA18747 | hp1 | a0001 | c0002 | t0002 | g0062 | EAS | CHB | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | CHB | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA18906 | hp1 | a0001 | c0001 | t0018 | g0283 | AFR | YRI | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA18906 | hp2 | a0001 | c0003 | t0005 | g0299 | AFR | YRI | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA18945 | hp1 | a0001 | c0001 | t0041 | g0036 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA18945 | hp2 | a0001 | c0002 | t0002 | g0294 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA18947 | hp1 | a0001 | c0001 | t0008 | g0263 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA18947 | hp2 | a0001 | c0001 | t0006 | g0201 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA18948 | hp1 | a0001 | c0002 | t0002 | g0126 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA18951 | hp1 | a0001 | c0001 | t0003 | g0202 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA18951 | hp2 | a0001 | c0002 | t0002 | g0087 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA18952 | hp1 | a0001 | c0002 | t0002 | g0032 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA18953 | hp1 | a0001 | c0001 | t0004 | g0214 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA18962 | hp1 | a0001 | c0001 | t0017 | g0259 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA18962 | hp2 | a0001 | c0002 | t0025 | g0169 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA18963 | hp1 | a0003 | c0006 | t0002 | g0195 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA18964 | hp1 | a0001 | c0002 | t0002 | g0159 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA18964 | hp2 | a0001 | c0001 | t0008 | g0273 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA18966 | hp1 | a0001 | c0001 | t0022 | g0175 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA18966 | hp2 | a0001 | c0001 | t0020 | g0047 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA18968 | hp1 | a0001 | c0001 | t0008 | g0262 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA18968 | hp2 | a0001 | c0002 | t0002 | g0124 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA18969 | hp2 | a0001 | c0001 | t0004 | g0061 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA18973 | hp1 | a0001 | c0002 | t0002 | g0293 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA18973 | hp2 | a0001 | c0002 | t0013 | g0267 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA18977 | hp1 | a0001 | c0002 | t0002 | g0291 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA18977 | hp2 | a0001 | c0001 | t0008 | g0265 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA18978 | hp1 | a0001 | c0001 | t0004 | g0057 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA18979 | hp1 | a0001 | c0001 | t0019 | g0196 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA18979 | hp2 | a0001 | c0001 | t0004 | g0054 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA18980 | hp1 | a0001 | c0001 | t0003 | g0041 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA18981 | hp1 | a0001 | c0002 | t0023 | g0052 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA18981 | hp2 | a0001 | c0001 | t0004 | g0296 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA18982 | hp1 | a0001 | c0001 | t0004 | g0136 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA18982 | hp2 | a0001 | c0002 | t0002 | g0200 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA18983 | hp1 | a0001 | c0001 | t0043 | g0184 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA18985 | hp1 | a0001 | c0001 | t0003 | g0112 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA18990 | hp1 | a0001 | c0001 | t0056 | g0274 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA18990 | hp2 | a0001 | c0001 | t0006 | g0132 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA18992 | hp1 | a0001 | c0001 | t0004 | g0161 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA18992 | hp2 | a0001 | c0001 | t0020 | g0034 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA18994 | hp1 | a0001 | c0001 | t0004 | g0143 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA18998 | hp1 | a0001 | c0002 | t0002 | g0039 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA18998 | hp2 | a0001 | c0001 | t0006 | g0215 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA19001 | hp1 | a0001 | c0002 | t0002 | g0060 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA19001 | hp2 | a0001 | c0002 | t0002 | g0217 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA19002 | hp2 | a0001 | c0001 | t0004 | g0152 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA19003 | hp1 | a0001 | c0001 | t0055 | g0270 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA19003 | hp2 | a0001 | c0002 | t0002 | g0155 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA19004 | hp1 | a0001 | c0002 | t0023 | g0044 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA19004 | hp2 | a0001 | c0002 | t0002 | g0209 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA19005 | hp1 | a0001 | c0001 | t0004 | g0043 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA19005 | hp2 | a0001 | c0002 | t0013 | g0266 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA19007 | hp1 | a0001 | c0001 | t0006 | g0288 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA19007 | hp2 | a0001 | c0001 | t0006 | g0040 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA19009 | hp1 | a0001 | c0002 | t0002 | g0297 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA19009 | hp2 | a0001 | c0001 | t0017 | g0260 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA19011 | hp1 | a0001 | c0002 | t0002 | g0289 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA19011 | hp2 | a0001 | c0001 | t0004 | g0048 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA19012 | hp2 | a0001 | c0001 | t0053 | g0271 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0310 | AFR | LWK | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | LWK | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA19043 | hp1 | a0001 | c0004 | t0011 | g0307 | AFR | LWK | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA19043 | hp2 | a0001 | c0001 | t0044 | g0081 | AFR | LWK | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA19056 | hp1 | a0001 | c0001 | t0006 | g0030 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA19056 | hp2 | a0001 | c0001 | t0008 | g0275 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA19060 | hp1 | a0001 | c0001 | t0004 | g0174 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA19060 | hp2 | a0001 | c0001 | t0029 | g0257 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA19065 | hp1 | a0001 | c0002 | t0013 | g0269 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA19065 | hp2 | a0001 | c0001 | t0032 | g0035 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA19066 | hp1 | a0001 | c0001 | t0004 | g0033 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA19066 | hp2 | a0001 | c0002 | t0002 | g0156 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA19068 | hp1 | a0001 | c0001 | t0008 | g0278 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA19074 | hp1 | a0001 | c0002 | t0002 | g0295 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA19074 | hp2 | a0001 | c0001 | t0008 | g0229 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA19077 | hp1 | a0001 | c0001 | t0058 | g0225 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA19077 | hp2 | a0001 | c0001 | t0006 | g0232 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA19078 | hp2 | a0001 | c0001 | t0057 | g0272 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA19081 | hp1 | a0001 | c0001 | t0006 | g0031 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA19082 | hp1 | a0001 | c0002 | t0002 | g0292 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA19082 | hp2 | a0001 | c0001 | t0008 | g0264 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA19083 | hp1 | a0001 | c0002 | t0002 | g0183 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA19083 | hp2 | a0001 | c0001 | t0052 | g0102 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA19087 | hp1 | a0001 | c0001 | t0054 | g0281 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA19087 | hp2 | a0001 | c0002 | t0002 | g0211 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA19091 | hp1 | a0001 | c0001 | t0022 | g0179 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA19091 | hp2 | a0001 | c0002 | t0002 | g0042 | EAS | JPT | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0235 | AFR | YRI | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA19240 | hp2 | a0001 | c0002 | t0002 | g0070 | AFR | YRI | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0118 | AFR | ASW | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA20129 | hp2 | a0001 | c0001 | t0009 | g0188 | AFR | ASW | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0141 | EUR | TSI | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0190 | EUR | TSI | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0142 | EUR | TSI | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0086 | EUR | TSI | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0053 | SAS | GIH | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | GIH | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG01123 | hp1 | a0001 | c0001 | t0003 | g0166 | AMR | CLM | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG01123 | hp2 | a0001 | c0001 | t0009 | g0227 | AMR | CLM | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG02109 | hp1 | a0001 | c0002 | t0002 | g0014 | AFR | ACB | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG02109 | hp2 | a0001 | c0001 | t0048 | g0162 | AFR | ACB | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0309 | AFR | ACB | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0171 | AFR | ACB | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG02559 | hp1 | a0001 | c0003 | t0005 | g0097 | AFR | ACB | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG02559 | hp2 | a0001 | c0001 | t0018 | g0099 | AFR | ACB | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0075 | AFR | MSL | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | MSL | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG06807 | hp1 | a0001 | c0001 | t0015 | g0246 | AFR | USA | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| HG06807 | hp2 | a0001 | c0001 | t0039 | g0024 | AFR | USA | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA20300 | hp1 | a0001 | c0001 | t0051 | g0096 | AFR | USA | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | USA | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA21309 | hp1 | a0001 | c0003 | t0005 | g0287 | AFR | LWK | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| NA21309 | hp2 | a0001 | c0001 | t0015 | g0073 | AFR | LWK | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0003 | g0146 | REF | REF | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| homoSapiens_grch38 | hp1 | a0001 | c0004 | t0011 | g0306 | REF | REF | TRIM71_chr3_32812997_32902824 | TRIM71 | chr3 | 32812997 | 32902824 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:32818133
|
T | G | 1 | a0003 | 1 | NA18963.hp1 | missense_variant | MODERATE | c.53T>G | p.Met18Arg | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/4 | 137/8704 | 53/2607 | 18/868 | chr3 | 32818133 | ||
| chr3:32890543
|
G | A | 1 | a0002 | 2 | HG00438.hp1 HG00621.hp1 |
missense_variant | MODERATE | c.1339G>A | p.Val447Met | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 1423/8704 | 1339/2607 | 447/868 | chr3 | 32890543 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:32818383
|
C | G | 1 | a0001c0008 | 1 | HG01884.hp2 | synonymous_variant | LOW | c.303C>G | p.Ala101Ala | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/4 | 387/8704 | 303/2607 | 101/868 | chr3 | 32818383 | ||
| chr3:32886017
|
G | T | 7 | a0001c0001a0001c0002a0001c0003others(4): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
synonymous_variant | LOW | c.1104G>T | p.Thr368Thr | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/4 | 1188/8704 | 1104/2607 | 368/868 | chr3 | 32886017 | ||
| chr3:32891163
|
C | T | 1 | a0001c0007 | 1 | HG00323.hp1 | synonymous_variant | LOW | c.1959C>T | p.Phe653Phe | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 2043/8704 | 1959/2607 | 653/868 | chr3 | 32891163 | ||
| chr3:32891544
|
G | A | 2 | a0001c0002a0003c0006 | 70 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(67): Show |
synonymous_variant | LOW | c.2340G>A | p.Ser780Ser | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 2424/8704 | 2340/2607 | 780/868 | chr3 | 32891544 | ||
| chr3:32891637
|
G | A | 1 | a0001c0003 | 16 | HG01891.hp2 HG01934.hp2 HG02559.hp1 others(13): Show |
synonymous_variant | LOW | c.2433G>A | p.Ala811Ala | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 2517/8704 | 2433/2607 | 811/868 | chr3 | 32891637 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:32818002
|
C | T | 1 | a0001c0001t0059 | 1 | HG01255.hp1 | 5_prime_UTR_variant | MODIFIER | c.-79C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/4 | 79 | chr3 | 32818002 | |||||
| chr3:32818028
|
C | T | 10 | a0001c0001t0008a0001c0001t0017a0001c0001t0027others(7): Show | 26 | HG00544.hp2 HG02074.hp2 HG02080.hp2 others(23): Show |
5_prime_UTR_variant | MODIFIER | c.-53C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/4 | 53 | chr3 | 32818028 | |||||
| chr3:32891852
|
G | GTC | 34 | a0001c0001t0001a0001c0001t0004a0001c0001t0006others(31): Show | 153 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(150): Show |
3_prime_UTR_variant | MODIFIER | c.*61_*62dupCT | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 63 | INFO_REALIGN_3_PRIME | chr3 | 32891852 | ||||
| chr3:32891852
|
G | GTCTC | 4 | a0001c0001t0010a0001c0001t0014a0001c0001t0018others(1): Show | 10 | HG00323.hp2 HG01175.hp2 HG01243.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*59_*62dupCTCT | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 63 | INFO_REALIGN_3_PRIME | chr3 | 32891852 | ||||
| chr3:32891870
|
C | T | 10 | a0001c0001t0003a0001c0001t0009a0001c0001t0012others(7): Show | 42 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*59C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 59 | chr3 | 32891870 | |||||
| chr3:32891874
|
T | C | 11 | a0001c0001t0003a0001c0001t0009a0001c0001t0012others(8): Show | 43 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*63T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 63 | chr3 | 32891874 | |||||
| chr3:32891876
|
C | T | 11 | a0001c0001t0003a0001c0001t0009a0001c0001t0012others(8): Show | 43 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*65C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 65 | chr3 | 32891876 | |||||
| chr3:32891880
|
T | C | 11 | a0001c0001t0003a0001c0001t0009a0001c0001t0012others(8): Show | 43 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*69T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 69 | chr3 | 32891880 | |||||
| chr3:32891890
|
T | C | 1 | a0001c0001t0048 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*79T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 79 | chr3 | 32891890 | |||||
| chr3:32892016
|
A | G | 1 | a0001c0001t0022 | 2 | NA18966.hp1 NA19091.hp1 |
3_prime_UTR_variant | MODIFIER | c.*205A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 205 | chr3 | 32892016 | |||||
| chr3:32892318
|
G | A | 1 | a0001c0001t0049 | 1 | HG03492.hp2 | 3_prime_UTR_variant | MODIFIER | c.*507G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 507 | chr3 | 32892318 | |||||
| chr3:32892719
|
A | G | 1 | a0001c0001t0044 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*908A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 908 | chr3 | 32892719 | |||||
| chr3:32892999
|
T | G | 1 | a0001c0003t0005 | 16 | HG01891.hp2 HG01934.hp2 HG02559.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1188T>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 1188 | chr3 | 32892999 | |||||
| chr3:32893011
|
A | G | 1 | a0001c0001t0043 | 1 | NA18983.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1200A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 1200 | chr3 | 32893011 | |||||
| chr3:32893251
|
G | A | 1 | a0001c0002t0023 | 2 | NA18981.hp1 NA19004.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1440G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 1440 | chr3 | 32893251 | |||||
| chr3:32893265
|
A | G | 1 | a0001c0001t0016 | 3 | HG02965.hp2 HG03139.hp1 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1454A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 1454 | chr3 | 32893265 | |||||
| chr3:32893290
|
C | T | 1 | a0001c0001t0021 | 2 | HG02015.hp2 HG02165.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1479C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 1479 | chr3 | 32893290 | |||||
| chr3:32893634
|
A | G | 12 | a0001c0001t0003a0001c0001t0009a0001c0001t0012others(9): Show | 44 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*1823A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 1823 | chr3 | 32893634 | |||||
| chr3:32893663
|
C | G | 2 | a0001c0001t0009a0001c0001t0042 | 9 | HG00140.hp1 HG01069.hp1 HG01123.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1852C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 1852 | chr3 | 32893663 | |||||
| chr3:32893719
|
T | C | 1 | a0001c0001t0016 | 3 | HG02965.hp2 HG03139.hp1 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1908T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 1908 | chr3 | 32893719 | |||||
| chr3:32893759
|
C | T | 3 | a0001c0001t0007a0001c0002t0047a0001c0008t0007 | 12 | HG00639.hp1 HG01884.hp2 HG02257.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1948C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 1948 | chr3 | 32893759 | |||||
| chr3:32893765
|
CCT | C | 8 | a0001c0001t0004a0001c0001t0008a0001c0001t0020others(5): Show | 35 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*1957_*1958delCT | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 1957 | INFO_REALIGN_3_PRIME | chr3 | 32893765 | ||||
| chr3:32894023
|
T | C | 14 | a0001c0001t0003a0001c0001t0009a0001c0001t0012others(11): Show | 46 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*2212T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 2212 | chr3 | 32894023 | |||||
| chr3:32894134
|
T | G | 1 | a0001c0002t0024 | 2 | HG01358.hp2 HG01952.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2323T>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 2323 | chr3 | 32894134 | |||||
| chr3:32894327
|
A | G | 13 | a0001c0001t0003a0001c0001t0009a0001c0001t0012others(10): Show | 45 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*2516A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 2516 | chr3 | 32894327 | |||||
| chr3:32894412
|
C | T | 1 | a0001c0003t0005 | 16 | HG01891.hp2 HG01934.hp2 HG02559.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*2601C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 2601 | chr3 | 32894412 | |||||
| chr3:32894750
|
G | A | 1 | a0001c0001t0032 | 1 | NA19065.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2939G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 2939 | chr3 | 32894750 | |||||
| chr3:32894863
|
G | T | 64 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(61): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
3_prime_UTR_variant | MODIFIER | c.*3052G>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 3052 | chr3 | 32894863 | |||||
| chr3:32894937
|
T | C | 2 | a0001c0001t0048a0001c0001t0050 | 2 | HG02109.hp2 HG03688.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3126T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 3126 | chr3 | 32894937 | |||||
| chr3:32895079
|
C | G | 2 | a0001c0001t0007a0001c0008t0007 | 11 | HG00639.hp1 HG01884.hp2 HG02257.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3268C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 3268 | chr3 | 32895079 | |||||
| chr3:32895080
|
T | C | 6 | a0001c0001t0006a0001c0001t0027a0001c0001t0028others(3): Show | 19 | HG00323.hp2 HG00544.hp2 HG02015.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*3269T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 3269 | chr3 | 32895080 | |||||
| chr3:32895313
|
G | A | 1 | a0001c0001t0054 | 1 | NA19087.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3502G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 3502 | chr3 | 32895313 | |||||
| chr3:32895511
|
T | G | 1 | a0001c0001t0034 | 1 | HG00140.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3700T>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 3700 | chr3 | 32895511 | |||||
| chr3:32895516
|
C | A | 22 | a0001c0001t0003a0001c0001t0004a0001c0001t0007others(19): Show | 100 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*3705C>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 3705 | chr3 | 32895516 | |||||
| chr3:32895549
|
T | C | 1 | a0001c0002t0023 | 2 | NA18981.hp1 NA19004.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3738T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 3738 | chr3 | 32895549 | |||||
| chr3:32895632
|
A | G | 1 | a0001c0001t0040 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3821A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 3821 | chr3 | 32895632 | |||||
| chr3:32895694
|
G | C | 1 | a0001c0001t0015 | 3 | HG02258.hp2 HG06807.hp1 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3883G>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 3883 | chr3 | 32895694 | |||||
| chr3:32895717
|
A | C | 2 | a0001c0001t0012a0001c0007t0012 | 4 | HG00323.hp1 HG01167.hp2 HG02615.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3906A>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 3906 | chr3 | 32895717 | |||||
| chr3:32896104
|
C | T | 36 | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(33): Show | 207 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(204): Show |
3_prime_UTR_variant | MODIFIER | c.*4293C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 4293 | chr3 | 32896104 | |||||
| chr3:32896162
|
C | G | 1 | a0001c0001t0026 | 2 | HG02723.hp1 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4351C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 4351 | chr3 | 32896162 | |||||
| chr3:32896183
|
T | G | 8 | a0001c0001t0004a0001c0001t0008a0001c0001t0020others(5): Show | 35 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*4372T>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 4372 | chr3 | 32896183 | |||||
| chr3:32896232
|
A | C | 1 | a0001c0002t0046 | 1 | HG01978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4421A>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 4421 | chr3 | 32896232 | |||||
| chr3:32896240
|
G | A | 1 | a0001c0001t0035 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4429G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 4429 | chr3 | 32896240 | |||||
| chr3:32896442
|
G | GT | 6 | a0001c0001t0019a0001c0001t0033a0001c0001t0039others(3): Show | 7 | HG02056.hp1 HG02056.hp2 HG06807.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4641dupT | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 4642 | INFO_REALIGN_3_PRIME | chr3 | 32896442 | ||||
| chr3:32896632
|
T | C | 1 | a0001c0001t0036 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4821T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 4821 | chr3 | 32896632 | |||||
| chr3:32896957
|
T | C | 4 | a0001c0001t0020a0001c0001t0055a0001c0001t0058others(1): Show | 6 | HG00544.hp1 NA18962.hp2 NA18966.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5146T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 5146 | chr3 | 32896957 | |||||
| chr3:32896976
|
ATTCCT | A | 9 | a0001c0001t0003a0001c0001t0012a0001c0001t0026others(6): Show | 34 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*5169_*5173delCTTT others(1): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 5169 | INFO_REALIGN_3_PRIME | chr3 | 32896976 | ||||
| chr3:32897010
|
G | A | 2 | a0001c0001t0037a0001c0001t0039 | 2 | HG02818.hp2 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5199G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 5199 | chr3 | 32897010 | |||||
| chr3:32897017
|
G | A | 2 | a0001c0001t0038a0001c0001t0045 | 2 | HG02647.hp2 HG03041.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5206G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 5206 | chr3 | 32897017 | |||||
| chr3:32897040
|
G | A | 1 | a0001c0001t0056 | 1 | NA18990.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5229G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 5229 | chr3 | 32897040 | |||||
| chr3:32897370
|
G | C | 1 | a0001c0001t0016 | 3 | HG02965.hp2 HG03139.hp1 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5559G>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 5559 | chr3 | 32897370 | |||||
| chr3:32897515
|
T | G | 1 | a0001c0001t0041 | 1 | NA18945.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5704T>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 5704 | chr3 | 32897515 | |||||
| chr3:32897521
|
TCC | T | 9 | a0001c0001t0004a0001c0001t0008a0001c0001t0020others(6): Show | 37 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*5715_*5716delCC | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 5715 | INFO_REALIGN_3_PRIME | chr3 | 32897521 | ||||
| chr3:32897561
|
T | C | 1 | a0001c0001t0018 | 2 | HG02559.hp2 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5750T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 4/4 | 5750 | chr3 | 32897561 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:32819052
|
C | T | 1 | a0001c0001t0019g0326 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.852+120C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32819052 | ||||||
| chr3:32819189
|
C | G | 1 | a0001c0001t0030g0325 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.852+257C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32819189 | ||||||
| chr3:32819206
|
G | T | 7 | a0001c0001t0002g0319a0001c0001t0002g0320a0001c0001t0026g0321others(4): Show | 7 | HG02717.hp1 HG02717.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.852+274G>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32819206 | ||||||
| chr3:32819237
|
G | A | 312 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(309): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.852+305G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32819237 | ||||||
| chr3:32819268
|
GCCTGCT | G | 312 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(309): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.852+344_852+349del others(6): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32819268 | |||||
| chr3:32819309
|
G | A | 1 | a0001c0001t0001g0003 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.852+377G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32819309 | ||||||
| chr3:32819479
|
G | T | 3 | a0001c0001t0001g0304a0001c0001t0016g0001a0001c0001t0036g0303 | 4 | HG02896.hp1 HG02976.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.852+547G>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32819479 | ||||||
| chr3:32819522
|
T | C | 3 | a0001c0001t0001g0004a0001c0001t0001g0006a0002c0005t0001g0005 | 3 | HG00423.hp1 HG00621.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.852+590T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32819522 | ||||||
| chr3:32819610
|
A | G | 4 | a0001c0003t0005g0299a0001c0003t0005g0300a0001c0003t0005g0301others(1): Show | 4 | HG01891.hp2 HG02622.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.852+678A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32819610 | ||||||
| chr3:32819634
|
C | G | 1 | a0001c0001t0002g0298 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.852+702C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32819634 | ||||||
| chr3:32819704
|
A | G | 9 | a0001c0001t0004g0296a0001c0002t0002g0289a0001c0002t0002g0290others(6): Show | 9 | HG02027.hp1 NA18945.hp2 NA18973.hp1 others(6): Show |
intron_variant | MODIFIER | c.852+772A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32819704 | ||||||
| chr3:32819968
|
C | T | 1 | a0001c0001t0006g0288 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.852+1036C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32819968 | ||||||
| chr3:32820025
|
T | G | 1 | a0001c0001t0001g0007 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.852+1093T>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32820025 | ||||||
| chr3:32820026
|
G | A | 1 | a0001c0001t0012g0008 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.852+1094G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32820026 | ||||||
| chr3:32820046
|
G | C | 1 | a0001c0001t0001g0009 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.852+1114G>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32820046 | ||||||
| chr3:32820064
|
G | T | 2 | a0001c0001t0007g0286a0001c0003t0005g0287 | 2 | HG03098.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.852+1132G>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32820064 | ||||||
| chr3:32820069
|
G | A | 1 | a0001c0001t0036g0303 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.852+1137G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32820069 | ||||||
| chr3:32820136
|
A | G | 58 | a0001c0001t0001g0003a0001c0001t0001g0230a0001c0001t0001g0231others(55): Show | 58 | HG00140.hp2 HG00544.hp2 HG00735.hp1 others(55): Show |
intron_variant | MODIFIER | c.852+1204A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32820136 | ||||||
| chr3:32820143
|
G | A | 1 | a0001c0001t0006g0010 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.852+1211G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32820143 | ||||||
| chr3:32820293
|
C | T | 2 | a0001c0003t0005g0284a0001c0003t0005g0285 | 2 | HG02647.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.852+1361C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32820293 | ||||||
| chr3:32820828
|
A | G | 3 | a0001c0001t0003g0226a0001c0001t0009g0227a0001c0001t0009g0228 | 3 | HG01069.hp1 HG01123.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.852+1896A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32820828 | ||||||
| chr3:32821043
|
G | C | 1 | a0001c0001t0001g0011 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.852+2111G>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32821043 | ||||||
| chr3:32821449
|
A | C | 3 | a0001c0001t0007g0286a0001c0003t0005g0287a0001c0003t0005g0302 | 3 | HG02809.hp2 HG03098.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.852+2517A>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32821449 | ||||||
| chr3:32821474
|
TA | T | 58 | a0001c0001t0001g0003a0001c0001t0001g0230a0001c0001t0001g0231others(55): Show | 58 | HG00140.hp2 HG00544.hp2 HG00735.hp1 others(55): Show |
intron_variant | MODIFIER | c.852+2546delA | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32821474 | |||||
| chr3:32821480
|
G | T | 3 | a0001c0003t0005g0299a0001c0003t0005g0300a0001c0003t0005g0301 | 3 | HG01891.hp2 HG02622.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.852+2548G>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32821480 | ||||||
| chr3:32821575
|
A | G | 1 | a0001c0002t0002g0324 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.852+2643A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32821575 | ||||||
| chr3:32821585
|
G | T | 312 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(309): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.852+2653G>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32821585 | ||||||
| chr3:32821789
|
A | C | 1 | a0001c0002t0002g0124 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.852+2857A>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32821789 | ||||||
| chr3:32821789
|
A | T | 119 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(116): Show | 119 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.852+2857A>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32821789 | ||||||
| chr3:32821998
|
T | C | 3 | a0001c0001t0001g0125a0001c0001t0001g0127a0001c0002t0002g0126 | 3 | NA18948.hp1 NA18969.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.852+3066T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32821998 | ||||||
| chr3:32822082
|
C | A | 1 | a0001c0001t0001g0007 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.852+3150C>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32822082 | ||||||
| chr3:32822515
|
C | A | 1 | a0001c0001t0008g0229 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.852+3583C>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32822515 | ||||||
| chr3:32822549
|
T | C | 1 | a0001c0002t0002g0324 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.852+3617T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32822549 | ||||||
| chr3:32822579
|
C | A | 11 | a0001c0001t0001g0012a0001c0002t0002g0014a0001c0002t0002g0015others(8): Show | 11 | HG01109.hp2 HG02109.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.852+3647C>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32822579 | ||||||
| chr3:32822584
|
G | A | 3 | a0001c0001t0001g0230a0001c0001t0001g0231a0001c0001t0006g0232 | 3 | HG02040.hp1 HG02129.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.852+3652G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32822584 | ||||||
| chr3:32822634
|
C | T | 3 | a0001c0001t0007g0121a0001c0001t0007g0123a0001c0003t0005g0122 | 3 | HG02451.hp2 HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.852+3702C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32822634 | ||||||
| chr3:32822652
|
A | AT | 69 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0230others(66): Show | 69 | HG00140.hp2 HG00544.hp2 HG00735.hp1 others(66): Show |
intron_variant | MODIFIER | c.852+3724dupT | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32822652 | |||||
| chr3:32822939
|
A | T | 9 | a0001c0002t0002g0014a0001c0002t0002g0015a0001c0002t0002g0016others(6): Show | 9 | HG01109.hp2 HG02109.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.852+4007A>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32822939 | ||||||
| chr3:32822946
|
A | T | 73 | a0001c0001t0001g0009a0001c0001t0001g0064a0001c0001t0001g0076others(70): Show | 74 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.852+4014A>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32822946 | ||||||
| chr3:32822958
|
G | T | 64 | a0001c0001t0001g0003a0001c0001t0001g0230a0001c0001t0001g0231others(61): Show | 64 | HG00140.hp2 HG00544.hp2 HG00735.hp1 others(61): Show |
intron_variant | MODIFIER | c.852+4026G>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32822958 | ||||||
| chr3:32822979
|
A | G | 1 | a0001c0001t0018g0283 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.852+4047A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32822979 | ||||||
| chr3:32823015
|
T | C | 65 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0230others(62): Show | 65 | HG00140.hp2 HG00544.hp2 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.852+4083T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32823015 | ||||||
| chr3:32823049
|
C | T | 73 | a0001c0001t0001g0009a0001c0001t0001g0064a0001c0001t0001g0076others(70): Show | 74 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.852+4117C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32823049 | ||||||
| chr3:32823198
|
G | T | 1 | a0001c0001t0014g0282 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.852+4266G>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32823198 | ||||||
| chr3:32823273
|
G | A | 1 | a0001c0001t0001g0128 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.852+4341G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32823273 | ||||||
| chr3:32823624
|
T | C | 1 | a0001c0001t0059g0129 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.852+4692T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32823624 | ||||||
| chr3:32823690
|
T | TTGCAGTG others(41): Show |
2 | a0001c0001t0001g0012a0001c0003t0005g0013 | 2 | HG02572.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.852+4773_852+4774i others(50): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32823690 | |||||
| chr3:32823708
|
G | A | 2 | a0001c0001t0001g0012a0001c0003t0005g0013 | 2 | HG02572.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.852+4776G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32823708 | ||||||
| chr3:32823708
|
G | GCAGTGAG others(25): Show |
1 | a0001c0002t0013g0258 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.852+4788_852+4789i others(34): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32823708 | |||||
| chr3:32823708
|
G | GCAGTGAG others(41): Show |
25 | a0001c0001t0008g0229a0001c0001t0008g0262a0001c0001t0008g0263others(22): Show | 25 | HG00544.hp2 HG02074.hp2 HG02080.hp2 others(22): Show |
intron_variant | MODIFIER | c.852+4788_852+4789i others(50): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32823708 | |||||
| chr3:32823850
|
G | C | 1 | a0001c0001t0049g0130 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.852+4918G>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32823850 | ||||||
| chr3:32823946
|
G | A | 1 | a0001c0002t0002g0131 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.852+5014G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32823946 | ||||||
| chr3:32824041
|
C | T | 26 | a0001c0001t0008g0229a0001c0001t0008g0262a0001c0001t0008g0263others(23): Show | 26 | HG00544.hp2 HG02074.hp2 HG02080.hp2 others(23): Show |
intron_variant | MODIFIER | c.852+5109C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32824041 | ||||||
| chr3:32824056
|
C | CAG | 312 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(309): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.852+5125_852+5126d others(4): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32824056 | |||||
| chr3:32824075
|
A | G | 3 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0006g0288 | 3 | HG02080.hp1 NA19007.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.852+5143A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32824075 | ||||||
| chr3:32824079
|
G | A | 1 | a0001c0002t0002g0060 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.852+5147G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32824079 | ||||||
| chr3:32824187
|
T | G | 4 | a0001c0001t0010g0237a0001c0001t0010g0238a0001c0001t0010g0239others(1): Show | 4 | HG01243.hp1 HG01255.hp2 HG01891.hp1 others(1): Show |
intron_variant | MODIFIER | c.852+5255T>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32824187 | ||||||
| chr3:32824258
|
A | C | 3 | a0001c0001t0007g0286a0001c0003t0005g0287a0001c0003t0005g0302 | 3 | HG02809.hp2 HG03098.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.852+5326A>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32824258 | ||||||
| chr3:32824265
|
C | T | 1 | a0001c0001t0001g0009 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.852+5333C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32824265 | ||||||
| chr3:32824294
|
C | A | 2 | a0001c0001t0004g0061a0001c0002t0002g0062 | 2 | NA18747.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.852+5362C>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32824294 | ||||||
| chr3:32824338
|
C | T | 1 | a0001c0001t0028g0222 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.852+5406C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32824338 | ||||||
| chr3:32824486
|
C | T | 3 | a0001c0001t0010g0237a0001c0001t0010g0238a0001c0001t0010g0239 | 3 | HG01243.hp1 HG01255.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.852+5554C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32824486 | ||||||
| chr3:32824495
|
C | T | 2 | a0001c0001t0001g0012a0001c0003t0005g0013 | 2 | HG02572.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.852+5563C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32824495 | ||||||
| chr3:32824775
|
C | T | 3 | a0001c0001t0003g0226a0001c0001t0009g0227a0001c0001t0009g0228 | 3 | HG01069.hp1 HG01123.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.852+5843C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32824775 | ||||||
| chr3:32824792
|
C | G | 124 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(121): Show | 124 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.852+5860C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32824792 | ||||||
| chr3:32825097
|
T | C | 3 | a0001c0001t0007g0121a0001c0001t0007g0123a0001c0003t0005g0122 | 3 | HG02451.hp2 HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.852+6165T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32825097 | ||||||
| chr3:32825236
|
G | A | 1 | a0001c0001t0012g0063 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.852+6304G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32825236 | ||||||
| chr3:32825293
|
A | G | 2 | a0001c0001t0001g0119a0001c0001t0001g0120 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.852+6361A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32825293 | ||||||
| chr3:32825310
|
C | T | 1 | a0001c0001t0002g0118 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.852+6378C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32825310 | ||||||
| chr3:32825500
|
G | A | 192 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(189): Show | 192 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.852+6568G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32825500 | ||||||
| chr3:32825520
|
G | A | 4 | a0001c0001t0001g0240a0001c0001t0001g0241a0001c0001t0001g0243others(1): Show | 4 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.852+6588G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32825520 | ||||||
| chr3:32825561
|
T | C | 3 | a0001c0001t0007g0286a0001c0003t0005g0287a0001c0003t0005g0302 | 3 | HG02809.hp2 HG03098.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.852+6629T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32825561 | ||||||
| chr3:32825612
|
C | T | 26 | a0001c0001t0001g0003a0001c0001t0001g0230a0001c0001t0001g0231others(23): Show | 26 | HG00140.hp2 HG00735.hp1 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.852+6680C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32825612 | ||||||
| chr3:32825633
|
T | G | 1 | a0001c0001t0001g0012 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.852+6701T>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32825633 | ||||||
| chr3:32825704
|
GATA | G | 3 | a0001c0001t0039g0024a0001c0003t0005g0025a0001c0008t0007g0023 | 3 | HG01884.hp2 HG01934.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.852+6775_852+6777d others(5): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32825704 | |||||
| chr3:32826186
|
C | T | 9 | a0001c0002t0002g0014a0001c0002t0002g0015a0001c0002t0002g0016others(6): Show | 9 | HG01109.hp2 HG02109.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.852+7254C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32826186 | ||||||
| chr3:32826187
|
G | A | 1 | a0001c0001t0001g0012 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.852+7255G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32826187 | ||||||
| chr3:32826196
|
C | T | 4 | a0001c0001t0001g0233a0001c0001t0002g0234a0001c0001t0002g0235others(1): Show | 4 | HG02258.hp1 HG02970.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.852+7264C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32826196 | ||||||
| chr3:32826212
|
A | G | 1 | a0001c0001t0003g0219 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.852+7280A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32826212 | ||||||
| chr3:32826221
|
G | A | 1 | a0001c0001t0006g0132 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.852+7289G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32826221 | ||||||
| chr3:32826227
|
C | T | 1 | a0001c0001t0004g0218 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.852+7295C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32826227 | ||||||
| chr3:32826398
|
A | G | 1 | a0001c0003t0005g0117 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.852+7466A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32826398 | ||||||
| chr3:32826582
|
C | CT | 123 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(120): Show | 124 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.852+7672dupT | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32826582 | |||||
| chr3:32826582
|
C | CTT | 8 | a0001c0001t0001g0216a0001c0001t0001g0317a0001c0001t0004g0214others(5): Show | 8 | HG02738.hp1 HG02976.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.852+7671_852+7672d others(4): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32826582 | |||||
| chr3:32826582
|
C | CTTT | 23 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0064others(20): Show | 23 | HG00558.hp1 HG01069.hp1 HG01123.hp2 others(20): Show |
intron_variant | MODIFIER | c.852+7670_852+7672d others(5): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32826582 | |||||
| chr3:32826582
|
C | CTTTT | 98 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0037others(95): Show | 99 | HG00099.hp2 HG00438.hp2 HG00609.hp1 others(96): Show |
intron_variant | MODIFIER | c.852+7669_852+7672d others(6): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32826582 | |||||
| chr3:32826582
|
C | CTTTTT | 42 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110others(39): Show | 42 | HG00544.hp2 HG01109.hp1 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.852+7668_852+7672d others(7): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32826582 | |||||
| chr3:32826582
|
C | CTTTTTT | 20 | a0001c0001t0001g0003a0001c0001t0001g0116a0001c0001t0001g0230others(17): Show | 20 | HG00140.hp2 HG00735.hp1 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.852+7667_852+7672d others(8): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32826582 | |||||
| chr3:32826582
|
C | CTTTTTTT others(9): Show |
1 | a0001c0001t0010g0237 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.852+7657_852+7672d others(18): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32826582 | |||||
| chr3:32826582
|
C | CTTTTTTT others(28): Show |
1 | a0001c0001t0010g0238 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.852+7672_852+7673i others(37): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32826582 | |||||
| chr3:32826582
|
C | CTTTTTTT others(30): Show |
1 | a0001c0001t0010g0239 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.852+7672_852+7673i others(39): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32826582 | |||||
| chr3:32826608
|
A | G | 1 | a0001c0001t0001g0213 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.852+7676A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32826608 | ||||||
| chr3:32826919
|
T | C | 28 | a0001c0001t0001g0012a0001c0001t0008g0229a0001c0001t0008g0262others(25): Show | 28 | HG00544.hp2 HG02074.hp2 HG02080.hp2 others(25): Show |
intron_variant | MODIFIER | c.852+7987T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32826919 | ||||||
| chr3:32826985
|
T | C | 26 | a0001c0001t0008g0229a0001c0001t0008g0262a0001c0001t0008g0263others(23): Show | 26 | HG00544.hp2 HG02074.hp2 HG02080.hp2 others(23): Show |
intron_variant | MODIFIER | c.852+8053T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32826985 | ||||||
| chr3:32827016
|
G | A | 1 | a0001c0001t0001g0247 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.852+8084G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32827016 | ||||||
| chr3:32827192
|
C | T | 1 | a0001c0001t0001g0012 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.852+8260C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32827192 | ||||||
| chr3:32827268
|
C | CTTTTTTT others(3): Show |
23 | a0001c0001t0008g0229a0001c0001t0008g0262a0001c0001t0008g0263others(20): Show | 23 | HG02074.hp2 HG02080.hp2 HG02132.hp1 others(20): Show |
intron_variant | MODIFIER | c.852+8341_852+8350d others(12): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32827268 | |||||
| chr3:32827268
|
C | CTTTTTTT others(4): Show |
1 | a0001c0001t0027g0279 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.852+8340_852+8350d others(13): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32827268 | |||||
| chr3:32827268
|
C | CTTTTTTT others(5): Show |
8 | a0001c0001t0001g0012a0001c0001t0001g0247a0001c0001t0001g0250others(5): Show | 8 | HG01243.hp1 HG01255.hp2 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.852+8339_852+8350d others(14): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32827268 | |||||
| chr3:32827268
|
C | CTTTTTTT others(6): Show |
19 | a0001c0001t0001g0003a0001c0001t0001g0230a0001c0001t0001g0231others(16): Show | 19 | HG00140.hp2 HG00735.hp1 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.852+8338_852+8350d others(15): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32827268 | |||||
| chr3:32827268
|
C | CTTTTTTT others(7): Show |
2 | a0001c0001t0001g0243a0001c0001t0029g0257 | 2 | HG01106.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.852+8337_852+8350d others(16): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32827268 | |||||
| chr3:32827337
|
C | A | 26 | a0001c0001t0008g0229a0001c0001t0008g0262a0001c0001t0008g0263others(23): Show | 26 | HG00544.hp2 HG02074.hp2 HG02080.hp2 others(23): Show |
intron_variant | MODIFIER | c.852+8405C>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32827337 | ||||||
| chr3:32827489
|
T | C | 26 | a0001c0001t0001g0003a0001c0001t0001g0230a0001c0001t0001g0231others(23): Show | 26 | HG00140.hp2 HG00735.hp1 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.852+8557T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32827489 | ||||||
| chr3:32827782
|
G | T | 74 | a0001c0001t0001g0009a0001c0001t0001g0064a0001c0001t0001g0076others(71): Show | 75 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.852+8850G>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32827782 | ||||||
| chr3:32828080
|
T | C | 1 | a0001c0002t0002g0059 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.852+9148T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32828080 | ||||||
| chr3:32828143
|
A | G | 1 | a0001c0001t0001g0028 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.852+9211A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32828143 | ||||||
| chr3:32828187
|
G | A | 26 | a0001c0001t0008g0229a0001c0001t0008g0262a0001c0001t0008g0263others(23): Show | 26 | HG00544.hp2 HG02074.hp2 HG02080.hp2 others(23): Show |
intron_variant | MODIFIER | c.852+9255G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32828187 | ||||||
| chr3:32828229
|
T | G | 2 | a0001c0001t0007g0286a0001c0003t0005g0287 | 2 | HG03098.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.852+9297T>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32828229 | ||||||
| chr3:32828248
|
G | A | 4 | a0001c0003t0005g0299a0001c0003t0005g0300a0001c0003t0005g0301others(1): Show | 4 | HG01891.hp2 HG02622.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.852+9316G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32828248 | ||||||
| chr3:32828402
|
C | T | 1 | a0001c0001t0001g0212 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.852+9470C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32828402 | ||||||
| chr3:32828430
|
G | A | 63 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0230others(60): Show | 63 | HG00140.hp2 HG00544.hp2 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.852+9498G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32828430 | ||||||
| chr3:32828458
|
A | G | 3 | a0001c0002t0002g0209a0001c0002t0002g0211a0001c0002t0025g0210 | 3 | HG00544.hp1 NA19004.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.852+9526A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32828458 | ||||||
| chr3:32828502
|
C | CT | 162 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(159): Show | 163 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.852+9593dupT | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32828502 | |||||
| chr3:32828502
|
C | CTT | 25 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0055others(22): Show | 25 | HG00609.hp2 HG01106.hp2 HG01175.hp1 others(22): Show |
intron_variant | MODIFIER | c.852+9592_852+9593d others(4): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32828502 | |||||
| chr3:32828502
|
CT | C | 27 | a0001c0001t0001g0012a0001c0001t0007g0286a0001c0001t0008g0229others(24): Show | 27 | HG00544.hp2 HG02074.hp2 HG02080.hp2 others(24): Show |
intron_variant | MODIFIER | c.852+9593delT | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32828502 | |||||
| chr3:32828606
|
C | G | 6 | a0001c0001t0003g0226a0001c0001t0007g0121a0001c0001t0007g0123others(3): Show | 6 | HG01069.hp1 HG01123.hp2 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.852+9674C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32828606 | ||||||
| chr3:32828665
|
A | T | 9 | a0001c0002t0002g0014a0001c0002t0002g0015a0001c0002t0002g0016others(6): Show | 9 | HG01109.hp2 HG02109.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.852+9733A>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32828665 | ||||||
| chr3:32828717
|
G | A | 1 | a0001c0002t0002g0138 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.852+9785G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32828717 | ||||||
| chr3:32828815
|
A | G | 1 | a0001c0001t0020g0047 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.852+9883A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32828815 | ||||||
| chr3:32828821
|
T | C | 1 | a0001c0001t0026g0066 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.852+9889T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32828821 | ||||||
| chr3:32828868
|
G | T | 1 | a0001c0001t0001g0012 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.852+9936G>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32828868 | ||||||
| chr3:32828939
|
G | T | 1 | a0001c0001t0004g0057 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.852+10007G>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32828939 | ||||||
| chr3:32828953
|
T | G | 1 | a0001c0001t0004g0057 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.852+10021T>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32828953 | ||||||
| chr3:32828955
|
G | C | 1 | a0001c0001t0004g0057 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.852+10023G>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32828955 | ||||||
| chr3:32828997
|
A | AT | 11 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0113others(8): Show | 11 | HG00099.hp2 HG01358.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.852+10079dupT | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32828997 | |||||
| chr3:32829033
|
G | T | 3 | a0001c0001t0001g0199a0001c0001t0006g0201a0001c0002t0002g0200 | 3 | HG00558.hp2 NA18947.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.852+10101G>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32829033 | ||||||
| chr3:32829063
|
G | A | 1 | a0001c0001t0002g0067 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.852+10131G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32829063 | ||||||
| chr3:32829149
|
A | G | 1 | a0001c0003t0005g0013 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.852+10217A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32829149 | ||||||
| chr3:32829168
|
TTTTTCTT others(5): Show |
T | 1 | a0001c0002t0047g0101 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.852+10248_852+1025 others(16): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32829168 | |||||
| chr3:32829185
|
CT | C | 52 | a0001c0001t0001g0003a0001c0001t0001g0230a0001c0001t0001g0231others(49): Show | 52 | HG00140.hp2 HG00544.hp2 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.852+10269delT | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32829185 | |||||
| chr3:32829235
|
A | G | 3 | a0001c0001t0026g0321a0001c0001t0037g0322a0001c0003t0005g0323 | 3 | HG02717.hp2 HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.852+10303A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32829235 | ||||||
| chr3:32829276
|
T | C | 26 | a0001c0001t0008g0229a0001c0001t0008g0262a0001c0001t0008g0263others(23): Show | 26 | HG00544.hp2 HG02074.hp2 HG02080.hp2 others(23): Show |
intron_variant | MODIFIER | c.852+10344T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32829276 | ||||||
| chr3:32829341
|
C | A | 1 | a0001c0001t0001g0233 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.852+10409C>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32829341 | ||||||
| chr3:32829342
|
A | G | 312 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(309): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.852+10410A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32829342 | ||||||
| chr3:32829505
|
T | C | 52 | a0001c0001t0001g0003a0001c0001t0001g0230a0001c0001t0001g0231others(49): Show | 52 | HG00140.hp2 HG00544.hp2 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.852+10573T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32829505 | ||||||
| chr3:32829544
|
A | G | 128 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(125): Show | 128 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.852+10612A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32829544 | ||||||
| chr3:32829561
|
A | G | 1 | a0001c0001t0003g0105 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.852+10629A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32829561 | ||||||
| chr3:32829626
|
T | TTG | 9 | a0001c0001t0001g0012a0001c0001t0001g0304a0001c0001t0003g0105others(6): Show | 10 | HG00099.hp1 HG02148.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.852+10718_852+1071 others(6): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32829626 | |||||
| chr3:32829626
|
T | TTGTG | 12 | a0001c0001t0001g0216a0001c0001t0003g0191a0001c0001t0003g0192others(9): Show | 12 | HG00741.hp1 HG01081.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.852+10716_852+1071 others(8): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32829626 | |||||
| chr3:32829626
|
T | TTGTGTG | 111 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(108): Show | 111 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.852+10714_852+1071 others(10): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32829626 | |||||
| chr3:32829626
|
T | TTGTGTGT others(3): Show |
3 | a0001c0001t0001g0140a0001c0001t0059g0129a0001c0002t0002g0290 | 3 | HG00280.hp1 HG01255.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.852+10710_852+1071 others(14): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32829626 | |||||
| chr3:32829626
|
T | TTGTGTGT others(5): Show |
13 | a0001c0001t0001g0230a0001c0001t0001g0231a0001c0001t0001g0247others(10): Show | 13 | HG00140.hp2 HG00735.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.852+10708_852+1071 others(16): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32829626 | |||||
| chr3:32829626
|
T | TTGTGTGT others(7): Show |
10 | a0001c0001t0001g0003a0001c0001t0001g0240a0001c0001t0001g0241others(7): Show | 10 | HG01069.hp2 HG01071.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.852+10706_852+1071 others(18): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32829626 | |||||
| chr3:32829626
|
T | TTGTGTGT others(9): Show |
16 | a0001c0001t0001g0243a0001c0001t0008g0262a0001c0001t0008g0263others(13): Show | 16 | HG01106.hp1 HG01255.hp2 HG02735.hp1 others(13): Show |
intron_variant | MODIFIER | c.852+10704_852+1071 others(20): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32829626 | |||||
| chr3:32829626
|
T | TTGTGTGT others(11): Show |
7 | a0001c0001t0001g0251a0001c0001t0008g0264a0001c0001t0008g0268others(4): Show | 7 | HG01081.hp1 HG01243.hp1 HG02074.hp2 others(4): Show |
intron_variant | MODIFIER | c.852+10702_852+1071 others(22): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32829626 | |||||
| chr3:32829626
|
T | TTGTGTGT others(13): Show |
2 | a0001c0002t0013g0258a0001c0002t0013g0266 | 2 | HG02155.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.852+10700_852+1071 others(24): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32829626 | |||||
| chr3:32829626
|
T | TTGTGTGT others(19): Show |
1 | a0001c0001t0027g0261 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.852+10719_852+1072 others(30): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32829626 | |||||
| chr3:32829626
|
TTG | T | 15 | a0001c0001t0001g0011a0001c0001t0001g0233a0001c0001t0002g0234others(12): Show | 15 | HG01109.hp2 HG02109.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.852+10718_852+1071 others(6): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32829626 | |||||
| chr3:32829626
|
TTGTGTGT others(3): Show |
T | 5 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0002g0316others(2): Show | 5 | HG02886.hp2 NA18747.hp2 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.852+10710_852+1071 others(14): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32829626 | |||||
| chr3:32829651
|
T | TGTGTGTG others(14): Show |
1 | a0001c0001t0008g0265 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.852+10719_852+1072 others(25): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32829651 | ||||||
| chr3:32829652
|
T | G | 5 | a0001c0001t0008g0229a0001c0001t0008g0262a0001c0001t0008g0263others(2): Show | 5 | HG00544.hp2 NA18947.hp1 NA18968.hp1 others(2): Show |
intron_variant | MODIFIER | c.852+10720T>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32829652 | ||||||
| chr3:32829654
|
G | A | 21 | a0001c0001t0008g0265a0001c0001t0008g0268a0001c0001t0008g0273others(18): Show | 21 | HG02074.hp2 HG02080.hp2 HG02132.hp1 others(18): Show |
intron_variant | MODIFIER | c.852+10722G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32829654 | ||||||
| chr3:32829659
|
T | TGTGTGTG others(11): Show |
1 | a0001c0001t0027g0279 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.852+10728_852+1072 others(22): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32829659 | |||||
| chr3:32829662
|
G | A | 1 | a0001c0001t0001g0199 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.852+10730G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32829662 | ||||||
| chr3:32829733
|
A | C | 1 | a0001c0001t0001g0028 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.852+10801A>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32829733 | ||||||
| chr3:32829759
|
C | G | 1 | a0001c0001t0001g0100 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.852+10827C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32829759 | ||||||
| chr3:32829827
|
T | C | 52 | a0001c0001t0001g0003a0001c0001t0001g0230a0001c0001t0001g0231others(49): Show | 52 | HG00140.hp2 HG00544.hp2 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.852+10895T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32829827 | ||||||
| chr3:32829922
|
A | AT | 23 | a0001c0001t0001g0127a0001c0001t0001g0216a0001c0001t0001g0304others(20): Show | 24 | HG01109.hp1 HG01243.hp2 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.852+11013dupT | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32829922 | |||||
| chr3:32829922
|
AT | A | 55 | a0001c0001t0001g0003a0001c0001t0001g0142a0001c0001t0001g0144others(52): Show | 55 | HG00140.hp2 HG00639.hp1 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.852+11013delT | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32829922 | |||||
| chr3:32829945
|
T | C | 32 | a0001c0001t0001g0003a0001c0001t0001g0028a0001c0001t0001g0141others(29): Show | 32 | HG00140.hp2 HG00735.hp1 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.852+11013T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32829945 | ||||||
| chr3:32829945
|
T | TC | 27 | a0001c0001t0001g0026a0001c0001t0001g0037a0001c0001t0001g0049others(24): Show | 27 | HG01106.hp2 HG01516.hp2 HG01517.hp2 others(24): Show |
intron_variant | MODIFIER | c.852+11014dupC | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32829945 | |||||
| chr3:32829967
|
C | T | 26 | a0001c0001t0001g0003a0001c0001t0001g0230a0001c0001t0001g0231others(23): Show | 26 | HG00140.hp2 HG00735.hp1 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.852+11035C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32829967 | ||||||
| chr3:32830165
|
C | T | 1 | a0001c0001t0017g0280 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.852+11233C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32830165 | ||||||
| chr3:32830166
|
G | A | 3 | a0001c0001t0007g0286a0001c0003t0005g0287a0001c0003t0005g0302 | 3 | HG02809.hp2 HG03098.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.852+11234G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32830166 | ||||||
| chr3:32830277
|
C | T | 3 | a0001c0001t0007g0286a0001c0003t0005g0287a0001c0003t0005g0302 | 3 | HG02809.hp2 HG03098.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.852+11345C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32830277 | ||||||
| chr3:32830356
|
C | T | 64 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0230others(61): Show | 64 | HG00140.hp2 HG00544.hp2 HG00735.hp1 others(61): Show |
intron_variant | MODIFIER | c.852+11424C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32830356 | ||||||
| chr3:32830400
|
C | A | 118 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(115): Show | 118 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.852+11468C>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32830400 | ||||||
| chr3:32830454
|
A | G | 1 | a0001c0002t0002g0106 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.852+11522A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32830454 | ||||||
| chr3:32830547
|
A | T | 1 | a0001c0001t0001g0189 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.852+11615A>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32830547 | ||||||
| chr3:32830654
|
A | G | 1 | a0001c0001t0015g0246 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.852+11722A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32830654 | ||||||
| chr3:32830779
|
C | T | 9 | a0001c0002t0002g0014a0001c0002t0002g0015a0001c0002t0002g0016others(6): Show | 9 | HG01109.hp2 HG02109.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.852+11847C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32830779 | ||||||
| chr3:32830820
|
T | A | 1 | a0001c0001t0004g0145 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.852+11888T>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32830820 | ||||||
| chr3:32830821
|
T | A | 129 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(126): Show | 129 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.852+11889T>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32830821 | ||||||
| chr3:32830844
|
T | C | 2 | a0001c0001t0007g0286a0001c0003t0005g0287 | 2 | HG03098.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.852+11912T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32830844 | ||||||
| chr3:32830895
|
C | G | 26 | a0001c0001t0001g0003a0001c0001t0001g0230a0001c0001t0001g0231others(23): Show | 26 | HG00140.hp2 HG00735.hp1 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.852+11963C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32830895 | ||||||
| chr3:32830985
|
A | AT | 9 | a0001c0002t0002g0014a0001c0002t0002g0015a0001c0002t0002g0016others(6): Show | 9 | HG01109.hp2 HG02109.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.852+12059dupT | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32830985 | |||||
| chr3:32830994
|
CAG | C | 26 | a0001c0001t0008g0229a0001c0001t0008g0262a0001c0001t0008g0263others(23): Show | 26 | HG00544.hp2 HG02074.hp2 HG02080.hp2 others(23): Show |
intron_variant | MODIFIER | c.852+12066_852+1206 others(6): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32830994 | |||||
| chr3:32831065
|
T | C | 26 | a0001c0001t0008g0229a0001c0001t0008g0262a0001c0001t0008g0263others(23): Show | 26 | HG00544.hp2 HG02074.hp2 HG02080.hp2 others(23): Show |
intron_variant | MODIFIER | c.852+12133T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32831065 | ||||||
| chr3:32831080
|
G | A | 1 | a0001c0002t0047g0101 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.852+12148G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32831080 | ||||||
| chr3:32831162
|
G | T | 4 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0012g0008others(1): Show | 4 | HG02615.hp1 HG03195.hp2 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.852+12230G>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32831162 | ||||||
| chr3:32831163
|
A | G | 26 | a0001c0001t0008g0229a0001c0001t0008g0262a0001c0001t0008g0263others(23): Show | 26 | HG00544.hp2 HG02074.hp2 HG02080.hp2 others(23): Show |
intron_variant | MODIFIER | c.852+12231A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32831163 | ||||||
| chr3:32831308
|
TTTCTGAC others(2): Show |
T | 22 | a0001c0001t0001g0003a0001c0001t0001g0230a0001c0001t0001g0231others(19): Show | 22 | HG00140.hp2 HG00735.hp1 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.852+12379_852+1238 others(13): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32831308 | |||||
| chr3:32831323
|
A | G | 1 | a0001c0003t0005g0013 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.852+12391A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32831323 | ||||||
| chr3:32831380
|
A | G | 1 | a0001c0001t0019g0326 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.852+12448A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32831380 | ||||||
| chr3:32831388
|
T | G | 54 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0230others(51): Show | 54 | HG00140.hp2 HG00544.hp2 HG00735.hp1 others(51): Show |
intron_variant | MODIFIER | c.852+12456T>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32831388 | ||||||
| chr3:32831536
|
C | CT | 15 | a0001c0001t0001g0012a0001c0001t0002g0316a0001c0001t0007g0286others(12): Show | 15 | HG01109.hp2 HG02109.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.852+12624dupT | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32831536 | |||||
| chr3:32831536
|
C | CTT | 24 | a0001c0001t0001g0003a0001c0001t0001g0240a0001c0001t0001g0241others(21): Show | 24 | HG00544.hp2 HG01069.hp2 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.852+12623_852+1262 others(6): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32831536 | |||||
| chr3:32831536
|
C | CTTT | 25 | a0001c0001t0001g0230a0001c0001t0001g0231a0001c0001t0001g0243others(22): Show | 25 | HG00140.hp2 HG00735.hp1 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.852+12622_852+1262 others(7): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32831536 | |||||
| chr3:32831536
|
C | CTTTT | 6 | a0001c0001t0001g0247a0001c0001t0008g0265a0001c0001t0008g0276others(3): Show | 6 | HG01981.hp1 HG02080.hp2 NA18973.hp2 others(3): Show |
intron_variant | MODIFIER | c.852+12621_852+1262 others(8): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32831536 | |||||
| chr3:32831536
|
CT | C | 215 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(212): Show | 216 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.852+12624delT | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32831536 | |||||
| chr3:32831536
|
CTT | C | 7 | a0001c0001t0001g0304a0001c0001t0003g0146a0001c0001t0003g0191others(4): Show | 7 | HG01081.hp2 HG01952.hp2 HG02132.hp2 others(4): Show |
intron_variant | MODIFIER | c.852+12623_852+1262 others(6): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32831536 | |||||
| chr3:32831602
|
G | A | 1 | a0001c0001t0039g0024 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.852+12670G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32831602 | ||||||
| chr3:32831682
|
G | A | 1 | a0001c0001t0002g0319 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.852+12750G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32831682 | ||||||
| chr3:32831842
|
T | C | 1 | a0001c0001t0001g0012 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.852+12910T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32831842 | ||||||
| chr3:32831947
|
G | A | 1 | a0001c0001t0017g0280 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.852+13015G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32831947 | ||||||
| chr3:32832100
|
T | G | 1 | a0001c0001t0004g0048 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.852+13168T>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32832100 | ||||||
| chr3:32832100
|
TG | T | 26 | a0001c0001t0008g0229a0001c0001t0008g0262a0001c0001t0008g0263others(23): Show | 26 | HG00544.hp2 HG02074.hp2 HG02080.hp2 others(23): Show |
intron_variant | MODIFIER | c.852+13176delG | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32832100 | |||||
| chr3:32832101
|
G | T | 1 | a0001c0001t0004g0048 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.852+13169G>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32832101 | ||||||
| chr3:32832106
|
G | C | 1 | a0001c0003t0005g0013 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.852+13174G>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32832106 | ||||||
| chr3:32832108
|
G | GA | 3 | a0001c0003t0005g0299a0001c0003t0005g0300a0001c0003t0005g0301 | 3 | HG01891.hp2 HG02622.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.852+13177dupA | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32832108 | |||||
| chr3:32832124
|
A | G | 1 | a0001c0003t0005g0013 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.852+13192A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32832124 | ||||||
| chr3:32832413
|
C | A | 28 | a0001c0001t0001g0012a0001c0001t0008g0229a0001c0001t0008g0262others(25): Show | 28 | HG00544.hp2 HG02074.hp2 HG02080.hp2 others(25): Show |
intron_variant | MODIFIER | c.852+13481C>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32832413 | ||||||
| chr3:32832470
|
A | G | 1 | a0001c0001t0001g0212 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.852+13538A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32832470 | ||||||
| chr3:32832532
|
C | A | 28 | a0001c0001t0001g0012a0001c0001t0008g0229a0001c0001t0008g0262others(25): Show | 28 | HG00544.hp2 HG02074.hp2 HG02080.hp2 others(25): Show |
intron_variant | MODIFIER | c.852+13600C>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32832532 | ||||||
| chr3:32832622
|
T | G | 1 | a0001c0001t0001g0011 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.852+13690T>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32832622 | ||||||
| chr3:32832692
|
A | G | 17 | a0001c0001t0001g0009a0001c0001t0001g0088a0001c0001t0001g0095others(14): Show | 17 | HG00609.hp1 HG01109.hp1 HG01952.hp1 others(14): Show |
intron_variant | MODIFIER | c.852+13760A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32832692 | ||||||
| chr3:32832944
|
A | G | 5 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0042g0107others(2): Show | 5 | HG03491.hp2 HG03710.hp1 HG03927.hp1 others(2): Show |
intron_variant | MODIFIER | c.852+14012A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32832944 | ||||||
| chr3:32833045
|
C | A | 1 | a0001c0002t0002g0147 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.852+14113C>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32833045 | ||||||
| chr3:32833058
|
C | A | 2 | a0001c0001t0008g0268a0001c0002t0013g0266 | 2 | HG02074.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.852+14126C>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32833058 | ||||||
| chr3:32833067
|
C | T | 9 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0185others(6): Show | 9 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(6): Show |
intron_variant | MODIFIER | c.852+14135C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32833067 | ||||||
| chr3:32833077
|
A | T | 3 | a0001c0001t0007g0286a0001c0003t0005g0287a0001c0003t0005g0302 | 3 | HG02809.hp2 HG03098.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.852+14145A>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32833077 | ||||||
| chr3:32833183
|
T | A | 1 | a0001c0001t0001g0213 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.852+14251T>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32833183 | ||||||
| chr3:32833184
|
T | A | 1 | a0001c0001t0001g0213 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.852+14252T>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32833184 | ||||||
| chr3:32833184
|
T | TA | 72 | a0001c0001t0001g0009a0001c0001t0001g0064a0001c0001t0001g0076others(69): Show | 73 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.852+14280dupA | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32833184 | |||||
| chr3:32833184
|
T | TAA | 24 | a0001c0001t0001g0055a0001c0001t0001g0085a0001c0001t0001g0100others(21): Show | 24 | HG01358.hp1 HG01516.hp2 HG01517.hp1 others(21): Show |
intron_variant | MODIFIER | c.852+14279_852+1428 others(6): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32833184 | |||||
| chr3:32833184
|
T | TAAA | 29 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0037others(26): Show | 29 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(26): Show |
intron_variant | MODIFIER | c.852+14278_852+1428 others(7): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32833184 | |||||
| chr3:32833184
|
T | TAAAA | 12 | a0001c0001t0001g0049a0001c0001t0003g0056a0001c0001t0003g0163others(9): Show | 12 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(9): Show |
intron_variant | MODIFIER | c.852+14277_852+1428 others(8): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32833184 | |||||
| chr3:32833184
|
T | TAAAAA | 10 | a0001c0001t0001g0216a0001c0001t0003g0190a0001c0001t0003g0194others(7): Show | 10 | HG00597.hp1 HG01516.hp1 HG02738.hp1 others(7): Show |
intron_variant | MODIFIER | c.852+14276_852+1428 others(9): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32833184 | |||||
| chr3:32833184
|
T | TAAAAAAA others(3): Show |
3 | a0001c0001t0006g0010a0001c0001t0009g0228a0001c0003t0005g0299 | 3 | HG01069.hp1 HG02165.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.852+14271_852+1428 others(14): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32833184 | |||||
| chr3:32833184
|
T | TAAAAAAA others(4): Show |
10 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0004g0161others(7): Show | 10 | HG00621.hp2 HG01123.hp2 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.852+14270_852+1428 others(15): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32833184 | |||||
| chr3:32833184
|
T | TAAAAAAA others(5): Show |
15 | a0001c0001t0001g0199a0001c0001t0003g0226a0001c0002t0002g0154others(12): Show | 15 | HG00423.hp2 HG00438.hp1 HG00558.hp2 others(12): Show |
intron_variant | MODIFIER | c.852+14269_852+1428 others(16): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32833184 | |||||
| chr3:32833184
|
T | TAAAAAAA others(6): Show |
1 | a0001c0001t0001g0007 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.852+14268_852+1428 others(17): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32833184 | |||||
| chr3:32833184
|
T | TAAAAAAA others(8): Show |
3 | a0001c0001t0001g0006a0001c0001t0001g0125a0001c0001t0001g0127 | 3 | NA18969.hp1 NA18975.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.852+14266_852+1428 others(19): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32833184 | |||||
| chr3:32833184
|
T | TAAAAAAA others(9): Show |
4 | a0001c0001t0001g0197a0001c0001t0001g0212a0001c0002t0002g0126others(1): Show | 4 | HG01884.hp2 HG03710.hp2 NA18948.hp1 others(1): Show |
intron_variant | MODIFIER | c.852+14265_852+1428 others(20): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32833184 | |||||
| chr3:32833184
|
T | TAAAAAAA others(10): Show |
4 | a0001c0001t0001g0004a0001c0001t0004g0152a0001c0001t0012g0153others(1): Show | 4 | HG00423.hp1 HG00621.hp1 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.852+14264_852+1428 others(21): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32833184 | |||||
| chr3:32833184
|
T | TAAAAAAA others(11): Show |
1 | a0001c0001t0031g0151 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.852+14263_852+1428 others(22): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32833184 | |||||
| chr3:32833184
|
T | TAAAAAAA others(13): Show |
1 | a0001c0001t0006g0288 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.852+14261_852+1428 others(24): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32833184 | |||||
| chr3:32833184
|
T | TAAAAAAA others(14): Show |
1 | a0001c0001t0001g0224 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.852+14260_852+1428 others(25): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32833184 | |||||
| chr3:32833184
|
T | TAAAAAAA others(16): Show |
2 | a0001c0002t0002g0200a0001c0002t0002g0206 | 2 | HG02027.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.852+14258_852+1428 others(27): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32833184 | |||||
| chr3:32833184
|
T | TAAAAAAA others(17): Show |
2 | a0001c0001t0019g0196a0001c0002t0002g0217 | 2 | NA18979.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.852+14257_852+1428 others(28): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32833184 | |||||
| chr3:32833184
|
T | TAAAAAAA others(18): Show |
2 | a0001c0001t0001g0128a0001c0001t0006g0150 | 2 | HG02015.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.852+14256_852+1428 others(29): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32833184 | |||||
| chr3:32833184
|
T | TAAAAAAA others(19): Show |
2 | a0001c0001t0001g0223a0001c0002t0002g0183 | 2 | HG02080.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.852+14255_852+1428 others(30): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32833184 | |||||
| chr3:32833184
|
T | TAAAAAAA others(21): Show |
2 | a0001c0001t0001g0148a0001c0001t0033g0149 | 2 | HG02056.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.852+14253_852+1428 others(32): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32833184 | |||||
| chr3:32833184
|
T | TAAAAAAA others(24): Show |
1 | a0001c0002t0024g0139 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.852+14280_852+1428 others(35): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32833184 | |||||
| chr3:32833184
|
T | TAAAAAAA others(28): Show |
1 | a0001c0001t0006g0201 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.852+14280_852+1428 others(39): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32833184 | |||||
| chr3:32833184
|
TA | T | 12 | a0001c0001t0001g0003a0001c0001t0001g0144a0001c0001t0001g0176others(9): Show | 12 | HG00735.hp2 HG01069.hp2 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.852+14280delA | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32833184 | |||||
| chr3:32833184
|
TAA | T | 20 | a0001c0001t0001g0140a0001c0001t0007g0098a0001c0001t0007g0286others(17): Show | 20 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(17): Show |
intron_variant | MODIFIER | c.852+14279_852+1428 others(6): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32833184 | |||||
| chr3:32833184
|
TAAA | T | 23 | a0001c0001t0001g0180a0001c0001t0001g0189a0001c0001t0008g0229others(20): Show | 23 | HG00544.hp2 HG02080.hp2 HG02132.hp1 others(20): Show |
intron_variant | MODIFIER | c.852+14278_852+1428 others(7): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32833184 | |||||
| chr3:32833184
|
TAAAAAAA others(1): Show |
T | 7 | a0001c0001t0001g0133a0001c0001t0001g0181a0001c0001t0001g0182others(4): Show | 7 | HG01934.hp1 HG01981.hp2 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.852+14273_852+1428 others(12): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32833184 | |||||
| chr3:32833184
|
TAAAAAAA others(3): Show |
T | 2 | a0001c0001t0001g0012a0001c0003t0005g0013 | 2 | HG02572.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.852+14271_852+1428 others(14): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32833184 | |||||
| chr3:32833213
|
G | A | 1 | a0001c0001t0004g0057 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.852+14281G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32833213 | ||||||
| chr3:32833294
|
G | A | 1 | a0001c0002t0002g0154 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.852+14362G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32833294 | ||||||
| chr3:32833414
|
G | T | 26 | a0001c0001t0008g0229a0001c0001t0008g0262a0001c0001t0008g0263others(23): Show | 26 | HG00544.hp2 HG02074.hp2 HG02080.hp2 others(23): Show |
intron_variant | MODIFIER | c.852+14482G>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32833414 | ||||||
| chr3:32833634
|
T | TTTTA | 79 | a0001c0001t0001g0012a0001c0001t0001g0037a0001c0001t0001g0064others(76): Show | 79 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.852+14742_852+1474 others(8): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32833634 | |||||
| chr3:32833634
|
T | TTTTATTT others(1): Show |
31 | a0001c0001t0001g0009a0001c0001t0001g0077a0001c0001t0001g0086others(28): Show | 31 | HG00280.hp2 HG01261.hp1 HG02080.hp2 others(28): Show |
intron_variant | MODIFIER | c.852+14738_852+1474 others(12): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32833634 | |||||
| chr3:32833634
|
T | TTTTATTT others(5): Show |
5 | a0001c0001t0001g0076a0001c0001t0002g0075a0001c0001t0017g0259others(2): Show | 5 | HG03471.hp1 HG03471.hp2 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.852+14734_852+1474 others(16): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32833634 | |||||
| chr3:32833634
|
TTTTA | T | 19 | a0001c0001t0001g0205a0001c0001t0001g0233a0001c0001t0001g0249others(16): Show | 21 | HG01069.hp1 HG01123.hp2 HG01361.hp2 others(18): Show |
intron_variant | MODIFIER | c.852+14742_852+1474 others(8): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32833634 | |||||
| chr3:32833634
|
TTTTATTT others(5): Show |
T | 5 | a0001c0001t0003g0093a0001c0001t0004g0143a0001c0001t0004g0214others(2): Show | 5 | HG02572.hp1 HG03669.hp1 HG03688.hp2 others(2): Show |
intron_variant | MODIFIER | c.852+14734_852+1474 others(16): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32833634 | |||||
| chr3:32833734
|
G | A | 1 | a0001c0001t0001g0077 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.852+14802G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32833734 | ||||||
| chr3:32833785
|
T | G | 2 | a0001c0001t0001g0012a0001c0003t0005g0013 | 2 | HG02572.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.852+14853T>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32833785 | ||||||
| chr3:32834034
|
T | C | 1 | a0001c0001t0001g0251 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.852+15102T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32834034 | ||||||
| chr3:32834394
|
A | AGTT | 28 | a0001c0001t0001g0012a0001c0001t0008g0229a0001c0001t0008g0262others(25): Show | 28 | HG00544.hp2 HG02074.hp2 HG02080.hp2 others(25): Show |
intron_variant | MODIFIER | c.852+15463_852+1546 others(7): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32834394 | |||||
| chr3:32834523
|
G | C | 1 | a0001c0001t0001g0088 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.852+15591G>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32834523 | ||||||
| chr3:32834546
|
G | C | 2 | a0001c0002t0002g0291a0001c0002t0002g0297 | 2 | NA18977.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.852+15614G>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32834546 | ||||||
| chr3:32834662
|
T | A | 1 | a0001c0001t0007g0098 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.852+15730T>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32834662 | ||||||
| chr3:32834694
|
T | G | 1 | a0001c0001t0002g0078 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.852+15762T>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32834694 | ||||||
| chr3:32834714
|
C | T | 1 | a0001c0001t0003g0053 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.852+15782C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32834714 | ||||||
| chr3:32834750
|
G | C | 3 | a0001c0001t0039g0024a0001c0003t0005g0025a0001c0008t0007g0023 | 3 | HG01884.hp2 HG01934.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.852+15818G>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32834750 | ||||||
| chr3:32834798
|
C | T | 1 | a0001c0001t0001g0116 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.852+15866C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32834798 | ||||||
| chr3:32834876
|
T | C | 3 | a0001c0001t0039g0024a0001c0003t0005g0025a0001c0008t0007g0023 | 3 | HG01884.hp2 HG01934.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.852+15944T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32834876 | ||||||
| chr3:32834916
|
C | T | 1 | a0001c0001t0001g0128 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.852+15984C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32834916 | ||||||
| chr3:32834919
|
A | G | 1 | a0001c0001t0014g0282 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.852+15987A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32834919 | ||||||
| chr3:32834946
|
C | T | 3 | a0001c0001t0007g0121a0001c0001t0007g0123a0001c0003t0005g0122 | 3 | HG02451.hp2 HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.852+16014C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32834946 | ||||||
| chr3:32835196
|
C | A | 47 | a0001c0001t0001g0012a0001c0001t0004g0033a0001c0001t0004g0038others(44): Show | 47 | HG00544.hp2 HG01109.hp2 HG02040.hp2 others(44): Show |
intron_variant | MODIFIER | c.852+16264C>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32835196 | ||||||
| chr3:32835247
|
T | C | 23 | a0001c0001t0001g0140a0001c0001t0001g0230a0001c0001t0001g0231others(20): Show | 23 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.852+16315T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32835247 | ||||||
| chr3:32835394
|
G | A | 1 | a0001c0001t0003g0253 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.852+16462G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32835394 | ||||||
| chr3:32835794
|
T | G | 6 | a0001c0001t0017g0259a0001c0001t0017g0260a0001c0001t0053g0271others(3): Show | 6 | NA18962.hp1 NA19003.hp1 NA19009.hp2 others(3): Show |
intron_variant | MODIFIER | c.852+16862T>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32835794 | ||||||
| chr3:32835830
|
C | CT | 127 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0064others(124): Show | 128 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(125): Show |
intron_variant | MODIFIER | c.852+16898_852+1689 others(5): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32835830 | ||||||
| chr3:32835831
|
G | A | 1 | a0001c0002t0002g0032 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.852+16899G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32835831 | ||||||
| chr3:32835868
|
G | A | 1 | a0001c0003t0005g0013 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.852+16936G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32835868 | ||||||
| chr3:32835933
|
T | C | 1 | a0001c0001t0001g0064 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.852+17001T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32835933 | ||||||
| chr3:32836073
|
C | G | 1 | a0001c0001t0001g0028 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.852+17141C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32836073 | ||||||
| chr3:32836160
|
G | A | 1 | a0001c0002t0002g0062 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.852+17228G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32836160 | ||||||
| chr3:32836337
|
T | C | 1 | a0001c0001t0001g0185 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.852+17405T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32836337 | ||||||
| chr3:32836411
|
A | G | 9 | a0001c0002t0002g0014a0001c0002t0002g0015a0001c0002t0002g0016others(6): Show | 9 | HG01109.hp2 HG02109.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.852+17479A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32836411 | ||||||
| chr3:32836642
|
C | T | 1 | a0001c0001t0001g0142 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.852+17710C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32836642 | ||||||
| chr3:32836648
|
T | A | 3 | a0001c0001t0010g0237a0001c0001t0010g0238a0001c0001t0010g0239 | 3 | HG01243.hp1 HG01255.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.852+17716T>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32836648 | ||||||
| chr3:32836667
|
G | T | 1 | a0001c0001t0004g0057 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.852+17735G>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32836667 | ||||||
| chr3:32836779
|
A | C | 3 | a0001c0002t0002g0209a0001c0002t0002g0211a0001c0002t0025g0210 | 3 | HG00544.hp1 NA19004.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.852+17847A>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32836779 | ||||||
| chr3:32836819
|
A | G | 79 | a0001c0001t0001g0009a0001c0001t0001g0064a0001c0001t0001g0076others(76): Show | 80 | HG00099.hp2 HG00609.hp1 HG01109.hp1 others(77): Show |
intron_variant | MODIFIER | c.852+17887A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32836819 | ||||||
| chr3:32836939
|
T | G | 1 | a0001c0001t0001g0304 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.852+18007T>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32836939 | ||||||
| chr3:32836941
|
C | A | 1 | a0001c0001t0004g0057 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.852+18009C>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32836941 | ||||||
| chr3:32837100
|
AAAC | A | 56 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0230others(53): Show | 56 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.852+18175_852+1817 others(7): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32837100 | |||||
| chr3:32837182
|
G | A | 1 | a0001c0001t0001g0100 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.852+18250G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32837182 | ||||||
| chr3:32837190
|
T | C | 56 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0230others(53): Show | 56 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.852+18258T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32837190 | ||||||
| chr3:32837426
|
G | A | 1 | a0001c0001t0004g0057 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.852+18494G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32837426 | ||||||
| chr3:32837427
|
T | G | 1 | a0001c0001t0004g0057 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.852+18495T>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32837427 | ||||||
| chr3:32837482
|
G | A | 1 | a0001c0001t0001g0095 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.852+18550G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32837482 | ||||||
| chr3:32837690
|
G | A | 3 | a0001c0001t0007g0286a0001c0003t0005g0287a0001c0003t0005g0302 | 3 | HG02809.hp2 HG03098.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.852+18758G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32837690 | ||||||
| chr3:32837813
|
G | A | 1 | a0001c0001t0003g0191 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.852+18881G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32837813 | ||||||
| chr3:32837813
|
GA | G | 126 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(123): Show | 126 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.852+18889delA | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32837813 | |||||
| chr3:32837814
|
A | G | 1 | a0001c0001t0003g0191 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.852+18882A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32837814 | ||||||
| chr3:32838004
|
G | T | 2 | a0001c0001t0006g0288a0001c0002t0002g0200 | 2 | NA18982.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.852+19072G>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32838004 | ||||||
| chr3:32838022
|
A | G | 1 | a0001c0001t0001g0173 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.852+19090A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32838022 | ||||||
| chr3:32838023
|
C | T | 1 | a0001c0001t0004g0174 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.852+19091C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32838023 | ||||||
| chr3:32838049
|
G | A | 1 | a0001c0002t0025g0169 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.852+19117G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32838049 | ||||||
| chr3:32838071
|
G | A | 1 | a0001c0001t0006g0215 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.852+19139G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32838071 | ||||||
| chr3:32838171
|
T | C | 121 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0037others(118): Show | 122 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.852+19239T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32838171 | ||||||
| chr3:32838233
|
A | G | 3 | a0001c0001t0007g0286a0001c0003t0005g0287a0001c0003t0005g0302 | 3 | HG02809.hp2 HG03098.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.852+19301A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32838233 | ||||||
| chr3:32838254
|
A | G | 1 | a0001c0001t0001g0100 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.852+19322A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32838254 | ||||||
| chr3:32838271
|
TGGAGTGC others(22): Show |
T | 1 | a0001c0001t0008g0265 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.852+19340_852+1936 others(33): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32838271 | ||||||
| chr3:32838331
|
A | T | 61 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0230others(58): Show | 61 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.852+19399A>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32838331 | ||||||
| chr3:32838461
|
G | A | 1 | a0001c0002t0002g0155 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.852+19529G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32838461 | ||||||
| chr3:32838522
|
C | CT | 84 | a0001c0001t0001g0009a0001c0001t0001g0064a0001c0001t0001g0076others(81): Show | 85 | HG00099.hp2 HG00609.hp1 HG01109.hp1 others(82): Show |
intron_variant | MODIFIER | c.852+19608dupT | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32838522 | |||||
| chr3:32838522
|
CT | C | 28 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0077others(25): Show | 28 | HG00140.hp2 HG00735.hp1 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.852+19608delT | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32838522 | |||||
| chr3:32838522
|
CTT | C | 123 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(120): Show | 123 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.852+19607_852+1960 others(6): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32838522 | |||||
| chr3:32838586
|
G | A | 118 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(115): Show | 118 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.852+19654G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32838586 | ||||||
| chr3:32838623
|
T | C | 33 | a0001c0001t0004g0033a0001c0001t0004g0038a0001c0001t0004g0043others(30): Show | 33 | HG00280.hp2 HG00544.hp2 HG02040.hp2 others(30): Show |
intron_variant | MODIFIER | c.852+19691T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32838623 | ||||||
| chr3:32838692
|
T | C | 5 | a0001c0001t0007g0286a0001c0002t0047g0101a0001c0003t0005g0013others(2): Show | 5 | HG02572.hp1 HG02683.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.852+19760T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32838692 | ||||||
| chr3:32838771
|
C | G | 33 | a0001c0001t0004g0033a0001c0001t0004g0038a0001c0001t0004g0043others(30): Show | 33 | HG00280.hp2 HG00544.hp2 HG02040.hp2 others(30): Show |
intron_variant | MODIFIER | c.852+19839C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32838771 | ||||||
| chr3:32838832
|
G | A | 1 | a0001c0001t0003g0079 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.852+19900G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32838832 | ||||||
| chr3:32838834
|
T | A | 1 | a0001c0001t0003g0079 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.852+19902T>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32838834 | ||||||
| chr3:32838838
|
T | A | 1 | a0001c0001t0003g0079 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.852+19906T>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32838838 | ||||||
| chr3:32838893
|
C | T | 4 | a0001c0001t0001g0133a0001c0001t0001g0181a0001c0001t0001g0182others(1): Show | 4 | HG01934.hp1 HG01981.hp2 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.852+19961C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32838893 | ||||||
| chr3:32838976
|
T | C | 1 | a0001c0001t0027g0261 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.852+20044T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32838976 | ||||||
| chr3:32839073
|
C | T | 1 | a0001c0001t0021g0172 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.852+20141C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32839073 | ||||||
| chr3:32839353
|
C | T | 1 | a0001c0003t0005g0013 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.852+20421C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32839353 | ||||||
| chr3:32839479
|
C | T | 3 | a0001c0001t0002g0074a0001c0001t0018g0099a0001c0003t0005g0084 | 3 | HG02145.hp1 HG02559.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.852+20547C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32839479 | ||||||
| chr3:32839506
|
A | G | 38 | a0001c0001t0004g0033a0001c0001t0004g0038a0001c0001t0004g0043others(35): Show | 38 | HG00280.hp2 HG00544.hp2 HG02015.hp2 others(35): Show |
intron_variant | MODIFIER | c.852+20574A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32839506 | ||||||
| chr3:32839550
|
A | G | 311 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(308): Show | 312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.852+20618A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32839550 | ||||||
| chr3:32839639
|
G | A | 1 | a0001c0001t0016g0080 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.852+20707G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32839639 | ||||||
| chr3:32839654
|
CT | C | 20 | a0001c0001t0001g0003a0001c0001t0001g0230a0001c0001t0001g0231others(17): Show | 20 | HG00140.hp2 HG00735.hp1 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.852+20729delT | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32839654 | |||||
| chr3:32839661
|
T | TG | 28 | a0001c0001t0002g0074a0001c0001t0003g0114a0001c0001t0004g0033others(25): Show | 28 | HG00280.hp2 HG01109.hp1 HG01123.hp2 others(25): Show |
intron_variant | MODIFIER | c.852+20739dupG | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32839661 | |||||
| chr3:32839661
|
TG | T | 139 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(136): Show | 139 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.852+20739delG | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32839661 | |||||
| chr3:32839667
|
G | T | 2 | a0001c0001t0001g0011a0001c0001t0001g0012 | 2 | HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.852+20735G>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32839667 | ||||||
| chr3:32839668
|
G | T | 3 | a0001c0003t0005g0299a0001c0003t0005g0300a0001c0003t0005g0301 | 3 | HG01891.hp2 HG02622.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.852+20736G>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32839668 | ||||||
| chr3:32839748
|
C | T | 2 | a0001c0001t0001g0007a0001c0001t0009g0167 | 2 | HG00741.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.852+20816C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32839748 | ||||||
| chr3:32839861
|
C | T | 1 | a0001c0001t0009g0167 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.852+20929C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32839861 | ||||||
| chr3:32839975
|
T | C | 311 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(308): Show | 312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.852+21043T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32839975 | ||||||
| chr3:32840014
|
A | C | 1 | a0001c0001t0004g0057 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.852+21082A>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32840014 | ||||||
| chr3:32840086
|
C | T | 1 | a0001c0001t0001g0180 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.852+21154C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32840086 | ||||||
| chr3:32840125
|
A | C | 2 | a0001c0001t0002g0067a0001c0001t0002g0083 | 2 | HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.852+21193A>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32840125 | ||||||
| chr3:32840157
|
A | G | 1 | a0001c0001t0001g0012 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.852+21225A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32840157 | ||||||
| chr3:32840179
|
A | C | 1 | a0001c0001t0001g0028 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.852+21247A>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32840179 | ||||||
| chr3:32840183
|
CAGGGAGG others(5): Show |
C | 1 | a0001c0002t0002g0217 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.852+21253_852+2126 others(16): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32840183 | |||||
| chr3:32840515
|
G | A | 121 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(118): Show | 121 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.852+21583G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32840515 | ||||||
| chr3:32840516
|
A | G | 8 | a0001c0001t0001g0133a0001c0001t0001g0181a0001c0001t0001g0182others(5): Show | 8 | HG01934.hp1 HG01981.hp2 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.852+21584A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32840516 | ||||||
| chr3:32840651
|
T | C | 1 | a0001c0002t0002g0324 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.852+21719T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32840651 | ||||||
| chr3:32840701
|
G | A | 1 | a0001c0001t0004g0057 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.852+21769G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32840701 | ||||||
| chr3:32840711
|
C | T | 2 | a0001c0001t0001g0119a0001c0001t0001g0120 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.852+21779C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32840711 | ||||||
| chr3:32840779
|
C | CACTGGTG | 22 | a0001c0001t0001g0003a0001c0001t0001g0230a0001c0001t0001g0231others(19): Show | 22 | HG00140.hp2 HG00735.hp1 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.852+21849_852+2185 others(11): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32840779 | |||||
| chr3:32840844
|
G | C | 1 | a0001c0001t0004g0174 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.852+21912G>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32840844 | ||||||
| chr3:32841138
|
G | A | 1 | a0001c0003t0005g0300 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.852+22206G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32841138 | ||||||
| chr3:32841200
|
G | A | 1 | a0001c0001t0014g0282 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.852+22268G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32841200 | ||||||
| chr3:32841354
|
G | T | 1 | a0001c0001t0008g0265 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.852+22422G>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32841354 | ||||||
| chr3:32841370
|
A | G | 34 | a0001c0001t0004g0033a0001c0001t0004g0038a0001c0001t0004g0043others(31): Show | 34 | HG00280.hp2 HG00544.hp2 HG02015.hp2 others(31): Show |
intron_variant | MODIFIER | c.852+22438A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32841370 | ||||||
| chr3:32841542
|
C | T | 1 | a0001c0001t0034g0254 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.852+22610C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32841542 | ||||||
| chr3:32841551
|
T | C | 9 | a0001c0002t0002g0014a0001c0002t0002g0015a0001c0002t0002g0016others(6): Show | 9 | HG01109.hp2 HG02109.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.852+22619T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32841551 | ||||||
| chr3:32841591
|
G | C | 277 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(274): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.852+22659G>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32841591 | ||||||
| chr3:32841618
|
A | C | 1 | a0001c0001t0004g0057 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.852+22686A>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32841618 | ||||||
| chr3:32841623
|
C | A | 1 | a0001c0001t0004g0057 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.852+22691C>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32841623 | ||||||
| chr3:32841624
|
A | C | 1 | a0001c0001t0004g0057 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.852+22692A>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32841624 | ||||||
| chr3:32841629
|
C | G | 1 | a0001c0002t0013g0267 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.852+22697C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32841629 | ||||||
| chr3:32841697
|
G | A | 277 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(274): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.852+22765G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32841697 | ||||||
| chr3:32841722
|
G | A | 1 | a0001c0001t0001g0086 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.852+22790G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32841722 | ||||||
| chr3:32841769
|
C | T | 1 | a0001c0001t0003g0194 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.852+22837C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32841769 | ||||||
| chr3:32841785
|
A | G | 1 | a0001c0002t0002g0217 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.852+22853A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32841785 | ||||||
| chr3:32841834
|
A | T | 1 | a0001c0001t0008g0278 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.852+22902A>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32841834 | ||||||
| chr3:32841883
|
A | G | 1 | a0001c0001t0004g0174 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.852+22951A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32841883 | ||||||
| chr3:32841917
|
C | T | 34 | a0001c0001t0004g0033a0001c0001t0004g0038a0001c0001t0004g0043others(31): Show | 34 | HG00280.hp2 HG00544.hp2 HG02015.hp2 others(31): Show |
intron_variant | MODIFIER | c.852+22985C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32841917 | ||||||
| chr3:32842089
|
G | A | 277 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(274): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.852+23157G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32842089 | ||||||
| chr3:32842104
|
G | A | 182 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(179): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.852+23172G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32842104 | ||||||
| chr3:32842269
|
A | C | 1 | a0001c0001t0002g0168 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.852+23337A>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32842269 | ||||||
| chr3:32842429
|
A | G | 3 | a0001c0001t0002g0305a0001c0001t0002g0309a0001c0001t0002g0310 | 3 | HG02451.hp1 HG02486.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.852+23497A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32842429 | ||||||
| chr3:32842546
|
C | T | 4 | a0001c0001t0001g0233a0001c0001t0002g0234a0001c0001t0002g0235others(1): Show | 4 | HG02258.hp1 HG02970.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.852+23614C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32842546 | ||||||
| chr3:32842587
|
C | T | 3 | a0001c0001t0010g0237a0001c0001t0010g0238a0001c0001t0010g0239 | 3 | HG01243.hp1 HG01255.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.852+23655C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32842587 | ||||||
| chr3:32842699
|
A | G | 1 | a0001c0001t0001g0197 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.852+23767A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32842699 | ||||||
| chr3:32842720
|
TACAG | T | 311 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(308): Show | 312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.852+23793_852+2379 others(8): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32842720 | |||||
| chr3:32842740
|
G | A | 1 | a0001c0002t0002g0062 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.852+23808G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32842740 | ||||||
| chr3:32842761
|
A | C | 1 | a0001c0001t0008g0265 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.852+23829A>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32842761 | ||||||
| chr3:32842861
|
C | T | 1 | a0001c0001t0001g0085 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.852+23929C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32842861 | ||||||
| chr3:32843016
|
G | C | 1 | a0001c0001t0008g0265 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.852+24084G>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32843016 | ||||||
| chr3:32843017
|
C | G | 1 | a0001c0001t0008g0265 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.852+24085C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32843017 | ||||||
| chr3:32843018
|
G | A | 2 | a0001c0001t0002g0067a0001c0001t0002g0083 | 2 | HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.852+24086G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32843018 | ||||||
| chr3:32843228
|
C | G | 1 | a0001c0001t0016g0080 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.852+24296C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32843228 | ||||||
| chr3:32843254
|
G | A | 18 | a0001c0001t0001g0003a0001c0001t0001g0243a0001c0001t0001g0247others(15): Show | 18 | HG00140.hp2 HG00735.hp1 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.852+24322G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32843254 | ||||||
| chr3:32843365
|
G | A | 1 | a0001c0001t0057g0272 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.852+24433G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32843365 | ||||||
| chr3:32843457
|
G | A | 3 | a0001c0003t0005g0299a0001c0003t0005g0300a0001c0003t0005g0301 | 3 | HG01891.hp2 HG02622.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.852+24525G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32843457 | ||||||
| chr3:32843575
|
C | T | 1 | a0001c0001t0001g0011 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.852+24643C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32843575 | ||||||
| chr3:32843815
|
A | G | 1 | a0001c0001t0006g0165 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.852+24883A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32843815 | ||||||
| chr3:32844043
|
C | T | 2 | a0001c0001t0018g0283a0001c0003t0005g0013 | 2 | HG02572.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.852+25111C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32844043 | ||||||
| chr3:32844092
|
C | T | 1 | a0001c0001t0003g0163 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.852+25160C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32844092 | ||||||
| chr3:32844100
|
G | T | 33 | a0001c0001t0004g0033a0001c0001t0004g0038a0001c0001t0004g0043others(30): Show | 33 | HG00280.hp2 HG00544.hp2 HG02015.hp2 others(30): Show |
intron_variant | MODIFIER | c.852+25168G>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32844100 | ||||||
| chr3:32844111
|
G | A | 27 | a0001c0001t0001g0003a0001c0001t0001g0243a0001c0001t0001g0247others(24): Show | 27 | HG00140.hp2 HG00735.hp1 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.852+25179G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32844111 | ||||||
| chr3:32844113
|
G | A | 1 | a0001c0001t0001g0110 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.852+25181G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32844113 | ||||||
| chr3:32844491
|
G | C | 46 | a0001c0001t0001g0028a0001c0001t0001g0037a0001c0001t0001g0049others(43): Show | 46 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.852+25559G>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32844491 | ||||||
| chr3:32844503
|
C | T | 1 | a0001c0001t0001g0088 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.852+25571C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32844503 | ||||||
| chr3:32844518
|
T | A | 58 | a0001c0001t0001g0050a0001c0001t0001g0055a0001c0001t0001g0064others(55): Show | 59 | HG00099.hp2 HG01261.hp1 HG01358.hp1 others(56): Show |
intron_variant | MODIFIER | c.852+25586T>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32844518 | ||||||
| chr3:32844519
|
C | T | 58 | a0001c0001t0001g0050a0001c0001t0001g0055a0001c0001t0001g0064others(55): Show | 59 | HG00099.hp2 HG01261.hp1 HG01358.hp1 others(56): Show |
intron_variant | MODIFIER | c.852+25587C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32844519 | ||||||
| chr3:32844717
|
A | G | 1 | a0001c0002t0002g0062 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.852+25785A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32844717 | ||||||
| chr3:32844835
|
A | G | 1 | a0001c0001t0004g0214 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.852+25903A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32844835 | ||||||
| chr3:32844903
|
C | T | 1 | a0001c0001t0002g0168 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.852+25971C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32844903 | ||||||
| chr3:32844944
|
T | G | 30 | a0001c0001t0001g0003a0001c0001t0001g0240a0001c0001t0001g0241others(27): Show | 30 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(27): Show |
intron_variant | MODIFIER | c.852+26012T>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32844944 | ||||||
| chr3:32844954
|
G | A | 172 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(169): Show | 173 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.852+26022G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32844954 | ||||||
| chr3:32845127
|
CCTGGAGG others(16): Show |
C | 5 | a0001c0003t0005g0097a0001c0003t0005g0299a0001c0003t0005g0300others(2): Show | 5 | HG01891.hp2 HG02559.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.852+26201_852+2622 others(27): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32845127 | |||||
| chr3:32845141
|
A | G | 1 | a0001c0001t0004g0218 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.852+26209A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32845141 | ||||||
| chr3:32845172
|
A | G | 323 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(320): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.852+26240A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32845172 | ||||||
| chr3:32845252
|
G | C | 1 | a0001c0002t0002g0126 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.852+26320G>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32845252 | ||||||
| chr3:32845502
|
A | C | 1 | a0001c0007t0012g0137 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.852+26570A>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32845502 | ||||||
| chr3:32845533
|
G | T | 1 | a0001c0001t0019g0326 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.852+26601G>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32845533 | ||||||
| chr3:32845602
|
T | C | 1 | a0001c0001t0001g0199 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.852+26670T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32845602 | ||||||
| chr3:32845608
|
A | T | 2 | a0001c0001t0002g0319a0001c0001t0002g0320 | 2 | HG02717.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.852+26676A>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32845608 | ||||||
| chr3:32845663
|
A | G | 59 | a0001c0001t0001g0050a0001c0001t0001g0055a0001c0001t0001g0064others(56): Show | 60 | HG00099.hp2 HG01081.hp1 HG01261.hp1 others(57): Show |
intron_variant | MODIFIER | c.852+26731A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32845663 | ||||||
| chr3:32845688
|
A | G | 5 | a0001c0003t0005g0097a0001c0003t0005g0299a0001c0003t0005g0300others(2): Show | 5 | HG01891.hp2 HG02559.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.852+26756A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32845688 | ||||||
| chr3:32845697
|
C | T | 1 | a0001c0001t0040g0256 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.852+26765C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32845697 | ||||||
| chr3:32845718
|
CT | C | 299 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(296): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.852+26799delT | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32845718 | |||||
| chr3:32845757
|
G | C | 3 | a0001c0001t0007g0121a0001c0001t0007g0123a0001c0003t0005g0122 | 3 | HG02451.hp2 HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.852+26825G>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32845757 | ||||||
| chr3:32845844
|
C | G | 1 | a0001c0001t0040g0256 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.852+26912C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32845844 | ||||||
| chr3:32845934
|
T | A | 60 | a0001c0001t0001g0050a0001c0001t0001g0055a0001c0001t0001g0064others(57): Show | 61 | HG00099.hp2 HG01261.hp1 HG01358.hp1 others(58): Show |
intron_variant | MODIFIER | c.852+27002T>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32845934 | ||||||
| chr3:32846000
|
TG | T | 109 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(106): Show | 109 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.852+27070delG | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32846000 | |||||
| chr3:32846036
|
T | C | 1 | a0001c0001t0027g0261 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.852+27104T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32846036 | ||||||
| chr3:32846072
|
CT | C | 87 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(84): Show | 88 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(85): Show |
intron_variant | MODIFIER | c.852+27161delT | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32846072 | |||||
| chr3:32846072
|
CTT | C | 29 | a0001c0001t0001g0050a0001c0001t0001g0055a0001c0001t0001g0095others(26): Show | 29 | HG01109.hp2 HG01358.hp1 HG01516.hp2 others(26): Show |
intron_variant | MODIFIER | c.852+27160_852+2716 others(6): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32846072 | |||||
| chr3:32846072
|
CTTT | C | 160 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(157): Show | 161 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(158): Show |
intron_variant | MODIFIER | c.852+27159_852+2716 others(7): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32846072 | |||||
| chr3:32846121
|
G | C | 5 | a0001c0003t0005g0097a0001c0003t0005g0299a0001c0003t0005g0300others(2): Show | 5 | HG01891.hp2 HG02559.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.852+27189G>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32846121 | ||||||
| chr3:32846171
|
G | T | 1 | a0001c0001t0001g0250 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.852+27239G>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32846171 | ||||||
| chr3:32846221
|
G | A | 1 | a0001c0001t0042g0107 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.852+27289G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32846221 | ||||||
| chr3:32846345
|
G | A | 2 | a0001c0001t0001g0007a0001c0001t0009g0167 | 2 | HG00741.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.852+27413G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32846345 | ||||||
| chr3:32846428
|
A | G | 2 | a0001c0001t0018g0283a0001c0001t0039g0024 | 2 | HG06807.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.853-27390A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32846428 | ||||||
| chr3:32846494
|
T | C | 3 | a0001c0001t0001g0304a0001c0001t0016g0001a0001c0003t0005g0025 | 4 | HG01934.hp2 HG02896.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.853-27324T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32846494 | ||||||
| chr3:32846573
|
G | C | 2 | a0001c0001t0002g0319a0001c0001t0002g0320 | 2 | HG02717.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.853-27245G>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32846573 | ||||||
| chr3:32846609
|
C | G | 2 | a0001c0001t0001g0251a0001c0001t0007g0311 | 2 | HG01081.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.853-27209C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32846609 | ||||||
| chr3:32846610
|
T | C | 1 | a0001c0001t0002g0067 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.853-27208T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32846610 | ||||||
| chr3:32846713
|
A | G | 1 | a0001c0001t0001g0012 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.853-27105A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32846713 | ||||||
| chr3:32846763
|
A | G | 1 | a0001c0001t0001g0012 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.853-27055A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32846763 | ||||||
| chr3:32846851
|
G | A | 1 | a0001c0001t0012g0063 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.853-26967G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32846851 | ||||||
| chr3:32846991
|
T | TG | 35 | a0001c0001t0001g0003a0001c0001t0001g0240a0001c0001t0001g0241others(32): Show | 36 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(33): Show |
intron_variant | MODIFIER | c.853-26823dupG | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32846991 | |||||
| chr3:32846994
|
G | A | 1 | a0001c0001t0004g0038 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.853-26824G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32846994 | ||||||
| chr3:32847190
|
A | AT | 19 | a0001c0001t0001g0304a0001c0001t0002g0118a0001c0001t0002g0234others(16): Show | 19 | HG01123.hp1 HG01192.hp1 HG01934.hp2 others(16): Show |
intron_variant | MODIFIER | c.853-26605dupT | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32847190 | |||||
| chr3:32847190
|
A | ATT | 8 | a0001c0001t0001g0110a0001c0001t0001g0233a0001c0001t0001g0247others(5): Show | 8 | HG01981.hp1 HG02145.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.853-26606_853-2660 others(6): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32847190 | |||||
| chr3:32847190
|
AT | A | 150 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(147): Show | 150 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.853-26605delT | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32847190 | |||||
| chr3:32847190
|
ATT | A | 11 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0197others(8): Show | 11 | HG01081.hp1 HG01123.hp2 HG01361.hp2 others(8): Show |
intron_variant | MODIFIER | c.853-26606_853-2660 others(6): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32847190 | |||||
| chr3:32847197
|
T | G | 1 | a0001c0001t0001g0108 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.853-26621T>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32847197 | ||||||
| chr3:32847273
|
C | T | 66 | a0001c0001t0001g0012a0001c0001t0001g0050a0001c0001t0001g0055others(63): Show | 66 | HG00099.hp2 HG01261.hp1 HG01358.hp1 others(63): Show |
intron_variant | MODIFIER | c.853-26545C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32847273 | ||||||
| chr3:32847288
|
C | G | 1 | a0001c0001t0003g0190 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.853-26530C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32847288 | ||||||
| chr3:32847359
|
G | A | 107 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(104): Show | 107 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.853-26459G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32847359 | ||||||
| chr3:32847387
|
G | A | 2 | a0001c0001t0001g0141a0001c0001t0001g0142 | 2 | NA20752.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.853-26431G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32847387 | ||||||
| chr3:32847437
|
C | T | 32 | a0001c0001t0004g0033a0001c0001t0004g0038a0001c0001t0004g0043others(29): Show | 32 | HG00280.hp2 HG00544.hp2 HG02015.hp2 others(29): Show |
intron_variant | MODIFIER | c.853-26381C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32847437 | ||||||
| chr3:32847484
|
C | T | 1 | a0001c0001t0007g0314 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.853-26334C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32847484 | ||||||
| chr3:32847551
|
G | A | 1 | a0001c0001t0006g0165 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.853-26267G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32847551 | ||||||
| chr3:32847606
|
A | G | 14 | a0001c0001t0001g0199a0001c0001t0003g0093a0001c0001t0004g0061others(11): Show | 14 | HG00558.hp2 HG00609.hp1 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.853-26212A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32847606 | ||||||
| chr3:32847646
|
T | C | 1 | a0001c0001t0001g0216 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.853-26172T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32847646 | ||||||
| chr3:32847662
|
G | T | 1 | a0001c0001t0004g0296 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.853-26156G>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32847662 | ||||||
| chr3:32847717
|
T | C | 2 | a0001c0001t0001g0243a0001c0001t0009g0242 | 2 | HG01106.hp1 HG01167.hp1 |
intron_variant | MODIFIER | c.853-26101T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32847717 | ||||||
| chr3:32847822
|
G | A | 1 | a0001c0001t0018g0283 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.853-25996G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32847822 | ||||||
| chr3:32847869
|
G | A | 5 | a0001c0003t0005g0097a0001c0003t0005g0299a0001c0003t0005g0300others(2): Show | 5 | HG01891.hp2 HG02559.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.853-25949G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32847869 | ||||||
| chr3:32847948
|
A | G | 71 | a0001c0001t0001g0012a0001c0001t0001g0028a0001c0001t0001g0050others(68): Show | 71 | HG00099.hp2 HG01261.hp1 HG01358.hp1 others(68): Show |
intron_variant | MODIFIER | c.853-25870A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32847948 | ||||||
| chr3:32848146
|
C | G | 35 | a0001c0001t0001g0003a0001c0001t0001g0185a0001c0001t0001g0240others(32): Show | 36 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(33): Show |
intron_variant | MODIFIER | c.853-25672C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32848146 | ||||||
| chr3:32848476
|
A | G | 32 | a0001c0001t0004g0033a0001c0001t0004g0038a0001c0001t0004g0043others(29): Show | 32 | HG00280.hp2 HG00544.hp2 HG02015.hp2 others(29): Show |
intron_variant | MODIFIER | c.853-25342A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32848476 | ||||||
| chr3:32848479
|
A | G | 1 | a0001c0001t0001g0216 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.853-25339A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32848479 | ||||||
| chr3:32848494
|
G | A | 3 | a0001c0001t0045g0071a0001c0002t0002g0070a0001c0003t0005g0117 | 3 | HG02630.hp1 HG02647.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.853-25324G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32848494 | ||||||
| chr3:32848503
|
G | A | 209 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(206): Show | 210 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.853-25315G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32848503 | ||||||
| chr3:32848581
|
G | C | 4 | a0001c0002t0002g0289a0001c0002t0002g0293a0001c0002t0002g0294others(1): Show | 4 | NA18945.hp2 NA18973.hp1 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.853-25237G>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32848581 | ||||||
| chr3:32848613
|
C | A | 1 | a0001c0001t0001g0028 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.853-25205C>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32848613 | ||||||
| chr3:32848627
|
A | G | 5 | a0001c0001t0001g0173a0001c0001t0001g0212a0001c0002t0002g0106others(2): Show | 5 | HG00639.hp2 HG01261.hp2 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.853-25191A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32848627 | ||||||
| chr3:32848710
|
C | G | 2 | a0001c0001t0014g0248a0001c0001t0014g0252 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.853-25108C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32848710 | ||||||
| chr3:32848822
|
C | A | 209 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(206): Show | 210 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.853-24996C>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32848822 | ||||||
| chr3:32848940
|
A | G | 1 | a0001c0001t0001g0110 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.853-24878A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32848940 | ||||||
| chr3:32848998
|
A | G | 2 | a0001c0001t0007g0286a0001c0003t0005g0287 | 2 | HG03098.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.853-24820A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32848998 | ||||||
| chr3:32849203
|
C | G | 37 | a0001c0001t0001g0028a0001c0001t0001g0233a0001c0001t0001g0249others(34): Show | 37 | HG00280.hp2 HG00544.hp2 HG02015.hp2 others(34): Show |
intron_variant | MODIFIER | c.853-24615C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32849203 | ||||||
| chr3:32849225
|
T | C | 5 | a0001c0003t0005g0097a0001c0003t0005g0299a0001c0003t0005g0300others(2): Show | 5 | HG01891.hp2 HG02559.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.853-24593T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32849225 | ||||||
| chr3:32849276
|
C | T | 1 | a0001c0004t0011g0245 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.853-24542C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32849276 | ||||||
| chr3:32849518
|
C | A | 106 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(103): Show | 106 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.853-24300C>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32849518 | ||||||
| chr3:32849617
|
C | T | 1 | a0001c0001t0018g0283 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.853-24201C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32849617 | ||||||
| chr3:32849699
|
T | TTG | 12 | a0001c0001t0001g0011a0001c0001t0001g0028a0001c0001t0001g0110others(9): Show | 12 | HG01884.hp2 HG01934.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.853-24118_853-2411 others(6): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32849699 | |||||
| chr3:32849784
|
C | T | 5 | a0001c0001t0001g0028a0001c0001t0001g0233a0001c0001t0001g0249others(2): Show | 5 | HG02258.hp1 HG03041.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.853-24034C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32849784 | ||||||
| chr3:32849834
|
A | G | 2 | a0001c0001t0002g0319a0001c0001t0002g0320 | 2 | HG02717.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.853-23984A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32849834 | ||||||
| chr3:32849931
|
A | G | 35 | a0001c0001t0001g0003a0001c0001t0001g0185a0001c0001t0001g0240others(32): Show | 36 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(33): Show |
intron_variant | MODIFIER | c.853-23887A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32849931 | ||||||
| chr3:32850017
|
T | C | 5 | a0001c0003t0005g0097a0001c0003t0005g0299a0001c0003t0005g0300others(2): Show | 5 | HG01891.hp2 HG02559.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.853-23801T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32850017 | ||||||
| chr3:32850112
|
C | T | 1 | a0001c0001t0001g0103 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.853-23706C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32850112 | ||||||
| chr3:32850265
|
A | AT | 54 | a0001c0001t0001g0037a0001c0001t0001g0049a0001c0001t0001g0140others(51): Show | 54 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.853-23544dupT | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32850265 | |||||
| chr3:32850273
|
T | G | 2 | a0001c0001t0001g0251a0001c0001t0003g0253 | 2 | HG00735.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.853-23545T>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32850273 | ||||||
| chr3:32850275
|
G | T | 61 | a0001c0001t0001g0028a0001c0001t0001g0050a0001c0001t0001g0055others(58): Show | 61 | HG00099.hp2 HG01261.hp1 HG01358.hp1 others(58): Show |
intron_variant | MODIFIER | c.853-23543G>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32850275 | ||||||
| chr3:32850947
|
G | A | 58 | a0001c0001t0001g0012a0001c0001t0001g0050a0001c0001t0001g0055others(55): Show | 58 | HG00099.hp2 HG01261.hp1 HG01358.hp1 others(55): Show |
intron_variant | MODIFIER | c.853-22871G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32850947 | ||||||
| chr3:32850968
|
T | C | 1 | a0001c0001t0034g0254 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.853-22850T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32850968 | ||||||
| chr3:32850971
|
A | G | 67 | a0001c0001t0001g0012a0001c0001t0001g0028a0001c0001t0001g0050others(64): Show | 67 | HG00099.hp2 HG01261.hp1 HG01358.hp1 others(64): Show |
intron_variant | MODIFIER | c.853-22847A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32850971 | ||||||
| chr3:32851143
|
G | A | 5 | a0001c0001t0003g0093a0001c0001t0009g0115a0001c0001t0050g0094others(2): Show | 5 | HG01109.hp1 HG02683.hp2 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.853-22675G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32851143 | ||||||
| chr3:32851512
|
C | G | 4 | a0001c0001t0001g0233a0001c0001t0001g0249a0001c0001t0002g0235others(1): Show | 4 | HG02258.hp1 HG03041.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.853-22306C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32851512 | ||||||
| chr3:32851559
|
A | G | 1 | a0001c0001t0051g0096 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.853-22259A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32851559 | ||||||
| chr3:32851562
|
G | A | 1 | a0001c0001t0001g0028 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.853-22256G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32851562 | ||||||
| chr3:32851593
|
C | T | 3 | a0001c0001t0010g0237a0001c0001t0010g0238a0001c0001t0010g0239 | 3 | HG01243.hp1 HG01255.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.853-22225C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32851593 | ||||||
| chr3:32851602
|
C | T | 1 | a0001c0001t0012g0008 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.853-22216C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32851602 | ||||||
| chr3:32851604
|
G | A | 1 | a0001c0001t0016g0080 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.853-22214G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32851604 | ||||||
| chr3:32851622
|
G | T | 1 | a0001c0002t0002g0290 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.853-22196G>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32851622 | ||||||
| chr3:32851626
|
C | T | 1 | a0001c0002t0002g0206 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.853-22192C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32851626 | ||||||
| chr3:32851627
|
C | A | 2 | a0001c0002t0002g0206a0001c0002t0002g0290 | 2 | HG02027.hp1 HG02027.hp2 |
intron_variant | MODIFIER | c.853-22191C>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32851627 | ||||||
| chr3:32851848
|
T | C | 4 | a0001c0001t0001g0304a0001c0001t0002g0118a0001c0001t0002g0168others(1): Show | 4 | HG01934.hp2 HG02896.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.853-21970T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32851848 | ||||||
| chr3:32851954
|
T | C | 1 | a0001c0002t0046g0065 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.853-21864T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32851954 | ||||||
| chr3:32852055
|
G | T | 1 | a0001c0001t0051g0096 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.853-21763G>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32852055 | ||||||
| chr3:32852279
|
C | A | 2 | a0001c0002t0002g0324a0001c0003t0005g0323 | 2 | HG02717.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.853-21539C>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32852279 | ||||||
| chr3:32852279
|
C | G | 1 | a0001c0008t0007g0023 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.853-21539C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32852279 | ||||||
| chr3:32852353
|
G | C | 1 | a0001c0002t0002g0135 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.853-21465G>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32852353 | ||||||
| chr3:32852363
|
C | CT | 4 | a0001c0001t0001g0077a0001c0001t0002g0075a0001c0001t0002g0078others(1): Show | 4 | HG02970.hp1 HG03471.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.853-21454dupT | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32852363 | |||||
| chr3:32852466
|
C | T | 1 | a0001c0001t0001g0189 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.853-21352C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32852466 | ||||||
| chr3:32852759
|
T | A | 2 | a0001c0001t0018g0283a0001c0002t0002g0014 | 2 | HG02109.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.853-21059T>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32852759 | ||||||
| chr3:32852759
|
T | TA | 181 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(178): Show | 181 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.853-21044dupA | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32852759 | |||||
| chr3:32852759
|
T | TAA | 12 | a0001c0001t0001g0006a0001c0001t0048g0162a0001c0002t0002g0015others(9): Show | 12 | HG01109.hp2 HG02109.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.853-21045_853-2104 others(6): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32852759 | |||||
| chr3:32852759
|
TA | T | 13 | a0001c0001t0001g0317a0001c0001t0002g0305a0001c0001t0002g0309others(10): Show | 14 | HG00639.hp1 HG02257.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.853-21044delA | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32852759 | |||||
| chr3:32852768
|
A | AC | 5 | a0001c0001t0001g0028a0001c0001t0001g0233a0001c0001t0001g0249others(2): Show | 5 | HG02258.hp1 HG03041.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.853-21050_853-2104 others(5): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32852768 | ||||||
| chr3:32852769
|
A | AC | 58 | a0001c0001t0001g0012a0001c0001t0001g0050a0001c0001t0001g0055others(55): Show | 58 | HG00099.hp2 HG01261.hp1 HG01358.hp1 others(55): Show |
intron_variant | MODIFIER | c.853-21049_853-2104 others(5): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32852769 | ||||||
| chr3:32852868
|
A | C | 5 | a0001c0001t0001g0028a0001c0001t0001g0233a0001c0001t0001g0249others(2): Show | 5 | HG02258.hp1 HG03041.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.853-20950A>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32852868 | ||||||
| chr3:32853104
|
TTC | T | 3 | a0001c0001t0001g0127a0001c0002t0002g0124a0001c0002t0002g0126 | 3 | NA18948.hp1 NA18968.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.853-20698_853-2069 others(6): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32853104 | |||||
| chr3:32853118
|
CTCT | C | 217 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(214): Show | 217 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.853-20698_853-2069 others(7): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32853118 | |||||
| chr3:32853120
|
CT | C | 17 | a0001c0001t0001g0317a0001c0001t0002g0305a0001c0001t0002g0309others(14): Show | 18 | HG00639.hp1 HG02257.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.853-20682delT | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32853120 | |||||
| chr3:32853120
|
CTT | C | 45 | a0001c0001t0001g0028a0001c0001t0001g0110a0001c0001t0001g0233others(42): Show | 45 | HG00544.hp2 HG01934.hp2 HG02015.hp2 others(42): Show |
intron_variant | MODIFIER | c.853-20683_853-2068 others(6): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32853120 | |||||
| chr3:32853120
|
CTTT | C | 35 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0185others(32): Show | 36 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(33): Show |
intron_variant | MODIFIER | c.853-20684_853-2068 others(7): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32853120 | |||||
| chr3:32853122
|
T | C | 4 | a0001c0001t0004g0218a0001c0001t0010g0237a0001c0001t0010g0238others(1): Show | 4 | HG00280.hp2 HG01243.hp1 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.853-20696T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32853122 | ||||||
| chr3:32853123
|
T | C | 2 | a0001c0001t0002g0319a0001c0001t0002g0320 | 2 | HG02717.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.853-20695T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32853123 | ||||||
| chr3:32853143
|
G | T | 1 | a0001c0001t0051g0096 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.853-20675G>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32853143 | ||||||
| chr3:32853286
|
T | C | 1 | a0001c0001t0030g0325 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.853-20532T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32853286 | ||||||
| chr3:32853338
|
C | T | 106 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(103): Show | 106 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.853-20480C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32853338 | ||||||
| chr3:32853342
|
C | T | 1 | a0001c0001t0031g0151 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.853-20476C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32853342 | ||||||
| chr3:32853479
|
T | C | 1 | a0001c0001t0001g0181 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.853-20339T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32853479 | ||||||
| chr3:32853707
|
T | C | 1 | a0001c0001t0006g0165 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.853-20111T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32853707 | ||||||
| chr3:32853965
|
C | T | 1 | a0001c0001t0051g0096 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.853-19853C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32853965 | ||||||
| chr3:32853991
|
G | A | 1 | a0001c0001t0001g0247 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.853-19827G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32853991 | ||||||
| chr3:32854650
|
A | G | 3 | a0001c0001t0004g0218a0001c0001t0008g0273a0001c0001t0008g0275 | 3 | HG00280.hp2 NA18964.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.853-19168A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32854650 | ||||||
| chr3:32855093
|
A | G | 1 | a0001c0002t0002g0158 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.853-18725A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32855093 | ||||||
| chr3:32855179
|
G | A | 1 | a0001c0001t0044g0081 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.853-18639G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32855179 | ||||||
| chr3:32855281
|
C | T | 1 | a0001c0001t0012g0008 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.853-18537C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32855281 | ||||||
| chr3:32855294
|
G | A | 1 | a0001c0001t0001g0011 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.853-18524G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32855294 | ||||||
| chr3:32855371
|
G | C | 1 | a0001c0001t0051g0096 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.853-18447G>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32855371 | ||||||
| chr3:32855376
|
A | G | 1 | a0001c0002t0002g0155 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.853-18442A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32855376 | ||||||
| chr3:32855377
|
G | A | 1 | a0001c0002t0002g0155 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.853-18441G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32855377 | ||||||
| chr3:32855494
|
G | A | 3 | a0001c0001t0003g0226a0001c0001t0009g0227a0001c0001t0009g0228 | 3 | HG01069.hp1 HG01123.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.853-18324G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32855494 | ||||||
| chr3:32855507
|
ATGTCTCT others(4): Show |
A | 1 | a0001c0001t0001g0011 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.853-18303_853-1829 others(15): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32855507 | |||||
| chr3:32855533
|
C | T | 1 | a0001c0001t0057g0272 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.853-18285C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32855533 | ||||||
| chr3:32855548
|
A | G | 4 | a0001c0001t0001g0240a0001c0001t0001g0241a0001c0001t0003g0192others(1): Show | 4 | HG00099.hp1 HG00741.hp1 HG01069.hp2 others(1): Show |
intron_variant | MODIFIER | c.853-18270A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32855548 | ||||||
| chr3:32855747
|
A | G | 1 | a0001c0001t0022g0179 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.853-18071A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32855747 | ||||||
| chr3:32855850
|
G | A | 1 | a0001c0002t0002g0039 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.853-17968G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32855850 | ||||||
| chr3:32855901
|
A | C | 6 | a0001c0001t0001g0144a0001c0001t0001g0176a0001c0001t0001g0177others(3): Show | 6 | HG00735.hp2 HG01071.hp1 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.853-17917A>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32855901 | ||||||
| chr3:32855990
|
T | TTTTA | 136 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(133): Show | 136 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.853-17804_853-1780 others(8): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32855990 | |||||
| chr3:32855990
|
T | TTTTATTT others(1): Show |
7 | a0001c0001t0001g0006a0001c0001t0001g0128a0001c0001t0004g0152others(4): Show | 7 | HG00621.hp1 HG02148.hp2 NA18966.hp1 others(4): Show |
intron_variant | MODIFIER | c.853-17808_853-1780 others(12): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32855990 | |||||
| chr3:32855990
|
T | TTTTATTT others(9): Show |
1 | a0001c0001t0001g0095 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.853-17816_853-1780 others(20): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32855990 | |||||
| chr3:32856178
|
C | T | 1 | a0001c0001t0001g0251 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.853-17640C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32856178 | ||||||
| chr3:32856180
|
G | A | 1 | a0001c0001t0016g0001 | 2 | HG03139.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.853-17638G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32856180 | ||||||
| chr3:32856365
|
C | T | 1 | a0001c0001t0001g0108 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.853-17453C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32856365 | ||||||
| chr3:32856519
|
A | G | 55 | a0001c0001t0001g0037a0001c0001t0001g0049a0001c0001t0001g0140others(52): Show | 55 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.853-17299A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32856519 | ||||||
| chr3:32856713
|
G | A | 224 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(221): Show | 224 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.853-17105G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32856713 | ||||||
| chr3:32856800
|
T | C | 1 | a0001c0001t0001g0110 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.853-17018T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32856800 | ||||||
| chr3:32856854
|
C | G | 1 | a0001c0001t0001g0212 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.853-16964C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32856854 | ||||||
| chr3:32856922
|
C | T | 2 | a0001c0001t0007g0286a0001c0003t0005g0287 | 2 | HG03098.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.853-16896C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32856922 | ||||||
| chr3:32856944
|
A | G | 1 | a0003c0006t0002g0195 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.853-16874A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32856944 | ||||||
| chr3:32857009
|
A | G | 2 | a0001c0001t0001g0003a0001c0001t0040g0256 | 2 | HG03834.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.853-16809A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32857009 | ||||||
| chr3:32857044
|
T | C | 2 | a0001c0001t0007g0286a0001c0003t0005g0287 | 2 | HG03098.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.853-16774T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32857044 | ||||||
| chr3:32857064
|
G | C | 1 | a0001c0002t0002g0155 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.853-16754G>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32857064 | ||||||
| chr3:32857066
|
C | G | 1 | a0001c0002t0002g0155 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.853-16752C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32857066 | ||||||
| chr3:32857219
|
A | G | 1 | a0001c0001t0003g0219 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.853-16599A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32857219 | ||||||
| chr3:32857383
|
C | G | 37 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0185others(34): Show | 38 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(35): Show |
intron_variant | MODIFIER | c.853-16435C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32857383 | ||||||
| chr3:32857405
|
T | C | 1 | a0001c0001t0015g0246 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.853-16413T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32857405 | ||||||
| chr3:32857428
|
A | G | 1 | a0001c0002t0013g0266 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.853-16390A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32857428 | ||||||
| chr3:32857447
|
C | T | 31 | a0001c0001t0004g0033a0001c0001t0004g0038a0001c0001t0004g0043others(28): Show | 31 | HG00280.hp2 HG00544.hp2 HG02015.hp2 others(28): Show |
intron_variant | MODIFIER | c.853-16371C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32857447 | ||||||
| chr3:32857496
|
A | C | 1 | a0001c0001t0004g0152 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.853-16322A>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32857496 | ||||||
| chr3:32857498
|
G | A | 1 | a0001c0002t0024g0139 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.853-16320G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32857498 | ||||||
| chr3:32857699
|
A | G | 5 | a0001c0001t0001g0007a0001c0001t0001g0128a0001c0001t0009g0167others(2): Show | 5 | HG00323.hp1 HG00741.hp2 HG01167.hp2 others(2): Show |
intron_variant | MODIFIER | c.853-16119A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32857699 | ||||||
| chr3:32857791
|
C | T | 1 | a0001c0001t0001g0076 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.853-16027C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32857791 | ||||||
| chr3:32857871
|
T | C | 1 | a0001c0004t0011g0245 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.853-15947T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32857871 | ||||||
| chr3:32857917
|
G | T | 1 | a0001c0001t0002g0298 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.853-15901G>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32857917 | ||||||
| chr3:32857919
|
C | T | 2 | a0001c0001t0003g0171a0001c0001t0003g0203 | 2 | HG02055.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.853-15899C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32857919 | ||||||
| chr3:32857926
|
G | A | 1 | a0001c0001t0018g0283 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.853-15892G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32857926 | ||||||
| chr3:32858007
|
G | A | 1 | a0001c0001t0002g0235 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.853-15811G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32858007 | ||||||
| chr3:32858018
|
T | A | 1 | a0001c0002t0002g0155 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.853-15800T>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32858018 | ||||||
| chr3:32858265
|
G | T | 28 | a0001c0001t0004g0033a0001c0001t0004g0038a0001c0001t0004g0043others(25): Show | 28 | HG00280.hp2 HG00544.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.853-15553G>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32858265 | ||||||
| chr3:32858320
|
T | C | 1 | a0001c0002t0002g0155 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.853-15498T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32858320 | ||||||
| chr3:32858321
|
G | T | 1 | a0001c0002t0002g0155 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.853-15497G>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32858321 | ||||||
| chr3:32858322
|
C | G | 1 | a0001c0002t0002g0155 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.853-15496C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32858322 | ||||||
| chr3:32858333
|
G | A | 1 | a0001c0002t0002g0070 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.853-15485G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32858333 | ||||||
| chr3:32858347
|
G | A | 5 | a0001c0001t0001g0110a0001c0001t0002g0118a0001c0001t0010g0237others(2): Show | 5 | HG01243.hp1 HG01255.hp2 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.853-15471G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32858347 | ||||||
| chr3:32858476
|
C | T | 1 | a0001c0001t0039g0024 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.853-15342C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32858476 | ||||||
| chr3:32858670
|
G | A | 1 | a0001c0001t0001g0108 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.853-15148G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32858670 | ||||||
| chr3:32858709
|
A | G | 3 | a0001c0001t0003g0219a0001c0002t0002g0058a0001c0002t0002g0059 | 3 | HG03710.hp1 HG03834.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.853-15109A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32858709 | ||||||
| chr3:32858753
|
T | C | 40 | a0001c0001t0001g0003a0001c0001t0001g0028a0001c0001t0001g0185others(37): Show | 41 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(38): Show |
intron_variant | MODIFIER | c.853-15065T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32858753 | ||||||
| chr3:32858756
|
G | A | 1 | a0001c0001t0006g0150 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.853-15062G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32858756 | ||||||
| chr3:32858781
|
G | T | 310 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(307): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.853-15037G>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32858781 | ||||||
| chr3:32858950
|
T | C | 28 | a0001c0001t0004g0033a0001c0001t0004g0038a0001c0001t0004g0043others(25): Show | 28 | HG00280.hp2 HG00544.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.853-14868T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32858950 | ||||||
| chr3:32859042
|
T | G | 28 | a0001c0001t0004g0033a0001c0001t0004g0038a0001c0001t0004g0043others(25): Show | 28 | HG00280.hp2 HG00544.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.853-14776T>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32859042 | ||||||
| chr3:32859234
|
C | T | 1 | a0001c0001t0006g0010 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.853-14584C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32859234 | ||||||
| chr3:32859251
|
C | T | 3 | a0001c0001t0001g0243a0001c0001t0003g0192a0001c0001t0009g0242 | 3 | HG00741.hp1 HG01106.hp1 HG01167.hp1 |
intron_variant | MODIFIER | c.853-14567C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32859251 | ||||||
| chr3:32859359
|
A | G | 28 | a0001c0001t0004g0033a0001c0001t0004g0038a0001c0001t0004g0043others(25): Show | 28 | HG00280.hp2 HG00544.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.853-14459A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32859359 | ||||||
| chr3:32859411
|
C | G | 1 | a0001c0001t0001g0109 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.853-14407C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32859411 | ||||||
| chr3:32859431
|
G | GT | 27 | a0001c0001t0004g0033a0001c0001t0004g0038a0001c0001t0004g0043others(24): Show | 27 | HG00280.hp2 HG00544.hp2 HG02015.hp2 others(24): Show |
intron_variant | MODIFIER | c.853-14380dupT | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32859431 | |||||
| chr3:32859626
|
T | G | 13 | a0001c0001t0001g0233a0001c0001t0001g0249a0001c0001t0002g0235others(10): Show | 13 | HG02258.hp1 HG02559.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.853-14192T>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32859626 | ||||||
| chr3:32859669
|
G | T | 28 | a0001c0001t0004g0033a0001c0001t0004g0038a0001c0001t0004g0043others(25): Show | 28 | HG00280.hp2 HG00544.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.853-14149G>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32859669 | ||||||
| chr3:32859681
|
G | C | 5 | a0001c0001t0001g0127a0001c0001t0004g0046a0001c0001t0006g0029others(2): Show | 5 | HG00438.hp2 HG02523.hp2 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.853-14137G>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32859681 | ||||||
| chr3:32859808
|
C | A | 45 | a0001c0001t0001g0011a0001c0001t0001g0110a0001c0001t0001g0233others(42): Show | 45 | HG00280.hp2 HG00544.hp2 HG01884.hp2 others(42): Show |
intron_variant | MODIFIER | c.853-14010C>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32859808 | ||||||
| chr3:32859875
|
G | A | 28 | a0001c0001t0004g0033a0001c0001t0004g0038a0001c0001t0004g0043others(25): Show | 28 | HG00280.hp2 HG00544.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.853-13943G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32859875 | ||||||
| chr3:32859894
|
G | A | 44 | a0001c0001t0001g0011a0001c0001t0001g0110a0001c0001t0001g0233others(41): Show | 44 | HG00280.hp2 HG00544.hp2 HG01884.hp2 others(41): Show |
intron_variant | MODIFIER | c.853-13924G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32859894 | ||||||
| chr3:32860137
|
TCCCTCCC others(5): Show |
T | 4 | a0001c0001t0020g0034a0001c0001t0020g0047a0001c0002t0002g0042others(1): Show | 4 | NA18966.hp2 NA18968.hp2 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.853-13667_853-1365 others(16): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32860137 | |||||
| chr3:32860215
|
A | G | 3 | a0001c0001t0001g0100a0001c0001t0001g0317a0001c0001t0037g0322 | 3 | HG02622.hp2 HG02818.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.853-13603A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32860215 | ||||||
| chr3:32860369
|
C | T | 312 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(309): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.853-13449C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32860369 | ||||||
| chr3:32860435
|
C | T | 3 | a0001c0001t0001g0304a0001c0001t0002g0168a0001c0003t0005g0025 | 3 | HG01934.hp2 HG02896.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.853-13383C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32860435 | ||||||
| chr3:32860463
|
C | T | 48 | a0001c0001t0001g0012a0001c0001t0001g0050a0001c0001t0001g0055others(45): Show | 48 | HG00099.hp2 HG01261.hp1 HG01358.hp1 others(45): Show |
intron_variant | MODIFIER | c.853-13355C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32860463 | ||||||
| chr3:32860506
|
T | C | 1 | a0001c0001t0001g0148 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.853-13312T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32860506 | ||||||
| chr3:32860530
|
TCTC | T | 220 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(217): Show | 220 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.853-13284_853-1328 others(7): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32860530 | |||||
| chr3:32860588
|
A | G | 1 | a0001c0001t0001g0250 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.853-13230A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32860588 | ||||||
| chr3:32860671
|
G | A | 28 | a0001c0001t0004g0033a0001c0001t0004g0038a0001c0001t0004g0043others(25): Show | 28 | HG00280.hp2 HG00544.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.853-13147G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32860671 | ||||||
| chr3:32860801
|
A | G | 1 | a0001c0001t0004g0152 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.853-13017A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32860801 | ||||||
| chr3:32860878
|
A | T | 1 | a0001c0002t0002g0292 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.853-12940A>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32860878 | ||||||
| chr3:32860888
|
C | T | 4 | a0001c0001t0001g0077a0001c0001t0002g0075a0001c0001t0002g0078others(1): Show | 4 | HG02970.hp1 HG03471.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.853-12930C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32860888 | ||||||
| chr3:32860940
|
C | T | 10 | a0001c0001t0001g0233a0001c0001t0001g0249a0001c0001t0002g0235others(7): Show | 10 | HG02258.hp1 HG02630.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.853-12878C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32860940 | ||||||
| chr3:32860982
|
C | T | 1 | a0001c0002t0002g0324 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.853-12836C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32860982 | ||||||
| chr3:32861067
|
CTG | C | 3 | a0001c0001t0001g0011a0001c0001t0018g0283a0001c0008t0007g0023 | 3 | HG01884.hp2 NA18906.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.853-12750_853-1274 others(6): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32861067 | ||||||
| chr3:32861080
|
C | T | 1 | a0001c0001t0001g0181 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.853-12738C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32861080 | ||||||
| chr3:32861096
|
T | A | 28 | a0001c0001t0004g0033a0001c0001t0004g0038a0001c0001t0004g0043others(25): Show | 28 | HG00280.hp2 HG00544.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.853-12722T>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32861096 | ||||||
| chr3:32861139
|
T | C | 311 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(308): Show | 312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.853-12679T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32861139 | ||||||
| chr3:32861224
|
C | A | 1 | a0001c0001t0020g0047 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.853-12594C>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32861224 | ||||||
| chr3:32861297
|
C | T | 1 | a0001c0003t0005g0323 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.853-12521C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32861297 | ||||||
| chr3:32861458
|
C | T | 2 | a0001c0001t0001g0026a0001c0001t0017g0280 | 2 | HG02735.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.853-12360C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32861458 | ||||||
| chr3:32861516
|
CCG | C | 28 | a0001c0001t0004g0033a0001c0001t0004g0038a0001c0001t0004g0043others(25): Show | 28 | HG00280.hp2 HG00544.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.853-12301_853-1230 others(6): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32861516 | ||||||
| chr3:32861525
|
A | C | 3 | a0001c0001t0001g0304a0001c0001t0002g0168a0001c0003t0005g0025 | 3 | HG01934.hp2 HG02896.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.853-12293A>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32861525 | ||||||
| chr3:32861525
|
A | G | 263 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(260): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.853-12293A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32861525 | ||||||
| chr3:32861610
|
C | T | 1 | a0001c0002t0023g0044 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.853-12208C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32861610 | ||||||
| chr3:32861639
|
C | G | 2 | a0001c0001t0002g0319a0001c0001t0002g0320 | 2 | HG02717.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.853-12179C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32861639 | ||||||
| chr3:32861833
|
C | T | 1 | a0001c0001t0001g0181 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.853-11985C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32861833 | ||||||
| chr3:32861913
|
C | T | 3 | a0001c0001t0007g0286a0001c0003t0005g0097a0001c0003t0005g0302 | 3 | HG02559.hp1 HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.853-11905C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32861913 | ||||||
| chr3:32861972
|
C | T | 1 | a0001c0001t0001g0076 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.853-11846C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32861972 | ||||||
| chr3:32862231
|
C | A | 220 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(217): Show | 220 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.853-11587C>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32862231 | ||||||
| chr3:32862335
|
C | G | 7 | a0001c0001t0001g0011a0001c0001t0001g0110a0001c0001t0001g0304others(4): Show | 7 | HG01884.hp2 HG01934.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.853-11483C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32862335 | ||||||
| chr3:32862456
|
G | A | 1 | a0001c0001t0003g0146 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.853-11362G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32862456 | ||||||
| chr3:32862715
|
G | A | 76 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0012others(73): Show | 76 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.853-11103G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32862715 | ||||||
| chr3:32862918
|
C | G | 28 | a0001c0001t0004g0033a0001c0001t0004g0038a0001c0001t0004g0043others(25): Show | 28 | HG00280.hp2 HG00544.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.853-10900C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32862918 | ||||||
| chr3:32862918
|
C | T | 76 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0012others(73): Show | 76 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.853-10900C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32862918 | ||||||
| chr3:32862925
|
T | G | 312 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(309): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.853-10893T>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32862925 | ||||||
| chr3:32863023
|
G | A | 28 | a0001c0001t0004g0033a0001c0001t0004g0038a0001c0001t0004g0043others(25): Show | 28 | HG00280.hp2 HG00544.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.853-10795G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32863023 | ||||||
| chr3:32863023
|
G | T | 4 | a0001c0001t0003g0226a0001c0001t0009g0227a0001c0001t0009g0228others(1): Show | 4 | HG01069.hp1 HG01123.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.853-10795G>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32863023 | ||||||
| chr3:32863058
|
A | T | 1 | a0001c0002t0002g0255 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.853-10760A>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32863058 | ||||||
| chr3:32863067
|
T | TTATTAGG others(3): Show |
1 | a0001c0002t0002g0155 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.853-10749_853-1074 others(14): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32863067 | |||||
| chr3:32863160
|
C | G | 28 | a0001c0001t0004g0033a0001c0001t0004g0038a0001c0001t0004g0043others(25): Show | 28 | HG00280.hp2 HG00544.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.853-10658C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32863160 | ||||||
| chr3:32863194
|
C | CTTT | 3 | a0001c0001t0001g0077a0001c0001t0002g0075a0001c0001t0002g0234 | 3 | HG02970.hp1 HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.853-10624_853-1062 others(7): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32863194 | ||||||
| chr3:32863195
|
C | CT | 72 | a0001c0001t0001g0049a0001c0001t0001g0110a0001c0001t0001g0140others(69): Show | 73 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.853-10597dupT | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32863195 | |||||
| chr3:32863195
|
C | CTT | 18 | a0001c0001t0001g0127a0001c0001t0001g0216a0001c0001t0002g0315others(15): Show | 18 | HG00280.hp2 HG01109.hp1 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.853-10598_853-1059 others(6): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32863195 | |||||
| chr3:32863195
|
C | T | 4 | a0001c0001t0001g0077a0001c0001t0002g0075a0001c0001t0002g0078others(1): Show | 4 | HG02970.hp1 HG03471.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.853-10623C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32863195 | ||||||
| chr3:32863195
|
CT | C | 122 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(119): Show | 122 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.853-10597delT | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32863195 | |||||
| chr3:32863195
|
CTT | C | 59 | a0001c0001t0001g0011a0001c0001t0001g0026a0001c0001t0001g0028others(56): Show | 60 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(57): Show |
intron_variant | MODIFIER | c.853-10598_853-1059 others(6): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32863195 | |||||
| chr3:32863195
|
CTTTTTTT others(6): Show |
C | 1 | a0001c0002t0002g0211 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.853-10609_853-1059 others(17): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32863195 | |||||
| chr3:32863397
|
T | C | 1 | a0001c0001t0001g0251 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.853-10421T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32863397 | ||||||
| chr3:32863405
|
G | A | 1 | a0001c0001t0021g0172 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.853-10413G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32863405 | ||||||
| chr3:32863425
|
C | G | 28 | a0001c0001t0004g0033a0001c0001t0004g0038a0001c0001t0004g0043others(25): Show | 28 | HG00280.hp2 HG00544.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.853-10393C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32863425 | ||||||
| chr3:32863527
|
C | T | 1 | a0001c0001t0008g0268 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.853-10291C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32863527 | ||||||
| chr3:32863528
|
G | A | 9 | a0001c0001t0001g0125a0001c0001t0001g0197a0001c0001t0001g0198others(6): Show | 9 | HG00558.hp2 HG02074.hp1 NA18747.hp2 others(6): Show |
intron_variant | MODIFIER | c.853-10290G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32863528 | ||||||
| chr3:32863586
|
A | T | 1 | a0001c0001t0001g0110 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.853-10232A>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32863586 | ||||||
| chr3:32863943
|
A | G | 2 | a0001c0001t0002g0067a0001c0001t0002g0083 | 2 | HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.853-9875A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32863943 | ||||||
| chr3:32863984
|
T | A | 28 | a0001c0001t0004g0033a0001c0001t0004g0038a0001c0001t0004g0043others(25): Show | 28 | HG00280.hp2 HG00544.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.853-9834T>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32863984 | ||||||
| chr3:32863985
|
C | A | 28 | a0001c0001t0004g0033a0001c0001t0004g0038a0001c0001t0004g0043others(25): Show | 28 | HG00280.hp2 HG00544.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.853-9833C>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32863985 | ||||||
| chr3:32864013
|
G | A | 308 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(305): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.853-9805G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32864013 | ||||||
| chr3:32864030
|
C | T | 1 | a0001c0001t0051g0096 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.853-9788C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32864030 | ||||||
| chr3:32864120
|
G | A | 28 | a0001c0001t0004g0033a0001c0001t0004g0038a0001c0001t0004g0043others(25): Show | 28 | HG00280.hp2 HG00544.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.853-9698G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32864120 | ||||||
| chr3:32864312
|
T | G | 4 | a0001c0001t0001g0011a0001c0001t0018g0283a0001c0003t0005g0025others(1): Show | 4 | HG01884.hp2 HG01934.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.853-9506T>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32864312 | ||||||
| chr3:32864314
|
G | C | 1 | a0001c0001t0001g0110 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.853-9504G>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32864314 | ||||||
| chr3:32864608
|
G | A | 1 | a0001c0001t0004g0038 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.853-9210G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32864608 | ||||||
| chr3:32864817
|
A | G | 10 | a0001c0001t0001g0233a0001c0001t0001g0249a0001c0001t0002g0235others(7): Show | 10 | HG02258.hp1 HG02630.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.853-9001A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32864817 | ||||||
| chr3:32864842
|
AGTGGTGT others(8): Show |
A | 1 | a0001c0003t0005g0084 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.853-8972_853-8958d others(17): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32864842 | |||||
| chr3:32864845
|
G | GGT | 13 | a0001c0001t0001g0144a0001c0001t0001g0176a0001c0001t0001g0178others(10): Show | 13 | HG00597.hp2 HG00621.hp2 HG00735.hp2 others(10): Show |
intron_variant | MODIFIER | c.853-8926_853-8925d others(4): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32864845 | |||||
| chr3:32864845
|
G | GGTGT | 4 | a0001c0001t0002g0309a0001c0001t0007g0313a0001c0002t0002g0138others(1): Show | 4 | HG00423.hp2 HG02074.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.853-8928_853-8925d others(6): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32864845 | |||||
| chr3:32864845
|
G | GGTGTGT | 4 | a0001c0002t0002g0289a0001c0002t0002g0293a0001c0002t0002g0294others(1): Show | 4 | NA18945.hp2 NA18973.hp1 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.853-8930_853-8925d others(8): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32864845 | |||||
| chr3:32864845
|
GGT | G | 31 | a0001c0001t0001g0108a0001c0001t0001g0116a0001c0001t0001g0180others(28): Show | 31 | HG00323.hp2 HG00438.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.853-8926_853-8925d others(4): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32864845 | |||||
| chr3:32864845
|
GGTGT | G | 24 | a0001c0001t0001g0026a0001c0001t0001g0189a0001c0001t0001g0216others(21): Show | 24 | HG00544.hp1 HG01993.hp1 HG02155.hp1 others(21): Show |
intron_variant | MODIFIER | c.853-8928_853-8925d others(6): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32864845 | |||||
| chr3:32864845
|
GGTGTGT | G | 36 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0086others(33): Show | 36 | HG00280.hp2 HG00323.hp1 HG00741.hp2 others(33): Show |
intron_variant | MODIFIER | c.853-8930_853-8925d others(8): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32864845 | |||||
| chr3:32864845
|
GGTGTGTG others(1): Show |
G | 8 | a0001c0001t0001g0113a0001c0001t0001g0125a0001c0001t0001g0197others(5): Show | 8 | HG00544.hp2 HG01081.hp1 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.853-8932_853-8925d others(10): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32864845 | |||||
| chr3:32864845
|
GGTGTGTG others(3): Show |
G | 9 | a0001c0001t0001g0140a0001c0001t0003g0056a0001c0001t0004g0046others(6): Show | 9 | HG00280.hp1 HG00438.hp2 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.853-8934_853-8925d others(12): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32864845 | |||||
| chr3:32864845
|
GGTGTGTG others(5): Show |
G | 57 | a0001c0001t0001g0028a0001c0001t0001g0037a0001c0001t0001g0049others(54): Show | 57 | HG00558.hp1 HG00609.hp1 HG01106.hp1 others(54): Show |
intron_variant | MODIFIER | c.853-8936_853-8925d others(14): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32864845 | |||||
| chr3:32864845
|
GGTGTGTG others(7): Show |
G | 94 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(91): Show | 95 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(92): Show |
intron_variant | MODIFIER | c.853-8938_853-8925d others(16): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32864845 | |||||
| chr3:32864845
|
GGTGTGTG others(9): Show |
G | 10 | a0001c0001t0002g0118a0001c0001t0002g0319a0001c0001t0002g0320others(7): Show | 10 | HG01109.hp2 HG02015.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.853-8940_853-8925d others(18): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32864845 | |||||
| chr3:32864845
|
GGTGTGTG others(11): Show |
G | 8 | a0001c0001t0001g0011a0001c0001t0001g0233a0001c0001t0001g0249others(5): Show | 8 | HG01081.hp2 HG02258.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.853-8942_853-8925d others(20): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32864845 | |||||
| chr3:32864845
|
GGTGTGTG others(13): Show |
G | 8 | a0001c0001t0010g0237a0001c0001t0010g0238a0001c0001t0010g0239others(5): Show | 8 | HG01243.hp1 HG01255.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.853-8944_853-8925d others(22): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32864845 | |||||
| chr3:32864845
|
GGTGTGTG others(17): Show |
G | 4 | a0001c0001t0015g0072a0001c0001t0015g0073a0001c0003t0005g0068others(1): Show | 4 | HG02258.hp2 HG02809.hp1 NA21309.hp1 others(1): Show |
intron_variant | MODIFIER | c.853-8948_853-8925d others(26): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32864845 | |||||
| chr3:32864892
|
G | C | 28 | a0001c0001t0004g0033a0001c0001t0004g0038a0001c0001t0004g0043others(25): Show | 28 | HG00280.hp2 HG00544.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.853-8926G>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32864892 | ||||||
| chr3:32865096
|
G | A | 1 | a0001c0001t0001g0243 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.853-8722G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32865096 | ||||||
| chr3:32865386
|
C | T | 53 | a0001c0001t0001g0037a0001c0001t0001g0049a0001c0001t0001g0127others(50): Show | 53 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.853-8432C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32865386 | ||||||
| chr3:32865410
|
T | G | 1 | a0001c0001t0001g0251 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.853-8408T>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32865410 | ||||||
| chr3:32865419
|
G | A | 28 | a0001c0001t0004g0033a0001c0001t0004g0038a0001c0001t0004g0043others(25): Show | 28 | HG00280.hp2 HG00544.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.853-8399G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32865419 | ||||||
| chr3:32865523
|
C | T | 28 | a0001c0001t0004g0033a0001c0001t0004g0038a0001c0001t0004g0043others(25): Show | 28 | HG00280.hp2 HG00544.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.853-8295C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32865523 | ||||||
| chr3:32865530
|
G | A | 9 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0095others(6): Show | 9 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(6): Show |
intron_variant | MODIFIER | c.853-8288G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32865530 | ||||||
| chr3:32865601
|
A | G | 1 | a0001c0001t0001g0037 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.853-8217A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32865601 | ||||||
| chr3:32865674
|
G | C | 1 | a0001c0001t0001g0095 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.853-8144G>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32865674 | ||||||
| chr3:32865737
|
G | A | 13 | a0001c0001t0001g0233a0001c0001t0001g0249a0001c0001t0002g0235others(10): Show | 13 | HG02258.hp1 HG02559.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.853-8081G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32865737 | ||||||
| chr3:32865790
|
CG | C | 23 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0001t0001g0086others(20): Show | 23 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(20): Show |
intron_variant | MODIFIER | c.853-8026delG | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32865790 | |||||
| chr3:32865791
|
G | GC | 13 | a0001c0001t0002g0320a0001c0001t0004g0161a0001c0001t0004g0296others(10): Show | 13 | HG00438.hp1 HG00544.hp1 HG00597.hp2 others(10): Show |
intron_variant | MODIFIER | c.853-8027_853-8026i others(3): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32865791 | ||||||
| chr3:32865791
|
G | GCC | 9 | a0001c0001t0001g0128a0001c0001t0003g0219a0001c0002t0002g0138others(6): Show | 9 | HG02074.hp1 HG02148.hp2 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.853-8027_853-8026i others(4): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32865791 | ||||||
| chr3:32865791
|
GGC | G | 31 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0148others(28): Show | 31 | HG00140.hp2 HG00280.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.853-8026_853-8025d others(4): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32865791 | ||||||
| chr3:32865791
|
GGCC | G | 31 | a0001c0001t0001g0028a0001c0001t0001g0144a0001c0001t0001g0178others(28): Show | 31 | HG00140.hp1 HG00323.hp1 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.853-8026_853-8024d others(5): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32865791 | ||||||
| chr3:32865791
|
GGCCC | G | 19 | a0001c0001t0001g0241a0001c0001t0001g0247a0001c0001t0003g0146others(16): Show | 20 | HG00099.hp1 HG01069.hp2 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.853-8026_853-8023d others(6): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32865791 | ||||||
| chr3:32865791
|
GGCCCCCC others(3): Show |
G | 5 | a0001c0001t0001g0077a0001c0001t0002g0075a0001c0001t0002g0078others(2): Show | 5 | HG02970.hp1 HG03471.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.853-8026_853-8017d others(12): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32865791 | ||||||
| chr3:32865791
|
GGCCCCCC others(4): Show |
G | 80 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0012others(77): Show | 80 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(77): Show |
intron_variant | MODIFIER | c.853-8026_853-8016d others(13): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32865791 | ||||||
| chr3:32865792
|
G | C | 41 | a0001c0001t0001g0108a0001c0001t0001g0128a0001c0001t0001g0213others(38): Show | 41 | HG00438.hp1 HG00544.hp1 HG00544.hp2 others(38): Show |
intron_variant | MODIFIER | c.853-8026G>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32865792 | ||||||
| chr3:32865792
|
GCC | G | 41 | a0001c0001t0001g0049a0001c0001t0001g0127a0001c0001t0001g0140others(38): Show | 41 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.853-8012_853-8011d others(4): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32865792 | |||||
| chr3:32865796
|
C | A | 2 | a0001c0001t0003g0203a0001c0002t0002g0255 | 2 | HG01192.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.853-8022C>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32865796 | ||||||
| chr3:32865797
|
C | A | 5 | a0001c0001t0003g0171a0001c0001t0014g0248a0001c0001t0014g0252others(2): Show | 5 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.853-8021C>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32865797 | ||||||
| chr3:32865799
|
C | G | 1 | a0001c0001t0003g0202 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.853-8019C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32865799 | ||||||
| chr3:32865803
|
C | A | 1 | a0001c0002t0023g0044 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.853-8015C>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32865803 | ||||||
| chr3:32865808
|
G | C | 1 | a0001c0001t0001g0110 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.853-8010G>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32865808 | ||||||
| chr3:32865813
|
A | G | 1 | a0001c0001t0001g0110 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.853-8005A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32865813 | ||||||
| chr3:32865815
|
C | CCCACCTT others(20): Show |
1 | a0001c0001t0001g0110 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.853-8003_853-8002i others(29): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32865815 | ||||||
| chr3:32865815
|
C | CT | 8 | a0001c0001t0001g0251a0001c0001t0003g0226a0001c0001t0009g0227others(5): Show | 8 | HG01081.hp1 HG01123.hp2 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.853-7975dupT | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32865815 | |||||
| chr3:32865815
|
C | CTT | 36 | a0001c0001t0001g0049a0001c0001t0001g0127a0001c0001t0001g0220others(33): Show | 36 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.853-7976_853-7975d others(4): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32865815 | |||||
| chr3:32865815
|
C | CTTT | 14 | a0001c0001t0001g0037a0001c0001t0001g0140a0001c0001t0003g0056others(11): Show | 14 | HG00280.hp1 HG01952.hp1 HG01978.hp1 others(11): Show |
intron_variant | MODIFIER | c.853-7977_853-7975d others(5): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32865815 | |||||
| chr3:32865815
|
CTT | C | 16 | a0001c0001t0001g0103a0001c0001t0001g0223a0001c0001t0001g0224others(13): Show | 16 | HG01256.hp1 HG01934.hp2 HG02040.hp1 others(13): Show |
intron_variant | MODIFIER | c.853-7976_853-7975d others(4): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32865815 | |||||
| chr3:32865815
|
CTTT | C | 98 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(95): Show | 98 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.853-7977_853-7975d others(5): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32865815 | |||||
| chr3:32865815
|
CTTTT | C | 92 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0026others(89): Show | 93 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(90): Show |
intron_variant | MODIFIER | c.853-7978_853-7975d others(6): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32865815 | |||||
| chr3:32865815
|
CTTTTT | C | 6 | a0001c0001t0001g0128a0001c0001t0007g0123a0001c0001t0008g0277others(3): Show | 6 | HG02132.hp1 HG02148.hp2 HG02155.hp1 others(3): Show |
intron_variant | MODIFIER | c.853-7979_853-7975d others(7): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32865815 | |||||
| chr3:32865815
|
CTTTTTT | C | 28 | a0001c0001t0004g0033a0001c0001t0004g0038a0001c0001t0004g0043others(25): Show | 28 | HG00280.hp2 HG00544.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.853-7980_853-7975d others(8): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32865815 | |||||
| chr3:32865815
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0004g0136 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.853-7985_853-7975d others(13): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32865815 | |||||
| chr3:32865815
|
CTTTTTTT others(5): Show |
C | 3 | a0001c0001t0001g0304a0001c0001t0002g0168a0001c0001t0002g0316 | 3 | HG02886.hp2 HG02896.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.853-7986_853-7975d others(14): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32865815 | |||||
| chr3:32865843
|
T | A | 1 | a0001c0001t0001g0076 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.853-7975T>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32865843 | ||||||
| chr3:32865936
|
C | T | 28 | a0001c0001t0004g0033a0001c0001t0004g0038a0001c0001t0004g0043others(25): Show | 28 | HG00280.hp2 HG00544.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.853-7882C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32865936 | ||||||
| chr3:32865967
|
C | T | 4 | a0001c0001t0001g0011a0001c0001t0018g0283a0001c0003t0005g0025others(1): Show | 4 | HG01884.hp2 HG01934.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.853-7851C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32865967 | ||||||
| chr3:32866133
|
C | T | 81 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0012others(78): Show | 81 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.853-7685C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32866133 | ||||||
| chr3:32866163
|
G | GT | 36 | a0001c0001t0001g0185a0001c0001t0001g0304a0001c0001t0002g0078others(33): Show | 36 | HG00280.hp2 HG00544.hp2 HG02015.hp2 others(33): Show |
intron_variant | MODIFIER | c.853-7645dupT | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32866163 | |||||
| chr3:32866165
|
T | G | 1 | a0001c0001t0001g0110 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.853-7653T>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32866165 | ||||||
| chr3:32866327
|
C | T | 1 | a0001c0001t0001g0251 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.853-7491C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32866327 | ||||||
| chr3:32866374
|
T | A | 10 | a0001c0001t0001g0233a0001c0001t0001g0249a0001c0001t0002g0235others(7): Show | 10 | HG02258.hp1 HG02630.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.853-7444T>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32866374 | ||||||
| chr3:32866507
|
G | A | 10 | a0001c0001t0001g0127a0001c0001t0001g0220a0001c0001t0001g0221others(7): Show | 10 | HG00438.hp2 HG01358.hp2 HG01952.hp2 others(7): Show |
intron_variant | MODIFIER | c.853-7311G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32866507 | ||||||
| chr3:32866518
|
C | T | 2 | a0001c0002t0002g0039a0001c0002t0046g0065 | 2 | HG01978.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.853-7300C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32866518 | ||||||
| chr3:32866701
|
A | G | 3 | a0001c0001t0001g0304a0001c0001t0002g0168a0001c0001t0051g0096 | 3 | HG02896.hp1 HG03453.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.853-7117A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32866701 | ||||||
| chr3:32866744
|
G | T | 9 | a0001c0002t0002g0014a0001c0002t0002g0015a0001c0002t0002g0016others(6): Show | 9 | HG01109.hp2 HG02109.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.853-7074G>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32866744 | ||||||
| chr3:32866941
|
AC | A | 3 | a0001c0001t0001g0230a0001c0001t0006g0232a0001c0001t0033g0149 | 3 | HG02056.hp1 HG02129.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.853-6876delC | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32866941 | ||||||
| chr3:32867001
|
T | A | 3 | a0001c0001t0001g0304a0001c0001t0002g0168a0001c0001t0051g0096 | 3 | HG02896.hp1 HG03453.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.853-6817T>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32867001 | ||||||
| chr3:32867041
|
C | T | 3 | a0001c0001t0003g0226a0001c0001t0009g0227a0001c0001t0009g0228 | 3 | HG01069.hp1 HG01123.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.853-6777C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32867041 | ||||||
| chr3:32867072
|
TC | T | 9 | a0001c0002t0002g0014a0001c0002t0002g0015a0001c0002t0002g0016others(6): Show | 9 | HG01109.hp2 HG02109.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.853-6745delC | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32867072 | ||||||
| chr3:32867140
|
C | T | 153 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(150): Show | 153 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.853-6678C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32867140 | ||||||
| chr3:32867171
|
A | AC | 16 | a0001c0001t0004g0038a0001c0001t0004g0136a0001c0001t0004g0145others(13): Show | 16 | HG00544.hp2 HG00597.hp1 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.853-6641dupC | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32867171 | |||||
| chr3:32867181
|
C | T | 1 | a0001c0002t0002g0324 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.853-6637C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32867181 | ||||||
| chr3:32867188
|
C | T | 322 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(319): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.853-6630C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32867188 | ||||||
| chr3:32867190
|
T | C | 5 | a0001c0001t0001g0012a0001c0001t0002g0067a0001c0001t0018g0099others(2): Show | 5 | HG01934.hp2 HG02559.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.853-6628T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32867190 | ||||||
| chr3:32867344
|
A | G | 1 | a0001c0008t0007g0023 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.853-6474A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32867344 | ||||||
| chr3:32867511
|
G | A | 4 | a0001c0001t0002g0319a0001c0001t0002g0320a0001c0001t0018g0099others(1): Show | 4 | HG02559.hp2 HG02717.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.853-6307G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32867511 | ||||||
| chr3:32867572
|
C | A | 32 | a0001c0001t0003g0041a0001c0001t0004g0033a0001c0001t0004g0038others(29): Show | 32 | HG00280.hp2 HG00544.hp2 HG02015.hp2 others(29): Show |
intron_variant | MODIFIER | c.853-6246C>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32867572 | ||||||
| chr3:32867644
|
A | G | 1 | a0001c0001t0001g0230 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.853-6174A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32867644 | ||||||
| chr3:32867708
|
C | A | 1 | a0001c0001t0008g0273 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.853-6110C>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32867708 | ||||||
| chr3:32867717
|
AT | A | 36 | a0001c0001t0003g0041a0001c0001t0004g0033a0001c0001t0004g0038others(33): Show | 36 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(33): Show |
intron_variant | MODIFIER | c.853-6094delT | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32867717 | |||||
| chr3:32867719
|
T | C | 36 | a0001c0001t0003g0041a0001c0001t0004g0033a0001c0001t0004g0038others(33): Show | 36 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(33): Show |
intron_variant | MODIFIER | c.853-6099T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32867719 | ||||||
| chr3:32867763
|
A | G | 1 | a0001c0001t0001g0221 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.853-6055A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32867763 | ||||||
| chr3:32867778
|
C | G | 36 | a0001c0001t0003g0041a0001c0001t0004g0033a0001c0001t0004g0038others(33): Show | 36 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(33): Show |
intron_variant | MODIFIER | c.853-6040C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32867778 | ||||||
| chr3:32867834
|
T | G | 1 | a0001c0001t0002g0168 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.853-5984T>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32867834 | ||||||
| chr3:32867931
|
T | C | 3 | a0001c0001t0014g0248a0001c0001t0014g0252a0001c0001t0014g0282 | 3 | HG01175.hp2 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.853-5887T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32867931 | ||||||
| chr3:32868028
|
T | G | 1 | a0001c0001t0016g0001 | 2 | HG03139.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.853-5790T>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32868028 | ||||||
| chr3:32868253
|
CT | C | 37 | a0001c0001t0001g0231a0001c0001t0003g0041a0001c0001t0004g0033others(34): Show | 37 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.853-5563delT | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32868253 | |||||
| chr3:32868450
|
A | G | 1 | a0001c0001t0042g0107 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.853-5368A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32868450 | ||||||
| chr3:32868516
|
A | G | 3 | a0001c0001t0001g0049a0001c0002t0023g0044a0001c0002t0023g0052 | 3 | NA18975.hp2 NA18981.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.853-5302A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32868516 | ||||||
| chr3:32868636
|
C | CT | 5 | a0001c0001t0002g0168a0001c0001t0016g0001a0001c0001t0051g0096others(2): Show | 6 | HG00609.hp2 HG01884.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.853-5170dupT | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32868636 | |||||
| chr3:32868661
|
GGAGACAA others(6): Show |
G | 41 | a0001c0001t0001g0231a0001c0001t0003g0041a0001c0001t0004g0033others(38): Show | 41 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.853-5150_853-5138d others(15): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32868661 | |||||
| chr3:32868686
|
G | GT | 34 | a0001c0001t0001g0006a0001c0001t0001g0251a0001c0001t0003g0041others(31): Show | 34 | HG00438.hp2 HG00597.hp1 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.853-5118dupT | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32868686 | |||||
| chr3:32868686
|
G | GTT | 8 | a0001c0001t0001g0231a0001c0001t0004g0061a0001c0001t0004g0218others(5): Show | 8 | HG00280.hp2 HG02040.hp1 NA18964.hp2 others(5): Show |
intron_variant | MODIFIER | c.853-5119_853-5118d others(4): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32868686 | |||||
| chr3:32868688
|
T | A | 1 | a0001c0001t0007g0286 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.853-5130T>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32868688 | ||||||
| chr3:32868699
|
T | A | 3 | a0001c0001t0007g0313a0001c0003t0005g0013a0001c0003t0005g0025 | 3 | HG01934.hp2 HG02572.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.853-5119T>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32868699 | ||||||
| chr3:32868700
|
T | A | 47 | a0001c0001t0001g0011a0001c0001t0001g0026a0001c0001t0001g0076others(44): Show | 48 | HG00323.hp1 HG00639.hp1 HG01167.hp2 others(45): Show |
intron_variant | MODIFIER | c.853-5118T>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32868700 | ||||||
| chr3:32868700
|
TA | T | 5 | a0001c0001t0001g0304a0001c0001t0002g0118a0001c0001t0015g0246others(2): Show | 5 | HG02647.hp2 HG02896.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.853-5112delA | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32868700 | |||||
| chr3:32868701
|
A | C | 1 | a0001c0001t0001g0251 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.853-5117A>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32868701 | ||||||
| chr3:32868701
|
A | T | 57 | a0001c0001t0001g0077a0001c0001t0001g0127a0001c0001t0001g0144others(54): Show | 57 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.853-5117A>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32868701 | ||||||
| chr3:32868702
|
A | T | 4 | a0001c0001t0004g0136a0001c0001t0004g0218a0001c0001t0008g0265others(1): Show | 4 | HG00280.hp2 HG02074.hp2 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.853-5116A>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32868702 | ||||||
| chr3:32868761
|
TA | T | 3 | a0001c0001t0015g0246a0001c0001t0045g0071a0001c0002t0002g0070 | 3 | HG02647.hp2 HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.853-5052delA | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32868761 | |||||
| chr3:32868789
|
T | C | 41 | a0001c0001t0001g0231a0001c0001t0003g0041a0001c0001t0004g0033others(38): Show | 41 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.853-5029T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32868789 | ||||||
| chr3:32868829
|
G | A | 2 | a0001c0001t0016g0001a0001c0008t0007g0023 | 3 | HG01884.hp2 HG03139.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.853-4989G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32868829 | ||||||
| chr3:32868968
|
A | G | 41 | a0001c0001t0001g0231a0001c0001t0003g0041a0001c0001t0004g0033others(38): Show | 41 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.853-4850A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32868968 | ||||||
| chr3:32869050
|
T | C | 15 | a0001c0001t0001g0077a0001c0001t0002g0067a0001c0001t0002g0075others(12): Show | 15 | HG01069.hp1 HG01123.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.853-4768T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32869050 | ||||||
| chr3:32869094
|
G | C | 3 | a0001c0001t0022g0175a0001c0001t0022g0179a0002c0005t0001g0157 | 3 | HG00438.hp1 NA18966.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.853-4724G>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32869094 | ||||||
| chr3:32869294
|
C | G | 4 | a0001c0001t0020g0034a0001c0001t0020g0047a0001c0001t0055g0270others(1): Show | 4 | NA18966.hp2 NA18992.hp2 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.853-4524C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32869294 | ||||||
| chr3:32869332
|
C | G | 3 | a0001c0001t0006g0134a0001c0001t0006g0215a0001c0002t0002g0131 | 3 | HG01993.hp1 HG02132.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.853-4486C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32869332 | ||||||
| chr3:32869397
|
G | A | 36 | a0001c0001t0001g0231a0001c0001t0003g0041a0001c0001t0004g0033others(33): Show | 36 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(33): Show |
intron_variant | MODIFIER | c.853-4421G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32869397 | ||||||
| chr3:32869424
|
T | A | 1 | a0001c0002t0002g0021 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.853-4394T>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32869424 | ||||||
| chr3:32869799
|
G | A | 1 | a0001c0001t0027g0261 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.853-4019G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32869799 | ||||||
| chr3:32869864
|
G | T | 1 | a0001c0001t0001g0110 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.853-3954G>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32869864 | ||||||
| chr3:32869892
|
T | C | 1 | a0001c0002t0002g0207 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.853-3926T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32869892 | ||||||
| chr3:32869906
|
C | T | 8 | a0001c0001t0001g0077a0001c0001t0002g0067a0001c0001t0002g0075others(5): Show | 8 | HG02970.hp1 HG03098.hp1 HG03471.hp1 others(5): Show |
intron_variant | MODIFIER | c.853-3912C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32869906 | ||||||
| chr3:32869912
|
G | A | 6 | a0001c0001t0007g0002a0001c0001t0007g0069a0001c0001t0007g0311others(3): Show | 7 | HG00639.hp1 HG02257.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.853-3906G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32869912 | ||||||
| chr3:32869919
|
A | T | 6 | a0001c0001t0007g0002a0001c0001t0007g0069a0001c0001t0007g0311others(3): Show | 7 | HG00639.hp1 HG02257.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.853-3899A>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32869919 | ||||||
| chr3:32870036
|
G | T | 3 | a0001c0001t0015g0246a0001c0001t0045g0071a0001c0002t0002g0070 | 3 | HG02647.hp2 HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.853-3782G>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32870036 | ||||||
| chr3:32870168
|
A | G | 1 | a0001c0001t0002g0168 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.853-3650A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32870168 | ||||||
| chr3:32870432
|
A | G | 1 | a0001c0001t0004g0143 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.853-3386A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32870432 | ||||||
| chr3:32870528
|
G | C | 1 | a0001c0001t0053g0271 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.853-3290G>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32870528 | ||||||
| chr3:32870836
|
C | T | 1 | a0001c0001t0016g0001 | 2 | HG03139.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.853-2982C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32870836 | ||||||
| chr3:32870896
|
T | G | 1 | a0001c0001t0016g0001 | 2 | HG03139.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.853-2922T>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32870896 | ||||||
| chr3:32870916
|
A | G | 202 | a0001c0001t0001g0011a0001c0001t0001g0049a0001c0001t0001g0076others(199): Show | 204 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.853-2902A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32870916 | ||||||
| chr3:32870968
|
A | AT | 87 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0076others(84): Show | 87 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.853-2833dupT | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32870968 | |||||
| chr3:32870968
|
A | ATT | 8 | a0001c0001t0007g0002a0001c0001t0007g0311a0001c0001t0007g0313others(5): Show | 9 | HG01884.hp2 HG02257.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.853-2834_853-2833d others(4): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32870968 | |||||
| chr3:32870968
|
AT | A | 11 | a0001c0001t0001g0113a0001c0001t0001g0148a0001c0001t0001g0177others(8): Show | 11 | HG01167.hp1 HG01358.hp1 HG01934.hp1 others(8): Show |
intron_variant | MODIFIER | c.853-2833delT | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32870968 | |||||
| chr3:32871107
|
G | A | 1 | a0001c0001t0002g0168 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.853-2711G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32871107 | ||||||
| chr3:32871155
|
A | G | 2 | a0001c0001t0007g0121a0001c0001t0007g0123 | 2 | HG02451.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.853-2663A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32871155 | ||||||
| chr3:32871159
|
A | G | 1 | a0001c0001t0008g0276 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.853-2659A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32871159 | ||||||
| chr3:32871258
|
C | T | 48 | a0001c0001t0001g0231a0001c0001t0001g0251a0001c0001t0003g0041others(45): Show | 49 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.853-2560C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32871258 | ||||||
| chr3:32871292
|
C | G | 1 | a0001c0001t0004g0161 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.853-2526C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32871292 | ||||||
| chr3:32871313
|
T | C | 1 | a0001c0001t0001g0026 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.853-2505T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32871313 | ||||||
| chr3:32871345
|
A | T | 5 | a0001c0001t0001g0144a0001c0001t0001g0176a0001c0001t0001g0178others(2): Show | 5 | HG00735.hp2 HG01071.hp1 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.853-2473A>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32871345 | ||||||
| chr3:32871355
|
C | A | 2 | a0001c0001t0014g0248a0001c0001t0014g0252 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.853-2463C>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32871355 | ||||||
| chr3:32871422
|
C | T | 1 | a0001c0003t0005g0308 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.853-2396C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32871422 | ||||||
| chr3:32871514
|
C | T | 1 | a0001c0001t0007g0286 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.853-2304C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32871514 | ||||||
| chr3:32871588
|
C | G | 2 | a0001c0001t0012g0153a0001c0007t0012g0137 | 2 | HG00323.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.853-2230C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32871588 | ||||||
| chr3:32871601
|
T | C | 191 | a0001c0001t0001g0011a0001c0001t0001g0049a0001c0001t0001g0076others(188): Show | 193 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.853-2217T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32871601 | ||||||
| chr3:32871910
|
A | G | 1 | a0001c0001t0026g0066 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.853-1908A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32871910 | ||||||
| chr3:32872002
|
G | A | 1 | a0001c0001t0031g0151 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.853-1816G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32872002 | ||||||
| chr3:32872096
|
G | A | 1 | a0001c0001t0057g0272 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.853-1722G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32872096 | ||||||
| chr3:32872122
|
C | T | 48 | a0001c0001t0001g0231a0001c0001t0001g0251a0001c0001t0003g0041others(45): Show | 49 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.853-1696C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32872122 | ||||||
| chr3:32872160
|
CAAAT | C | 10 | a0001c0001t0012g0153a0001c0002t0002g0014a0001c0002t0002g0015others(7): Show | 10 | HG01109.hp2 HG01167.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.853-1654_853-1651d others(6): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32872160 | |||||
| chr3:32872212
|
A | T | 322 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(319): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.853-1606A>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32872212 | ||||||
| chr3:32872246
|
G | C | 41 | a0001c0001t0001g0231a0001c0001t0003g0041a0001c0001t0004g0033others(38): Show | 41 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.853-1572G>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32872246 | ||||||
| chr3:32872266
|
G | A | 3 | a0001c0001t0016g0001a0001c0001t0051g0096a0001c0008t0007g0023 | 4 | HG01884.hp2 HG03139.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.853-1552G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32872266 | ||||||
| chr3:32872404
|
T | C | 1 | a0001c0001t0002g0319 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.853-1414T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32872404 | ||||||
| chr3:32872518
|
T | A | 1 | a0001c0001t0001g0231 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.853-1300T>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32872518 | ||||||
| chr3:32872820
|
G | C | 1 | a0001c0001t0039g0024 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.853-998G>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32872820 | ||||||
| chr3:32872914
|
C | G | 1 | a0001c0003t0005g0013 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.853-904C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32872914 | ||||||
| chr3:32873056
|
T | TCTCCCTC others(9): Show |
1 | a0001c0001t0002g0118 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.853-759_853-758ins others(16): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32873056 | |||||
| chr3:32873056
|
TCTCTCTT others(5): Show |
T | 2 | a0001c0001t0001g0249a0001c0001t0038g0318 | 2 | HG03041.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.853-758_853-747del others(12): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32873056 | |||||
| chr3:32873059
|
CTCTT | C | 3 | a0001c0001t0018g0099a0001c0001t0018g0283a0001c0002t0023g0052 | 3 | HG02559.hp2 NA18906.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.853-758_853-755del others(4): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32873059 | ||||||
| chr3:32873060
|
T | C | 2 | a0001c0001t0001g0304a0001c0001t0002g0118 | 2 | HG02896.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.853-758T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32873060 | ||||||
| chr3:32873060
|
T | TCTCCCTC others(5): Show |
1 | a0001c0001t0001g0077 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.853-756_853-755ins others(12): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32873060 | |||||
| chr3:32873060
|
TCTTC | T | 4 | a0001c0001t0004g0033a0001c0001t0004g0161a0001c0002t0002g0155others(1): Show | 4 | NA18992.hp1 NA19003.hp2 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.853-755_853-752del others(4): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32873060 | |||||
| chr3:32873060
|
TCTTCCTC others(1): Show |
T | 34 | a0001c0001t0001g0012a0001c0001t0001g0141a0001c0001t0001g0142others(31): Show | 34 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.853-755_853-748del others(8): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32873060 | |||||
| chr3:32873060
|
TCTTCCTC others(9): Show |
T | 1 | a0001c0001t0014g0282 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.853-755_853-740del others(16): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32873060 | |||||
| chr3:32873063
|
T | C | 10 | a0001c0001t0001g0077a0001c0001t0001g0304a0001c0001t0002g0118others(7): Show | 10 | HG01256.hp2 HG01258.hp1 HG02698.hp2 others(7): Show |
intron_variant | MODIFIER | c.853-755T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32873063 | ||||||
| chr3:32873063
|
T | TCCTC | 125 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(122): Show | 125 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.853-724_853-721dup others(4): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32873063 | |||||
| chr3:32873063
|
T | TCCTCCCT others(1): Show |
15 | a0001c0001t0001g0199a0001c0001t0006g0134a0001c0001t0006g0150others(12): Show | 15 | HG00140.hp1 HG00558.hp2 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.853-728_853-721dup others(8): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32873063 | |||||
| chr3:32873063
|
T | TCCTCCCT others(5): Show |
22 | a0001c0001t0001g0007a0001c0001t0001g0050a0001c0001t0001g0055others(19): Show | 22 | HG00099.hp2 HG00558.hp1 HG00621.hp1 others(19): Show |
intron_variant | MODIFIER | c.853-732_853-721dup others(12): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32873063 | |||||
| chr3:32873063
|
T | TCCTCCCT others(9): Show |
2 | a0001c0001t0009g0089a0001c0001t0009g0188 | 2 | HG03239.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.853-736_853-721dup others(16): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32873063 | |||||
| chr3:32873063
|
T | TCCTCCCT others(13): Show |
4 | a0001c0001t0001g0049a0001c0001t0016g0001a0001c0001t0045g0071others(1): Show | 5 | HG02647.hp2 HG03139.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.853-740_853-721dup others(20): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32873063 | |||||
| chr3:32873063
|
T | TCCTCCCT others(17): Show |
5 | a0001c0001t0002g0078a0001c0001t0002g0234a0001c0001t0007g0286others(2): Show | 5 | HG02559.hp1 HG02809.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.853-744_853-721dup others(24): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32873063 | |||||
| chr3:32873063
|
T | TCCTCCCT others(21): Show |
1 | a0001c0001t0002g0075 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.853-748_853-721dup others(28): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32873063 | |||||
| chr3:32873063
|
TCCTC | T | 46 | a0001c0001t0001g0009a0001c0001t0001g0088a0001c0001t0001g0125others(43): Show | 46 | HG00438.hp2 HG00597.hp1 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.853-724_853-721del others(4): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32873063 | |||||
| chr3:32873063
|
TCCTCCCT others(1): Show |
T | 6 | a0001c0001t0001g0205a0001c0001t0001g0251a0001c0002t0002g0062others(3): Show | 6 | HG01081.hp1 HG01109.hp1 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.853-728_853-721del others(8): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32873063 | |||||
| chr3:32873063
|
TCCTCCCT others(5): Show |
T | 1 | a0001c0001t0002g0235 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.853-732_853-721del others(12): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 32873063 | |||||
| chr3:32873116
|
G | A | 10 | a0001c0001t0001g0077a0001c0001t0002g0067a0001c0001t0002g0075others(7): Show | 10 | HG02559.hp1 HG02809.hp2 HG02970.hp1 others(7): Show |
intron_variant | MODIFIER | c.853-702G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32873116 | ||||||
| chr3:32873161
|
C | G | 1 | a0001c0001t0002g0083 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.853-657C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32873161 | ||||||
| chr3:32873362
|
A | G | 1 | a0001c0001t0026g0321 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.853-456A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32873362 | ||||||
| chr3:32873589
|
C | T | 9 | a0001c0001t0002g0067a0001c0001t0002g0075a0001c0001t0002g0078others(6): Show | 9 | HG02559.hp1 HG02809.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.853-229C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32873589 | ||||||
| chr3:32873605
|
T | G | 8 | a0001c0001t0003g0226a0001c0001t0009g0089a0001c0001t0009g0115others(5): Show | 8 | HG01069.hp1 HG01123.hp2 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.853-213T>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32873605 | ||||||
| chr3:32873722
|
C | G | 322 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(319): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.853-96C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32873722 | ||||||
| chr3:32873726
|
C | T | 1 | a0001c0001t0007g0069 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.853-92C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32873726 | ||||||
| chr3:32873804
|
T | G | 10 | a0001c0001t0001g0009a0001c0001t0001g0037a0001c0001t0001g0127others(7): Show | 10 | HG00544.hp2 HG00621.hp1 HG02129.hp1 others(7): Show |
intron_variant | MODIFIER | c.853-14T>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32873804 | ||||||
| chr3:32873811
|
T | C | 3 | a0001c0001t0010g0237a0001c0001t0010g0238a0001c0001t0010g0239 | 3 | HG01243.hp1 HG01255.hp2 HG01891.hp1 |
splice_region_variant&intron_variant | LOW | c.853-7T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 1/3 | chr3 | 32873811 | ||||||
| chr3:32874150
|
C | T | 1 | a0001c0001t0001g0317 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1020+165C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32874150 | ||||||
| chr3:32874165
|
G | C | 8 | a0001c0001t0003g0226a0001c0001t0009g0089a0001c0001t0009g0115others(5): Show | 8 | HG01069.hp1 HG01123.hp2 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.1020+180G>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32874165 | ||||||
| chr3:32874183
|
G | C | 42 | a0001c0001t0003g0041a0001c0001t0004g0033a0001c0001t0004g0038others(39): Show | 42 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.1020+198G>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32874183 | ||||||
| chr3:32874320
|
C | CTTA | 9 | a0001c0001t0004g0033a0001c0001t0004g0054a0001c0001t0004g0057others(6): Show | 9 | NA18945.hp1 NA18966.hp2 NA18969.hp2 others(6): Show |
intron_variant | MODIFIER | c.1020+339_1020+341d others(5): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 32874320 | |||||
| chr3:32874320
|
C | CTTATTA | 27 | a0001c0001t0003g0041a0001c0001t0004g0038a0001c0001t0004g0043others(24): Show | 27 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(24): Show |
intron_variant | MODIFIER | c.1020+336_1020+341d others(8): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 32874320 | |||||
| chr3:32874320
|
CTTA | C | 16 | a0001c0001t0001g0077a0001c0001t0001g0100a0001c0001t0001g0233others(13): Show | 16 | HG00323.hp1 HG01167.hp2 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.1020+339_1020+341d others(5): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 32874320 | |||||
| chr3:32874321
|
TTATTAC | T | 16 | a0001c0001t0015g0072a0001c0001t0015g0073a0001c0002t0002g0111others(13): Show | 16 | HG01109.hp1 HG01891.hp2 HG01934.hp2 others(13): Show |
intron_variant | MODIFIER | c.1020+339_1020+344d others(8): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 32874321 | |||||
| chr3:32874324
|
T | C | 9 | a0001c0001t0001g0011a0001c0001t0001g0249a0001c0001t0001g0251others(6): Show | 9 | HG01081.hp1 HG02615.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.1020+339T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32874324 | ||||||
| chr3:32874324
|
T | TTAC | 4 | a0001c0001t0001g0127a0001c0001t0001g0185a0001c0003t0005g0097others(1): Show | 4 | HG02559.hp1 HG02809.hp2 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.1020+382_1020+384d others(5): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 32874324 | |||||
| chr3:32874324
|
T | TTATTAC | 3 | a0001c0001t0004g0143a0001c0001t0004g0152a0001c0001t0004g0214 | 3 | NA18953.hp1 NA18994.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.1020+341_1020+342i others(8): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 32874324 | |||||
| chr3:32874324
|
T | TTATTATT others(2): Show |
3 | a0001c0001t0006g0030a0001c0001t0006g0040a0001c0001t0008g0278 | 3 | NA19007.hp2 NA19056.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.1020+341_1020+342i others(11): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 32874324 | |||||
| chr3:32874324
|
TTAC | T | 97 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0026others(94): Show | 97 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.1020+382_1020+384d others(5): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 32874324 | |||||
| chr3:32874324
|
TTACTAC | T | 48 | a0001c0001t0001g0012a0001c0001t0001g0049a0001c0001t0003g0226others(45): Show | 48 | HG00544.hp1 HG00609.hp1 HG01069.hp1 others(45): Show |
intron_variant | MODIFIER | c.1020+379_1020+384d others(8): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 32874324 | |||||
| chr3:32874324
|
TTACTACT others(2): Show |
T | 4 | a0001c0001t0015g0246a0001c0001t0016g0001a0001c0001t0045g0071others(1): Show | 5 | HG02647.hp2 HG03139.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.1020+376_1020+384d others(11): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 32874324 | |||||
| chr3:32874324
|
TTACTACT others(8): Show |
T | 1 | a0001c0001t0001g0004 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1020+370_1020+384d others(17): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 32874324 | |||||
| chr3:32874327
|
C | T | 12 | a0001c0001t0004g0033a0001c0001t0004g0054a0001c0001t0004g0057others(9): Show | 12 | HG01243.hp1 HG01255.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.1020+342C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32874327 | ||||||
| chr3:32874330
|
C | T | 3 | a0001c0001t0010g0237a0001c0001t0010g0238a0001c0001t0010g0239 | 3 | HG01243.hp1 HG01255.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.1020+345C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32874330 | ||||||
| chr3:32874352
|
TACTACTA others(11): Show |
T | 3 | a0001c0001t0010g0237a0001c0001t0010g0238a0001c0001t0010g0239 | 3 | HG01243.hp1 HG01255.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.1020+370_1020+387d others(20): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 32874352 | |||||
| chr3:32874358
|
TACTACTA others(5): Show |
T | 1 | a0001c0003t0005g0308 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1020+376_1020+387d others(14): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 32874358 | |||||
| chr3:32874364
|
T | A | 33 | a0001c0001t0001g0011a0001c0001t0001g0077a0001c0001t0001g0100others(30): Show | 33 | HG00323.hp1 HG01081.hp1 HG01167.hp2 others(30): Show |
intron_variant | MODIFIER | c.1020+379T>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32874364 | ||||||
| chr3:32874367
|
T | A | 110 | a0001c0001t0001g0011a0001c0001t0001g0049a0001c0001t0001g0077others(107): Show | 110 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.1020+382T>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32874367 | ||||||
| chr3:32874367
|
T | TACA | 12 | a0001c0001t0003g0114a0001c0001t0003g0163a0001c0001t0003g0166others(9): Show | 13 | HG01123.hp1 HG01175.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.1020+386_1020+388d others(5): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 32874367 | |||||
| chr3:32874370
|
A | T | 42 | a0001c0001t0003g0041a0001c0001t0004g0033a0001c0001t0004g0038others(39): Show | 42 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.1020+385A>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32874370 | ||||||
| chr3:32874559
|
G | C | 1 | a0001c0001t0003g0192 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1020+574G>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32874559 | ||||||
| chr3:32874663
|
C | G | 1 | a0001c0001t0001g0012 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1020+678C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32874663 | ||||||
| chr3:32874667
|
C | A | 42 | a0001c0001t0003g0041a0001c0001t0004g0033a0001c0001t0004g0038others(39): Show | 42 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.1020+682C>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32874667 | ||||||
| chr3:32874672
|
A | G | 42 | a0001c0001t0003g0041a0001c0001t0004g0033a0001c0001t0004g0038others(39): Show | 42 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.1020+687A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32874672 | ||||||
| chr3:32874841
|
A | T | 2 | a0001c0002t0002g0126a0001c0002t0002g0154 | 2 | HG00423.hp2 NA18948.hp1 |
intron_variant | MODIFIER | c.1020+856A>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32874841 | ||||||
| chr3:32874907
|
G | A | 3 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0017g0260 | 3 | HG02080.hp1 NA19009.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.1020+922G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32874907 | ||||||
| chr3:32874966
|
G | A | 2 | a0001c0001t0003g0171a0001c0001t0003g0203 | 2 | HG02055.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1020+981G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32874966 | ||||||
| chr3:32875035
|
G | A | 30 | a0001c0001t0001g0240a0001c0001t0001g0241a0001c0001t0003g0053others(27): Show | 30 | HG00099.hp1 HG00735.hp1 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.1020+1050G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32875035 | ||||||
| chr3:32875225
|
C | T | 1 | a0001c0001t0001g0212 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1020+1240C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32875225 | ||||||
| chr3:32875229
|
A | G | 1 | a0001c0001t0001g0012 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1020+1244A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32875229 | ||||||
| chr3:32875476
|
A | G | 45 | a0001c0001t0003g0041a0001c0001t0004g0033a0001c0001t0004g0038others(42): Show | 45 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(42): Show |
intron_variant | MODIFIER | c.1020+1491A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32875476 | ||||||
| chr3:32875547
|
G | A | 45 | a0001c0001t0003g0041a0001c0001t0004g0033a0001c0001t0004g0038others(42): Show | 45 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(42): Show |
intron_variant | MODIFIER | c.1020+1562G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32875547 | ||||||
| chr3:32875596
|
G | T | 45 | a0001c0001t0003g0041a0001c0001t0004g0033a0001c0001t0004g0038others(42): Show | 45 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(42): Show |
intron_variant | MODIFIER | c.1020+1611G>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32875596 | ||||||
| chr3:32875664
|
A | G | 1 | a0001c0001t0004g0145 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1020+1679A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32875664 | ||||||
| chr3:32875910
|
A | C | 1 | a0001c0001t0001g0006 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1020+1925A>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32875910 | ||||||
| chr3:32875923
|
G | A | 111 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0009others(108): Show | 111 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.1020+1938G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32875923 | ||||||
| chr3:32875925
|
T | A | 1 | a0001c0001t0001g0006 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1020+1940T>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32875925 | ||||||
| chr3:32876016
|
T | C | 21 | a0001c0001t0001g0011a0001c0001t0001g0077a0001c0001t0001g0100others(18): Show | 21 | HG00323.hp1 HG01081.hp1 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.1020+2031T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32876016 | ||||||
| chr3:32876090
|
T | C | 2 | a0001c0002t0001g0236a0001c0002t0002g0324 | 2 | HG02258.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1020+2105T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32876090 | ||||||
| chr3:32876252
|
C | T | 1 | a0001c0001t0002g0118 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1020+2267C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32876252 | ||||||
| chr3:32876382
|
G | A | 1 | a0001c0001t0033g0149 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1020+2397G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32876382 | ||||||
| chr3:32876413
|
G | A | 1 | a0001c0001t0001g0133 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1020+2428G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32876413 | ||||||
| chr3:32876562
|
C | T | 7 | a0001c0001t0002g0067a0001c0001t0002g0075a0001c0001t0002g0078others(4): Show | 7 | HG02970.hp1 HG03098.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.1020+2577C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32876562 | ||||||
| chr3:32876582
|
T | TCAAA | 5 | a0001c0002t0002g0042a0001c0002t0002g0124a0001c0002t0002g0211others(2): Show | 5 | HG00544.hp1 NA18962.hp2 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.1020+2608_1020+261 others(8): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 32876582 | |||||
| chr3:32876667
|
A | G | 2 | a0001c0001t0001g0076a0001c0001t0051g0096 | 2 | HG03471.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1020+2682A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32876667 | ||||||
| chr3:32876718
|
G | A | 1 | a0001c0008t0007g0023 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1020+2733G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32876718 | ||||||
| chr3:32876743
|
C | T | 42 | a0001c0001t0003g0041a0001c0001t0004g0033a0001c0001t0004g0038others(39): Show | 42 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.1020+2758C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32876743 | ||||||
| chr3:32876745
|
C | A | 9 | a0001c0001t0007g0002a0001c0001t0007g0069a0001c0001t0007g0098others(6): Show | 10 | HG00639.hp1 HG01884.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1020+2760C>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32876745 | ||||||
| chr3:32876969
|
G | A | 15 | a0001c0003t0005g0013a0001c0003t0005g0025a0001c0003t0005g0068others(12): Show | 15 | HG01891.hp2 HG01934.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.1020+2984G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32876969 | ||||||
| chr3:32877005
|
G | C | 1 | a0001c0002t0013g0258 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1020+3020G>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32877005 | ||||||
| chr3:32877234
|
G | C | 2 | a0001c0003t0005g0117a0001c0003t0005g0323 | 2 | HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1020+3249G>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32877234 | ||||||
| chr3:32877369
|
G | T | 1 | a0001c0001t0001g0141 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1020+3384G>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32877369 | ||||||
| chr3:32877404
|
A | AT | 40 | a0001c0001t0001g0011a0001c0001t0001g0077a0001c0001t0001g0100others(37): Show | 40 | HG00323.hp1 HG01081.hp1 HG01167.hp2 others(37): Show |
intron_variant | MODIFIER | c.1020+3430dupT | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 32877404 | |||||
| chr3:32877404
|
A | T | 1 | a0001c0001t0002g0234 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1020+3419A>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32877404 | ||||||
| chr3:32877434
|
C | G | 1 | a0001c0001t0008g0275 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1020+3449C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32877434 | ||||||
| chr3:32877483
|
G | A | 11 | a0001c0001t0001g0076a0001c0001t0002g0074a0001c0001t0002g0118others(8): Show | 11 | HG02145.hp1 HG02451.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.1020+3498G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32877483 | ||||||
| chr3:32877578
|
C | T | 9 | a0001c0001t0002g0067a0001c0001t0002g0075a0001c0001t0002g0078others(6): Show | 9 | HG02970.hp1 HG03098.hp1 HG03098.hp2 others(6): Show |
intron_variant | MODIFIER | c.1020+3593C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32877578 | ||||||
| chr3:32877699
|
A | G | 42 | a0001c0001t0003g0041a0001c0001t0004g0033a0001c0001t0004g0038others(39): Show | 42 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.1020+3714A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32877699 | ||||||
| chr3:32877795
|
C | T | 3 | a0001c0001t0007g0098a0001c0001t0007g0121a0001c0001t0007g0123 | 3 | HG02451.hp2 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1020+3810C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32877795 | ||||||
| chr3:32878254
|
C | T | 9 | a0001c0001t0002g0067a0001c0001t0002g0075a0001c0001t0002g0078others(6): Show | 9 | HG02970.hp1 HG03098.hp1 HG03098.hp2 others(6): Show |
intron_variant | MODIFIER | c.1020+4269C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32878254 | ||||||
| chr3:32878327
|
C | T | 1 | a0001c0001t0010g0244 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1020+4342C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32878327 | ||||||
| chr3:32878366
|
T | A | 1 | a0001c0001t0001g0116 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1020+4381T>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32878366 | ||||||
| chr3:32878624
|
A | AAATG | 25 | a0001c0001t0001g0011a0001c0001t0001g0077a0001c0001t0001g0100others(22): Show | 25 | HG00323.hp1 HG01081.hp1 HG01167.hp2 others(22): Show |
intron_variant | MODIFIER | c.1020+4643_1020+464 others(8): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 32878624 | |||||
| chr3:32878808
|
A | G | 1 | a0001c0001t0051g0096 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1020+4823A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32878808 | ||||||
| chr3:32878865
|
C | A | 3 | a0001c0001t0010g0237a0001c0001t0010g0238a0001c0001t0010g0239 | 3 | HG01243.hp1 HG01255.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.1020+4880C>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32878865 | ||||||
| chr3:32878888
|
C | G | 55 | a0001c0001t0002g0067a0001c0001t0002g0075a0001c0001t0002g0078others(52): Show | 55 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.1020+4903C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32878888 | ||||||
| chr3:32879018
|
C | T | 37 | a0001c0001t0003g0041a0001c0001t0004g0033a0001c0001t0004g0038others(34): Show | 37 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.1020+5033C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32879018 | ||||||
| chr3:32879082
|
TGTTTTCT others(2): Show |
T | 9 | a0001c0001t0007g0002a0001c0001t0007g0069a0001c0001t0007g0098others(6): Show | 10 | HG00639.hp1 HG01884.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1020+5098_1020+510 others(13): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32879082 | ||||||
| chr3:32879110
|
G | C | 172 | a0001c0001t0001g0011a0001c0001t0001g0049a0001c0001t0001g0077others(169): Show | 173 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.1020+5125G>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32879110 | ||||||
| chr3:32879112
|
C | G | 46 | a0001c0001t0002g0067a0001c0001t0002g0075a0001c0001t0002g0078others(43): Show | 46 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.1020+5127C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32879112 | ||||||
| chr3:32879288
|
C | T | 4 | a0001c0001t0016g0001a0001c0001t0045g0071a0001c0002t0002g0070others(1): Show | 5 | HG02630.hp1 HG02647.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1020+5303C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32879288 | ||||||
| chr3:32879402
|
C | T | 1 | a0001c0001t0007g0286 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1020+5417C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32879402 | ||||||
| chr3:32879409
|
C | G | 122 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(119): Show | 122 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.1020+5424C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32879409 | ||||||
| chr3:32879430
|
A | G | 2 | a0001c0001t0018g0099a0001c0001t0018g0283 | 2 | HG02559.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1020+5445A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32879430 | ||||||
| chr3:32879550
|
T | C | 9 | a0001c0001t0007g0002a0001c0001t0007g0069a0001c0001t0007g0098others(6): Show | 10 | HG00639.hp1 HG01884.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1020+5565T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32879550 | ||||||
| chr3:32879654
|
C | G | 1 | a0001c0001t0001g0103 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1020+5669C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32879654 | ||||||
| chr3:32879672
|
TA | T | 45 | a0001c0001t0001g0076a0001c0001t0001g0240a0001c0001t0001g0241others(42): Show | 46 | HG00099.hp1 HG00639.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.1020+5703delA | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 32879672 | |||||
| chr3:32879672
|
TAA | T | 182 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(179): Show | 183 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.1020+5702_1020+570 others(6): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 32879672 | |||||
| chr3:32879672
|
TAAA | T | 41 | a0001c0001t0001g0006a0001c0001t0003g0041a0001c0001t0004g0033others(38): Show | 41 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.1020+5701_1020+570 others(7): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 32879672 | |||||
| chr3:32879675
|
A | T | 4 | a0001c0002t0002g0289a0001c0002t0002g0293a0001c0002t0002g0294others(1): Show | 4 | NA18945.hp2 NA18973.hp1 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.1020+5690A>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32879675 | ||||||
| chr3:32879684
|
A | C | 39 | a0001c0001t0001g0011a0001c0001t0001g0077a0001c0001t0001g0100others(36): Show | 39 | HG00323.hp1 HG01081.hp1 HG01167.hp2 others(36): Show |
intron_variant | MODIFIER | c.1020+5699A>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32879684 | ||||||
| chr3:32879687
|
A | T | 9 | a0001c0001t0010g0237a0001c0001t0010g0238a0001c0001t0010g0239others(6): Show | 10 | HG01243.hp1 HG01255.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.1020+5702A>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32879687 | ||||||
| chr3:32879696
|
A | T | 1 | a0001c0002t0002g0131 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1020+5711A>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32879696 | ||||||
| chr3:32879987
|
T | C | 2 | a0001c0001t0018g0099a0001c0001t0018g0283 | 2 | HG02559.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1021-5947T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32879987 | ||||||
| chr3:32879998
|
T | C | 4 | a0001c0001t0016g0001a0001c0001t0045g0071a0001c0002t0002g0070others(1): Show | 5 | HG02630.hp1 HG02647.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1021-5936T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32879998 | ||||||
| chr3:32880094
|
G | C | 9 | a0001c0001t0007g0002a0001c0001t0007g0069a0001c0001t0007g0098others(6): Show | 10 | HG00639.hp1 HG01884.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1021-5840G>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32880094 | ||||||
| chr3:32880276
|
G | A | 8 | a0001c0001t0012g0008a0001c0001t0012g0063a0001c0001t0012g0153others(5): Show | 8 | HG00323.hp1 HG01167.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1021-5658G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32880276 | ||||||
| chr3:32880390
|
C | T | 1 | a0002c0005t0001g0157 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1021-5544C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32880390 | ||||||
| chr3:32880435
|
T | A | 1 | a0001c0001t0007g0098 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1021-5499T>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32880435 | ||||||
| chr3:32880504
|
T | A | 1 | a0001c0001t0002g0118 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1021-5430T>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32880504 | ||||||
| chr3:32880511
|
A | T | 1 | a0001c0001t0001g0181 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1021-5423A>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32880511 | ||||||
| chr3:32880826
|
A | G | 3 | a0001c0001t0010g0237a0001c0001t0010g0238a0001c0001t0010g0239 | 3 | HG01243.hp1 HG01255.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.1021-5108A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32880826 | ||||||
| chr3:32880917
|
G | T | 3 | a0001c0001t0016g0080a0001c0001t0026g0066a0001c0001t0026g0321 | 3 | HG02723.hp1 HG02965.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1021-5017G>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32880917 | ||||||
| chr3:32880968
|
A | G | 1 | a0001c0001t0001g0213 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1021-4966A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32880968 | ||||||
| chr3:32881009
|
TTA | T | 4 | a0001c0001t0016g0001a0001c0001t0045g0071a0001c0002t0002g0070others(1): Show | 5 | HG02630.hp1 HG02647.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1021-4919_1021-491 others(6): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 32881009 | |||||
| chr3:32881017
|
G | GTA | 8 | a0001c0001t0002g0075a0001c0001t0002g0078a0001c0001t0002g0234others(5): Show | 8 | HG02559.hp1 HG02809.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.1021-4905_1021-490 others(6): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 32881017 | |||||
| chr3:32881029
|
A | ATT | 38 | a0001c0001t0002g0083a0001c0001t0002g0315a0001c0001t0003g0041others(35): Show | 38 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.1021-4899_1021-489 others(6): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 32881029 | |||||
| chr3:32881029
|
A | T | 15 | a0001c0001t0006g0029a0001c0001t0006g0030a0001c0001t0006g0040others(12): Show | 15 | HG00609.hp2 HG01243.hp1 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.1021-4905A>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32881029 | ||||||
| chr3:32881031
|
T | A | 4 | a0001c0001t0001g0076a0001c0001t0018g0099a0001c0001t0018g0283others(1): Show | 4 | HG02559.hp2 HG03471.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1021-4903T>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32881031 | ||||||
| chr3:32881093
|
A | C | 54 | a0001c0001t0001g0049a0001c0001t0001g0220a0001c0001t0001g0221others(51): Show | 54 | HG00140.hp1 HG00544.hp1 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.1021-4841A>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32881093 | ||||||
| chr3:32881310
|
C | T | 8 | a0001c0001t0007g0002a0001c0001t0007g0098a0001c0001t0007g0121others(5): Show | 9 | HG01884.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1021-4624C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32881310 | ||||||
| chr3:32881692
|
A | G | 1 | a0001c0001t0016g0080 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1021-4242A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32881692 | ||||||
| chr3:32881839
|
G | T | 8 | a0001c0001t0002g0075a0001c0001t0002g0078a0001c0001t0002g0083others(5): Show | 8 | HG02970.hp1 HG03098.hp2 HG03471.hp1 others(5): Show |
intron_variant | MODIFIER | c.1021-4095G>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32881839 | ||||||
| chr3:32881846
|
C | T | 2 | a0001c0001t0001g0076a0001c0001t0051g0096 | 2 | HG03471.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1021-4088C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32881846 | ||||||
| chr3:32881852
|
T | A | 2 | a0001c0001t0001g0240a0001c0001t0001g0241 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1021-4082T>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32881852 | ||||||
| chr3:32881924
|
T | C | 1 | a0001c0001t0002g0316 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1021-4010T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32881924 | ||||||
| chr3:32881934
|
T | C | 217 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(214): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.1021-4000T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32881934 | ||||||
| chr3:32882148
|
C | CA | 28 | a0001c0001t0001g0240a0001c0001t0001g0241a0001c0001t0003g0053others(25): Show | 28 | HG00099.hp1 HG00735.hp1 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.1021-3785dupA | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 32882148 | |||||
| chr3:32882179
|
C | CT | 45 | a0001c0001t0002g0075a0001c0001t0002g0078a0001c0001t0002g0083others(42): Show | 45 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(42): Show |
intron_variant | MODIFIER | c.1021-3746dupT | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 32882179 | |||||
| chr3:32882188
|
T | C | 8 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0028others(5): Show | 8 | HG00140.hp2 HG00741.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.1021-3746T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32882188 | ||||||
| chr3:32882257
|
TAGAA | T | 37 | a0001c0001t0003g0041a0001c0001t0004g0033a0001c0001t0004g0038others(34): Show | 37 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.1021-3674_1021-367 others(8): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 32882257 | |||||
| chr3:32882542
|
T | C | 2 | a0001c0001t0045g0071a0001c0003t0005g0117 | 2 | HG02630.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1021-3392T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32882542 | ||||||
| chr3:32882598
|
C | T | 18 | a0001c0001t0001g0011a0001c0001t0001g0076a0001c0001t0002g0067others(15): Show | 18 | HG01192.hp1 HG02145.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.1021-3336C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32882598 | ||||||
| chr3:32882727
|
A | G | 1 | a0001c0001t0009g0242 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1021-3207A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32882727 | ||||||
| chr3:32882733
|
G | A | 91 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0002g0083others(88): Show | 91 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.1021-3201G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32882733 | ||||||
| chr3:32882803
|
G | A | 322 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(319): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.1021-3131G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32882803 | ||||||
| chr3:32882845
|
A | G | 2 | a0001c0001t0045g0071a0001c0003t0005g0117 | 2 | HG02630.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1021-3089A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32882845 | ||||||
| chr3:32882882
|
A | C | 139 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(136): Show | 139 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.1021-3052A>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32882882 | ||||||
| chr3:32882892
|
A | T | 1 | a0001c0001t0027g0261 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1021-3042A>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32882892 | ||||||
| chr3:32882985
|
C | A | 9 | a0001c0002t0002g0014a0001c0002t0002g0015a0001c0002t0002g0016others(6): Show | 9 | HG01109.hp2 HG02109.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1021-2949C>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32882985 | ||||||
| chr3:32883019
|
ACT | A | 4 | a0001c0001t0009g0167a0001c0001t0009g0227a0001c0001t0009g0228others(1): Show | 4 | HG01069.hp1 HG01123.hp2 HG01167.hp1 others(1): Show |
intron_variant | MODIFIER | c.1021-2910_1021-290 others(6): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 32883019 | |||||
| chr3:32883034
|
G | A | 37 | a0001c0001t0003g0041a0001c0001t0004g0033a0001c0001t0004g0038others(34): Show | 37 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.1021-2900G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32883034 | ||||||
| chr3:32883091
|
T | A | 1 | a0001c0002t0002g0255 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1021-2843T>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32883091 | ||||||
| chr3:32883110
|
A | T | 3 | a0001c0001t0002g0083a0001c0001t0002g0315a0001c0003t0005g0308 | 3 | HG03516.hp1 HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1021-2824A>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32883110 | ||||||
| chr3:32883249
|
T | C | 2 | a0001c0001t0004g0061a0001c0001t0004g0296 | 2 | NA18969.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.1021-2685T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32883249 | ||||||
| chr3:32883310
|
C | T | 14 | a0001c0003t0005g0013a0001c0003t0005g0025a0001c0003t0005g0068others(11): Show | 14 | HG01891.hp2 HG01934.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.1021-2624C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32883310 | ||||||
| chr3:32883312
|
G | A | 3 | a0001c0001t0003g0171a0001c0001t0003g0203a0001c0001t0003g0253 | 3 | HG00735.hp1 HG02055.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1021-2622G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32883312 | ||||||
| chr3:32883330
|
A | G | 1 | a0001c0001t0001g0249 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1021-2604A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32883330 | ||||||
| chr3:32883375
|
C | T | 1 | a0001c0001t0001g0233 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1021-2559C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32883375 | ||||||
| chr3:32883542
|
C | A | 13 | a0001c0001t0002g0067a0001c0001t0002g0074a0001c0001t0002g0075others(10): Show | 13 | HG02145.hp1 HG02451.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.1021-2392C>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32883542 | ||||||
| chr3:32884098
|
C | T | 3 | a0001c0001t0002g0083a0001c0001t0002g0315a0001c0003t0005g0308 | 3 | HG03516.hp1 HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1021-1836C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32884098 | ||||||
| chr3:32884298
|
A | G | 1 | a0001c0001t0006g0150 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1021-1636A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32884298 | ||||||
| chr3:32884314
|
T | C | 3 | a0001c0001t0002g0083a0001c0001t0002g0315a0001c0003t0005g0308 | 3 | HG03516.hp1 HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1021-1620T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32884314 | ||||||
| chr3:32884317
|
T | C | 3 | a0001c0001t0010g0237a0001c0001t0010g0238a0001c0001t0010g0239 | 3 | HG01243.hp1 HG01255.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.1021-1617T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32884317 | ||||||
| chr3:32884433
|
C | G | 107 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(104): Show | 107 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.1021-1501C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32884433 | ||||||
| chr3:32884456
|
T | G | 40 | a0001c0001t0002g0083a0001c0001t0002g0315a0001c0001t0003g0041others(37): Show | 40 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.1021-1478T>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32884456 | ||||||
| chr3:32884540
|
GA | G | 318 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(315): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.1021-1380delA | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 32884540 | |||||
| chr3:32884574
|
A | G | 1 | a0001c0001t0012g0008 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1021-1360A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32884574 | ||||||
| chr3:32884613
|
C | T | 1 | a0001c0002t0002g0106 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1021-1321C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32884613 | ||||||
| chr3:32884614
|
G | T | 14 | a0001c0003t0005g0013a0001c0003t0005g0025a0001c0003t0005g0068others(11): Show | 14 | HG01891.hp2 HG01934.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.1021-1320G>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32884614 | ||||||
| chr3:32884668
|
G | C | 1 | a0001c0001t0002g0316 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1021-1266G>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32884668 | ||||||
| chr3:32884671
|
T | C | 6 | a0001c0001t0002g0074a0001c0001t0002g0305a0001c0001t0002g0309others(3): Show | 6 | HG02145.hp1 HG02451.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1021-1263T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32884671 | ||||||
| chr3:32885058
|
C | A | 1 | a0001c0001t0045g0071 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1021-876C>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32885058 | ||||||
| chr3:32885063
|
C | T | 1 | a0001c0001t0001g0076 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1021-871C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32885063 | ||||||
| chr3:32885284
|
T | TTTTTATG | 40 | a0001c0001t0002g0083a0001c0001t0002g0315a0001c0001t0003g0041others(37): Show | 40 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.1021-650_1021-649i others(9): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32885284 | ||||||
| chr3:32885491
|
C | T | 3 | a0001c0001t0002g0083a0001c0001t0002g0315a0001c0003t0005g0308 | 3 | HG03516.hp1 HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1021-443C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32885491 | ||||||
| chr3:32885494
|
G | A | 15 | a0001c0003t0005g0013a0001c0003t0005g0025a0001c0003t0005g0068others(12): Show | 15 | HG01891.hp2 HG01934.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.1021-440G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32885494 | ||||||
| chr3:32885496
|
C | T | 9 | a0001c0001t0007g0002a0001c0001t0007g0098a0001c0001t0007g0121others(6): Show | 10 | HG01884.hp2 HG02257.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1021-438C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32885496 | ||||||
| chr3:32885575
|
G | T | 1 | a0001c0001t0003g0191 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1021-359G>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32885575 | ||||||
| chr3:32885660
|
G | C | 1 | a0001c0001t0002g0316 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1021-274G>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32885660 | ||||||
| chr3:32885833
|
G | A | 9 | a0001c0002t0002g0014a0001c0002t0002g0015a0001c0002t0002g0016others(6): Show | 9 | HG01109.hp2 HG02109.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1021-101G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32885833 | ||||||
| chr3:32885908
|
G | A | 67 | a0001c0002t0001g0236a0001c0002t0002g0014a0001c0002t0002g0015others(64): Show | 67 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.1021-26G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 2/3 | chr3 | 32885908 | ||||||
| chr3:32886180
|
A | G | 2 | a0001c0003t0005g0117a0001c0003t0005g0323 | 2 | HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1155+112A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | chr3 | 32886180 | ||||||
| chr3:32886310
|
T | C | 2 | a0001c0001t0018g0099a0001c0001t0018g0283 | 2 | HG02559.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1155+242T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | chr3 | 32886310 | ||||||
| chr3:32886468
|
C | T | 15 | a0001c0003t0005g0013a0001c0003t0005g0025a0001c0003t0005g0068others(12): Show | 15 | HG01891.hp2 HG01934.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.1155+400C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | chr3 | 32886468 | ||||||
| chr3:32886593
|
A | G | 3 | a0001c0001t0010g0237a0001c0001t0010g0238a0001c0001t0010g0239 | 3 | HG01243.hp1 HG01255.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.1155+525A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | chr3 | 32886593 | ||||||
| chr3:32886672
|
A | G | 32 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0002t0002g0032others(29): Show | 32 | HG00423.hp2 HG00597.hp2 HG00621.hp2 others(29): Show |
intron_variant | MODIFIER | c.1155+604A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | chr3 | 32886672 | ||||||
| chr3:32887322
|
A | G | 1 | a0001c0001t0008g0273 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1155+1254A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | chr3 | 32887322 | ||||||
| chr3:32887422
|
T | C | 1 | a0001c0003t0005g0308 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1155+1354T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | chr3 | 32887422 | ||||||
| chr3:32887481
|
C | CT | 39 | a0001c0001t0002g0074a0001c0001t0002g0305a0001c0001t0002g0309others(36): Show | 40 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.1155+1434dupT | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr3 | 32887481 | |||||
| chr3:32887481
|
CT | C | 86 | a0001c0001t0001g0011a0001c0001t0001g0076a0001c0001t0001g0077others(83): Show | 87 | HG00423.hp2 HG00544.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1155+1434delT | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr3 | 32887481 | |||||
| chr3:32887481
|
CTT | C | 137 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(134): Show | 137 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.1155+1433_1155+143 others(6): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr3 | 32887481 | |||||
| chr3:32887623
|
T | C | 115 | a0001c0001t0003g0041a0001c0001t0003g0053a0001c0001t0003g0056others(112): Show | 117 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.1155+1555T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | chr3 | 32887623 | ||||||
| chr3:32887660
|
C | G | 1 | a0001c0001t0001g0189 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1155+1592C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | chr3 | 32887660 | ||||||
| chr3:32887711
|
C | CAT | 3 | a0001c0001t0016g0001a0001c0001t0016g0080a0001c0001t0045g0071 | 4 | HG02647.hp2 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1155+1651_1155+165 others(6): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr3 | 32887711 | |||||
| chr3:32887783
|
C | T | 1 | a0001c0001t0001g0009 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1155+1715C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | chr3 | 32887783 | ||||||
| chr3:32887789
|
T | C | 3 | a0001c0001t0001g0100a0001c0001t0001g0304a0001c0001t0001g0317 | 3 | HG02622.hp2 HG02896.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1155+1721T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | chr3 | 32887789 | ||||||
| chr3:32887836
|
A | G | 1 | a0001c0001t0007g0286 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1155+1768A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | chr3 | 32887836 | ||||||
| chr3:32887850
|
G | A | 9 | a0001c0001t0009g0089a0001c0001t0009g0115a0001c0001t0009g0164others(6): Show | 9 | HG00140.hp1 HG01069.hp1 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.1155+1782G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | chr3 | 32887850 | ||||||
| chr3:32887991
|
A | G | 1 | a0001c0002t0002g0207 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1155+1923A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | chr3 | 32887991 | ||||||
| chr3:32888105
|
T | C | 1 | a0001c0001t0002g0118 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1155+2037T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | chr3 | 32888105 | ||||||
| chr3:32888208
|
T | G | 1 | a0001c0001t0051g0096 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1155+2140T>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | chr3 | 32888208 | ||||||
| chr3:32888407
|
G | A | 1 | a0001c0001t0020g0034 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1156-1953G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | chr3 | 32888407 | ||||||
| chr3:32888427
|
T | C | 1 | a0001c0001t0009g0188 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1156-1933T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | chr3 | 32888427 | ||||||
| chr3:32888434
|
CAAAAAAA others(3): Show |
C | 10 | a0001c0001t0002g0067a0001c0001t0002g0074a0001c0001t0002g0075others(7): Show | 10 | HG02040.hp2 HG02145.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1156-1896_1156-188 others(14): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr3 | 32888434 | |||||
| chr3:32888434
|
CAAAAAAA others(4): Show |
C | 31 | a0001c0001t0002g0234a0001c0001t0002g0235a0001c0001t0002g0309others(28): Show | 31 | HG00438.hp2 HG01891.hp2 HG01934.hp2 others(28): Show |
intron_variant | MODIFIER | c.1156-1897_1156-188 others(15): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr3 | 32888434 | |||||
| chr3:32888434
|
CAAAAAAA others(5): Show |
C | 43 | a0001c0001t0002g0305a0001c0001t0002g0310a0001c0001t0002g0320others(40): Show | 43 | HG00280.hp2 HG00597.hp1 HG01106.hp2 others(40): Show |
intron_variant | MODIFIER | c.1156-1898_1156-188 others(16): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr3 | 32888434 | |||||
| chr3:32888434
|
CAAAAAAA others(6): Show |
C | 58 | a0001c0001t0001g0148a0001c0001t0001g0178a0001c0001t0001g0220others(55): Show | 58 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.1156-1899_1156-188 others(17): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr3 | 32888434 | |||||
| chr3:32888434
|
CAAAAAAA others(7): Show |
C | 17 | a0001c0001t0001g0085a0001c0001t0001g0095a0001c0001t0001g0110others(14): Show | 17 | HG01175.hp1 HG01255.hp1 HG01981.hp1 others(14): Show |
intron_variant | MODIFIER | c.1156-1900_1156-188 others(18): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr3 | 32888434 | |||||
| chr3:32888434
|
CAAAAAAA others(8): Show |
C | 97 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(94): Show | 98 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(95): Show |
intron_variant | MODIFIER | c.1156-1901_1156-188 others(19): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr3 | 32888434 | |||||
| chr3:32888434
|
CAAAAAAA others(9): Show |
C | 6 | a0001c0001t0001g0088a0001c0001t0001g0140a0001c0001t0001g0304others(3): Show | 6 | HG00280.hp1 HG02735.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1156-1902_1156-188 others(20): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr3 | 32888434 | |||||
| chr3:32888434
|
CAAAAAAA others(10): Show |
C | 9 | a0001c0001t0007g0002a0001c0001t0007g0069a0001c0001t0007g0098others(6): Show | 10 | HG00639.hp1 HG01884.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1156-1903_1156-188 others(21): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr3 | 32888434 | |||||
| chr3:32888434
|
CAAAAAAA others(12): Show |
C | 1 | a0001c0001t0002g0118 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1156-1905_1156-188 others(23): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr3 | 32888434 | |||||
| chr3:32888434
|
CAAAAAAA others(16): Show |
C | 36 | a0001c0001t0003g0041a0001c0001t0003g0053a0001c0001t0003g0056others(33): Show | 36 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.1156-1909_1156-188 others(27): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr3 | 32888434 | |||||
| chr3:32888434
|
CAAAAAAA others(20): Show |
C | 1 | a0001c0001t0009g0188 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1156-1913_1156-188 others(31): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr3 | 32888434 | |||||
| chr3:32888473
|
A | T | 106 | a0001c0001t0003g0041a0001c0001t0003g0053a0001c0001t0003g0056others(103): Show | 108 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.1156-1887A>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | chr3 | 32888473 | ||||||
| chr3:32888532
|
T | TTTG | 14 | a0001c0001t0001g0011a0001c0001t0001g0076a0001c0001t0001g0077others(11): Show | 15 | HG02258.hp2 HG02647.hp2 HG02818.hp2 others(12): Show |
intron_variant | MODIFIER | c.1156-1807_1156-180 others(7): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr3 | 32888532 | |||||
| chr3:32888622
|
C | A | 1 | a0001c0001t0008g0268 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1156-1738C>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | chr3 | 32888622 | ||||||
| chr3:32888702
|
G | A | 118 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(115): Show | 118 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(115): Show |
intron_variant | MODIFIER | c.1156-1658G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | chr3 | 32888702 | ||||||
| chr3:32888755
|
G | A | 13 | a0001c0001t0001g0011a0001c0001t0001g0076a0001c0001t0001g0077others(10): Show | 13 | HG01081.hp1 HG02258.hp2 HG02818.hp2 others(10): Show |
intron_variant | MODIFIER | c.1156-1605G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | chr3 | 32888755 | ||||||
| chr3:32888839
|
T | A | 37 | a0001c0001t0003g0041a0001c0001t0003g0053a0001c0001t0003g0056others(34): Show | 37 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.1156-1521T>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | chr3 | 32888839 | ||||||
| chr3:32888893
|
G | A | 19 | a0001c0001t0016g0001a0001c0001t0016g0080a0001c0001t0045g0071others(16): Show | 20 | HG01891.hp2 HG01934.hp2 HG02559.hp1 others(17): Show |
intron_variant | MODIFIER | c.1156-1467G>A | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | chr3 | 32888893 | ||||||
| chr3:32889007
|
C | T | 4 | a0001c0003t0005g0068a0001c0003t0005g0284a0001c0003t0005g0285others(1): Show | 4 | HG02647.hp1 HG02809.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1156-1353C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | chr3 | 32889007 | ||||||
| chr3:32889077
|
C | G | 1 | a0001c0001t0001g0189 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1156-1283C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | chr3 | 32889077 | ||||||
| chr3:32889338
|
C | T | 55 | a0001c0001t0003g0041a0001c0001t0003g0053a0001c0001t0003g0056others(52): Show | 56 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(53): Show |
intron_variant | MODIFIER | c.1156-1022C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | chr3 | 32889338 | ||||||
| chr3:32889360
|
C | T | 1 | a0001c0001t0021g0172 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1156-1000C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | chr3 | 32889360 | ||||||
| chr3:32889501
|
G | GTAA | 55 | a0001c0001t0003g0041a0001c0001t0003g0053a0001c0001t0003g0056others(52): Show | 56 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(53): Show |
intron_variant | MODIFIER | c.1156-856_1156-854d others(5): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr3 | 32889501 | |||||
| chr3:32889513
|
C | G | 1 | a0001c0001t0001g0140 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1156-847C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | chr3 | 32889513 | ||||||
| chr3:32889548
|
C | T | 6 | a0001c0001t0010g0237a0001c0001t0010g0238a0001c0001t0010g0239others(3): Show | 6 | HG01243.hp1 HG01255.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.1156-812C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | chr3 | 32889548 | ||||||
| chr3:32889559
|
A | AATT | 125 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0026others(122): Show | 125 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.1156-758_1156-756d others(5): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr3 | 32889559 | |||||
| chr3:32889559
|
A | AATTATT | 23 | a0001c0001t0001g0110a0001c0001t0001g0181a0001c0001t0001g0216others(20): Show | 23 | HG00140.hp1 HG00323.hp1 HG01123.hp1 others(20): Show |
intron_variant | MODIFIER | c.1156-761_1156-756d others(8): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr3 | 32889559 | |||||
| chr3:32889559
|
A | AATTATTA others(2): Show |
4 | a0001c0001t0003g0203a0001c0001t0008g0276a0001c0001t0008g0278others(1): Show | 4 | HG00609.hp2 HG02055.hp1 HG02080.hp2 others(1): Show |
intron_variant | MODIFIER | c.1156-764_1156-756d others(11): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr3 | 32889559 | |||||
| chr3:32889559
|
AATT | A | 37 | a0001c0001t0002g0315a0001c0001t0007g0002a0001c0001t0007g0121others(34): Show | 39 | HG00423.hp2 HG00597.hp2 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.1156-758_1156-756d others(5): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr3 | 32889559 | |||||
| chr3:32889559
|
AATTATT | A | 7 | a0001c0001t0001g0037a0001c0001t0001g0197a0001c0001t0001g0198others(4): Show | 7 | NA18747.hp2 NA18966.hp1 NA18979.hp1 others(4): Show |
intron_variant | MODIFIER | c.1156-761_1156-756d others(8): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr3 | 32889559 | |||||
| chr3:32889617
|
C | T | 1 | a0001c0002t0002g0154 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1156-743C>T | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | chr3 | 32889617 | ||||||
| chr3:32889628
|
C | G | 105 | a0001c0001t0003g0041a0001c0001t0003g0053a0001c0001t0003g0056others(102): Show | 107 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.1156-732C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | chr3 | 32889628 | ||||||
| chr3:32889645
|
A | G | 6 | a0001c0001t0007g0002a0001c0001t0007g0069a0001c0001t0007g0311others(3): Show | 7 | HG00639.hp1 HG01884.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1156-715A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | chr3 | 32889645 | ||||||
| chr3:32889766
|
T | C | 1 | a0001c0001t0001g0224 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1156-594T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | chr3 | 32889766 | ||||||
| chr3:32889843
|
A | G | 54 | a0001c0001t0003g0041a0001c0001t0003g0053a0001c0001t0003g0056others(51): Show | 55 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.1156-517A>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | chr3 | 32889843 | ||||||
| chr3:32889886
|
A | ATG | 7 | a0001c0001t0002g0316a0001c0001t0010g0237a0001c0001t0010g0238others(4): Show | 7 | HG01243.hp1 HG01255.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.1156-460_1156-459d others(4): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr3 | 32889886 | |||||
| chr3:32889898
|
GTGTA | G | 35 | a0001c0001t0003g0041a0001c0001t0003g0053a0001c0001t0003g0056others(32): Show | 35 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.1156-442_1156-439d others(6): Show |
TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr3 | 32889898 | |||||
| chr3:32890173
|
C | G | 16 | a0001c0003t0005g0013a0001c0003t0005g0025a0001c0003t0005g0068others(13): Show | 16 | HG01891.hp2 HG01934.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.1156-187C>G | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | chr3 | 32890173 | ||||||
| chr3:32890179
|
T | C | 2 | a0001c0002t0002g0155a0001c0002t0002g0156 | 2 | NA19003.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.1156-181T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | chr3 | 32890179 | ||||||
| chr3:32890257
|
T | C | 4 | a0001c0001t0001g0247a0001c0001t0001g0249a0001c0001t0001g0251others(1): Show | 4 | HG01081.hp1 HG01981.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1156-103T>C | TRIM71 | ENSG00000206557.6 | transcript | ENST00000383763.6 | protein_coding | 3/3 | chr3 | 32890257 |