Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 440730 |
|---|---|
| ensemblid | ENSG00000119283.16 |
| hgncid | 31859 |
| symbol | TRIM67 |
| name | tripartite motif containing 67 |
| refseq_nuc | NM_001004342.5 |
| refseq_prot | NP_001004342.3 |
| ensembl_nuc | ENST00000366653.6 |
| ensembl_prot | ENSP00000355613.5 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 231162058 |
| end | 231221565 |
| strand | + |
| ver | v1.2 |
| region | chr1:231162058-231221565 |
| region5000 | chr1:231157058-231226565 |
| regionname0 | TRIM67_chr1_231162058_231221565 |
| regionname5000 | TRIM67_chr1_231157058_231226565 |
| 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 | 783 | 344 | 88 | 63 | 146 | 12 | 33 | 100 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0002 | 0/0 | 783 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0003 | 0/0 | 783 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0004 | 0/0 | 783 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0005 | 0/0 | 783 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0006 | 0/0 | 783 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0007 | 0/0 | 783 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0008 | 0/0 | 783 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| 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 | 1/1 | 2352 | 211 | 47 | 50 | 80 | 11 | 21 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| c0002 | 0/0 | 2352 | 50 | 13 | 1 | 28 | 0 | 8 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| c0003 | 0/0 | 2352 | 44 | 1 | 9 | 32 | 0 | 2 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| c0004 | 0/0 | 2352 | 19 | 18 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| c0005 | 0/0 | 2352 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| c0006 | 0/0 | 2352 | 3 | 0 | 2 | 0 | 1 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| c0007 | 0/0 | 2352 | 3 | 0 | 3 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| c0008 | 0/0 | 2352 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| c0009 | 0/0 | 2352 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| c0010 | 0/0 | 2352 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| c0011 | 0/0 | 2352 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| c0012 | 0/0 | 2352 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| c0013 | 0/0 | 2352 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| c0014 | 0/0 | 2352 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| c0015 | 0/0 | 2352 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| c0016 | 0/0 | 2352 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| c0017 | 0/0 | 2352 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| c0018 | 0/0 | 2352 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| c0019 | 0/0 | 2352 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| c0020 | 0/0 | 2352 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| c0021 | 0/0 | 2352 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| c0022 | 0/0 | 2352 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| c0023 | 0/0 | 2352 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| c0024 | 0/0 | 2352 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| c0025 | 0/0 | 2352 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| c0026 | 0/0 | 2352 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| 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 | 0/1 | 7038 | 103 | 18 | 29 | 36 | 5 | 14 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| t0002 | 0/0 | 7038 | 36 | 1 | 7 | 25 | 2 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| t0003 | 0/0 | 7038 | 26 | 0 | 0 | 19 | 0 | 7 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| t0004 | 0/0 | 7038 | 25 | 3 | 8 | 8 | 1 | 5 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| t0005 | 0/0 | 7039 | 23 | 16 | 1 | 6 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| t0006 | 0/0 | 7038 | 22 | 0 | 5 | 16 | 0 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| t0007 | 0/0 | 7038 | 12 | 0 | 3 | 8 | 0 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| t0008 | 0/0 | 7038 | 7 | 5 | 1 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| t0009 | 0/0 | 7039 | 7 | 7 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| t0010 | 0/0 | 7039 | 6 | 6 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| t0011 | 0/0 | 7038 | 5 | 0 | 0 | 5 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| t0012 | 0/0 | 7038 | 5 | 0 | 0 | 5 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| t0013 | 0/0 | 7038 | 4 | 4 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| t0014 | 0/0 | 7038 | 4 | 0 | 0 | 4 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| t0015 | 0/0 | 7038 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| t0016 | 0/0 | 7038 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| t0017 | 0/0 | 7038 | 3 | 2 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| t0018 | 0/0 | 7038 | 3 | 0 | 3 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| t0019 | 0/0 | 7038 | 3 | 0 | 3 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| t0020 | 0/0 | 7038 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| t0021 | 0/0 | 7039 | 3 | 0 | 0 | 2 | 0 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| t0022 | 0/0 | 7039 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| t0023 | 0/0 | 7038 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| t0024 | 0/0 | 7035 | 2 | 0 | 0 | 0 | 1 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| t0025 | 0/0 | 7038 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| t0026 | 0/0 | 7038 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| t0027 | 0/0 | 7038 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| t0028 | 1/0 | 7038 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| t0029 | 0/0 | 7038 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| t0030 | 0/0 | 7038 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| t0031 | 0/0 | 7038 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| t0032 | 0/0 | 7038 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| t0033 | 0/0 | 7038 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| t0034 | 0/0 | 7039 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| t0035 | 0/0 | 7039 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| t0036 | 0/0 | 7039 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| t0037 | 0/0 | 7039 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| t0038 | 0/0 | 7039 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| t0039 | 0/0 | 7038 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| t0040 | 0/0 | 7038 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| t0041 | 0/0 | 7038 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| t0042 | 0/0 | 7038 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| t0043 | 0/0 | 7038 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| t0044 | 0/0 | 7038 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| t0045 | 0/0 | 7035 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| t0046 | 0/0 | 7038 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| t0047 | 0/0 | 7038 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| t0048 | 0/0 | 7038 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| t0049 | 0/0 | 7038 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| t0050 | 0/0 | 7038 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| t0051 | 0/0 | 7038 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| t0052 | 0/0 | 7038 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| t0053 | 0/0 | 7035 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| t0054 | 0/0 | 7038 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| t0055 | 0/0 | 7038 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| t0056 | 0/0 | 7039 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| t0057 | 0/0 | 7038 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| t0058 | 0/0 | 7038 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| t0059 | 0/0 | 7038 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| t0060 | 0/0 | 7038 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| t0061 | 0/0 | 7038 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| t0062 | 0/0 | 7038 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| t0063 | 0/0 | 7038 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| 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 | 0 | 1 | 0 | 0 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0003 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0038 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0048 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| 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 | 1/1 | 2352 | 211 | 47 | 50 | 80 | 11 | 21 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0001c0002 | 0/0 | 2352 | 50 | 13 | 1 | 28 | 0 | 8 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0001c0003 | 0/0 | 2352 | 44 | 1 | 9 | 32 | 0 | 2 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0001c0004 | 0/0 | 2352 | 19 | 18 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0001c0005 | 0/0 | 2352 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0001c0006 | 0/0 | 2352 | 3 | 0 | 2 | 0 | 1 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0001c0009 | 0/0 | 2352 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0001c0010 | 0/0 | 2352 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0001c0011 | 0/0 | 2352 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0001c0012 | 0/0 | 2352 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0001c0014 | 0/0 | 2352 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0001c0017 | 0/0 | 2352 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0001c0018 | 0/0 | 2352 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0001c0019 | 0/0 | 2352 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0001c0020 | 0/0 | 2352 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0001c0022 | 0/0 | 2352 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0001c0023 | 0/0 | 2352 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0001c0024 | 0/0 | 2352 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0001c0026 | 0/0 | 2352 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0002c0007 | 0/0 | 2352 | 3 | 0 | 3 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0003c0008 | 0/0 | 2352 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0004c0013 | 0/0 | 2352 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0005c0021 | 0/0 | 2352 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0006c0025 | 0/0 | 2352 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0007c0016 | 0/0 | 2352 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0008c0015 | 0/0 | 2352 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 9389 | 89 | 13 | 27 | 34 | 4 | 10 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0001c0001t0002 | 0/0 | 9389 | 36 | 1 | 7 | 25 | 2 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0001c0001t0004 | 0/0 | 9389 | 23 | 1 | 8 | 8 | 1 | 5 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0001c0001t0005 | 0/0 | 9390 | 8 | 8 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0001c0001t0008 | 0/0 | 9389 | 7 | 5 | 1 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0001c0001t0011 | 0/0 | 9389 | 5 | 0 | 0 | 5 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0001c0001t0013 | 0/0 | 9389 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0001c0001t0014 | 0/0 | 9389 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0001c0001t0015 | 0/0 | 9389 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0001c0001t0016 | 0/0 | 9389 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0001c0001t0017 | 0/0 | 9389 | 3 | 2 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0001c0001t0018 | 0/0 | 9389 | 3 | 0 | 3 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0001c0001t0022 | 0/0 | 9390 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0001c0001t0023 | 0/0 | 9389 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0001c0001t0024 | 0/0 | 9386 | 2 | 0 | 0 | 0 | 1 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0001c0001t0025 | 0/0 | 9389 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0001c0001t0026 | 0/0 | 9389 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0001c0001t0027 | 0/0 | 9389 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0001c0001t0028 | 1/0 | 9389 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0001c0001t0029 | 0/0 | 9389 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0001c0001t0030 | 0/0 | 9389 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0001c0001t0032 | 0/0 | 9389 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0001c0001t0034 | 0/0 | 9390 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0001c0001t0037 | 0/0 | 9390 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0001c0001t0040 | 0/0 | 9389 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0001c0001t0043 | 0/0 | 9389 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0001c0001t0044 | 0/0 | 9389 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0001c0001t0045 | 0/0 | 9386 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0001c0001t0046 | 0/0 | 9389 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0001c0001t0047 | 0/0 | 9389 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0001c0001t0048 | 0/0 | 9389 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0001c0001t0049 | 0/0 | 9389 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0001c0001t0050 | 0/0 | 9389 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0001c0001t0052 | 0/0 | 9389 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0001c0001t0053 | 0/0 | 9386 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0001c0001t0054 | 0/0 | 9389 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0001c0001t0062 | 0/0 | 9389 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0001c0001t0063 | 0/0 | 9389 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0001c0002t0001 | 0/0 | 9389 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0001c0002t0003 | 0/0 | 9389 | 24 | 0 | 0 | 17 | 0 | 7 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0001c0002t0005 | 0/0 | 9390 | 12 | 5 | 1 | 6 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0001c0002t0009 | 0/0 | 9390 | 7 | 7 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0001c0002t0014 | 0/0 | 9389 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0001c0002t0036 | 0/0 | 9390 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0001c0002t0038 | 0/0 | 9390 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0001c0002t0051 | 0/0 | 9389 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0001c0003t0006 | 0/0 | 9389 | 21 | 0 | 5 | 15 | 0 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0001c0003t0007 | 0/0 | 9389 | 12 | 0 | 3 | 8 | 0 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0001c0003t0012 | 0/0 | 9389 | 5 | 0 | 0 | 5 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0001c0003t0055 | 0/0 | 9389 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0001c0003t0056 | 0/0 | 9390 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0001c0003t0057 | 0/0 | 9389 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0001c0003t0058 | 0/0 | 9389 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0001c0003t0059 | 0/0 | 9389 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0001c0003t0060 | 0/0 | 9389 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0001c0004t0001 | 0/0 | 9389 | 4 | 4 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0001c0004t0005 | 0/0 | 9390 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0001c0004t0010 | 0/0 | 9390 | 5 | 5 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0001c0004t0013 | 0/0 | 9389 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0001c0004t0015 | 0/0 | 9389 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0001c0004t0020 | 0/0 | 9389 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0001c0004t0041 | 0/0 | 9389 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0001c0005t0021 | 0/0 | 9390 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0001c0005t0061 | 0/0 | 9389 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0001c0006t0001 | 0/0 | 9389 | 3 | 0 | 2 | 0 | 1 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0001c0009t0005 | 0/0 | 9390 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0001c0009t0035 | 0/0 | 9390 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0001c0010t0021 | 0/0 | 9390 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0001c0011t0006 | 0/0 | 9389 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0001c0012t0004 | 0/0 | 9389 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0001c0014t0016 | 0/0 | 9389 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0001c0017t0001 | 0/0 | 9389 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0001c0018t0003 | 0/0 | 9389 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0001c0019t0033 | 0/0 | 9389 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0001c0020t0001 | 0/0 | 9389 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0001c0022t0005 | 0/0 | 9390 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0001c0023t0039 | 0/0 | 9389 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0001c0024t0004 | 0/0 | 9389 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0001c0026t0042 | 0/0 | 9389 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0002c0007t0019 | 0/0 | 9389 | 3 | 0 | 3 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0003c0008t0001 | 0/0 | 9389 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0004c0013t0001 | 0/0 | 9389 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0005c0021t0031 | 0/0 | 9389 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0006c0025t0010 | 0/0 | 9390 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0007c0016t0001 | 0/0 | 9389 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| a0008c0015t0003 | 0/0 | 9389 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | copy fasta | chr1 | 231157058 | 231226565 |
| 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 | 2 | 1 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0001g0038 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0002g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0002g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0004g0001 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0004g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0004g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0004g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0004g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0004g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0004g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0004g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0004g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0004g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0004g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0004g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0004g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0004g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0004g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0004g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0004g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0004g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0004g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0004g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0004g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0004g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0005g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0005g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0005g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0005g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0005g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0005g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0005g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0005g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0008g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0008g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0008g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0008g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0008g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0008g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0008g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0011g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0011g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0011g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0011g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0011g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0013g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0014g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0015g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0016g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0016g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0017g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0017g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0017g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0018g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0018g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0018g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0022g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0022g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0023g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0023g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0024g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0024g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0025g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0025g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0026g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0026g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0027g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0027g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0028g0048 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0029g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0030g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0032g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0034g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0037g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0040g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0043g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0044g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0045g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0046g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0047g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0048g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0049g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0050g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0052g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0053g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0054g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0062g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0001t0063g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0002t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0002t0003g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0002t0003g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0002t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0002t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0002t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0002t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0002t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0002t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0002t0003g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0002t0003g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0002t0003g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0002t0003g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0002t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0002t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0002t0003g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0002t0003g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0002t0003g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0002t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0002t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0002t0003g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0002t0003g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0002t0003g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0002t0003g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0002t0005g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0002t0005g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0002t0005g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0002t0005g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0002t0005g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0002t0005g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0002t0005g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0002t0005g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0002t0005g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0002t0005g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0002t0005g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0002t0005g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0002t0009g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0002t0009g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0002t0009g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0002t0009g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0002t0009g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0002t0009g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0002t0009g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0002t0014g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0002t0014g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0002t0014g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0002t0036g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0002t0038g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0002t0051g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0003t0006g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0003t0006g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0003t0006g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0003t0006g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0003t0006g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0003t0006g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0003t0006g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0003t0006g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0003t0006g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0003t0006g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0003t0006g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0003t0006g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0003t0006g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0003t0006g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0003t0006g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0003t0006g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0003t0006g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0003t0006g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0003t0006g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0003t0006g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0003t0006g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0003t0007g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0003t0007g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0003t0007g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0003t0007g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0003t0007g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0003t0007g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0003t0007g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0003t0007g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0003t0007g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0003t0007g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0003t0007g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0003t0007g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0003t0012g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0003t0012g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0003t0012g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0003t0012g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0003t0012g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0003t0055g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0003t0056g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0003t0057g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0003t0058g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0003t0059g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0003t0060g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0004t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0004t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0004t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0004t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0004t0005g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0004t0010g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0004t0010g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0004t0010g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0004t0010g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0004t0010g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0004t0013g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0004t0013g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0004t0013g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0004t0015g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0004t0015g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0004t0020g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0004t0020g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0004t0020g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0004t0041g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0005t0021g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0005t0021g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0005t0061g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0006t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0006t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0006t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0009t0005g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0009t0035g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0010t0021g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0011t0006g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0012t0004g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0014t0016g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0017t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0018t0003g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0019t0033g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0020t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0022t0005g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0023t0039g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0024t0004g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0001c0026t0042g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0002c0007t0019g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0002c0007t0019g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0003c0008t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0003c0008t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0004c0013t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0005c0021t0031g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0006c0025t0010g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0007c0016t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| a0008c0015t0003g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0264 | EUR | GBR | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0030 | EUR | GBR | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG00140 | hp1 | a0001 | c0001 | t0043 | g0262 | EUR | GBR | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG00140 | hp2 | a0001 | c0001 | t0004 | g0152 | EUR | GBR | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG00280 | hp1 | a0001 | c0001 | t0024 | g0247 | EUR | FIN | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0232 | EUR | FIN | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG00323 | hp1 | a0001 | c0006 | t0001 | g0305 | EUR | FIN | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG00323 | hp2 | a0001 | c0001 | t0045 | g0169 | EUR | FIN | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | CHS | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG00408 | hp2 | a0001 | c0002 | t0003 | g0257 | EAS | CHS | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG00423 | hp1 | a0001 | c0002 | t0003 | g0317 | EAS | CHS | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG00423 | hp2 | a0001 | c0003 | t0006 | g0089 | EAS | CHS | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG00438 | hp1 | a0001 | c0002 | t0005 | g0258 | EAS | CHS | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG00438 | hp2 | a0001 | c0003 | t0006 | g0077 | EAS | CHS | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG00544 | hp1 | a0001 | c0003 | t0007 | g0098 | EAS | CHS | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | CHS | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0311 | EAS | CHS | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | CHS | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0198 | EAS | CHS | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0313 | EAS | CHS | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG00609 | hp1 | a0001 | c0002 | t0005 | g0120 | EAS | CHS | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | CHS | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG00621 | hp1 | a0001 | c0003 | t0006 | g0095 | EAS | CHS | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0321 | EAS | CHS | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0128 | AMR | PUR | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG00639 | hp2 | a0001 | c0003 | t0055 | g0112 | AMR | PUR | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG00642 | hp1 | a0001 | c0002 | t0005 | g0157 | AMR | PUR | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG00642 | hp2 | a0001 | c0006 | t0001 | g0306 | AMR | PUR | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | CHS | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | CHS | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG00733 | hp1 | a0001 | c0003 | t0007 | g0073 | AMR | PUR | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0234 | AMR | PUR | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0272 | AMR | PUR | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG00741 | hp1 | a0001 | c0001 | t0018 | g0327 | AMR | PUR | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG00741 | hp2 | a0001 | c0006 | t0001 | g0325 | AMR | PUR | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG01069 | hp1 | a0001 | c0003 | t0006 | g0085 | AMR | PUR | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0273 | AMR | PUR | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG01070 | hp1 | a0001 | c0001 | t0018 | g0266 | AMR | PUR | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0260 | AMR | PUR | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0286 | AMR | PUR | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG01071 | hp2 | a0001 | c0003 | t0006 | g0084 | AMR | PUR | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG01074 | hp1 | a0001 | c0001 | t0004 | g0276 | AMR | PUR | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0285 | AMR | PUR | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG01081 | hp1 | a0001 | c0003 | t0006 | g0079 | AMR | PUR | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0281 | AMR | PUR | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG01099 | hp1 | a0001 | c0001 | t0008 | g0344 | AMR | PUR | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0287 | AMR | PUR | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG01106 | hp1 | a0001 | c0001 | t0017 | g0137 | AMR | PUR | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0326 | AMR | PUR | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG01169 | hp1 | a0001 | c0001 | t0023 | g0133 | AMR | PUR | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0323 | AMR | PUR | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG01243 | hp1 | a0001 | c0004 | t0041 | g0006 | AMR | PUR | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0223 | AMR | CLM | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0292 | AMR | CLM | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG01256 | hp1 | a0002 | c0007 | t0019 | g0002 | AMR | CLM | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | CLM | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | CLM | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | CLM | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG01258 | hp1 | a0002 | c0007 | t0019 | g0002 | AMR | CLM | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0309 | AMR | CLM | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | CLM | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0282 | AMR | CLM | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG01346 | hp1 | a0001 | c0003 | t0007 | g0105 | AMR | CLM | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | CLM | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG01361 | hp1 | a0002 | c0007 | t0019 | g0316 | AMR | CLM | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0336 | AMR | CLM | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG01433 | hp1 | a0001 | c0003 | t0006 | g0075 | AMR | CLM | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0296 | AMR | CLM | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG01496 | hp1 | a0001 | c0001 | t0023 | g0140 | AMR | CLM | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG01496 | hp2 | a0001 | c0001 | t0004 | g0126 | AMR | CLM | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG01516 | hp1 | a0001 | c0001 | t0047 | g0059 | EUR | IBS | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0224 | EUR | IBS | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG01884 | hp1 | a0001 | c0001 | t0008 | g0345 | AFR | ACB | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG01884 | hp2 | a0001 | c0023 | t0039 | g0005 | AFR | ACB | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG01891 | hp1 | a0001 | c0004 | t0005 | g0016 | AFR | ACB | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | ACB | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG01928 | hp1 | a0001 | c0003 | t0006 | g0080 | AMR | PEL | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG01928 | hp2 | a0001 | c0001 | t0004 | g0167 | AMR | PEL | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0206 | AMR | PEL | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG01934 | hp2 | a0001 | c0001 | t0029 | g0283 | AMR | PEL | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG01943 | hp1 | a0001 | c0001 | t0004 | g0001 | AMR | PEL | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | PEL | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG01952 | hp2 | a0001 | c0003 | t0007 | g0104 | AMR | PEL | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG01981 | hp1 | a0001 | c0001 | t0004 | g0150 | AMR | PEL | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0329 | AMR | PEL | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0263 | AMR | PEL | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG01993 | hp2 | a0001 | c0001 | t0004 | g0166 | AMR | PEL | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | KHV | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG02040 | hp2 | a0001 | c0003 | t0060 | g0101 | EAS | KHV | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG02055 | hp1 | a0001 | c0001 | t0026 | g0061 | AFR | ACB | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG02055 | hp2 | a0001 | c0004 | t0010 | g0027 | AFR | ACB | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | KHV | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG02056 | hp2 | a0001 | c0001 | t0004 | g0175 | EAS | KHV | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | KHV | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG02071 | hp2 | a0001 | c0001 | t0040 | g0196 | EAS | KHV | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG02074 | hp1 | a0001 | c0003 | t0012 | g0102 | EAS | KHV | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG02074 | hp2 | a0001 | c0003 | t0007 | g0094 | EAS | KHV | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG02080 | hp1 | a0001 | c0002 | t0003 | g0124 | EAS | KHV | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | KHV | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0280 | EAS | KHV | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG02083 | hp2 | a0001 | c0003 | t0007 | g0074 | EAS | KHV | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0270 | EAS | KHV | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG02129 | hp2 | a0001 | c0002 | t0005 | g0275 | EAS | KHV | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | KHV | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG02132 | hp2 | a0001 | c0005 | t0061 | g0103 | EAS | KHV | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG02135 | hp1 | a0001 | c0018 | t0003 | g0320 | EAS | KHV | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | KHV | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PEL | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG02148 | hp2 | a0001 | c0001 | t0004 | g0162 | AMR | PEL | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG02155 | hp1 | a0001 | c0019 | t0033 | g0348 | EAS | CDX | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | CDX | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | CDX | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG02165 | hp2 | a0001 | c0003 | t0012 | g0072 | EAS | CDX | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG02257 | hp1 | a0001 | c0001 | t0062 | g0067 | AFR | ACB | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG02257 | hp2 | a0001 | c0001 | t0005 | g0229 | AFR | ACB | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG02258 | hp1 | a0001 | c0004 | t0015 | g0017 | AFR | ACB | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG02258 | hp2 | a0001 | c0001 | t0004 | g0333 | AFR | ACB | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG02280 | hp1 | a0001 | c0004 | t0001 | g0010 | AFR | ACB | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG02280 | hp2 | a0001 | c0001 | t0016 | g0210 | AFR | ACB | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG02300 | hp1 | a0001 | c0001 | t0018 | g0165 | AMR | PEL | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PEL | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG02451 | hp1 | a0001 | c0004 | t0001 | g0011 | AFR | ACB | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | ACB | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG02523 | hp1 | a0001 | c0003 | t0006 | g0083 | EAS | KHV | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG02523 | hp2 | a0001 | c0001 | t0004 | g0297 | EAS | KHV | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG02602 | hp1 | a0001 | c0001 | t0024 | g0043 | SAS | PJL | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0053 | SAS | PJL | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG02615 | hp1 | a0001 | c0001 | t0005 | g0225 | AFR | GWD | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG02615 | hp2 | a0001 | c0004 | t0020 | g0025 | AFR | GWD | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG02622 | hp1 | a0001 | c0012 | t0004 | g0351 | AFR | GWD | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG02622 | hp2 | a0001 | c0001 | t0015 | g0136 | AFR | GWD | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG02630 | hp1 | a0001 | c0001 | t0034 | g0063 | AFR | GWD | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG02630 | hp2 | a0001 | c0002 | t0038 | g0060 | AFR | GWD | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG02647 | hp1 | a0001 | c0004 | t0010 | g0022 | AFR | GWD | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG02647 | hp2 | a0001 | c0001 | t0063 | g0004 | AFR | GWD | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG02698 | hp1 | a0001 | c0001 | t0044 | g0177 | SAS | PJL | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG02698 | hp2 | a0001 | c0001 | t0004 | g0001 | SAS | PJL | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG02717 | hp1 | a0001 | c0002 | t0009 | g0208 | AFR | GWD | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0334 | AFR | GWD | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG02738 | hp1 | a0001 | c0003 | t0006 | g0114 | SAS | PJL | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG02738 | hp2 | a0003 | c0008 | t0001 | g0240 | SAS | PJL | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG02809 | hp1 | a0001 | c0002 | t0005 | g0122 | AFR | GWD | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG02809 | hp2 | a0001 | c0001 | t0048 | g0237 | AFR | GWD | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG02818 | hp1 | a0001 | c0001 | t0005 | g0215 | AFR | GWD | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG02818 | hp2 | a0001 | c0001 | t0005 | g0293 | AFR | GWD | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG02886 | hp1 | a0001 | c0001 | t0005 | g0331 | AFR | GWD | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG02886 | hp2 | a0001 | c0001 | t0054 | g0322 | AFR | GWD | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG02895 | hp1 | a0001 | c0004 | t0020 | g0023 | AFR | GWD | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG02895 | hp2 | a0001 | c0002 | t0009 | g0171 | AFR | GWD | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | GWD | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG02896 | hp2 | a0001 | c0001 | t0008 | g0339 | AFR | GWD | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG02922 | hp1 | a0001 | c0009 | t0005 | g0018 | AFR | ESN | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG02922 | hp2 | a0001 | c0001 | t0017 | g0332 | AFR | ESN | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG02965 | hp1 | a0001 | c0004 | t0010 | g0007 | AFR | ESN | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG02965 | hp2 | a0001 | c0004 | t0015 | g0009 | AFR | ESN | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | ESN | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG02970 | hp2 | a0001 | c0004 | t0010 | g0013 | AFR | ESN | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG02976 | hp1 | a0001 | c0001 | t0016 | g0211 | AFR | ESN | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | ESN | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG03017 | hp2 | a0001 | c0001 | t0004 | g0058 | SAS | PJL | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG03041 | hp1 | a0001 | c0002 | t0005 | g0129 | AFR | GWD | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG03041 | hp2 | a0001 | c0001 | t0030 | g0340 | AFR | GWD | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG03098 | hp1 | a0001 | c0004 | t0001 | g0019 | AFR | MSL | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG03098 | hp2 | a0001 | c0004 | t0013 | g0021 | AFR | MSL | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG03130 | hp1 | a0001 | c0004 | t0013 | g0012 | AFR | ESN | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG03130 | hp2 | a0001 | c0002 | t0009 | g0209 | AFR | ESN | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG03195 | hp1 | a0001 | c0001 | t0017 | g0338 | AFR | ESN | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG03195 | hp2 | a0001 | c0004 | t0001 | g0008 | AFR | ESN | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | MSL | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | MSL | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG03225 | hp1 | a0001 | c0001 | t0013 | g0123 | AFR | MSL | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG03225 | hp2 | a0001 | c0001 | t0050 | g0168 | AFR | MSL | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0268 | SAS | PJL | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG03453 | hp1 | a0001 | c0026 | t0042 | g0028 | AFR | MSL | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | MSL | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG03486 | hp1 | a0001 | c0017 | t0001 | g0231 | AFR | MSL | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG03486 | hp2 | a0001 | c0001 | t0008 | g0341 | AFR | MSL | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG03490 | hp1 | a0001 | c0010 | t0021 | g0097 | SAS | PJL | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG03490 | hp2 | a0001 | c0001 | t0022 | g0176 | SAS | PJL | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG03492 | hp1 | a0001 | c0002 | t0003 | g0160 | SAS | PJL | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG03492 | hp2 | a0001 | c0001 | t0022 | g0131 | SAS | PJL | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG03516 | hp1 | a0001 | c0002 | t0009 | g0139 | AFR | ESN | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG03516 | hp2 | a0001 | c0022 | t0005 | g0154 | AFR | ESN | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | GWD | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG03540 | hp2 | a0001 | c0002 | t0009 | g0330 | AFR | GWD | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG03579 | hp1 | a0001 | c0024 | t0004 | g0026 | AFR | MSL | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG03579 | hp2 | a0001 | c0002 | t0009 | g0156 | AFR | MSL | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG03669 | hp1 | a0003 | c0008 | t0001 | g0241 | SAS | PJL | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG03669 | hp2 | a0001 | c0002 | t0003 | g0051 | SAS | PJL | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG03704 | hp1 | a0001 | c0002 | t0003 | g0159 | SAS | PJL | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG03704 | hp2 | a0001 | c0002 | t0003 | g0158 | SAS | PJL | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG03831 | hp1 | a0001 | c0003 | t0007 | g0113 | SAS | BEB | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG03831 | hp2 | a0001 | c0001 | t0004 | g0153 | SAS | BEB | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0039 | SAS | BEB | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0144 | SAS | BEB | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG03927 | hp1 | a0001 | c0001 | t0004 | g0180 | SAS | BEB | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG03927 | hp2 | a0001 | c0020 | t0001 | g0267 | SAS | BEB | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG03942 | hp1 | a0001 | c0002 | t0003 | g0044 | SAS | BEB | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0318 | SAS | BEB | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0049 | SAS | BEB | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG04184 | hp2 | a0001 | c0002 | t0003 | g0197 | SAS | BEB | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG04199 | hp1 | a0001 | c0002 | t0051 | g0181 | SAS | STU | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG04199 | hp2 | a0001 | c0001 | t0004 | g0179 | SAS | STU | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG04204 | hp1 | a0001 | c0001 | t0053 | g0052 | SAS | STU | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | STU | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG04228 | hp1 | a0001 | c0002 | t0003 | g0172 | SAS | STU | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0182 | SAS | STU | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA18522 | hp1 | a0001 | c0001 | t0027 | g0065 | AFR | YRI | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA18522 | hp2 | a0001 | c0002 | t0005 | g0170 | AFR | YRI | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | CHB | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA18612 | hp2 | a0001 | c0002 | t0003 | g0132 | EAS | CHB | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA18747 | hp1 | a0001 | c0002 | t0005 | g0036 | EAS | CHB | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA18747 | hp2 | a0001 | c0002 | t0003 | g0265 | EAS | CHB | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA18906 | hp1 | a0001 | c0004 | t0010 | g0014 | AFR | YRI | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA18906 | hp2 | a0001 | c0001 | t0037 | g0236 | AFR | YRI | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA18940 | hp1 | a0001 | c0001 | t0008 | g0347 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA18940 | hp2 | a0001 | c0003 | t0007 | g0107 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA18941 | hp2 | a0001 | c0003 | t0006 | g0069 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA18942 | hp1 | a0001 | c0005 | t0021 | g0096 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA18942 | hp2 | a0001 | c0002 | t0003 | g0125 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA18944 | hp1 | a0001 | c0001 | t0011 | g0251 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA18945 | hp1 | a0001 | c0002 | t0036 | g0274 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA18945 | hp2 | a0001 | c0001 | t0004 | g0195 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA18950 | hp1 | a0001 | c0001 | t0046 | g0324 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA18950 | hp2 | a0001 | c0002 | t0014 | g0203 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA18951 | hp1 | a0001 | c0002 | t0003 | g0191 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA18951 | hp2 | a0001 | c0003 | t0006 | g0082 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA18952 | hp1 | a0001 | c0003 | t0006 | g0100 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA18952 | hp2 | a0001 | c0001 | t0025 | g0244 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA18954 | hp2 | a0001 | c0002 | t0003 | g0033 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0307 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA18961 | hp1 | a0001 | c0003 | t0056 | g0091 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA18961 | hp2 | a0001 | c0003 | t0012 | g0070 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA18964 | hp1 | a0001 | c0003 | t0007 | g0109 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA18966 | hp1 | a0001 | c0001 | t0032 | g0349 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA18966 | hp2 | a0001 | c0002 | t0003 | g0143 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA18967 | hp2 | a0001 | c0002 | t0003 | g0301 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA18970 | hp1 | a0001 | c0001 | t0004 | g0142 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA18970 | hp2 | a0001 | c0003 | t0006 | g0081 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA18971 | hp2 | a0001 | c0003 | t0007 | g0078 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA18977 | hp1 | a0001 | c0001 | t0004 | g0163 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA18977 | hp2 | a0001 | c0003 | t0006 | g0099 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA18981 | hp1 | a0001 | c0002 | t0003 | g0253 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA18981 | hp2 | a0001 | c0001 | t0049 | g0202 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA18984 | hp2 | a0001 | c0003 | t0006 | g0087 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA18985 | hp1 | a0008 | c0015 | t0003 | g0300 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA18986 | hp1 | a0001 | c0002 | t0001 | g0178 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA18990 | hp2 | a0001 | c0001 | t0011 | g0288 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA18993 | hp2 | a0001 | c0001 | t0011 | g0185 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA18995 | hp1 | a0001 | c0003 | t0006 | g0115 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA18995 | hp2 | a0001 | c0001 | t0011 | g0184 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA18997 | hp1 | a0001 | c0003 | t0007 | g0108 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA18999 | hp2 | a0001 | c0003 | t0012 | g0068 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA19002 | hp2 | a0001 | c0001 | t0004 | g0141 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA19004 | hp1 | a0001 | c0003 | t0006 | g0110 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA19009 | hp2 | a0001 | c0001 | t0004 | g0151 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA19010 | hp1 | a0001 | c0002 | t0003 | g0278 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA19010 | hp2 | a0001 | c0011 | t0006 | g0093 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA19030 | hp1 | a0001 | c0002 | t0005 | g0138 | AFR | LWK | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA19030 | hp2 | a0005 | c0021 | t0031 | g0346 | AFR | LWK | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA19043 | hp1 | a0001 | c0009 | t0035 | g0029 | AFR | LWK | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA19043 | hp2 | a0001 | c0001 | t0005 | g0233 | AFR | LWK | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA19055 | hp1 | a0001 | c0002 | t0014 | g0193 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA19055 | hp2 | a0001 | c0003 | t0058 | g0076 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA19057 | hp1 | a0001 | c0001 | t0014 | g0218 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA19057 | hp2 | a0001 | c0002 | t0005 | g0031 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA19058 | hp1 | a0001 | c0003 | t0012 | g0071 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA19060 | hp1 | a0001 | c0001 | t0004 | g0164 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA19060 | hp2 | a0007 | c0016 | t0001 | g0155 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA19063 | hp2 | a0001 | c0003 | t0059 | g0086 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA19065 | hp2 | a0001 | c0002 | t0003 | g0134 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA19066 | hp2 | a0001 | c0002 | t0005 | g0299 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA19070 | hp1 | a0001 | c0003 | t0006 | g0092 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA19070 | hp2 | a0001 | c0002 | t0014 | g0056 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA19074 | hp1 | a0001 | c0001 | t0025 | g0245 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA19074 | hp2 | a0001 | c0002 | t0003 | g0256 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA19077 | hp1 | a0001 | c0003 | t0006 | g0088 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA19077 | hp2 | a0001 | c0003 | t0007 | g0106 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA19079 | hp2 | a0001 | c0001 | t0011 | g0201 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA19081 | hp1 | a0001 | c0003 | t0006 | g0090 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA19081 | hp2 | a0001 | c0002 | t0003 | g0190 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA19087 | hp2 | a0001 | c0002 | t0003 | g0146 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA19240 | hp1 | a0001 | c0001 | t0008 | g0342 | AFR | YRI | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA19240 | hp2 | a0001 | c0004 | t0013 | g0020 | AFR | YRI | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | ASW | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA20129 | hp2 | a0001 | c0004 | t0020 | g0024 | AFR | ASW | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0055 | EUR | TSI | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0221 | EUR | TSI | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA20905 | hp1 | a0004 | c0013 | t0001 | g0291 | SAS | GIH | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0337 | SAS | GIH | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | CLM | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG01123 | hp2 | a0001 | c0001 | t0004 | g0335 | AMR | CLM | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG02109 | hp1 | a0001 | c0001 | t0026 | g0062 | AFR | ACB | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG02109 | hp2 | a0001 | c0001 | t0027 | g0066 | AFR | ACB | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG02486 | hp1 | a0006 | c0025 | t0010 | g0015 | AFR | ACB | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG02486 | hp2 | a0001 | c0002 | t0005 | g0295 | AFR | ACB | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG02559 | hp1 | a0001 | c0001 | t0005 | g0238 | AFR | ACB | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0319 | AFR | ACB | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG03471 | hp1 | a0001 | c0014 | t0016 | g0328 | AFR | MSL | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | MSL | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG06807 | hp1 | a0001 | c0001 | t0005 | g0230 | AFR | USA | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| HG06807 | hp2 | a0001 | c0003 | t0057 | g0064 | AFR | USA | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA18955 | hp1 | a0001 | c0002 | t0003 | g0304 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA18955 | hp2 | a0001 | c0005 | t0021 | g0111 | EAS | JPT | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | USA | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA20300 | hp2 | a0001 | c0002 | t0009 | g0116 | AFR | USA | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA21309 | hp1 | a0001 | c0001 | t0052 | g0350 | AFR | LWK | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| NA21309 | hp2 | a0001 | c0001 | t0008 | g0343 | AFR | LWK | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0038 | REF | REF | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0028 | g0048 | REF | REF | TRIM67_chr1_231157058_231226565 | TRIM67 | chr1 | 231157058 | 231226565 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:231163787
|
G | A | 1 | a0004 | 1 | NA20905.hp1 | missense_variant | MODERATE | c.818G>A | p.Gly273Asp | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/10 | 1730/9389 | 818/2352 | 273/783 | chr1 | 231163787 | ||
| chr1:231163797
|
C | G | 1 | a0005 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.828C>G | p.Ser276Arg | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/10 | 1740/9389 | 828/2352 | 276/783 | chr1 | 231163797 | ||
| chr1:231200203
|
T | A | 1 | a0008 | 1 | NA18985.hp1 | missense_variant | MODERATE | c.1319T>A | p.Leu440Gln | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 4/10 | 2231/9389 | 1319/2352 | 440/783 | chr1 | 231200203 | ||
| chr1:231200240
|
C | A | 1 | a0007 | 1 | NA19060.hp2 | missense_variant | MODERATE | c.1356C>A | p.Asp452Glu | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 4/10 | 2268/9389 | 1356/2352 | 452/783 | chr1 | 231200240 | ||
| chr1:231206722
|
G | A | 1 | a0003 | 2 | HG02738.hp2 HG03669.hp1 |
missense_variant | MODERATE | c.1751G>A | p.Arg584Gln | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 7/10 | 2663/9389 | 1751/2352 | 584/783 | chr1 | 231206722 | ||
| chr1:231209162
|
A | G | 1 | a0002 | 3 | HG01256.hp1 HG01258.hp1 HG01361.hp1 |
missense_variant | MODERATE | c.2035A>G | p.Met679Val | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 8/10 | 2947/9389 | 2035/2352 | 679/783 | chr1 | 231209162 | ||
| chr1:231209214
|
G | A | 1 | a0006 | 1 | HG02486.hp1 | missense_variant | MODERATE | c.2087G>A | p.Arg696His | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 8/10 | 2999/9389 | 2087/2352 | 696/783 | chr1 | 231209214 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:231163152
|
C | A | 4 | a0001c0003a0001c0005a0001c0010others(1): Show | 49 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(46): Show |
synonymous_variant | LOW | c.183C>A | p.Ala61Ala | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/10 | 1095/9389 | 183/2352 | 61/783 | chr1 | 231163152 | ||
| chr1:231163191
|
C | T | 6 | a0001c0004a0001c0009a0001c0023others(3): Show | 25 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(22): Show |
synonymous_variant | LOW | c.222C>T | p.Gly74Gly | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/10 | 1134/9389 | 222/2352 | 74/783 | chr1 | 231163191 | ||
| chr1:231163224
|
T | C | 1 | a0001c0012 | 1 | HG02622.hp1 | synonymous_variant | LOW | c.255T>C | p.Ala85Ala | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/10 | 1167/9389 | 255/2352 | 85/783 | chr1 | 231163224 | ||
| chr1:231163245
|
G | C | 1 | a0001c0023 | 1 | HG01884.hp2 | synonymous_variant | LOW | c.276G>C | p.Ala92Ala | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/10 | 1188/9389 | 276/2352 | 92/783 | chr1 | 231163245 | ||
| chr1:231163584
|
G | C | 1 | a0001c0010 | 1 | HG03490.hp1 | synonymous_variant | LOW | c.615G>C | p.Val205Val | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/10 | 1527/9389 | 615/2352 | 205/783 | chr1 | 231163584 | ||
| chr1:231163638
|
C | T | 1 | a0001c0026 | 1 | HG03453.hp1 | synonymous_variant | LOW | c.669C>T | p.Cys223Cys | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/10 | 1581/9389 | 669/2352 | 223/783 | chr1 | 231163638 | ||
| chr1:231163794
|
C | T | 1 | a0001c0022 | 1 | HG03516.hp2 | synonymous_variant | LOW | c.825C>T | p.Pro275Pro | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/10 | 1737/9389 | 825/2352 | 275/783 | chr1 | 231163794 | ||
| chr1:231163827
|
C | A | 1 | a0001c0024 | 1 | HG03579.hp1 | synonymous_variant | LOW | c.858C>A | p.Gly286Gly | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/10 | 1770/9389 | 858/2352 | 286/783 | chr1 | 231163827 | ||
| chr1:231163932
|
G | A | 1 | a0001c0014 | 1 | HG03471.hp1 | synonymous_variant | LOW | c.963G>A | p.Pro321Pro | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/10 | 1875/9389 | 963/2352 | 321/783 | chr1 | 231163932 | ||
| chr1:231200237
|
C | T | 1 | a0001c0020 | 1 | HG03927.hp2 | synonymous_variant | LOW | c.1353C>T | p.Asn451Asn | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 4/10 | 2265/9389 | 1353/2352 | 451/783 | chr1 | 231200237 | ||
| chr1:231200246
|
C | A | 1 | a0008c0015 | 1 | NA18985.hp1 | synonymous_variant | LOW | c.1362C>A | p.Ser454Ser | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 4/10 | 2274/9389 | 1362/2352 | 454/783 | chr1 | 231200246 | ||
| chr1:231201480
|
C | T | 1 | a0001c0019 | 1 | HG02155.hp1 | synonymous_variant | LOW | c.1497C>T | p.Ala499Ala | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 5/10 | 2409/9389 | 1497/2352 | 499/783 | chr1 | 231201480 | ||
| chr1:231203961
|
C | G | 1 | a0001c0011 | 1 | NA19010.hp2 | synonymous_variant | LOW | c.1629C>G | p.Pro543Pro | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 6/10 | 2541/9389 | 1629/2352 | 543/783 | chr1 | 231203961 | ||
| chr1:231203967
|
C | T | 8 | a0001c0002a0001c0005a0001c0009others(5): Show | 62 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(59): Show |
synonymous_variant | LOW | c.1635C>T | p.Asp545Asp | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 6/10 | 2547/9389 | 1635/2352 | 545/783 | chr1 | 231203967 | ||
| chr1:231204009
|
C | T | 1 | a0001c0017 | 1 | HG03486.hp1 | synonymous_variant | LOW | c.1677C>T | p.Phe559Phe | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 6/10 | 2589/9389 | 1677/2352 | 559/783 | chr1 | 231204009 | ||
| chr1:231209062
|
G | A | 1 | a0001c0018 | 1 | HG02135.hp1 | synonymous_variant | LOW | c.1935G>A | p.Ala645Ala | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 8/10 | 2847/9389 | 1935/2352 | 645/783 | chr1 | 231209062 | ||
| chr1:231209149
|
C | T | 1 | a0001c0022 | 1 | HG03516.hp2 | synonymous_variant | LOW | c.2022C>T | p.Ser674Ser | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 8/10 | 2934/9389 | 2022/2352 | 674/783 | chr1 | 231209149 | ||
| chr1:231215404
|
G | A | 1 | a0001c0006 | 3 | HG00323.hp1 HG00642.hp2 HG00741.hp2 |
synonymous_variant | LOW | c.2316G>A | p.Pro772Pro | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 10/10 | 3228/9389 | 2316/2352 | 772/783 | chr1 | 231215404 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:231162068
|
G | T | 1 | a0001c0001t0063 | 1 | HG02647.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-902G>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/10 | chr1 | 231162068 | ||||||
| chr1:231162083
|
G | A | 1 | a0001c0001t0022 | 2 | HG03490.hp2 HG03492.hp2 |
5_prime_UTR_variant | MODIFIER | c.-887G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/10 | 887 | chr1 | 231162083 | |||||
| chr1:231162238
|
G | T | 16 | a0001c0001t0026a0001c0001t0027a0001c0001t0062others(13): Show | 54 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(51): Show |
5_prime_UTR_variant | MODIFIER | c.-732G>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/10 | 732 | chr1 | 231162238 | |||||
| chr1:231162246
|
A | G | 85 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(82): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
5_prime_UTR_variant | MODIFIER | c.-724A>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/10 | 724 | chr1 | 231162246 | |||||
| chr1:231162257
|
G | A | 13 | a0001c0003t0006a0001c0003t0007a0001c0003t0012others(10): Show | 49 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(46): Show |
5_prime_UTR_variant | MODIFIER | c.-713G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/10 | 713 | chr1 | 231162257 | |||||
| chr1:231162263
|
T | C | 1 | a0001c0001t0029 | 1 | HG01934.hp2 | 5_prime_UTR_variant | MODIFIER | c.-707T>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/10 | 707 | chr1 | 231162263 | |||||
| chr1:231162285
|
C | G | 85 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(82): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
5_prime_UTR_variant | MODIFIER | c.-685C>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/10 | 685 | chr1 | 231162285 | |||||
| chr1:231162291
|
T | G | 85 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(82): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
5_prime_UTR_variant | MODIFIER | c.-679T>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/10 | 679 | chr1 | 231162291 | |||||
| chr1:231162509
|
T | C | 22 | a0001c0001t0008a0001c0001t0026a0001c0001t0027others(19): Show | 66 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(63): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-461T>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/10 | chr1 | 231162509 | ||||||
| chr1:231162516
|
G | T | 1 | a0001c0001t0054 | 1 | HG02886.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-454G>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/10 | chr1 | 231162516 | ||||||
| chr1:231162549
|
C | T | 1 | a0001c0004t0020 | 3 | HG02615.hp2 HG02895.hp1 NA20129.hp2 |
5_prime_UTR_variant | MODIFIER | c.-421C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/10 | 421 | chr1 | 231162549 | |||||
| chr1:231162682
|
G | T | 1 | a0001c0001t0053 | 1 | HG04204.hp1 | 5_prime_UTR_variant | MODIFIER | c.-288G>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/10 | 288 | chr1 | 231162682 | |||||
| chr1:231162774
|
C | T | 1 | a0001c0001t0052 | 1 | NA21309.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-196C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/10 | chr1 | 231162774 | ||||||
| chr1:231162830
|
C | G | 2 | a0001c0001t0027a0001c0001t0062 | 3 | HG02109.hp2 HG02257.hp1 NA18522.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-140C>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/10 | chr1 | 231162830 | ||||||
| chr1:231162851
|
C | T | 1 | a0001c0001t0034 | 1 | HG02630.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-119C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/10 | chr1 | 231162851 | ||||||
| chr1:231162865
|
G | A | 1 | a0001c0003t0055 | 1 | HG00639.hp2 | 5_prime_UTR_variant | MODIFIER | c.-105G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/10 | 105 | chr1 | 231162865 | |||||
| chr1:231162889
|
C | A | 1 | a0001c0001t0023 | 2 | HG01169.hp1 HG01496.hp1 |
5_prime_UTR_variant | MODIFIER | c.-81C>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/10 | 81 | chr1 | 231162889 | |||||
| chr1:231162953
|
T | G | 22 | a0001c0001t0008a0001c0001t0026a0001c0001t0027others(19): Show | 66 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(63): Show |
5_prime_UTR_variant | MODIFIER | c.-17T>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/10 | 17 | chr1 | 231162953 | |||||
| chr1:231215744
|
T | A | 13 | a0001c0001t0005a0001c0001t0034a0001c0001t0037others(10): Show | 38 | HG00438.hp1 HG00609.hp1 HG00642.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*304T>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 10/10 | 304 | chr1 | 231215744 | |||||
| chr1:231215817
|
C | T | 12 | a0001c0001t0005a0001c0001t0034a0001c0001t0037others(9): Show | 37 | HG00438.hp1 HG00609.hp1 HG00642.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*377C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 10/10 | 377 | chr1 | 231215817 | |||||
| chr1:231215991
|
C | G | 9 | a0001c0001t0014a0001c0002t0003a0001c0002t0014others(6): Show | 36 | HG00408.hp2 HG00423.hp1 HG01256.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*551C>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 10/10 | 551 | chr1 | 231215991 | |||||
| chr1:231216196
|
C | G | 3 | a0001c0001t0014a0001c0002t0014a0001c0005t0061 | 5 | HG02132.hp2 NA18950.hp2 NA19055.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*756C>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 10/10 | 756 | chr1 | 231216196 | |||||
| chr1:231216233
|
T | A | 2 | a0001c0004t0010a0006c0025t0010 | 6 | HG02055.hp2 HG02486.hp1 HG02647.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*793T>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 10/10 | 793 | chr1 | 231216233 | |||||
| chr1:231216280
|
C | T | 1 | a0001c0001t0062 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*840C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 10/10 | 840 | chr1 | 231216280 | |||||
| chr1:231216294
|
T | A | 1 | a0001c0001t0011 | 5 | NA18944.hp1 NA18990.hp2 NA18993.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*854T>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 10/10 | 854 | chr1 | 231216294 | |||||
| chr1:231216432
|
G | A | 11 | a0001c0001t0005a0001c0001t0034a0001c0001t0037others(8): Show | 36 | HG00438.hp1 HG00609.hp1 HG00642.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*992G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 10/10 | 992 | chr1 | 231216432 | |||||
| chr1:231216586
|
C | T | 1 | a0001c0001t0050 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1146C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 10/10 | 1146 | chr1 | 231216586 | |||||
| chr1:231216625
|
C | T | 1 | a0001c0002t0038 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1185C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 10/10 | 1185 | chr1 | 231216625 | |||||
| chr1:231216673
|
T | C | 2 | a0001c0001t0026a0001c0023t0039 | 3 | HG01884.hp2 HG02055.hp1 HG02109.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1233T>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 10/10 | 1233 | chr1 | 231216673 | |||||
| chr1:231216854
|
T | C | 1 | a0001c0002t0038 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1414T>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 10/10 | 1414 | chr1 | 231216854 | |||||
| chr1:231217021
|
A | G | 42 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(39): Show | 176 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(173): Show |
3_prime_UTR_variant | MODIFIER | c.*1581A>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 10/10 | 1581 | chr1 | 231217021 | |||||
| chr1:231217112
|
C | G | 1 | a0001c0001t0047 | 1 | HG01516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1672C>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 10/10 | 1672 | chr1 | 231217112 | |||||
| chr1:231217116
|
T | C | 1 | a0001c0001t0040 | 1 | HG02071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1676T>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 10/10 | 1676 | chr1 | 231217116 | |||||
| chr1:231217263
|
C | T | 2 | a0001c0001t0046a0001c0002t0051 | 2 | HG04199.hp1 NA18950.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1823C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 10/10 | 1823 | chr1 | 231217263 | |||||
| chr1:231217589
|
G | GA | 17 | a0001c0001t0005a0001c0001t0022a0001c0001t0034others(14): Show | 47 | HG00438.hp1 HG00609.hp1 HG00642.hp1 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*2158dupA | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 10/10 | 2159 | INFO_REALIGN_3_PRIME | chr1 | 231217589 | ||||
| chr1:231217702
|
C | A | 5 | a0001c0001t0013a0001c0001t0030a0001c0003t0057others(2): Show | 7 | HG01243.hp1 HG03041.hp2 HG03098.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2262C>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 10/10 | 2262 | chr1 | 231217702 | |||||
| chr1:231217716
|
A | G | 24 | a0001c0001t0005a0001c0001t0014a0001c0001t0034others(21): Show | 80 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*2276A>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 10/10 | 2276 | chr1 | 231217716 | |||||
| chr1:231217843
|
A | G | 18 | a0001c0001t0002a0001c0001t0004a0001c0001t0017others(15): Show | 96 | HG00140.hp2 HG00544.hp1 HG00558.hp1 others(93): Show |
3_prime_UTR_variant | MODIFIER | c.*2403A>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 10/10 | 2403 | chr1 | 231217843 | |||||
| chr1:231217866
|
G | T | 2 | a0001c0001t0016a0001c0014t0016 | 3 | HG02280.hp2 HG02976.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2426G>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 10/10 | 2426 | chr1 | 231217866 | |||||
| chr1:231219004
|
C | A | 1 | a0001c0004t0041 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3564C>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 10/10 | 3564 | chr1 | 231219004 | |||||
| chr1:231219122
|
G | A | 2 | a0001c0001t0015a0001c0004t0015 | 3 | HG02258.hp1 HG02622.hp2 HG02965.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3682G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 10/10 | 3682 | chr1 | 231219122 | |||||
| chr1:231219230
|
A | C | 3 | a0001c0001t0024a0001c0001t0045a0001c0001t0053 | 4 | HG00280.hp1 HG00323.hp2 HG02602.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3790A>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 10/10 | 3790 | chr1 | 231219230 | |||||
| chr1:231219312
|
C | T | 18 | a0001c0001t0002a0001c0001t0004a0001c0001t0017others(15): Show | 96 | HG00140.hp2 HG00544.hp1 HG00558.hp1 others(93): Show |
3_prime_UTR_variant | MODIFIER | c.*3872C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 10/10 | 3872 | chr1 | 231219312 | |||||
| chr1:231219313
|
G | A | 2 | a0001c0004t0010a0006c0025t0010 | 6 | HG02055.hp2 HG02486.hp1 HG02647.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3873G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 10/10 | 3873 | chr1 | 231219313 | |||||
| chr1:231219324
|
G | A | 48 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(45): Show | 184 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(181): Show |
3_prime_UTR_variant | MODIFIER | c.*3884G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 10/10 | 3884 | chr1 | 231219324 | |||||
| chr1:231219788
|
G | A | 1 | a0001c0002t0036 | 1 | NA18945.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4348G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 10/10 | 4348 | chr1 | 231219788 | |||||
| chr1:231219892
|
T | C | 2 | a0001c0001t0026a0001c0023t0039 | 3 | HG01884.hp2 HG02055.hp1 HG02109.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4452T>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 10/10 | 4452 | chr1 | 231219892 | |||||
| chr1:231219954
|
C | T | 1 | a0001c0001t0025 | 2 | NA18952.hp2 NA19074.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4514C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 10/10 | 4514 | chr1 | 231219954 | |||||
| chr1:231220166
|
G | T | 11 | a0001c0001t0002a0001c0001t0017a0001c0001t0018others(8): Show | 66 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(63): Show |
3_prime_UTR_variant | MODIFIER | c.*4726G>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 10/10 | 4726 | chr1 | 231220166 | |||||
| chr1:231220172
|
C | G | 39 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(36): Show | 148 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(145): Show |
3_prime_UTR_variant | MODIFIER | c.*4732C>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 10/10 | 4732 | chr1 | 231220172 | |||||
| chr1:231220173
|
G | T | 39 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(36): Show | 148 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(145): Show |
3_prime_UTR_variant | MODIFIER | c.*4733G>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 10/10 | 4733 | chr1 | 231220173 | |||||
| chr1:231220240
|
G | T | 3 | a0001c0001t0024a0001c0001t0045a0001c0001t0053 | 4 | HG00280.hp1 HG00323.hp2 HG02602.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4800G>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 10/10 | 4800 | chr1 | 231220240 | |||||
| chr1:231220261
|
C | T | 1 | a0001c0001t0044 | 1 | HG02698.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4821C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 10/10 | 4821 | chr1 | 231220261 | |||||
| chr1:231220336
|
T | C | 5 | a0001c0001t0024a0001c0001t0045a0001c0001t0053others(2): Show | 10 | HG00280.hp1 HG00323.hp2 HG02055.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*4896T>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 10/10 | 4896 | chr1 | 231220336 | |||||
| chr1:231220356
|
A | G | 5 | a0001c0001t0024a0001c0001t0045a0001c0001t0053others(2): Show | 10 | HG00280.hp1 HG00323.hp2 HG02055.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*4916A>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 10/10 | 4916 | chr1 | 231220356 | |||||
| chr1:231220388
|
G | A | 1 | a0001c0001t0043 | 1 | HG00140.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4948G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 10/10 | 4948 | chr1 | 231220388 | |||||
| chr1:231220555
|
C | T | 5 | a0001c0001t0024a0001c0001t0045a0001c0001t0053others(2): Show | 10 | HG00280.hp1 HG00323.hp2 HG02055.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*5115C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 10/10 | 5115 | chr1 | 231220555 | |||||
| chr1:231220571
|
G | A | 2 | a0001c0001t0017a0005c0021t0031 | 4 | HG01106.hp1 HG02922.hp2 HG03195.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5131G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 10/10 | 5131 | chr1 | 231220571 | |||||
| chr1:231220621
|
C | T | 1 | a0001c0003t0058 | 1 | NA19055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5181C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 10/10 | 5181 | chr1 | 231220621 | |||||
| chr1:231220688
|
A | G | 1 | a0001c0001t0037 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5248A>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 10/10 | 5248 | chr1 | 231220688 | |||||
| chr1:231220813
|
A | G | 39 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(36): Show | 152 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(149): Show |
3_prime_UTR_variant | MODIFIER | c.*5373A>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 10/10 | 5373 | chr1 | 231220813 | |||||
| chr1:231220817
|
G | A | 3 | a0001c0001t0024a0001c0001t0045a0001c0001t0053 | 4 | HG00280.hp1 HG00323.hp2 HG02602.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5377G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 10/10 | 5377 | chr1 | 231220817 | |||||
| chr1:231220913
|
G | A | 1 | a0002c0007t0019 | 3 | HG01256.hp1 HG01258.hp1 HG01361.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5473G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 10/10 | 5473 | chr1 | 231220913 | |||||
| chr1:231220980
|
G | A | 1 | a0001c0001t0024 | 2 | HG00280.hp1 HG02602.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5540G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 10/10 | 5540 | chr1 | 231220980 | |||||
| chr1:231221049
|
CAGA | C | 3 | a0001c0001t0024a0001c0001t0045a0001c0001t0053 | 4 | HG00280.hp1 HG00323.hp2 HG02602.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5615_*5617delAAG | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 10/10 | 5615 | INFO_REALIGN_3_PRIME | chr1 | 231221049 | ||||
| chr1:231221053
|
A | G | 18 | a0001c0001t0005a0001c0001t0026a0001c0001t0034others(15): Show | 48 | HG00438.hp1 HG00609.hp1 HG00642.hp1 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*5613A>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 10/10 | 5613 | chr1 | 231221053 | |||||
| chr1:231221066
|
G | A | 3 | a0001c0001t0024a0001c0001t0045a0001c0001t0053 | 4 | HG00280.hp1 HG00323.hp2 HG02602.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5626G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 10/10 | 5626 | chr1 | 231221066 | |||||
| chr1:231221356
|
G | C | 17 | a0001c0001t0002a0001c0001t0004a0001c0001t0011others(14): Show | 99 | HG00140.hp2 HG00544.hp1 HG00558.hp1 others(96): Show |
3_prime_UTR_variant | MODIFIER | c.*5916G>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 10/10 | 5916 | chr1 | 231221356 | |||||
| chr1:231221363
|
C | A | 1 | a0001c0003t0060 | 1 | HG02040.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5923C>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 10/10 | 5923 | chr1 | 231221363 | |||||
| chr1:231221363
|
C | G | 16 | a0001c0001t0002a0001c0001t0004a0001c0001t0011others(13): Show | 98 | HG00140.hp2 HG00544.hp1 HG00558.hp1 others(95): Show |
3_prime_UTR_variant | MODIFIER | c.*5923C>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 10/10 | 5923 | chr1 | 231221363 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:231164157
|
C | G | 1 | a0001c0012t0004g0351 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1044+144C>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231164157 | ||||||
| chr1:231164558
|
T | C | 1 | a0001c0001t0063g0004 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1044+545T>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231164558 | ||||||
| chr1:231164565
|
T | C | 25 | a0001c0004t0001g0008a0001c0004t0001g0010a0001c0004t0001g0011others(22): Show | 25 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.1044+552T>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231164565 | ||||||
| chr1:231164904
|
C | T | 321 | a0001c0001t0001g0003a0001c0001t0001g0117a0001c0001t0001g0118others(318): Show | 324 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(321): Show |
intron_variant | MODIFIER | c.1044+891C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231164904 | ||||||
| chr1:231165207
|
G | C | 1 | a0001c0001t0001g0030 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1044+1194G>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231165207 | ||||||
| chr1:231165223
|
A | G | 1 | a0001c0001t0052g0350 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1044+1210A>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231165223 | ||||||
| chr1:231165281
|
A | T | 1 | a0001c0001t0047g0059 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1044+1268A>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231165281 | ||||||
| chr1:231165385
|
G | A | 1 | a0001c0002t0038g0060 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1044+1372G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231165385 | ||||||
| chr1:231165920
|
A | G | 11 | a0001c0001t0008g0339a0001c0001t0008g0341a0001c0001t0008g0342others(8): Show | 11 | HG01099.hp1 HG01884.hp1 HG02155.hp1 others(8): Show |
intron_variant | MODIFIER | c.1044+1907A>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231165920 | ||||||
| chr1:231166143
|
C | A | 55 | a0001c0001t0026g0061a0001c0001t0026g0062a0001c0001t0027g0065others(52): Show | 55 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.1044+2130C>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231166143 | ||||||
| chr1:231166157
|
A | G | 48 | a0001c0003t0006g0069a0001c0003t0006g0075a0001c0003t0006g0077others(45): Show | 48 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(45): Show |
intron_variant | MODIFIER | c.1044+2144A>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231166157 | ||||||
| chr1:231166276
|
GTTC | G | 3 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0002t0009g0116 | 3 | HG02451.hp2 HG03209.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1044+2270_1044+227 others(7): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 231166276 | |||||
| chr1:231166368
|
G | T | 3 | a0001c0001t0027g0065a0001c0001t0027g0066a0001c0001t0062g0067 | 3 | HG02109.hp2 HG02257.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1044+2355G>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231166368 | ||||||
| chr1:231166404
|
T | G | 1 | a0001c0001t0001g0119 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1044+2391T>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231166404 | ||||||
| chr1:231166503
|
T | A | 1 | a0001c0002t0005g0120 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1044+2490T>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231166503 | ||||||
| chr1:231166545
|
T | TTTGTTG | 234 | a0001c0001t0001g0003a0001c0001t0001g0117a0001c0001t0001g0118others(231): Show | 236 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.1044+2538_1044+254 others(10): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 231166545 | |||||
| chr1:231166610
|
T | C | 38 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0212others(35): Show | 38 | HG00280.hp2 HG00738.hp1 HG01106.hp2 others(35): Show |
intron_variant | MODIFIER | c.1044+2597T>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231166610 | ||||||
| chr1:231166611
|
T | A | 5 | a0001c0001t0026g0061a0001c0001t0026g0062a0001c0001t0027g0065others(2): Show | 5 | HG02055.hp1 HG02109.hp1 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.1044+2598T>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231166611 | ||||||
| chr1:231166657
|
C | T | 1 | a0001c0002t0038g0060 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1044+2644C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231166657 | ||||||
| chr1:231166664
|
G | T | 9 | a0001c0001t0001g0334a0001c0001t0001g0337a0001c0001t0002g0336others(6): Show | 9 | HG01123.hp2 HG01361.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1044+2651G>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231166664 | ||||||
| chr1:231166670
|
C | T | 1 | a0001c0001t0001g0207 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1044+2657C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231166670 | ||||||
| chr1:231166701
|
A | G | 66 | a0001c0001t0008g0339a0001c0001t0008g0341a0001c0001t0008g0342others(63): Show | 66 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.1044+2688A>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231166701 | ||||||
| chr1:231166744
|
C | T | 1 | a0001c0009t0035g0029 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1044+2731C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231166744 | ||||||
| chr1:231166770
|
T | A | 7 | a0001c0001t0001g0212a0001c0001t0001g0213a0001c0001t0001g0214others(4): Show | 7 | HG01106.hp2 HG01891.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1044+2757T>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231166770 | ||||||
| chr1:231166810
|
G | A | 4 | a0001c0003t0006g0069a0001c0003t0012g0068a0001c0003t0012g0070others(1): Show | 4 | NA18941.hp2 NA18961.hp2 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.1044+2797G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231166810 | ||||||
| chr1:231166900
|
T | C | 1 | a0001c0001t0002g0121 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1044+2887T>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231166900 | ||||||
| chr1:231167279
|
G | C | 1 | a0001c0001t0005g0215 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1044+3266G>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231167279 | ||||||
| chr1:231167319
|
C | CT | 21 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0194others(18): Show | 21 | HG00597.hp1 HG01261.hp1 HG02071.hp2 others(18): Show |
intron_variant | MODIFIER | c.1044+3327dupT | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 231167319 | |||||
| chr1:231167319
|
C | CTT | 6 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0252others(3): Show | 6 | HG00673.hp1 HG00673.hp2 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.1044+3326_1044+332 others(6): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 231167319 | |||||
| chr1:231167319
|
C | CTTTTTTT others(4): Show |
2 | a0001c0001t0004g0333a0001c0001t0063g0004 | 2 | HG02258.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1044+3317_1044+332 others(15): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 231167319 | |||||
| chr1:231167319
|
C | CTTTTTTT others(11): Show |
1 | a0001c0002t0003g0253 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1044+3310_1044+332 others(22): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 231167319 | |||||
| chr1:231167319
|
C | CTTTTTTT others(12): Show |
4 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0014g0218others(1): Show | 4 | HG01257.hp1 NA19012.hp1 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.1044+3309_1044+332 others(23): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 231167319 | |||||
| chr1:231167319
|
C | CTTTTTTT others(13): Show |
42 | a0001c0001t0001g0119a0001c0001t0001g0259a0001c0001t0001g0260others(39): Show | 43 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(40): Show |
intron_variant | MODIFIER | c.1044+3308_1044+332 others(24): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 231167319 | |||||
| chr1:231167319
|
C | CTTTTTTT others(14): Show |
45 | a0001c0001t0001g0003a0001c0001t0001g0117a0001c0001t0001g0118others(42): Show | 46 | HG00323.hp1 HG00423.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.1044+3307_1044+332 others(25): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 231167319 | |||||
| chr1:231167319
|
C | CTTTTTTT others(15): Show |
17 | a0001c0001t0001g0232a0001c0001t0001g0235a0001c0001t0001g0323others(14): Show | 17 | HG00280.hp2 HG00738.hp1 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.1044+3327_1044+332 others(26): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 231167319 | |||||
| chr1:231167319
|
C | CTTTTTTT others(16): Show |
3 | a0001c0001t0001g0337a0001c0001t0002g0336a0001c0001t0005g0215 | 3 | HG01361.hp2 HG02818.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1044+3327_1044+332 others(27): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 231167319 | |||||
| chr1:231167319
|
C | CTTTTTTT others(17): Show |
2 | a0001c0001t0001g0239a0001c0001t0001g0329 | 2 | HG01981.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1044+3327_1044+332 others(28): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 231167319 | |||||
| chr1:231167319
|
C | CTTTTTTT others(19): Show |
6 | a0001c0001t0001g0212a0001c0001t0016g0210a0001c0001t0016g0211others(3): Show | 6 | HG01106.hp2 HG02280.hp2 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.1044+3327_1044+332 others(30): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 231167319 | |||||
| chr1:231167319
|
C | CTTTTTTT others(20): Show |
2 | a0001c0001t0001g0213a0001c0001t0001g0214 | 2 | HG01891.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1044+3327_1044+332 others(31): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 231167319 | |||||
| chr1:231167319
|
C | CTTTTTTT others(22): Show |
1 | a0001c0001t0017g0338 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1044+3327_1044+332 others(33): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 231167319 | |||||
| chr1:231167319
|
CTTTTTTT others(299): Show |
C | 91 | a0001c0001t0008g0339a0001c0001t0008g0341a0001c0001t0008g0342others(88): Show | 91 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.1044+3318_1044+362 others(4): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 231167319 | |||||
| chr1:231167467
|
C | T | 1 | a0001c0001t0001g0186 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1044+3454C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231167467 | ||||||
| chr1:231167512
|
C | T | 2 | a0001c0002t0005g0295a0001c0014t0016g0328 | 2 | HG02486.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1044+3499C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231167512 | ||||||
| chr1:231167535
|
G | C | 1 | a0001c0017t0001g0231 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1044+3522G>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231167535 | ||||||
| chr1:231167621
|
C | T | 1 | a0001c0002t0014g0203 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1044+3608C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231167621 | ||||||
| chr1:231167807
|
G | T | 24 | a0001c0004t0001g0008a0001c0004t0001g0010a0001c0004t0001g0011others(21): Show | 24 | HG01243.hp1 HG01891.hp1 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.1044+3794G>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231167807 | ||||||
| chr1:231167860
|
A | G | 3 | a0001c0001t0008g0347a0001c0001t0032g0349a0001c0019t0033g0348 | 3 | HG02155.hp1 NA18940.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.1044+3847A>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231167860 | ||||||
| chr1:231167869
|
C | G | 1 | a0001c0023t0039g0005 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1044+3856C>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231167869 | ||||||
| chr1:231167880
|
G | T | 11 | a0001c0001t0008g0339a0001c0001t0008g0341a0001c0001t0008g0342others(8): Show | 11 | HG01099.hp1 HG01884.hp1 HG02155.hp1 others(8): Show |
intron_variant | MODIFIER | c.1044+3867G>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231167880 | ||||||
| chr1:231167891
|
C | T | 1 | a0001c0026t0042g0028 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1044+3878C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231167891 | ||||||
| chr1:231167959
|
C | CT | 8 | a0001c0001t0001g0250a0001c0001t0002g0321a0001c0001t0011g0184others(5): Show | 8 | HG00621.hp2 HG06807.hp2 NA18981.hp1 others(5): Show |
intron_variant | MODIFIER | c.1044+3958dupT | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 231167959 | |||||
| chr1:231168080
|
G | A | 1 | a0001c0004t0041g0006 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1044+4067G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231168080 | ||||||
| chr1:231168243
|
C | T | 1 | a0001c0001t0001g0294 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1044+4230C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231168243 | ||||||
| chr1:231168253
|
C | T | 1 | a0001c0001t0001g0212 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1044+4240C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231168253 | ||||||
| chr1:231168292
|
C | T | 55 | a0001c0001t0026g0061a0001c0001t0026g0062a0001c0001t0027g0065others(52): Show | 55 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.1044+4279C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231168292 | ||||||
| chr1:231168568
|
T | A | 11 | a0001c0001t0008g0339a0001c0001t0008g0341a0001c0001t0008g0342others(8): Show | 11 | HG01099.hp1 HG01884.hp1 HG02155.hp1 others(8): Show |
intron_variant | MODIFIER | c.1044+4555T>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231168568 | ||||||
| chr1:231168793
|
G | T | 1 | a0001c0023t0039g0005 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1044+4780G>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231168793 | ||||||
| chr1:231168881
|
G | A | 1 | a0001c0002t0005g0122 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1044+4868G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231168881 | ||||||
| chr1:231168890
|
T | C | 1 | a0001c0001t0001g0232 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1044+4877T>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231168890 | ||||||
| chr1:231168990
|
G | A | 1 | a0001c0002t0005g0031 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1044+4977G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231168990 | ||||||
| chr1:231168996
|
C | G | 55 | a0001c0001t0026g0061a0001c0001t0026g0062a0001c0001t0027g0065others(52): Show | 55 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.1044+4983C>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231168996 | ||||||
| chr1:231169031
|
A | G | 1 | a0001c0001t0052g0350 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1044+5018A>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231169031 | ||||||
| chr1:231169056
|
TTTTTTTA | T | 55 | a0001c0001t0026g0061a0001c0001t0026g0062a0001c0001t0027g0065others(52): Show | 55 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.1044+5049_1044+505 others(11): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 231169056 | |||||
| chr1:231169070
|
T | C | 11 | a0001c0001t0008g0339a0001c0001t0008g0341a0001c0001t0008g0342others(8): Show | 11 | HG01099.hp1 HG01884.hp1 HG02155.hp1 others(8): Show |
intron_variant | MODIFIER | c.1044+5057T>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231169070 | ||||||
| chr1:231169142
|
C | T | 1 | a0001c0001t0002g0055 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1044+5129C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231169142 | ||||||
| chr1:231169181
|
G | T | 1 | a0001c0001t0001g0183 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1044+5168G>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231169181 | ||||||
| chr1:231169240
|
A | G | 2 | a0001c0001t0026g0061a0001c0001t0026g0062 | 2 | HG02055.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.1044+5227A>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231169240 | ||||||
| chr1:231169310
|
C | G | 11 | a0001c0001t0008g0339a0001c0001t0008g0341a0001c0001t0008g0342others(8): Show | 11 | HG01099.hp1 HG01884.hp1 HG02155.hp1 others(8): Show |
intron_variant | MODIFIER | c.1044+5297C>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231169310 | ||||||
| chr1:231169319
|
T | A | 1 | a0001c0001t0013g0123 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1044+5306T>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231169319 | ||||||
| chr1:231169368
|
C | CT | 115 | a0001c0001t0001g0003a0001c0001t0001g0054a0001c0001t0001g0117others(112): Show | 117 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.1044+5380dupT | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 231169368 | |||||
| chr1:231169368
|
CT | C | 27 | a0001c0001t0001g0032a0001c0001t0001g0127a0001c0001t0001g0242others(24): Show | 27 | HG00639.hp1 HG00733.hp2 HG01123.hp2 others(24): Show |
intron_variant | MODIFIER | c.1044+5380delT | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 231169368 | |||||
| chr1:231169368
|
CTT | C | 30 | a0001c0001t0008g0341a0001c0001t0008g0342a0001c0001t0008g0343others(27): Show | 30 | HG01099.hp1 HG01243.hp1 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.1044+5379_1044+538 others(6): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 231169368 | |||||
| chr1:231169368
|
CTTT | C | 6 | a0001c0001t0008g0339a0001c0004t0001g0008a0001c0004t0001g0010others(3): Show | 6 | HG02280.hp1 HG02451.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1044+5378_1044+538 others(7): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 231169368 | |||||
| chr1:231169368
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0002t0003g0124 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1044+5371_1044+538 others(14): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 231169368 | |||||
| chr1:231169369
|
T | TC | 46 | a0001c0003t0006g0069a0001c0003t0006g0075a0001c0003t0006g0077others(43): Show | 46 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(43): Show |
intron_variant | MODIFIER | c.1044+5356_1044+535 others(5): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231169369 | ||||||
| chr1:231169370
|
T | C | 4 | a0001c0001t0027g0066a0001c0001t0062g0067a0001c0003t0012g0072others(1): Show | 4 | HG02109.hp2 HG02165.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.1044+5357T>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231169370 | ||||||
| chr1:231169371
|
T | C | 3 | a0001c0001t0026g0061a0001c0001t0026g0062a0001c0001t0027g0065 | 3 | HG02055.hp1 HG02109.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1044+5358T>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231169371 | ||||||
| chr1:231169485
|
T | TTC | 55 | a0001c0001t0026g0061a0001c0001t0026g0062a0001c0001t0027g0065others(52): Show | 55 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.1044+5475_1044+547 others(6): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 231169485 | |||||
| chr1:231169504
|
A | G | 1 | a0001c0024t0004g0026 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1044+5491A>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231169504 | ||||||
| chr1:231169536
|
G | A | 5 | a0001c0001t0026g0061a0001c0001t0026g0062a0001c0001t0027g0065others(2): Show | 5 | HG02055.hp1 HG02109.hp1 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.1044+5523G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231169536 | ||||||
| chr1:231169679
|
G | A | 50 | a0001c0001t0034g0063a0001c0003t0006g0069a0001c0003t0006g0075others(47): Show | 50 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.1044+5666G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231169679 | ||||||
| chr1:231169851
|
T | TCAC | 49 | a0001c0003t0006g0069a0001c0003t0006g0075a0001c0003t0006g0077others(46): Show | 49 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.1044+5839_1044+584 others(7): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 231169851 | |||||
| chr1:231169991
|
C | CTTTTTTT others(5): Show |
1 | a0001c0003t0007g0073 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1044+5979_1044+598 others(16): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 231169991 | |||||
| chr1:231169991
|
C | CTTTTTTT others(6): Show |
39 | a0001c0003t0006g0069a0001c0003t0006g0075a0001c0003t0006g0077others(36): Show | 39 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(36): Show |
intron_variant | MODIFIER | c.1044+5979_1044+598 others(17): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 231169991 | |||||
| chr1:231169991
|
C | CTTTTTTT others(7): Show |
9 | a0001c0003t0006g0110a0001c0003t0006g0114a0001c0003t0007g0107others(6): Show | 9 | HG00639.hp2 HG02738.hp1 HG03831.hp1 others(6): Show |
intron_variant | MODIFIER | c.1044+5979_1044+598 others(18): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 231169991 | |||||
| chr1:231169993
|
C | CTTTTTTT others(7): Show |
1 | a0001c0001t0054g0322 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1044+5990_1044+599 others(18): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 231169993 | |||||
| chr1:231169993
|
C | CTTTTTTT others(8): Show |
1 | a0001c0001t0034g0063 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1044+5990_1044+599 others(19): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 231169993 | |||||
| chr1:231169993
|
C | CTTTTTTT others(10): Show |
12 | a0001c0001t0001g0334a0001c0001t0001g0337a0001c0001t0002g0336others(9): Show | 12 | HG01123.hp2 HG01361.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1044+5990_1044+599 others(21): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 231169993 | |||||
| chr1:231169993
|
C | CTTTTTTT others(11): Show |
26 | a0001c0001t0001g0242a0001c0001t0026g0061a0001c0001t0062g0067others(23): Show | 26 | HG01243.hp1 HG01243.hp2 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.1044+5990_1044+599 others(22): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 231169993 | |||||
| chr1:231169993
|
C | CTTTTTTT others(12): Show |
7 | a0001c0001t0026g0062a0001c0001t0032g0349a0001c0004t0010g0022others(4): Show | 7 | HG02109.hp1 HG02155.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1044+5990_1044+599 others(23): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 231169993 | |||||
| chr1:231169993
|
C | CTTTTTTT others(13): Show |
8 | a0001c0001t0008g0339a0001c0001t0008g0341a0001c0001t0008g0342others(5): Show | 8 | HG01099.hp1 HG01884.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1044+5990_1044+599 others(24): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 231169993 | |||||
| chr1:231169993
|
C | T | 49 | a0001c0003t0006g0069a0001c0003t0006g0075a0001c0003t0006g0077others(46): Show | 49 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.1044+5980C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231169993 | ||||||
| chr1:231170070
|
T | C | 1 | a0001c0001t0054g0322 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1044+6057T>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231170070 | ||||||
| chr1:231170098
|
T | C | 1 | a0001c0026t0042g0028 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1044+6085T>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231170098 | ||||||
| chr1:231170210
|
T | C | 10 | a0001c0001t0008g0339a0001c0001t0008g0341a0001c0001t0008g0342others(7): Show | 10 | HG01099.hp1 HG01884.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.1044+6197T>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231170210 | ||||||
| chr1:231170217
|
C | T | 1 | a0001c0002t0038g0060 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1044+6204C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231170217 | ||||||
| chr1:231170497
|
A | G | 1 | a0001c0001t0001g0053 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1044+6484A>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231170497 | ||||||
| chr1:231170509
|
G | A | 49 | a0001c0003t0006g0069a0001c0003t0006g0075a0001c0003t0006g0077others(46): Show | 49 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.1044+6496G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231170509 | ||||||
| chr1:231170562
|
G | C | 25 | a0001c0003t0006g0075a0001c0003t0006g0077a0001c0003t0006g0079others(22): Show | 25 | HG00423.hp2 HG00438.hp2 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.1044+6549G>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231170562 | ||||||
| chr1:231170656
|
T | C | 3 | a0001c0001t0026g0061a0001c0001t0026g0062a0001c0023t0039g0005 | 3 | HG01884.hp2 HG02055.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.1044+6643T>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231170656 | ||||||
| chr1:231170762
|
G | A | 10 | a0001c0001t0008g0339a0001c0001t0008g0341a0001c0001t0008g0342others(7): Show | 10 | HG01099.hp1 HG01884.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.1044+6749G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231170762 | ||||||
| chr1:231170891
|
C | T | 1 | a0001c0001t0002g0055 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1044+6878C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231170891 | ||||||
| chr1:231171056
|
G | A | 10 | a0001c0001t0008g0339a0001c0001t0008g0341a0001c0001t0008g0342others(7): Show | 10 | HG01099.hp1 HG01884.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.1044+7043G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231171056 | ||||||
| chr1:231171111
|
A | C | 66 | a0001c0001t0008g0339a0001c0001t0008g0341a0001c0001t0008g0342others(63): Show | 66 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.1044+7098A>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231171111 | ||||||
| chr1:231171336
|
G | A | 3 | a0001c0001t0027g0065a0001c0001t0027g0066a0001c0001t0062g0067 | 3 | HG02109.hp2 HG02257.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1044+7323G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231171336 | ||||||
| chr1:231171822
|
T | C | 1 | a0001c0020t0001g0267 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1044+7809T>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231171822 | ||||||
| chr1:231172046
|
C | T | 5 | a0001c0001t0002g0130a0001c0001t0002g0173a0001c0001t0002g0174others(2): Show | 5 | HG00597.hp1 HG02056.hp2 NA18941.hp1 others(2): Show |
intron_variant | MODIFIER | c.1044+8033C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231172046 | ||||||
| chr1:231172235
|
T | G | 23 | a0001c0004t0001g0008a0001c0004t0001g0010a0001c0004t0001g0011others(20): Show | 23 | HG01243.hp1 HG01891.hp1 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.1044+8222T>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231172235 | ||||||
| chr1:231172263
|
C | G | 2 | a0001c0001t0001g0329a0001c0001t0024g0247 | 2 | HG00280.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.1044+8250C>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231172263 | ||||||
| chr1:231172391
|
A | C | 3 | a0001c0001t0027g0065a0001c0001t0027g0066a0001c0001t0062g0067 | 3 | HG02109.hp2 HG02257.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1044+8378A>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231172391 | ||||||
| chr1:231172493
|
T | A | 1 | a0001c0002t0005g0295 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1044+8480T>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231172493 | ||||||
| chr1:231172647
|
C | T | 19 | a0001c0001t0001g0212a0001c0001t0001g0213a0001c0001t0001g0214others(16): Show | 19 | HG01106.hp2 HG01891.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.1044+8634C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231172647 | ||||||
| chr1:231172854
|
T | C | 66 | a0001c0001t0008g0339a0001c0001t0008g0341a0001c0001t0008g0342others(63): Show | 66 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.1044+8841T>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231172854 | ||||||
| chr1:231173340
|
G | A | 65 | a0001c0001t0008g0339a0001c0001t0008g0341a0001c0001t0008g0342others(62): Show | 65 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.1044+9327G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231173340 | ||||||
| chr1:231173359
|
T | C | 24 | a0001c0004t0001g0008a0001c0004t0001g0010a0001c0004t0001g0011others(21): Show | 24 | HG01243.hp1 HG01891.hp1 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.1044+9346T>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231173359 | ||||||
| chr1:231173465
|
A | C | 1 | a0001c0001t0004g0333 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1044+9452A>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231173465 | ||||||
| chr1:231173563
|
C | T | 1 | a0001c0001t0034g0063 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1044+9550C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231173563 | ||||||
| chr1:231173643
|
G | C | 2 | a0001c0001t0022g0131a0001c0001t0022g0176 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1044+9630G>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231173643 | ||||||
| chr1:231173660
|
A | G | 1 | a0001c0026t0042g0028 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1044+9647A>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231173660 | ||||||
| chr1:231173680
|
G | A | 1 | a0001c0001t0001g0268 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1044+9667G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231173680 | ||||||
| chr1:231173713
|
G | T | 26 | a0001c0003t0006g0075a0001c0003t0006g0077a0001c0003t0006g0079others(23): Show | 26 | HG00423.hp2 HG00438.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.1044+9700G>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231173713 | ||||||
| chr1:231173722
|
G | A | 6 | a0001c0001t0001g0269a0001c0001t0001g0271a0001c0001t0001g0298others(3): Show | 6 | HG00408.hp2 HG00438.hp1 HG02071.hp1 others(3): Show |
intron_variant | MODIFIER | c.1044+9709G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231173722 | ||||||
| chr1:231173742
|
A | G | 6 | a0001c0001t0001g0269a0001c0001t0001g0271a0001c0001t0001g0298others(3): Show | 6 | HG00408.hp2 HG00438.hp1 HG02071.hp1 others(3): Show |
intron_variant | MODIFIER | c.1044+9729A>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231173742 | ||||||
| chr1:231173809
|
G | A | 1 | a0001c0001t0026g0061 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1044+9796G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231173809 | ||||||
| chr1:231173881
|
A | G | 1 | a0001c0001t0001g0205 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1044+9868A>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231173881 | ||||||
| chr1:231173885
|
G | C | 3 | a0001c0002t0003g0124a0001c0002t0003g0125a0001c0002t0003g0132 | 3 | HG02080.hp1 NA18612.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.1044+9872G>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231173885 | ||||||
| chr1:231173938
|
G | T | 1 | a0001c0002t0003g0172 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1044+9925G>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231173938 | ||||||
| chr1:231173957
|
C | A | 1 | a0005c0021t0031g0346 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1044+9944C>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231173957 | ||||||
| chr1:231174058
|
A | G | 13 | a0001c0001t0001g0334a0001c0001t0001g0337a0001c0001t0002g0336others(10): Show | 13 | HG01123.hp2 HG01361.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.1044+10045A>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231174058 | ||||||
| chr1:231174151
|
TC | T | 6 | a0001c0003t0006g0089a0001c0003t0006g0090a0001c0003t0006g0092others(3): Show | 6 | HG00423.hp2 NA18961.hp1 NA18995.hp1 others(3): Show |
intron_variant | MODIFIER | c.1044+10139delC | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231174151 | ||||||
| chr1:231174152
|
CT | C | 126 | a0001c0001t0001g0003a0001c0001t0001g0119a0001c0001t0001g0212others(123): Show | 128 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.1044+10156delT | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 231174152 | |||||
| chr1:231174152
|
CTT | C | 24 | a0001c0001t0001g0334a0001c0001t0001g0337a0001c0001t0002g0336others(21): Show | 24 | HG01099.hp1 HG01123.hp2 HG01361.hp2 others(21): Show |
intron_variant | MODIFIER | c.1044+10155_1044+10 others(8): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 231174152 | |||||
| chr1:231174210
|
G | A | 1 | a0001c0001t0004g0126 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1044+10197G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231174210 | ||||||
| chr1:231174290
|
C | T | 1 | a0001c0001t0002g0321 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1044+10277C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231174290 | ||||||
| chr1:231174333
|
A | AT | 10 | a0001c0001t0002g0130a0001c0001t0053g0052a0001c0001t0054g0322others(7): Show | 10 | HG02080.hp1 HG02486.hp2 HG02738.hp1 others(7): Show |
intron_variant | MODIFIER | c.1044+10335dupT | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 231174333 | |||||
| chr1:231174423
|
C | A | 1 | a0001c0001t0001g0268 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1044+10410C>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231174423 | ||||||
| chr1:231174486
|
T | C | 3 | a0001c0001t0026g0061a0001c0001t0026g0062a0001c0023t0039g0005 | 3 | HG01884.hp2 HG02055.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.1044+10473T>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231174486 | ||||||
| chr1:231174597
|
T | C | 29 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0034others(26): Show | 29 | HG00099.hp2 HG00597.hp1 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.1044+10584T>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231174597 | ||||||
| chr1:231174606
|
C | T | 1 | a0001c0001t0063g0004 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1044+10593C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231174606 | ||||||
| chr1:231174680
|
T | C | 1 | a0001c0002t0003g0197 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1044+10667T>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231174680 | ||||||
| chr1:231174839
|
A | C | 28 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0226others(25): Show | 28 | HG00280.hp2 HG01243.hp1 HG01891.hp1 others(25): Show |
intron_variant | MODIFIER | c.1044+10826A>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231174839 | ||||||
| chr1:231174929
|
T | A | 130 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0034others(127): Show | 130 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.1044+10916T>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231174929 | ||||||
| chr1:231175047
|
T | C | 144 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0034others(141): Show | 145 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.1044+11034T>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231175047 | ||||||
| chr1:231175111
|
C | T | 1 | a0001c0001t0001g0050 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1044+11098C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231175111 | ||||||
| chr1:231175265
|
G | A | 1 | a0001c0001t0054g0322 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1044+11252G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231175265 | ||||||
| chr1:231175367
|
G | A | 1 | a0001c0001t0052g0350 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1044+11354G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231175367 | ||||||
| chr1:231175424
|
G | A | 10 | a0001c0001t0025g0244a0001c0001t0025g0245a0001c0001t0045g0169others(7): Show | 10 | HG00323.hp2 HG00609.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1044+11411G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231175424 | ||||||
| chr1:231175476
|
T | C | 1 | a0001c0026t0042g0028 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1044+11463T>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231175476 | ||||||
| chr1:231175612
|
G | A | 1 | a0001c0003t0055g0112 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1044+11599G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231175612 | ||||||
| chr1:231175679
|
A | G | 1 | a0001c0001t0017g0332 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1044+11666A>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231175679 | ||||||
| chr1:231175721
|
C | A | 3 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0002t0009g0116 | 3 | HG02451.hp2 HG03209.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1044+11708C>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231175721 | ||||||
| chr1:231175874
|
G | A | 2 | a0001c0001t0001g0187a0001c0001t0015g0136 | 2 | HG01261.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1044+11861G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231175874 | ||||||
| chr1:231175950
|
G | A | 1 | a0001c0001t0008g0339 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1044+11937G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231175950 | ||||||
| chr1:231176121
|
A | G | 144 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040others(141): Show | 145 | HG00140.hp2 HG00408.hp2 HG00597.hp1 others(142): Show |
intron_variant | MODIFIER | c.1044+12108A>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231176121 | ||||||
| chr1:231176217
|
T | A | 152 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040others(149): Show | 153 | HG00140.hp2 HG00408.hp2 HG00597.hp1 others(150): Show |
intron_variant | MODIFIER | c.1044+12204T>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231176217 | ||||||
| chr1:231176324
|
A | G | 144 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040others(141): Show | 145 | HG00140.hp2 HG00408.hp2 HG00597.hp1 others(142): Show |
intron_variant | MODIFIER | c.1044+12311A>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231176324 | ||||||
| chr1:231176343
|
A | G | 148 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040others(145): Show | 149 | HG00140.hp2 HG00408.hp2 HG00597.hp1 others(146): Show |
intron_variant | MODIFIER | c.1044+12330A>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231176343 | ||||||
| chr1:231176349
|
A | G | 3 | a0001c0001t0026g0061a0001c0001t0026g0062a0001c0023t0039g0005 | 3 | HG01884.hp2 HG02055.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.1044+12336A>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231176349 | ||||||
| chr1:231176453
|
C | T | 240 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040others(237): Show | 241 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(238): Show |
intron_variant | MODIFIER | c.1044+12440C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231176453 | ||||||
| chr1:231176466
|
G | T | 3 | a0001c0001t0054g0322a0001c0001t0063g0004a0001c0026t0042g0028 | 3 | HG02647.hp2 HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1044+12453G>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231176466 | ||||||
| chr1:231176629
|
G | T | 4 | a0001c0003t0006g0069a0001c0003t0012g0068a0001c0003t0012g0070others(1): Show | 4 | NA18941.hp2 NA18961.hp2 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.1044+12616G>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231176629 | ||||||
| chr1:231176710
|
G | A | 2 | a0001c0001t0054g0322a0001c0001t0063g0004 | 2 | HG02647.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1044+12697G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231176710 | ||||||
| chr1:231176830
|
G | A | 1 | a0001c0001t0052g0350 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1044+12817G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231176830 | ||||||
| chr1:231176906
|
C | CA | 14 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0302others(11): Show | 14 | HG02071.hp1 HG02155.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.1044+12910dupA | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 231176906 | |||||
| chr1:231176906
|
C | CAAAAAA | 9 | a0001c0001t0001g0207a0001c0001t0002g0128a0001c0001t0004g0001others(6): Show | 10 | HG00639.hp1 HG01074.hp1 HG01346.hp2 others(7): Show |
intron_variant | MODIFIER | c.1044+12905_1044+12 others(12): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 231176906 | |||||
| chr1:231176906
|
C | CAAAAAAA | 27 | a0001c0001t0001g0047a0001c0001t0001g0135a0001c0001t0001g0194others(24): Show | 27 | HG01106.hp2 HG01123.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.1044+12904_1044+12 others(13): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 231176906 | |||||
| chr1:231176906
|
C | CAAAAAAA others(1): Show |
36 | a0001c0001t0001g0187a0001c0001t0001g0216a0001c0001t0001g0217others(33): Show | 36 | HG00642.hp1 HG00738.hp1 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.1044+12903_1044+12 others(14): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 231176906 | |||||
| chr1:231176906
|
C | CAAAAAAA others(2): Show |
32 | a0001c0001t0001g0041a0001c0001t0001g0204a0001c0001t0001g0227others(29): Show | 32 | HG00140.hp2 HG00673.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.1044+12902_1044+12 others(15): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 231176906 | |||||
| chr1:231176906
|
C | CAAAAAAA others(3): Show |
23 | a0001c0001t0001g0040a0001c0001t0001g0054a0001c0001t0001g0117others(20): Show | 23 | HG00597.hp1 HG00673.hp2 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.1044+12901_1044+12 others(16): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 231176906 | |||||
| chr1:231176906
|
C | CAAAAAAA others(4): Show |
20 | a0001c0001t0001g0226a0001c0001t0001g0232a0001c0001t0001g0235others(17): Show | 20 | HG00280.hp2 HG00621.hp1 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.1044+12900_1044+12 others(17): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 231176906 | |||||
| chr1:231176906
|
C | CAAAAAAA others(5): Show |
42 | a0001c0001t0001g0127a0001c0001t0001g0144a0001c0001t0002g0045others(39): Show | 42 | HG00733.hp1 HG01069.hp1 HG01071.hp2 others(39): Show |
intron_variant | MODIFIER | c.1044+12899_1044+12 others(18): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 231176906 | |||||
| chr1:231176906
|
C | CAAAAAAA others(6): Show |
17 | a0001c0001t0004g0335a0001c0001t0008g0341a0001c0001t0030g0340others(14): Show | 17 | HG00423.hp2 HG00438.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.1044+12898_1044+12 others(19): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 231176906 | |||||
| chr1:231176906
|
C | CAAAAAAA others(7): Show |
3 | a0001c0001t0024g0043a0001c0002t0005g0295a0001c0003t0006g0075 | 3 | HG01433.hp1 HG02486.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.1044+12897_1044+12 others(20): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 231176906 | |||||
| chr1:231176906
|
C | CAAAAAAA others(8): Show |
1 | a0001c0003t0007g0098 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1044+12896_1044+12 others(21): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 231176906 | |||||
| chr1:231176906
|
C | CAAAAAAA others(9): Show |
4 | a0001c0001t0001g0039a0001c0001t0004g0142a0001c0002t0003g0143others(1): Show | 4 | HG03834.hp1 HG06807.hp2 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.1044+12895_1044+12 others(22): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 231176906 | |||||
| chr1:231176906
|
C | CAAAAAAA others(10): Show |
7 | a0001c0001t0001g0038a0001c0001t0004g0141a0001c0001t0017g0332others(4): Show | 7 | HG01169.hp1 HG02922.hp2 NA18612.hp2 others(4): Show |
intron_variant | MODIFIER | c.1044+12894_1044+12 others(23): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 231176906 | |||||
| chr1:231176906
|
C | CAAAAAAA others(11): Show |
2 | a0001c0001t0023g0140a0001c0002t0003g0124 | 2 | HG01496.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.1044+12910_1044+12 others(24): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 231176906 | |||||
| chr1:231176906
|
C | CAAAAAAA others(12): Show |
2 | a0001c0001t0002g0219a0001c0002t0003g0257 | 2 | HG00408.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.1044+12910_1044+12 others(25): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 231176906 | |||||
| chr1:231176906
|
C | CAAAAAAA others(14): Show |
1 | a0001c0001t0014g0218 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1044+12910_1044+12 others(27): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 231176906 | |||||
| chr1:231176912
|
A | AAAAAAAA others(16): Show |
1 | a0001c0001t0052g0350 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1044+12910_1044+12 others(29): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 231176912 | |||||
| chr1:231176912
|
A | AAAAAAAA others(12): Show |
3 | a0001c0001t0027g0065a0001c0001t0027g0066a0001c0001t0062g0067 | 3 | HG02109.hp2 HG02257.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1044+12908_1044+12 others(25): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 231176912 | |||||
| chr1:231176968
|
G | C | 1 | a0001c0001t0004g0335 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1044+12955G>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231176968 | ||||||
| chr1:231176992
|
C | T | 1 | a0001c0003t0059g0086 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1044+12979C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231176992 | ||||||
| chr1:231177279
|
C | T | 1 | a0001c0001t0052g0350 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1044+13266C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231177279 | ||||||
| chr1:231177343
|
T | C | 1 | a0001c0001t0001g0334 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1044+13330T>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231177343 | ||||||
| chr1:231177446
|
T | C | 2 | a0001c0001t0027g0065a0001c0001t0027g0066 | 2 | HG02109.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1044+13433T>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231177446 | ||||||
| chr1:231177483
|
A | C | 4 | a0001c0001t0001g0292a0001c0001t0002g0224a0001c0001t0005g0293others(1): Show | 4 | HG01255.hp2 HG01516.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1044+13470A>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231177483 | ||||||
| chr1:231177508
|
T | C | 1 | a0001c0003t0006g0114 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1044+13495T>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231177508 | ||||||
| chr1:231177694
|
A | G | 6 | a0001c0004t0010g0007a0001c0004t0010g0013a0001c0004t0010g0014others(3): Show | 6 | HG02055.hp2 HG02486.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1044+13681A>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231177694 | ||||||
| chr1:231178092
|
A | G | 1 | a0001c0001t0001g0242 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1044+14079A>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231178092 | ||||||
| chr1:231178113
|
T | C | 241 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040others(238): Show | 242 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(239): Show |
intron_variant | MODIFIER | c.1044+14100T>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231178113 | ||||||
| chr1:231178447
|
C | T | 1 | a0001c0001t0002g0223 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1044+14434C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231178447 | ||||||
| chr1:231178462
|
C | T | 5 | a0001c0003t0007g0073a0001c0003t0007g0104a0001c0003t0007g0105others(2): Show | 5 | HG00639.hp2 HG00733.hp1 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.1044+14449C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231178462 | ||||||
| chr1:231178475
|
A | G | 144 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040others(141): Show | 145 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.1044+14462A>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231178475 | ||||||
| chr1:231178476
|
C | T | 1 | a0001c0001t0001g0242 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1044+14463C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231178476 | ||||||
| chr1:231178502
|
G | A | 1 | a0001c0001t0017g0332 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1044+14489G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231178502 | ||||||
| chr1:231178546
|
A | G | 2 | a0001c0001t0001g0222a0001c0001t0002g0223 | 2 | HG01168.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.1044+14533A>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231178546 | ||||||
| chr1:231178583
|
C | T | 6 | a0001c0004t0010g0007a0001c0004t0010g0013a0001c0004t0010g0014others(3): Show | 6 | HG02055.hp2 HG02486.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1044+14570C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231178583 | ||||||
| chr1:231178746
|
C | G | 1 | a0001c0001t0001g0035 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1044+14733C>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231178746 | ||||||
| chr1:231178829
|
G | A | 70 | a0001c0001t0001g0127a0001c0001t0001g0204a0001c0001t0001g0242others(67): Show | 70 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.1044+14816G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231178829 | ||||||
| chr1:231178965
|
A | T | 3 | a0001c0001t0001g0243a0001c0001t0001g0250a0001c0001t0046g0324 | 3 | NA18950.hp1 NA18973.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.1044+14952A>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231178965 | ||||||
| chr1:231179154
|
G | A | 1 | a0001c0001t0052g0350 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1044+15141G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231179154 | ||||||
| chr1:231179161
|
C | T | 2 | a0001c0001t0054g0322a0001c0001t0063g0004 | 2 | HG02647.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1044+15148C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231179161 | ||||||
| chr1:231179167
|
T | A | 67 | a0001c0001t0001g0127a0001c0001t0001g0204a0001c0001t0002g0045others(64): Show | 67 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.1044+15154T>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231179167 | ||||||
| chr1:231179231
|
G | A | 6 | a0001c0004t0010g0007a0001c0004t0010g0013a0001c0004t0010g0014others(3): Show | 6 | HG02055.hp2 HG02486.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1044+15218G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231179231 | ||||||
| chr1:231179309
|
T | C | 2 | a0001c0001t0027g0065a0001c0001t0027g0066 | 2 | HG02109.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1044+15296T>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231179309 | ||||||
| chr1:231179423
|
C | T | 2 | a0001c0001t0004g0163a0001c0001t0004g0164 | 2 | NA18977.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.1044+15410C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231179423 | ||||||
| chr1:231179527
|
G | A | 2 | a0001c0001t0001g0041a0001c0001t0001g0054 | 2 | HG02148.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.1044+15514G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231179527 | ||||||
| chr1:231179572
|
A | G | 4 | a0001c0001t0001g0220a0001c0001t0001g0221a0003c0008t0001g0240others(1): Show | 4 | HG01256.hp2 HG02738.hp2 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.1044+15559A>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231179572 | ||||||
| chr1:231179765
|
C | A | 1 | a0001c0001t0034g0063 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1044+15752C>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231179765 | ||||||
| chr1:231179827
|
G | A | 4 | a0001c0001t0002g0234a0001c0001t0002g0319a0001c0001t0018g0266others(1): Show | 4 | HG00738.hp1 HG00741.hp1 HG01070.hp1 others(1): Show |
intron_variant | MODIFIER | c.1044+15814G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231179827 | ||||||
| chr1:231179969
|
T | C | 1 | a0001c0001t0052g0350 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1044+15956T>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231179969 | ||||||
| chr1:231180144
|
T | A | 1 | a0001c0001t0034g0063 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1044+16131T>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231180144 | ||||||
| chr1:231180158
|
T | C | 27 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0226others(24): Show | 27 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.1044+16145T>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231180158 | ||||||
| chr1:231180364
|
C | A | 2 | a0001c0001t0002g0277a0001c0001t0008g0347 | 2 | NA18940.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.1044+16351C>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231180364 | ||||||
| chr1:231180387
|
A | G | 1 | a0001c0003t0055g0112 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1044+16374A>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231180387 | ||||||
| chr1:231180428
|
T | G | 68 | a0001c0001t0001g0117a0001c0001t0001g0127a0001c0001t0001g0204others(65): Show | 68 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.1044+16415T>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231180428 | ||||||
| chr1:231180478
|
C | A | 1 | a0001c0001t0052g0350 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1044+16465C>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231180478 | ||||||
| chr1:231180709
|
T | G | 2 | a0001c0001t0054g0322a0001c0001t0063g0004 | 2 | HG02647.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1045-16662T>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231180709 | ||||||
| chr1:231180740
|
G | A | 1 | a0001c0001t0052g0350 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1045-16631G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231180740 | ||||||
| chr1:231180952
|
GGTTTTTT others(9): Show |
G | 129 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040others(126): Show | 130 | HG00140.hp2 HG00280.hp2 HG00597.hp1 others(127): Show |
intron_variant | MODIFIER | c.1045-16414_1045-16 others(22): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 231180952 | |||||
| chr1:231180953
|
GTTTT | G | 6 | a0001c0004t0010g0007a0001c0004t0010g0013a0001c0004t0010g0014others(3): Show | 6 | HG02055.hp2 HG02486.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1045-16414_1045-16 others(10): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 231180953 | |||||
| chr1:231180957
|
TTTTG | T | 110 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0127others(107): Show | 110 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.1045-16388_1045-16 others(10): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 231180957 | |||||
| chr1:231180999
|
C | T | 2 | a0001c0001t0024g0043a0001c0002t0003g0044 | 2 | HG02602.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.1045-16372C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231180999 | ||||||
| chr1:231181423
|
A | G | 2 | a0001c0003t0006g0084a0001c0003t0006g0085 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1045-15948A>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231181423 | ||||||
| chr1:231181425
|
C | A | 71 | a0001c0001t0001g0127a0001c0001t0001g0204a0001c0001t0002g0045others(68): Show | 71 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.1045-15946C>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231181425 | ||||||
| chr1:231181433
|
G | A | 131 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040others(128): Show | 132 | HG00140.hp2 HG00280.hp2 HG00597.hp1 others(129): Show |
intron_variant | MODIFIER | c.1045-15938G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231181433 | ||||||
| chr1:231181437
|
G | A | 10 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0135others(7): Show | 10 | HG00280.hp2 HG01169.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.1045-15934G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231181437 | ||||||
| chr1:231181464
|
G | A | 3 | a0001c0001t0027g0065a0001c0001t0027g0066a0001c0001t0062g0067 | 3 | HG02109.hp2 HG02257.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1045-15907G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231181464 | ||||||
| chr1:231181698
|
C | T | 1 | a0001c0002t0009g0209 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1045-15673C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231181698 | ||||||
| chr1:231181752
|
T | A | 1 | a0001c0001t0052g0350 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1045-15619T>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231181752 | ||||||
| chr1:231181858
|
T | C | 1 | a0001c0001t0027g0065 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1045-15513T>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231181858 | ||||||
| chr1:231181964
|
G | T | 1 | a0001c0001t0034g0063 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1045-15407G>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231181964 | ||||||
| chr1:231181969
|
T | A | 1 | a0001c0003t0007g0104 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1045-15402T>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231181969 | ||||||
| chr1:231182001
|
T | A | 1 | a0001c0002t0009g0330 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1045-15370T>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231182001 | ||||||
| chr1:231182029
|
C | T | 1 | a0001c0001t0034g0063 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1045-15342C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231182029 | ||||||
| chr1:231182169
|
G | T | 1 | a0001c0026t0042g0028 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1045-15202G>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231182169 | ||||||
| chr1:231182441
|
G | C | 106 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0127others(103): Show | 106 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.1045-14930G>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231182441 | ||||||
| chr1:231182492
|
T | A | 4 | a0001c0001t0001g0216a0001c0001t0001g0227a0001c0001t0037g0236others(1): Show | 4 | HG02809.hp2 HG03209.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1045-14879T>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231182492 | ||||||
| chr1:231182594
|
A | G | 1 | a0001c0001t0002g0130 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1045-14777A>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231182594 | ||||||
| chr1:231182608
|
A | G | 1 | a0001c0001t0004g0333 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1045-14763A>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231182608 | ||||||
| chr1:231182849
|
C | T | 2 | a0001c0001t0027g0066a0001c0001t0062g0067 | 2 | HG02109.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.1045-14522C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231182849 | ||||||
| chr1:231182932
|
C | T | 102 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0127others(99): Show | 102 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.1045-14439C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231182932 | ||||||
| chr1:231182978
|
C | T | 2 | a0001c0001t0026g0062a0001c0023t0039g0005 | 2 | HG01884.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.1045-14393C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231182978 | ||||||
| chr1:231183056
|
G | A | 6 | a0001c0004t0010g0007a0001c0004t0010g0013a0001c0004t0010g0014others(3): Show | 6 | HG02055.hp2 HG02486.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1045-14315G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231183056 | ||||||
| chr1:231183073
|
A | G | 1 | a0001c0001t0001g0318 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1045-14298A>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231183073 | ||||||
| chr1:231183074
|
G | C | 2 | a0001c0001t0054g0322a0001c0001t0063g0004 | 2 | HG02647.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1045-14297G>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231183074 | ||||||
| chr1:231183221
|
G | C | 1 | a0001c0002t0003g0301 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1045-14150G>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231183221 | ||||||
| chr1:231183277
|
T | C | 3 | a0001c0001t0002g0182a0001c0001t0004g0153a0001c0001t0004g0180 | 3 | HG03831.hp2 HG03927.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1045-14094T>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231183277 | ||||||
| chr1:231183557
|
T | C | 4 | a0001c0001t0017g0332a0001c0001t0026g0061a0001c0001t0026g0062others(1): Show | 4 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.1045-13814T>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231183557 | ||||||
| chr1:231183585
|
G | A | 9 | a0001c0001t0026g0061a0001c0001t0026g0062a0001c0004t0010g0007others(6): Show | 9 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.1045-13786G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231183585 | ||||||
| chr1:231183599
|
A | G | 350 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0032others(347): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.1045-13772A>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231183599 | ||||||
| chr1:231183684
|
G | C | 1 | a0001c0001t0001g0040 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1045-13687G>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231183684 | ||||||
| chr1:231184059
|
G | A | 1 | a0001c0002t0003g0158 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1045-13312G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231184059 | ||||||
| chr1:231184145
|
GAGACTCA others(2097): Show |
G | 6 | a0001c0004t0010g0007a0001c0004t0010g0013a0001c0004t0010g0014others(3): Show | 6 | HG02055.hp2 HG02486.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1045-13223_1045-11 others(6): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 231184145 | |||||
| chr1:231184236
|
A | G | 1 | a0001c0001t0013g0123 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1045-13135A>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231184236 | ||||||
| chr1:231184321
|
T | C | 1 | a0001c0004t0020g0023 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1045-13050T>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231184321 | ||||||
| chr1:231184349
|
A | G | 9 | a0001c0001t0001g0228a0001c0001t0001g0334a0001c0001t0004g0333others(6): Show | 9 | HG02257.hp1 HG02258.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1045-13022A>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231184349 | ||||||
| chr1:231184406
|
C | T | 1 | a0001c0001t0001g0255 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1045-12965C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231184406 | ||||||
| chr1:231184498
|
T | G | 1 | a0001c0001t0002g0336 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1045-12873T>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231184498 | ||||||
| chr1:231184644
|
C | G | 15 | a0001c0001t0001g0127a0001c0003t0006g0069a0001c0003t0006g0077others(12): Show | 15 | HG00423.hp2 HG00438.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.1045-12727C>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231184644 | ||||||
| chr1:231184691
|
G | A | 1 | a0001c0003t0007g0108 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1045-12680G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231184691 | ||||||
| chr1:231184720
|
G | A | 7 | a0001c0001t0001g0187a0001c0001t0001g0227a0001c0004t0001g0008others(4): Show | 7 | HG01261.hp1 HG02280.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1045-12651G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231184720 | ||||||
| chr1:231184798
|
C | T | 1 | a0001c0024t0004g0026 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1045-12573C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231184798 | ||||||
| chr1:231184873
|
G | C | 1 | a0001c0002t0003g0256 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1045-12498G>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231184873 | ||||||
| chr1:231184905
|
G | A | 1 | a0001c0001t0004g0142 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1045-12466G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231184905 | ||||||
| chr1:231184931
|
C | A | 1 | a0001c0001t0001g0049 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1045-12440C>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231184931 | ||||||
| chr1:231184974
|
A | T | 55 | a0001c0001t0004g0141a0001c0001t0005g0230a0001c0001t0017g0338others(52): Show | 56 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.1045-12397A>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231184974 | ||||||
| chr1:231185059
|
T | A | 1 | a0001c0001t0001g0334 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1045-12312T>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231185059 | ||||||
| chr1:231185068
|
G | C | 1 | a0001c0001t0001g0334 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1045-12303G>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231185068 | ||||||
| chr1:231185074
|
C | T | 5 | a0001c0001t0001g0249a0001c0001t0001g0269a0001c0001t0001g0271others(2): Show | 5 | HG00408.hp1 HG02071.hp1 NA18944.hp2 others(2): Show |
intron_variant | MODIFIER | c.1045-12297C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231185074 | ||||||
| chr1:231185174
|
C | T | 6 | a0001c0002t0009g0116a0001c0002t0009g0139a0001c0002t0009g0156others(3): Show | 6 | HG02895.hp2 HG03130.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.1045-12197C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231185174 | ||||||
| chr1:231185175
|
G | A | 1 | a0001c0001t0017g0137 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1045-12196G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231185175 | ||||||
| chr1:231185302
|
G | C | 1 | a0001c0001t0047g0059 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1045-12069G>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231185302 | ||||||
| chr1:231185469
|
G | A | 6 | a0001c0001t0001g0296a0001c0001t0001g0323a0001c0001t0001g0326others(3): Show | 6 | HG00323.hp1 HG00642.hp2 HG00741.hp2 others(3): Show |
intron_variant | MODIFIER | c.1045-11902G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231185469 | ||||||
| chr1:231185531
|
T | C | 38 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0054others(35): Show | 38 | HG00673.hp2 HG01106.hp2 HG01169.hp1 others(35): Show |
intron_variant | MODIFIER | c.1045-11840T>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231185531 | ||||||
| chr1:231185566
|
A | G | 111 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0054others(108): Show | 112 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.1045-11805A>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231185566 | ||||||
| chr1:231185595
|
C | A | 1 | a0001c0002t0005g0120 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1045-11776C>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231185595 | ||||||
| chr1:231185749
|
C | T | 1 | a0001c0001t0008g0345 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1045-11622C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231185749 | ||||||
| chr1:231185792
|
G | A | 52 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0054others(49): Show | 52 | HG00280.hp1 HG00323.hp2 HG00673.hp2 others(49): Show |
intron_variant | MODIFIER | c.1045-11579G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231185792 | ||||||
| chr1:231185896
|
T | C | 108 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0054others(105): Show | 109 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.1045-11475T>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231185896 | ||||||
| chr1:231185913
|
G | T | 1 | a0001c0014t0016g0328 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1045-11458G>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231185913 | ||||||
| chr1:231186113
|
T | C | 1 | a0001c0003t0006g0099 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1045-11258T>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231186113 | ||||||
| chr1:231186159
|
C | T | 1 | a0001c0002t0005g0138 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1045-11212C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231186159 | ||||||
| chr1:231186164
|
C | G | 1 | a0001c0001t0063g0004 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1045-11207C>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231186164 | ||||||
| chr1:231186197
|
C | A | 108 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0054others(105): Show | 109 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.1045-11174C>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231186197 | ||||||
| chr1:231186202
|
G | A | 1 | a0001c0001t0047g0059 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1045-11169G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231186202 | ||||||
| chr1:231186297
|
A | G | 108 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0054others(105): Show | 109 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.1045-11074A>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231186297 | ||||||
| chr1:231186471
|
C | T | 55 | a0001c0001t0004g0141a0001c0001t0017g0338a0001c0001t0032g0349others(52): Show | 56 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.1045-10900C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231186471 | ||||||
| chr1:231186741
|
T | A | 1 | a0001c0003t0007g0108 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1045-10630T>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231186741 | ||||||
| chr1:231186765
|
C | T | 4 | a0001c0001t0001g0041a0001c0001t0001g0054a0001c0001t0001g0135others(1): Show | 4 | HG02148.hp1 HG02300.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.1045-10606C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231186765 | ||||||
| chr1:231186882
|
T | C | 20 | a0001c0001t0017g0338a0001c0002t0005g0031a0001c0002t0005g0036others(17): Show | 20 | HG00438.hp1 HG00609.hp1 HG00642.hp1 others(17): Show |
intron_variant | MODIFIER | c.1045-10489T>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231186882 | ||||||
| chr1:231186885
|
GATGA | G | 6 | a0001c0004t0010g0007a0001c0004t0010g0013a0001c0004t0010g0014others(3): Show | 6 | HG02055.hp2 HG02486.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1045-10485_1045-10 others(10): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231186885 | ||||||
| chr1:231186890
|
T | C | 6 | a0001c0004t0010g0007a0001c0004t0010g0013a0001c0004t0010g0014others(3): Show | 6 | HG02055.hp2 HG02486.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1045-10481T>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231186890 | ||||||
| chr1:231186957
|
C | T | 1 | a0001c0001t0011g0251 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1045-10414C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231186957 | ||||||
| chr1:231186963
|
C | A | 2 | a0002c0007t0019g0002a0002c0007t0019g0316 | 3 | HG01256.hp1 HG01258.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.1045-10408C>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231186963 | ||||||
| chr1:231186980
|
G | A | 1 | a0001c0001t0027g0066 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1045-10391G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231186980 | ||||||
| chr1:231187003
|
T | C | 36 | a0001c0001t0004g0141a0001c0001t0032g0349a0001c0001t0037g0236others(33): Show | 37 | HG00408.hp2 HG00423.hp1 HG01256.hp1 others(34): Show |
intron_variant | MODIFIER | c.1045-10368T>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231187003 | ||||||
| chr1:231187035
|
C | G | 2 | a0001c0001t0001g0127a0001c0003t0006g0110 | 2 | NA18954.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1045-10336C>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231187035 | ||||||
| chr1:231187081
|
C | G | 11 | a0001c0001t0001g0047a0001c0001t0004g0001a0001c0001t0004g0126others(8): Show | 12 | HG01074.hp1 HG01123.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.1045-10290C>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231187081 | ||||||
| chr1:231187092
|
G | A | 4 | a0001c0001t0001g0040a0001c0001t0001g0205a0001c0001t0023g0133others(1): Show | 4 | HG00673.hp2 HG01169.hp1 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.1045-10279G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231187092 | ||||||
| chr1:231187108
|
G | A | 3 | a0001c0001t0004g0162a0001c0001t0004g0166a0001c0001t0004g0276 | 3 | HG01074.hp1 HG01993.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.1045-10263G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231187108 | ||||||
| chr1:231187146
|
G | A | 3 | a0001c0001t0004g0333a0001c0001t0048g0237a0001c0012t0004g0351 | 3 | HG02258.hp2 HG02622.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1045-10225G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231187146 | ||||||
| chr1:231187272
|
G | A | 52 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0054others(49): Show | 52 | HG00280.hp1 HG00323.hp2 HG00673.hp2 others(49): Show |
intron_variant | MODIFIER | c.1045-10099G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231187272 | ||||||
| chr1:231187401
|
T | A | 2 | a0001c0001t0001g0298a0001c0001t0001g0334 | 2 | HG02717.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.1045-9970T>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231187401 | ||||||
| chr1:231187515
|
A | G | 1 | a0001c0001t0005g0331 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1045-9856A>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231187515 | ||||||
| chr1:231187593
|
A | G | 50 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0054others(47): Show | 50 | HG00280.hp1 HG00323.hp2 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.1045-9778A>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231187593 | ||||||
| chr1:231187620
|
G | A | 1 | a0001c0001t0004g0151 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1045-9751G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231187620 | ||||||
| chr1:231187756
|
G | A | 2 | a0001c0001t0001g0186a0001c0002t0003g0051 | 2 | HG03669.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.1045-9615G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231187756 | ||||||
| chr1:231187822
|
A | C | 15 | a0001c0001t0032g0349a0001c0002t0001g0178a0001c0002t0003g0033others(12): Show | 15 | HG00408.hp2 HG00423.hp1 HG02155.hp1 others(12): Show |
intron_variant | MODIFIER | c.1045-9549A>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231187822 | ||||||
| chr1:231187830
|
A | C | 1 | a0001c0001t0002g0224 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1045-9541A>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231187830 | ||||||
| chr1:231187947
|
A | G | 55 | a0001c0001t0004g0141a0001c0001t0017g0338a0001c0001t0032g0349others(52): Show | 56 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.1045-9424A>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231187947 | ||||||
| chr1:231188038
|
C | G | 1 | a0001c0001t0001g0186 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1045-9333C>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231188038 | ||||||
| chr1:231188258
|
G | T | 6 | a0001c0004t0010g0007a0001c0004t0010g0013a0001c0004t0010g0014others(3): Show | 6 | HG02055.hp2 HG02486.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1045-9113G>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231188258 | ||||||
| chr1:231188383
|
G | A | 1 | a0001c0001t0001g0334 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1045-8988G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231188383 | ||||||
| chr1:231188511
|
G | A | 35 | a0001c0001t0004g0141a0001c0001t0032g0349a0001c0001t0037g0236others(32): Show | 36 | HG00408.hp2 HG00423.hp1 HG01256.hp1 others(33): Show |
intron_variant | MODIFIER | c.1045-8860G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231188511 | ||||||
| chr1:231188737
|
G | A | 108 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0054others(105): Show | 109 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.1045-8634G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231188737 | ||||||
| chr1:231188753
|
T | C | 20 | a0001c0001t0017g0338a0001c0002t0005g0031a0001c0002t0005g0036others(17): Show | 20 | HG00438.hp1 HG00609.hp1 HG00642.hp1 others(17): Show |
intron_variant | MODIFIER | c.1045-8618T>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231188753 | ||||||
| chr1:231188795
|
G | A | 108 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0054others(105): Show | 109 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.1045-8576G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231188795 | ||||||
| chr1:231188804
|
C | G | 108 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0054others(105): Show | 109 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.1045-8567C>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231188804 | ||||||
| chr1:231188852
|
C | T | 6 | a0001c0004t0010g0007a0001c0004t0010g0013a0001c0004t0010g0014others(3): Show | 6 | HG02055.hp2 HG02486.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1045-8519C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231188852 | ||||||
| chr1:231189344
|
C | T | 53 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0054others(50): Show | 53 | HG00280.hp1 HG00323.hp2 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.1045-8027C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231189344 | ||||||
| chr1:231189521
|
T | C | 2 | a0001c0002t0005g0138a0001c0009t0005g0018 | 2 | HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1045-7850T>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231189521 | ||||||
| chr1:231189865
|
C | A | 1 | a0001c0001t0011g0201 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1045-7506C>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231189865 | ||||||
| chr1:231189866
|
G | A | 1 | a0001c0001t0011g0201 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1045-7505G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231189866 | ||||||
| chr1:231189883
|
G | A | 56 | a0001c0001t0004g0141a0001c0001t0017g0338a0001c0001t0032g0349others(53): Show | 57 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.1045-7488G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231189883 | ||||||
| chr1:231190033
|
A | G | 117 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0054others(114): Show | 118 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.1045-7338A>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231190033 | ||||||
| chr1:231190090
|
A | G | 55 | a0001c0001t0004g0141a0001c0001t0017g0338a0001c0001t0032g0349others(52): Show | 56 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.1045-7281A>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231190090 | ||||||
| chr1:231190340
|
G | A | 254 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0047others(251): Show | 256 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(253): Show |
intron_variant | MODIFIER | c.1045-7031G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231190340 | ||||||
| chr1:231190470
|
G | A | 1 | a0001c0001t0001g0050 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1045-6901G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231190470 | ||||||
| chr1:231190513
|
A | T | 1 | a0001c0001t0001g0194 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1045-6858A>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231190513 | ||||||
| chr1:231190548
|
C | T | 1 | a0001c0002t0038g0060 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1045-6823C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231190548 | ||||||
| chr1:231190598
|
GTAGCCAA others(8): Show |
G | 55 | a0001c0001t0004g0141a0001c0001t0017g0338a0001c0001t0032g0349others(52): Show | 56 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.1045-6771_1045-675 others(19): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 231190598 | |||||
| chr1:231190648
|
G | A | 4 | a0001c0001t0002g0234a0001c0001t0002g0319a0001c0001t0018g0266others(1): Show | 4 | HG00738.hp1 HG00741.hp1 HG01070.hp1 others(1): Show |
intron_variant | MODIFIER | c.1045-6723G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231190648 | ||||||
| chr1:231190846
|
C | T | 6 | a0001c0001t0001g0329a0001c0001t0024g0043a0001c0001t0024g0247others(3): Show | 6 | HG00280.hp1 HG00323.hp2 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.1045-6525C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231190846 | ||||||
| chr1:231190948
|
C | T | 1 | a0001c0001t0053g0052 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1045-6423C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231190948 | ||||||
| chr1:231190995
|
G | A | 2 | a0001c0001t0005g0215a0001c0001t0034g0063 | 2 | HG02630.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1045-6376G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231190995 | ||||||
| chr1:231191015
|
A | G | 1 | a0001c0002t0009g0208 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1045-6356A>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231191015 | ||||||
| chr1:231191043
|
C | T | 1 | a0001c0001t0004g0175 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1045-6328C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231191043 | ||||||
| chr1:231191160
|
C | G | 3 | a0001c0004t0020g0023a0001c0004t0020g0024a0001c0004t0020g0025 | 3 | HG02615.hp2 HG02895.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1045-6211C>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231191160 | ||||||
| chr1:231191278
|
T | A | 20 | a0001c0001t0001g0041a0001c0001t0001g0054a0001c0001t0001g0135others(17): Show | 20 | HG01243.hp1 HG02148.hp1 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.1045-6093T>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231191278 | ||||||
| chr1:231191282
|
C | T | 55 | a0001c0001t0004g0141a0001c0001t0017g0338a0001c0001t0032g0349others(52): Show | 56 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.1045-6089C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231191282 | ||||||
| chr1:231191312
|
G | A | 1 | a0001c0001t0001g0334 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1045-6059G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231191312 | ||||||
| chr1:231191320
|
C | T | 55 | a0001c0001t0004g0141a0001c0001t0017g0338a0001c0001t0032g0349others(52): Show | 56 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.1045-6051C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231191320 | ||||||
| chr1:231191443
|
G | A | 53 | a0001c0001t0004g0141a0001c0001t0017g0338a0001c0001t0032g0349others(50): Show | 54 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.1045-5928G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231191443 | ||||||
| chr1:231191453
|
G | A | 54 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0054others(51): Show | 54 | HG00280.hp1 HG00323.hp2 HG00673.hp2 others(51): Show |
intron_variant | MODIFIER | c.1045-5918G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231191453 | ||||||
| chr1:231191458
|
G | A | 2 | a0001c0001t0005g0215a0001c0001t0034g0063 | 2 | HG02630.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1045-5913G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231191458 | ||||||
| chr1:231191589
|
C | T | 1 | a0001c0001t0053g0052 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1045-5782C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231191589 | ||||||
| chr1:231191800
|
A | G | 1 | a0001c0001t0004g0179 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1045-5571A>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231191800 | ||||||
| chr1:231191866
|
T | C | 2 | a0001c0001t0005g0225a0001c0022t0005g0154 | 2 | HG02615.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1045-5505T>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231191866 | ||||||
| chr1:231191920
|
T | A | 57 | a0001c0001t0004g0141a0001c0001t0005g0215a0001c0001t0017g0338others(54): Show | 58 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.1045-5451T>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231191920 | ||||||
| chr1:231191951
|
A | C | 2 | a0001c0001t0015g0136a0001c0004t0015g0017 | 2 | HG02258.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1045-5420A>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231191951 | ||||||
| chr1:231192032
|
G | A | 2 | a0001c0001t0005g0215a0001c0001t0034g0063 | 2 | HG02630.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1045-5339G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231192032 | ||||||
| chr1:231192035
|
A | G | 109 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0054others(106): Show | 110 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.1045-5336A>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231192035 | ||||||
| chr1:231192042
|
C | T | 54 | a0001c0001t0004g0141a0001c0001t0017g0338a0001c0001t0032g0349others(51): Show | 55 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.1045-5329C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231192042 | ||||||
| chr1:231192067
|
G | A | 2 | a0001c0002t0005g0138a0001c0009t0005g0018 | 2 | HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1045-5304G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231192067 | ||||||
| chr1:231192113
|
A | G | 55 | a0001c0001t0004g0141a0001c0001t0017g0338a0001c0001t0032g0349others(52): Show | 56 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.1045-5258A>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231192113 | ||||||
| chr1:231192162
|
A | G | 1 | a0001c0001t0023g0133 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1045-5209A>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231192162 | ||||||
| chr1:231192202
|
G | GTC | 20 | a0001c0001t0017g0338a0001c0002t0005g0031a0001c0002t0005g0036others(17): Show | 20 | HG00438.hp1 HG00609.hp1 HG00642.hp1 others(17): Show |
intron_variant | MODIFIER | c.1045-5151_1045-515 others(6): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 231192202 | |||||
| chr1:231192202
|
GTC | G | 45 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0054others(42): Show | 45 | HG00280.hp1 HG00323.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.1045-5151_1045-515 others(6): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 231192202 | |||||
| chr1:231192247
|
G | T | 20 | a0001c0001t0017g0338a0001c0002t0005g0031a0001c0002t0005g0036others(17): Show | 20 | HG00438.hp1 HG00609.hp1 HG00642.hp1 others(17): Show |
intron_variant | MODIFIER | c.1045-5124G>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231192247 | ||||||
| chr1:231192300
|
A | G | 20 | a0001c0001t0001g0041a0001c0001t0001g0054a0001c0001t0001g0135others(17): Show | 20 | HG01243.hp1 HG02148.hp1 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.1045-5071A>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231192300 | ||||||
| chr1:231192340
|
A | G | 1 | a0001c0001t0004g0141 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1045-5031A>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231192340 | ||||||
| chr1:231192571
|
C | T | 9 | a0001c0001t0015g0136a0001c0002t0009g0116a0001c0002t0009g0139others(6): Show | 9 | HG02258.hp1 HG02622.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1045-4800C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231192571 | ||||||
| chr1:231192659
|
C | T | 2 | a0001c0001t0004g0163a0001c0001t0004g0164 | 2 | NA18977.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.1045-4712C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231192659 | ||||||
| chr1:231193071
|
G | C | 3 | a0001c0001t0004g0333a0001c0001t0048g0237a0001c0012t0004g0351 | 3 | HG02258.hp2 HG02622.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1045-4300G>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231193071 | ||||||
| chr1:231193113
|
C | G | 1 | a0001c0001t0017g0332 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1045-4258C>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231193113 | ||||||
| chr1:231193143
|
C | A | 113 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0054others(110): Show | 114 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.1045-4228C>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231193143 | ||||||
| chr1:231193188
|
C | T | 1 | a0001c0004t0013g0021 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1045-4183C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231193188 | ||||||
| chr1:231193431
|
G | A | 1 | a0001c0001t0004g0179 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1045-3940G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231193431 | ||||||
| chr1:231193491
|
A | ACT | 6 | a0001c0001t0001g0249a0001c0001t0001g0269a0001c0001t0001g0271others(3): Show | 6 | HG00408.hp1 HG02071.hp1 NA18944.hp1 others(3): Show |
intron_variant | MODIFIER | c.1045-3872_1045-387 others(6): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 231193491 | |||||
| chr1:231193503
|
G | GCT | 37 | a0001c0001t0001g0003a0001c0001t0001g0035a0001c0001t0001g0049others(34): Show | 39 | HG00738.hp2 HG01070.hp2 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.1045-3822_1045-382 others(6): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 231193503 | |||||
| chr1:231193503
|
G | GCTCT | 19 | a0001c0001t0001g0032a0001c0001t0001g0050a0001c0001t0001g0207others(16): Show | 19 | HG00408.hp1 HG00733.hp2 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.1045-3824_1045-382 others(8): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 231193503 | |||||
| chr1:231193503
|
G | GCTCTCT | 34 | a0001c0001t0001g0037a0001c0001t0001g0186a0001c0001t0001g0212others(31): Show | 34 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.1045-3826_1045-382 others(10): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 231193503 | |||||
| chr1:231193503
|
G | GCTCTCTC others(1): Show |
45 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0144others(42): Show | 45 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(42): Show |
intron_variant | MODIFIER | c.1045-3828_1045-382 others(12): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 231193503 | |||||
| chr1:231193503
|
G | GCTCTCTC others(3): Show |
32 | a0001c0001t0001g0047a0001c0001t0001g0053a0001c0001t0001g0204others(29): Show | 32 | HG00099.hp1 HG00544.hp2 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.1045-3830_1045-382 others(14): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 231193503 | |||||
| chr1:231193503
|
G | GCTCTCTC others(5): Show |
35 | a0001c0001t0001g0119a0001c0001t0001g0242a0001c0001t0001g0249others(32): Show | 35 | HG00438.hp1 HG00639.hp1 HG01081.hp1 others(32): Show |
intron_variant | MODIFIER | c.1045-3832_1045-382 others(16): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 231193503 | |||||
| chr1:231193503
|
G | GCTCTCTC others(7): Show |
22 | a0001c0001t0001g0039a0001c0001t0001g0235a0001c0001t0001g0282others(19): Show | 22 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(19): Show |
intron_variant | MODIFIER | c.1045-3834_1045-382 others(18): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 231193503 | |||||
| chr1:231193503
|
G | GCTCTCTC others(9): Show |
18 | a0001c0001t0001g0117a0001c0001t0002g0046a0001c0001t0002g0149others(15): Show | 18 | HG01069.hp1 HG01106.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.1045-3836_1045-382 others(20): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 231193503 | |||||
| chr1:231193503
|
G | GCTCTCTC others(11): Show |
7 | a0001c0001t0002g0057a0001c0001t0002g0219a0001c0001t0027g0066others(4): Show | 7 | HG00642.hp1 HG02040.hp1 HG02071.hp2 others(4): Show |
intron_variant | MODIFIER | c.1045-3838_1045-382 others(22): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 231193503 | |||||
| chr1:231193503
|
G | GCTCTCTC others(13): Show |
3 | a0001c0001t0001g0038a0001c0001t0004g0152a0001c0010t0021g0097 | 3 | HG00140.hp2 HG03490.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1045-3840_1045-382 others(24): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 231193503 | |||||
| chr1:231193503
|
G | GCTCTCTC others(15): Show |
6 | a0001c0001t0001g0118a0001c0001t0001g0329a0001c0001t0008g0342others(3): Show | 6 | HG00639.hp2 HG01981.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1045-3842_1045-382 others(26): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 231193503 | |||||
| chr1:231193503
|
G | GCTCTCTC others(17): Show |
2 | a0001c0001t0008g0343a0001c0001t0024g0247 | 2 | HG00280.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1045-3844_1045-382 others(28): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 231193503 | |||||
| chr1:231193503
|
G | GCTCTCTC others(19): Show |
1 | a0001c0002t0005g0036 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1045-3846_1045-382 others(30): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 231193503 | |||||
| chr1:231193503
|
GCT | G | 6 | a0001c0001t0001g0227a0001c0001t0029g0283a0001c0002t0003g0256others(3): Show | 6 | HG01934.hp2 HG03540.hp1 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.1045-3822_1045-382 others(6): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 231193503 | |||||
| chr1:231193503
|
GCTCT | G | 13 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0205others(10): Show | 13 | HG00673.hp2 HG01169.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.1045-3824_1045-382 others(8): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 231193503 | |||||
| chr1:231193503
|
GCTCTCT | G | 38 | a0001c0001t0001g0054a0001c0001t0001g0135a0001c0001t0001g0252others(35): Show | 39 | HG00423.hp1 HG00609.hp2 HG01256.hp1 others(36): Show |
intron_variant | MODIFIER | c.1045-3826_1045-382 others(10): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 231193503 | |||||
| chr1:231193503
|
GCTCTCTC others(1): Show |
G | 11 | a0001c0001t0001g0226a0001c0001t0005g0225a0001c0001t0005g0229others(8): Show | 11 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.1045-3828_1045-382 others(12): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 231193503 | |||||
| chr1:231193503
|
GCTCTCTC others(3): Show |
G | 2 | a0001c0002t0038g0060a0001c0017t0001g0231 | 2 | HG02630.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1045-3830_1045-382 others(14): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 231193503 | |||||
| chr1:231193503
|
GCTCTCTC others(5): Show |
G | 3 | a0001c0002t0003g0033a0001c0002t0003g0197a0001c0002t0003g0257 | 3 | HG00408.hp2 HG04184.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.1045-3832_1045-382 others(16): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 231193503 | |||||
| chr1:231193523
|
T | TCTCTCTC others(3): Show |
2 | a0001c0001t0002g0147a0001c0001t0002g0199 | 2 | NA19012.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1045-3839_1045-383 others(14): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 231193523 | |||||
| chr1:231193524
|
C | CTCTCTCT others(9): Show |
1 | a0001c0001t0017g0332 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1045-3832_1045-383 others(20): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 231193524 | |||||
| chr1:231193550
|
C | CTCTCTCT others(6): Show |
1 | a0001c0001t0002g0321 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1045-3821_1045-382 others(17): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231193550 | ||||||
| chr1:231193550
|
C | CTCTCTCT others(10): Show |
1 | a0001c0003t0006g0069 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1045-3821_1045-382 others(21): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231193550 | ||||||
| chr1:231193675
|
G | A | 1 | a0001c0001t0001g0334 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1045-3696G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231193675 | ||||||
| chr1:231193729
|
C | T | 1 | a0001c0001t0027g0066 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1045-3642C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231193729 | ||||||
| chr1:231193780
|
T | C | 1 | a0001c0002t0005g0120 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1045-3591T>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231193780 | ||||||
| chr1:231194007
|
C | T | 1 | a0001c0001t0001g0284 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1045-3364C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231194007 | ||||||
| chr1:231194020
|
A | C | 2 | a0001c0002t0003g0159a0001c0002t0003g0160 | 2 | HG03492.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.1045-3351A>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231194020 | ||||||
| chr1:231194052
|
C | T | 7 | a0001c0001t0013g0123a0001c0001t0030g0340a0001c0003t0057g0064others(4): Show | 7 | HG01243.hp1 HG03041.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.1045-3319C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231194052 | ||||||
| chr1:231194053
|
G | A | 1 | a0001c0001t0001g0259 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1045-3318G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231194053 | ||||||
| chr1:231194336
|
G | A | 50 | a0001c0001t0001g0282a0001c0001t0002g0045a0001c0001t0002g0046others(47): Show | 50 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.1045-3035G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231194336 | ||||||
| chr1:231194360
|
G | C | 2 | a0001c0001t0005g0215a0001c0001t0034g0063 | 2 | HG02630.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1045-3011G>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231194360 | ||||||
| chr1:231194691
|
T | C | 2 | a0001c0002t0038g0060a0001c0017t0001g0231 | 2 | HG02630.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1045-2680T>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231194691 | ||||||
| chr1:231194842
|
C | T | 1 | a0001c0002t0003g0044 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1045-2529C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231194842 | ||||||
| chr1:231194913
|
G | A | 5 | a0001c0001t0001g0040a0001c0001t0001g0205a0001c0001t0001g0255others(2): Show | 5 | HG00673.hp2 HG01169.hp1 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.1045-2458G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231194913 | ||||||
| chr1:231195116
|
G | A | 1 | a0001c0002t0003g0197 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1045-2255G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231195116 | ||||||
| chr1:231195117
|
A | T | 1 | a0001c0002t0003g0197 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1045-2254A>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231195117 | ||||||
| chr1:231195341
|
A | G | 25 | a0001c0001t0001g0003a0001c0001t0001g0183a0001c0001t0001g0207others(22): Show | 26 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.1045-2030A>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231195341 | ||||||
| chr1:231195369
|
T | A | 1 | a0001c0001t0005g0215 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1045-2002T>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231195369 | ||||||
| chr1:231195376
|
C | A | 1 | a0001c0001t0005g0215 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1045-1995C>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231195376 | ||||||
| chr1:231195450
|
G | C | 9 | a0001c0001t0001g0187a0001c0001t0001g0212a0001c0001t0001g0227others(6): Show | 9 | HG01106.hp2 HG01261.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1045-1921G>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231195450 | ||||||
| chr1:231195580
|
T | A | 4 | a0001c0002t0003g0124a0001c0002t0003g0132a0001c0002t0003g0265others(1): Show | 4 | HG02080.hp1 HG02135.hp1 NA18612.hp2 others(1): Show |
intron_variant | MODIFIER | c.1045-1791T>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231195580 | ||||||
| chr1:231195595
|
C | T | 1 | a0001c0001t0001g0226 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1045-1776C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231195595 | ||||||
| chr1:231195694
|
T | C | 1 | a0001c0001t0002g0057 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1045-1677T>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231195694 | ||||||
| chr1:231195790
|
G | A | 8 | a0001c0001t0001g0040a0001c0001t0001g0205a0001c0001t0001g0217others(5): Show | 8 | HG00673.hp2 HG01169.hp1 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.1045-1581G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231195790 | ||||||
| chr1:231195803
|
G | A | 1 | a0001c0001t0026g0061 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1045-1568G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231195803 | ||||||
| chr1:231195803
|
G | T | 1 | a0001c0002t0005g0157 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1045-1568G>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231195803 | ||||||
| chr1:231195880
|
C | T | 2 | a0001c0001t0005g0215a0001c0001t0034g0063 | 2 | HG02630.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1045-1491C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231195880 | ||||||
| chr1:231195938
|
T | C | 1 | a0001c0004t0020g0024 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1045-1433T>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231195938 | ||||||
| chr1:231196342
|
T | C | 5 | a0001c0001t0005g0229a0001c0001t0005g0230a0001c0001t0005g0233others(2): Show | 5 | HG02257.hp2 HG02559.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1045-1029T>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231196342 | ||||||
| chr1:231196432
|
C | T | 6 | a0001c0001t0001g0250a0001c0003t0012g0068a0001c0003t0012g0070others(3): Show | 6 | HG02074.hp1 HG02165.hp2 NA18961.hp2 others(3): Show |
intron_variant | MODIFIER | c.1045-939C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231196432 | ||||||
| chr1:231196575
|
C | CA | 6 | a0001c0001t0049g0202a0001c0003t0012g0068a0001c0003t0012g0070others(3): Show | 6 | NA18955.hp2 NA18961.hp2 NA18981.hp2 others(3): Show |
intron_variant | MODIFIER | c.1045-782dupA | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 231196575 | |||||
| chr1:231196575
|
CA | C | 28 | a0001c0001t0001g0127a0001c0001t0001g0216a0001c0001t0001g0254others(25): Show | 29 | HG00140.hp2 HG01074.hp1 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.1045-782delA | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 231196575 | |||||
| chr1:231196651
|
G | A | 14 | a0001c0001t0001g0041a0001c0001t0001g0054a0001c0001t0001g0135others(11): Show | 14 | HG01243.hp1 HG02148.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.1045-720G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231196651 | ||||||
| chr1:231197115
|
C | T | 1 | a0001c0001t0037g0236 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1045-256C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231197115 | ||||||
| chr1:231197116
|
G | A | 1 | a0001c0001t0001g0318 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1045-255G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231197116 | ||||||
| chr1:231197201
|
C | T | 2 | a0001c0001t0017g0338a0005c0021t0031g0346 | 2 | HG03195.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1045-170C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231197201 | ||||||
| chr1:231197261
|
G | A | 1 | a0001c0003t0059g0086 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1045-110G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 1/9 | chr1 | 231197261 | ||||||
| chr1:231197553
|
C | T | 5 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0235others(2): Show | 5 | HG02109.hp2 HG02451.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1140+87C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 2/9 | chr1 | 231197553 | ||||||
| chr1:231197625
|
A | C | 1 | a0001c0009t0035g0029 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1140+159A>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 2/9 | chr1 | 231197625 | ||||||
| chr1:231197700
|
C | A | 1 | a0001c0001t0001g0222 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1140+234C>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 2/9 | chr1 | 231197700 | ||||||
| chr1:231197756
|
C | T | 1 | a0001c0009t0035g0029 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1140+290C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 2/9 | chr1 | 231197756 | ||||||
| chr1:231197835
|
A | G | 2 | a0001c0001t0005g0215a0001c0001t0034g0063 | 2 | HG02630.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1140+369A>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 2/9 | chr1 | 231197835 | ||||||
| chr1:231197847
|
A | AAGAAGG | 37 | a0001c0001t0001g0287a0001c0001t0004g0141a0001c0001t0017g0338others(34): Show | 38 | HG00408.hp2 HG00423.hp1 HG01099.hp2 others(35): Show |
intron_variant | MODIFIER | c.1140+405_1140+410d others(8): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 231197847 | |||||
| chr1:231197847
|
A | AAGAAGGA others(5): Show |
3 | a0001c0001t0001g0334a0001c0002t0003g0134a0001c0002t0003g0146 | 3 | HG02717.hp2 NA19065.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.1140+399_1140+410d others(14): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 231197847 | |||||
| chr1:231197847
|
A | G | 1 | a0008c0015t0003g0300 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1140+381A>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 2/9 | chr1 | 231197847 | ||||||
| chr1:231197847
|
AAGAAGG | A | 12 | a0001c0001t0001g0329a0001c0001t0016g0210a0001c0001t0016g0211others(9): Show | 12 | HG00280.hp1 HG00323.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.1140+405_1140+410d others(8): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 231197847 | |||||
| chr1:231198006
|
T | C | 114 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0054others(111): Show | 115 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.1140+540T>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 2/9 | chr1 | 231198006 | ||||||
| chr1:231198260
|
T | A | 1 | a0008c0015t0003g0300 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1141-787T>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 2/9 | chr1 | 231198260 | ||||||
| chr1:231198393
|
T | C | 1 | a0001c0002t0005g0129 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1141-654T>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 2/9 | chr1 | 231198393 | ||||||
| chr1:231198394
|
C | CT | 18 | a0001c0001t0011g0185a0001c0002t0005g0031a0001c0002t0005g0036others(15): Show | 18 | HG00438.hp1 HG00609.hp1 HG00642.hp1 others(15): Show |
intron_variant | MODIFIER | c.1141-643dupT | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 231198394 | |||||
| chr1:231198477
|
C | T | 1 | a0001c0001t0014g0218 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1141-570C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 2/9 | chr1 | 231198477 | ||||||
| chr1:231198813
|
A | T | 1 | a0001c0002t0003g0301 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1141-234A>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 2/9 | chr1 | 231198813 | ||||||
| chr1:231199032
|
C | T | 1 | a0001c0001t0002g0055 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1141-15C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 2/9 | chr1 | 231199032 | ||||||
| chr1:231199034
|
C | A | 38 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0054others(35): Show | 38 | HG00673.hp2 HG01169.hp1 HG01243.hp1 others(35): Show |
intron_variant | MODIFIER | c.1141-13C>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 2/9 | chr1 | 231199034 | ||||||
| chr1:231199267
|
A | G | 2 | a0001c0001t0005g0215a0001c0001t0034g0063 | 2 | HG02630.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1263+98A>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 3/9 | chr1 | 231199267 | ||||||
| chr1:231199441
|
T | C | 1 | a0001c0001t0046g0324 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1263+272T>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 3/9 | chr1 | 231199441 | ||||||
| chr1:231199531
|
C | G | 1 | a0001c0001t0001g0252 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1263+362C>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 3/9 | chr1 | 231199531 | ||||||
| chr1:231199556
|
A | C | 5 | a0001c0001t0001g0183a0001c0001t0001g0243a0001c0001t0001g0250others(2): Show | 5 | NA18950.hp1 NA18973.hp2 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.1263+387A>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 3/9 | chr1 | 231199556 | ||||||
| chr1:231199594
|
C | T | 1 | a0001c0001t0037g0236 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1263+425C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 3/9 | chr1 | 231199594 | ||||||
| chr1:231199611
|
G | A | 37 | a0001c0001t0004g0141a0001c0001t0032g0349a0001c0001t0037g0236others(34): Show | 38 | HG00408.hp2 HG00423.hp1 HG01256.hp1 others(35): Show |
intron_variant | MODIFIER | c.1263+442G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 3/9 | chr1 | 231199611 | ||||||
| chr1:231199661
|
A | G | 2 | a0001c0002t0003g0197a0001c0002t0003g0257 | 2 | HG00408.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.1264-487A>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 3/9 | chr1 | 231199661 | ||||||
| chr1:231199695
|
A | G | 5 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0235others(2): Show | 5 | HG02109.hp2 HG02451.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1264-453A>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 3/9 | chr1 | 231199695 | ||||||
| chr1:231199800
|
A | T | 1 | a0001c0001t0017g0137 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1264-348A>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 3/9 | chr1 | 231199800 | ||||||
| chr1:231199851
|
G | C | 113 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0054others(110): Show | 114 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.1264-297G>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 3/9 | chr1 | 231199851 | ||||||
| chr1:231199933
|
T | C | 3 | a0001c0002t0003g0033a0001c0002t0003g0197a0001c0002t0003g0257 | 3 | HG00408.hp2 HG04184.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.1264-215T>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 3/9 | chr1 | 231199933 | ||||||
| chr1:231200016
|
A | C | 1 | a0008c0015t0003g0300 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1264-132A>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 3/9 | chr1 | 231200016 | ||||||
| chr1:231200045
|
C | G | 1 | a0008c0015t0003g0300 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1264-103C>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 3/9 | chr1 | 231200045 | ||||||
| chr1:231200045
|
C | T | 1 | a0001c0001t0001g0039 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1264-103C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 3/9 | chr1 | 231200045 | ||||||
| chr1:231200046
|
G | C | 1 | a0008c0015t0003g0300 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1264-102G>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 3/9 | chr1 | 231200046 | ||||||
| chr1:231200047
|
C | G | 1 | a0008c0015t0003g0300 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1264-101C>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 3/9 | chr1 | 231200047 | ||||||
| chr1:231200083
|
C | G | 1 | a0001c0001t0001g0054 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1264-65C>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 3/9 | chr1 | 231200083 | ||||||
| chr1:231200103
|
C | T | 1 | a0008c0015t0003g0300 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1264-45C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 3/9 | chr1 | 231200103 | ||||||
| chr1:231200106
|
C | T | 1 | a0008c0015t0003g0300 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1264-42C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 3/9 | chr1 | 231200106 | ||||||
| chr1:231200378
|
T | C | 56 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0054others(53): Show | 56 | HG00280.hp1 HG00323.hp2 HG00673.hp2 others(53): Show |
intron_variant | MODIFIER | c.1374+120T>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 4/9 | chr1 | 231200378 | ||||||
| chr1:231200422
|
C | T | 5 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0235others(2): Show | 5 | HG02109.hp2 HG02451.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1374+164C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 4/9 | chr1 | 231200422 | ||||||
| chr1:231200663
|
C | T | 56 | a0001c0001t0004g0141a0001c0001t0017g0338a0001c0001t0032g0349others(53): Show | 57 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.1374+405C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 4/9 | chr1 | 231200663 | ||||||
| chr1:231200785
|
G | C | 56 | a0001c0001t0004g0141a0001c0001t0017g0338a0001c0001t0032g0349others(53): Show | 57 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.1374+527G>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 4/9 | chr1 | 231200785 | ||||||
| chr1:231200787
|
C | T | 114 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0054others(111): Show | 115 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.1374+529C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 4/9 | chr1 | 231200787 | ||||||
| chr1:231200791
|
C | T | 1 | a0001c0001t0001g0255 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1374+533C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 4/9 | chr1 | 231200791 | ||||||
| chr1:231200805
|
G | T | 1 | a0001c0009t0035g0029 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1374+547G>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 4/9 | chr1 | 231200805 | ||||||
| chr1:231200815
|
C | T | 2 | a0001c0001t0005g0215a0001c0001t0034g0063 | 2 | HG02630.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1375-543C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 4/9 | chr1 | 231200815 | ||||||
| chr1:231200877
|
A | T | 1 | a0001c0001t0032g0349 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1375-481A>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 4/9 | chr1 | 231200877 | ||||||
| chr1:231200924
|
G | A | 2 | a0001c0001t0005g0215a0001c0001t0034g0063 | 2 | HG02630.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1375-434G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 4/9 | chr1 | 231200924 | ||||||
| chr1:231200989
|
G | T | 2 | a0001c0002t0014g0193a0001c0002t0014g0203 | 2 | NA18950.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.1375-369G>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 4/9 | chr1 | 231200989 | ||||||
| chr1:231201058
|
T | C | 5 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0235others(2): Show | 5 | HG02109.hp2 HG02451.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1375-300T>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 4/9 | chr1 | 231201058 | ||||||
| chr1:231201200
|
G | A | 56 | a0001c0001t0004g0141a0001c0001t0017g0338a0001c0001t0032g0349others(53): Show | 57 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.1375-158G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 4/9 | chr1 | 231201200 | ||||||
| chr1:231201285
|
C | A | 56 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0054others(53): Show | 56 | HG00280.hp1 HG00323.hp2 HG00673.hp2 others(53): Show |
intron_variant | MODIFIER | c.1375-73C>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 4/9 | chr1 | 231201285 | ||||||
| chr1:231201291
|
C | T | 8 | a0001c0001t0001g0040a0001c0001t0001g0205a0001c0001t0001g0217others(5): Show | 8 | HG00673.hp2 HG01169.hp1 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.1375-67C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 4/9 | chr1 | 231201291 | ||||||
| chr1:231201622
|
T | A | 3 | a0001c0001t0026g0061a0001c0001t0026g0062a0001c0023t0039g0005 | 3 | HG01884.hp2 HG02055.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.1534+105T>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 5/9 | chr1 | 231201622 | ||||||
| chr1:231201645
|
G | A | 1 | a0001c0001t0001g0248 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1534+128G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 5/9 | chr1 | 231201645 | ||||||
| chr1:231201696
|
G | A | 1 | a0001c0020t0001g0267 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1534+179G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 5/9 | chr1 | 231201696 | ||||||
| chr1:231201707
|
T | C | 2 | a0001c0001t0001g0254a0001c0001t0001g0309 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1534+190T>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 5/9 | chr1 | 231201707 | ||||||
| chr1:231201821
|
G | A | 1 | a0001c0002t0003g0124 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1534+304G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 5/9 | chr1 | 231201821 | ||||||
| chr1:231201991
|
G | A | 1 | a0001c0001t0002g0055 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1534+474G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 5/9 | chr1 | 231201991 | ||||||
| chr1:231201995
|
G | A | 1 | a0001c0018t0003g0320 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1534+478G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 5/9 | chr1 | 231201995 | ||||||
| chr1:231202065
|
A | G | 1 | a0001c0001t0047g0059 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1534+548A>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 5/9 | chr1 | 231202065 | ||||||
| chr1:231202070
|
G | GGAGGAGG others(374): Show |
1 | a0001c0002t0001g0178 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1534+562_1534+563i others(383): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr1 | 231202070 | |||||
| chr1:231202070
|
G | GGAGGAGG others(372): Show |
2 | a0001c0001t0001g0204a0001c0001t0002g0174 | 2 | HG00673.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.1534+563_1534+564i others(381): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr1 | 231202070 | |||||
| chr1:231202070
|
G | GGAGGAGG others(375): Show |
1 | a0001c0002t0003g0044 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1534+563_1534+564i others(384): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr1 | 231202070 | |||||
| chr1:231202070
|
G | GGAGGAGG others(375): Show |
1 | a0001c0002t0005g0295 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1534+563_1534+564i others(384): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr1 | 231202070 | |||||
| chr1:231202070
|
G | GGAGGAGG others(371): Show |
1 | a0001c0001t0001g0220 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1534+563_1534+564i others(380): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr1 | 231202070 | |||||
| chr1:231202070
|
G | GGAGGAGG others(371): Show |
1 | a0007c0016t0001g0155 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1534+563_1534+564i others(380): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr1 | 231202070 | |||||
| chr1:231202070
|
G | GGAGGAGG others(371): Show |
1 | a0001c0001t0001g0279 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1534+563_1534+564i others(380): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr1 | 231202070 | |||||
| chr1:231202070
|
G | GGAGGAGG others(372): Show |
1 | a0001c0001t0001g0302 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1534+563_1534+564i others(381): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr1 | 231202070 | |||||
| chr1:231202070
|
G | GGAGGAGG others(371): Show |
224 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0032others(221): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.1534+563_1534+564i others(380): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr1 | 231202070 | |||||
| chr1:231202070
|
G | GGAGGAGG others(587): Show |
7 | a0001c0002t0009g0116a0001c0002t0009g0139a0001c0002t0009g0156others(4): Show | 7 | HG02717.hp1 HG02895.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.1534+563_1534+564i others(596): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr1 | 231202070 | |||||
| chr1:231202070
|
G | GGAGGAGG others(374): Show |
36 | a0001c0001t0004g0141a0001c0001t0017g0338a0001c0001t0032g0349others(33): Show | 37 | HG00408.hp2 HG00423.hp1 HG01256.hp1 others(34): Show |
intron_variant | MODIFIER | c.1534+563_1534+564i others(383): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr1 | 231202070 | |||||
| chr1:231202070
|
G | GGAGGAGG others(375): Show |
1 | a0001c0004t0013g0021 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1534+563_1534+564i others(384): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr1 | 231202070 | |||||
| chr1:231202070
|
G | GGAGGAGG others(374): Show |
53 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0054others(50): Show | 53 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.1534+563_1534+564i others(383): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr1 | 231202070 | |||||
| chr1:231202070
|
G | GGAGGAGG others(590): Show |
10 | a0001c0001t0005g0215a0001c0001t0034g0063a0001c0002t0005g0036others(7): Show | 10 | HG00438.hp1 HG00642.hp1 HG02129.hp2 others(7): Show |
intron_variant | MODIFIER | c.1534+563_1534+564i others(599): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr1 | 231202070 | |||||
| chr1:231202070
|
G | GGAGGAGG others(371): Show |
2 | a0001c0002t0038g0060a0001c0004t0010g0014 | 2 | HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1534+563_1534+564i others(380): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr1 | 231202070 | |||||
| chr1:231202070
|
G | GGAGGAGG others(374): Show |
1 | a0001c0001t0001g0334 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1534+563_1534+564i others(383): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr1 | 231202070 | |||||
| chr1:231202070
|
G | GGAGGAGG others(368): Show |
5 | a0001c0004t0010g0007a0001c0004t0010g0013a0001c0004t0010g0022others(2): Show | 5 | HG02055.hp2 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1534+563_1534+564i others(377): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr1 | 231202070 | |||||
| chr1:231202070
|
G | GGAGGAGG others(365): Show |
1 | a0001c0009t0035g0029 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1534+563_1534+564i others(374): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr1 | 231202070 | |||||
| chr1:231202070
|
G | GGAGGAGG others(374): Show |
1 | a0001c0002t0005g0170 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1534+563_1534+564i others(383): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr1 | 231202070 | |||||
| chr1:231202089
|
A | G | 350 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0032others(347): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.1534+572A>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 5/9 | chr1 | 231202089 | ||||||
| chr1:231202114
|
T | C | 1 | a0001c0001t0002g0219 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1534+597T>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 5/9 | chr1 | 231202114 | ||||||
| chr1:231202176
|
G | A | 1 | a0001c0001t0008g0343 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1534+659G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 5/9 | chr1 | 231202176 | ||||||
| chr1:231202218
|
G | A | 4 | a0001c0002t0005g0031a0001c0005t0021g0096a0001c0005t0021g0111others(1): Show | 4 | HG03490.hp1 NA18942.hp1 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.1534+701G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 5/9 | chr1 | 231202218 | ||||||
| chr1:231202231
|
G | A | 4 | a0001c0002t0005g0031a0001c0005t0021g0096a0001c0005t0021g0111others(1): Show | 4 | HG03490.hp1 NA18942.hp1 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.1534+714G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 5/9 | chr1 | 231202231 | ||||||
| chr1:231202232
|
A | G | 4 | a0001c0002t0005g0031a0001c0005t0021g0096a0001c0005t0021g0111others(1): Show | 4 | HG03490.hp1 NA18942.hp1 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.1534+715A>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 5/9 | chr1 | 231202232 | ||||||
| chr1:231202233
|
G | C | 4 | a0001c0002t0005g0031a0001c0005t0021g0096a0001c0005t0021g0111others(1): Show | 4 | HG03490.hp1 NA18942.hp1 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.1534+716G>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 5/9 | chr1 | 231202233 | ||||||
| chr1:231202238
|
G | GA | 4 | a0001c0002t0005g0031a0001c0005t0021g0096a0001c0005t0021g0111others(1): Show | 4 | HG03490.hp1 NA18942.hp1 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.1534+721_1534+722i others(3): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 5/9 | chr1 | 231202238 | ||||||
| chr1:231202239
|
G | A | 4 | a0001c0002t0005g0031a0001c0005t0021g0096a0001c0005t0021g0111others(1): Show | 4 | HG03490.hp1 NA18942.hp1 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.1534+722G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 5/9 | chr1 | 231202239 | ||||||
| chr1:231202247
|
G | A | 4 | a0001c0002t0005g0031a0001c0005t0021g0096a0001c0005t0021g0111others(1): Show | 4 | HG03490.hp1 NA18942.hp1 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.1534+730G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 5/9 | chr1 | 231202247 | ||||||
| chr1:231202253
|
A | G | 4 | a0001c0002t0005g0031a0001c0005t0021g0096a0001c0005t0021g0111others(1): Show | 4 | HG03490.hp1 NA18942.hp1 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.1534+736A>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 5/9 | chr1 | 231202253 | ||||||
| chr1:231202253
|
AAGGAGGA others(14): Show |
A | 14 | a0001c0001t0001g0041a0001c0001t0001g0054a0001c0001t0001g0135others(11): Show | 14 | HG01243.hp1 HG02148.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.1534+749_1534+769d others(23): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr1 | 231202253 | |||||
| chr1:231202260
|
A | ACATAGTG others(188): Show |
1 | a0001c0005t0021g0111 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1534+743_1534+744i others(197): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 5/9 | chr1 | 231202260 | ||||||
| chr1:231202260
|
A | ACATAGTG others(187): Show |
3 | a0001c0002t0005g0031a0001c0005t0021g0096a0001c0010t0021g0097 | 3 | HG03490.hp1 NA18942.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.1534+743_1534+744i others(196): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 5/9 | chr1 | 231202260 | ||||||
| chr1:231202263
|
T | G | 4 | a0001c0002t0005g0031a0001c0005t0021g0096a0001c0005t0021g0111others(1): Show | 4 | HG03490.hp1 NA18942.hp1 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.1534+746T>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 5/9 | chr1 | 231202263 | ||||||
| chr1:231202266
|
TGGCGGAG others(14): Show |
T | 18 | a0001c0001t0001g0040a0001c0001t0001g0205a0001c0001t0001g0255others(15): Show | 18 | HG00438.hp1 HG00609.hp1 HG00642.hp1 others(15): Show |
intron_variant | MODIFIER | c.1534+753_1534+773d others(23): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr1 | 231202266 | |||||
| chr1:231202267
|
G | A | 4 | a0001c0002t0005g0031a0001c0005t0021g0096a0001c0005t0021g0111others(1): Show | 4 | HG03490.hp1 NA18942.hp1 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.1534+750G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 5/9 | chr1 | 231202267 | ||||||
| chr1:231202269
|
C | T | 4 | a0001c0002t0005g0031a0001c0005t0021g0096a0001c0005t0021g0111others(1): Show | 4 | HG03490.hp1 NA18942.hp1 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.1534+752C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 5/9 | chr1 | 231202269 | ||||||
| chr1:231202274
|
G | A | 4 | a0001c0002t0005g0031a0001c0005t0021g0096a0001c0005t0021g0111others(1): Show | 4 | HG03490.hp1 NA18942.hp1 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.1534+757G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 5/9 | chr1 | 231202274 | ||||||
| chr1:231202287
|
A | T | 10 | a0001c0001t0001g0217a0001c0001t0026g0061a0001c0001t0026g0062others(7): Show | 10 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.1534+770A>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 5/9 | chr1 | 231202287 | ||||||
| chr1:231202329
|
AGGAG | A | 48 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0054others(45): Show | 48 | HG00438.hp1 HG00609.hp1 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.1534+817_1534+820d others(6): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr1 | 231202329 | |||||
| chr1:231202387
|
A | G | 16 | a0001c0001t0001g0040a0001c0001t0001g0144a0001c0001t0001g0205others(13): Show | 16 | HG00673.hp2 HG01169.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.1534+870A>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 5/9 | chr1 | 231202387 | ||||||
| chr1:231202398
|
G | T | 1 | a0001c0002t0003g0051 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1534+881G>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 5/9 | chr1 | 231202398 | ||||||
| chr1:231202744
|
G | A | 1 | a0001c0001t0001g0216 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1535-1123G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 5/9 | chr1 | 231202744 | ||||||
| chr1:231202767
|
C | T | 1 | a0001c0011t0006g0093 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1535-1100C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 5/9 | chr1 | 231202767 | ||||||
| chr1:231202831
|
A | G | 1 | a0001c0001t0001g0039 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1535-1036A>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 5/9 | chr1 | 231202831 | ||||||
| chr1:231203070
|
G | T | 50 | a0001c0001t0001g0282a0001c0001t0002g0045a0001c0001t0002g0046others(47): Show | 50 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.1535-797G>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 5/9 | chr1 | 231203070 | ||||||
| chr1:231203152
|
T | TA | 61 | a0001c0001t0004g0141a0001c0002t0001g0178a0001c0002t0003g0033others(58): Show | 62 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.1535-706dupA | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr1 | 231203152 | |||||
| chr1:231203446
|
C | T | 1 | a0001c0009t0035g0029 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1535-421C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 5/9 | chr1 | 231203446 | ||||||
| chr1:231203475
|
G | A | 3 | a0001c0001t0026g0061a0001c0001t0026g0062a0001c0023t0039g0005 | 3 | HG01884.hp2 HG02055.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.1535-392G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 5/9 | chr1 | 231203475 | ||||||
| chr1:231203582
|
G | C | 5 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0235others(2): Show | 5 | HG02109.hp2 HG02451.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1535-285G>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 5/9 | chr1 | 231203582 | ||||||
| chr1:231203687
|
T | C | 1 | a0001c0009t0035g0029 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1535-180T>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 5/9 | chr1 | 231203687 | ||||||
| chr1:231203692
|
A | G | 1 | a0001c0009t0035g0029 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1535-175A>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 5/9 | chr1 | 231203692 | ||||||
| chr1:231204064
|
A | C | 8 | a0001c0001t0005g0225a0001c0001t0005g0229a0001c0001t0005g0230others(5): Show | 8 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1680+52A>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 6/9 | chr1 | 231204064 | ||||||
| chr1:231204268
|
T | G | 1 | a0001c0001t0001g0323 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1680+256T>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 6/9 | chr1 | 231204268 | ||||||
| chr1:231204351
|
A | T | 1 | a0001c0001t0001g0318 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1680+339A>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 6/9 | chr1 | 231204351 | ||||||
| chr1:231204369
|
T | C | 2 | a0001c0004t0010g0007a0001c0004t0010g0013 | 2 | HG02965.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1680+357T>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 6/9 | chr1 | 231204369 | ||||||
| chr1:231204393
|
G | A | 1 | a0001c0009t0035g0029 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1680+381G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 6/9 | chr1 | 231204393 | ||||||
| chr1:231204425
|
C | T | 1 | a0001c0002t0003g0172 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1680+413C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 6/9 | chr1 | 231204425 | ||||||
| chr1:231204460
|
G | T | 2 | a0001c0002t0005g0138a0001c0009t0005g0018 | 2 | HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1680+448G>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 6/9 | chr1 | 231204460 | ||||||
| chr1:231204639
|
T | C | 2 | a0001c0001t0001g0228a0001c0001t0008g0339 | 2 | HG02896.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1680+627T>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 6/9 | chr1 | 231204639 | ||||||
| chr1:231204650
|
C | T | 60 | a0001c0002t0001g0178a0001c0002t0003g0033a0001c0002t0003g0044others(57): Show | 61 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.1680+638C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 6/9 | chr1 | 231204650 | ||||||
| chr1:231204661
|
G | A | 1 | a0001c0002t0003g0125 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1680+649G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 6/9 | chr1 | 231204661 | ||||||
| chr1:231204687
|
C | T | 49 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0117others(46): Show | 49 | HG00140.hp2 HG00673.hp2 HG01169.hp1 others(46): Show |
intron_variant | MODIFIER | c.1680+675C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 6/9 | chr1 | 231204687 | ||||||
| chr1:231204763
|
A | G | 1 | a0001c0019t0033g0348 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1680+751A>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 6/9 | chr1 | 231204763 | ||||||
| chr1:231204829
|
T | C | 1 | a0001c0009t0035g0029 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1680+817T>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 6/9 | chr1 | 231204829 | ||||||
| chr1:231204841
|
A | G | 1 | a0001c0002t0038g0060 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1680+829A>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 6/9 | chr1 | 231204841 | ||||||
| chr1:231204902
|
T | C | 1 | a0001c0003t0055g0112 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1680+890T>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 6/9 | chr1 | 231204902 | ||||||
| chr1:231204960
|
T | C | 1 | a0001c0014t0016g0328 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1680+948T>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 6/9 | chr1 | 231204960 | ||||||
| chr1:231205059
|
C | T | 6 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0235others(3): Show | 6 | HG02109.hp2 HG02451.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1680+1047C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 6/9 | chr1 | 231205059 | ||||||
| chr1:231205361
|
A | G | 1 | a0001c0001t0001g0289 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1681-1291A>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 6/9 | chr1 | 231205361 | ||||||
| chr1:231205468
|
G | A | 1 | a0001c0024t0004g0026 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1681-1184G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 6/9 | chr1 | 231205468 | ||||||
| chr1:231205528
|
C | A | 3 | a0001c0001t0026g0061a0001c0001t0026g0062a0001c0023t0039g0005 | 3 | HG01884.hp2 HG02055.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.1681-1124C>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 6/9 | chr1 | 231205528 | ||||||
| chr1:231205594
|
C | T | 2 | a0001c0001t0001g0279a0001c0001t0001g0294 | 2 | NA18986.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.1681-1058C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 6/9 | chr1 | 231205594 | ||||||
| chr1:231205696
|
A | C | 1 | a0001c0001t0002g0224 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1681-956A>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 6/9 | chr1 | 231205696 | ||||||
| chr1:231205725
|
C | CA | 12 | a0001c0001t0002g0206a0001c0001t0024g0043a0001c0001t0024g0247others(9): Show | 12 | HG00280.hp1 HG00323.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.1681-911dupA | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr1 | 231205725 | |||||
| chr1:231205725
|
CA | C | 64 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0117others(61): Show | 64 | HG00140.hp2 HG00438.hp1 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.1681-911delA | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr1 | 231205725 | |||||
| chr1:231205725
|
CAA | C | 35 | a0001c0002t0001g0178a0001c0002t0003g0033a0001c0002t0003g0044others(32): Show | 36 | HG00408.hp2 HG00423.hp1 HG01256.hp1 others(33): Show |
intron_variant | MODIFIER | c.1681-912_1681-911d others(4): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr1 | 231205725 | |||||
| chr1:231205765
|
A | G | 110 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0117others(107): Show | 111 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.1681-887A>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 6/9 | chr1 | 231205765 | ||||||
| chr1:231205823
|
G | T | 60 | a0001c0002t0001g0178a0001c0002t0003g0033a0001c0002t0003g0044others(57): Show | 61 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.1681-829G>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 6/9 | chr1 | 231205823 | ||||||
| chr1:231205841
|
T | C | 1 | a0001c0001t0001g0312 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1681-811T>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 6/9 | chr1 | 231205841 | ||||||
| chr1:231205844
|
C | T | 6 | a0001c0001t0001g0186a0001c0001t0011g0184a0001c0001t0011g0185others(3): Show | 6 | NA18944.hp1 NA18984.hp1 NA18990.hp2 others(3): Show |
intron_variant | MODIFIER | c.1681-808C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 6/9 | chr1 | 231205844 | ||||||
| chr1:231206010
|
G | A | 61 | a0001c0002t0001g0178a0001c0002t0003g0033a0001c0002t0003g0044others(58): Show | 62 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.1681-642G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 6/9 | chr1 | 231206010 | ||||||
| chr1:231206020
|
G | T | 1 | a0001c0001t0045g0169 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1681-632G>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 6/9 | chr1 | 231206020 | ||||||
| chr1:231206059
|
G | A | 8 | a0001c0001t0005g0225a0001c0001t0005g0229a0001c0001t0005g0230others(5): Show | 8 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1681-593G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 6/9 | chr1 | 231206059 | ||||||
| chr1:231206223
|
T | A | 60 | a0001c0002t0001g0178a0001c0002t0003g0033a0001c0002t0003g0044others(57): Show | 61 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.1681-429T>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 6/9 | chr1 | 231206223 | ||||||
| chr1:231206293
|
T | C | 1 | a0001c0002t0003g0033 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1681-359T>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 6/9 | chr1 | 231206293 | ||||||
| chr1:231206372
|
C | A | 1 | a0001c0003t0007g0078 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1681-280C>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 6/9 | chr1 | 231206372 | ||||||
| chr1:231206398
|
G | A | 1 | a0001c0001t0001g0272 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1681-254G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 6/9 | chr1 | 231206398 | ||||||
| chr1:231206863
|
T | C | 2 | a0001c0001t0016g0210a0001c0001t0016g0211 | 2 | HG02280.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1819+73T>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 7/9 | chr1 | 231206863 | ||||||
| chr1:231206908
|
C | T | 1 | a0001c0002t0003g0051 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1819+118C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 7/9 | chr1 | 231206908 | ||||||
| chr1:231206950
|
G | A | 25 | a0001c0002t0005g0031a0001c0002t0005g0036a0001c0002t0005g0120others(22): Show | 25 | HG00438.hp1 HG00609.hp1 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.1819+160G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 7/9 | chr1 | 231206950 | ||||||
| chr1:231207111
|
T | C | 112 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0117others(109): Show | 113 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.1819+321T>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 7/9 | chr1 | 231207111 | ||||||
| chr1:231207125
|
A | G | 112 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0117others(109): Show | 113 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.1819+335A>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 7/9 | chr1 | 231207125 | ||||||
| chr1:231207166
|
G | A | 1 | a0001c0009t0035g0029 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1819+376G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 7/9 | chr1 | 231207166 | ||||||
| chr1:231207265
|
G | A | 1 | a0001c0001t0001g0119 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1819+475G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 7/9 | chr1 | 231207265 | ||||||
| chr1:231207508
|
G | A | 1 | a0001c0001t0004g0179 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1819+718G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 7/9 | chr1 | 231207508 | ||||||
| chr1:231207736
|
T | C | 1 | a0001c0002t0005g0157 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1819+946T>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 7/9 | chr1 | 231207736 | ||||||
| chr1:231207855
|
T | A | 28 | a0001c0001t0005g0215a0001c0001t0034g0063a0001c0002t0005g0031others(25): Show | 28 | HG00438.hp1 HG00609.hp1 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.1819+1065T>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 7/9 | chr1 | 231207855 | ||||||
| chr1:231207941
|
A | G | 28 | a0001c0001t0005g0215a0001c0001t0034g0063a0001c0002t0005g0031others(25): Show | 28 | HG00438.hp1 HG00609.hp1 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.1820-1006A>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 7/9 | chr1 | 231207941 | ||||||
| chr1:231207986
|
A | C | 1 | a0001c0001t0005g0225 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1820-961A>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 7/9 | chr1 | 231207986 | ||||||
| chr1:231207991
|
T | C | 2 | a0001c0002t0003g0159a0001c0002t0003g0160 | 2 | HG03492.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.1820-956T>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 7/9 | chr1 | 231207991 | ||||||
| chr1:231208004
|
C | T | 3 | a0001c0001t0026g0061a0001c0001t0026g0062a0001c0023t0039g0005 | 3 | HG01884.hp2 HG02055.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.1820-943C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 7/9 | chr1 | 231208004 | ||||||
| chr1:231208009
|
C | CT | 24 | a0001c0001t0001g0255a0001c0001t0001g0271a0001c0001t0001g0302others(21): Show | 24 | HG00280.hp1 HG00323.hp2 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.1820-920dupT | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr1 | 231208009 | |||||
| chr1:231208009
|
CT | C | 7 | a0001c0001t0001g0117a0001c0001t0001g0213a0001c0001t0001g0260others(4): Show | 7 | HG01070.hp2 HG01071.hp1 HG01993.hp2 others(4): Show |
intron_variant | MODIFIER | c.1820-920delT | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr1 | 231208009 | |||||
| chr1:231208009
|
CTT | C | 27 | a0001c0001t0001g0285a0001c0001t0005g0215a0001c0001t0034g0063others(24): Show | 27 | HG00438.hp1 HG00609.hp1 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.1820-921_1820-920d others(4): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr1 | 231208009 | |||||
| chr1:231208015
|
T | TA | 35 | a0001c0002t0001g0178a0001c0002t0003g0033a0001c0002t0003g0044others(32): Show | 36 | HG00408.hp2 HG00423.hp1 HG01256.hp1 others(33): Show |
intron_variant | MODIFIER | c.1820-932_1820-931i others(3): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 7/9 | chr1 | 231208015 | ||||||
| chr1:231208083
|
C | G | 1 | a0001c0001t0001g0032 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1820-864C>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 7/9 | chr1 | 231208083 | ||||||
| chr1:231208087
|
G | T | 120 | a0001c0001t0001g0054a0001c0001t0001g0216a0001c0001t0001g0282others(117): Show | 121 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.1820-860G>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 7/9 | chr1 | 231208087 | ||||||
| chr1:231208097
|
C | T | 1 | a0001c0003t0007g0078 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1820-850C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 7/9 | chr1 | 231208097 | ||||||
| chr1:231208175
|
A | AT | 23 | a0001c0001t0001g0040a0001c0001t0001g0255a0001c0001t0001g0272others(20): Show | 23 | HG00597.hp2 HG00738.hp2 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.1820-756dupT | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr1 | 231208175 | |||||
| chr1:231208175
|
AT | A | 51 | a0001c0001t0001g0127a0001c0001t0001g0213a0001c0001t0004g0333others(48): Show | 52 | HG00408.hp2 HG00423.hp1 HG01256.hp1 others(49): Show |
intron_variant | MODIFIER | c.1820-756delT | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr1 | 231208175 | |||||
| chr1:231208421
|
G | C | 3 | a0001c0001t0026g0061a0001c0001t0026g0062a0001c0023t0039g0005 | 3 | HG01884.hp2 HG02055.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.1820-526G>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 7/9 | chr1 | 231208421 | ||||||
| chr1:231208476
|
G | A | 1 | a0001c0001t0004g0163 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1820-471G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 7/9 | chr1 | 231208476 | ||||||
| chr1:231208537
|
G | C | 76 | a0001c0001t0005g0215a0001c0001t0005g0225a0001c0001t0005g0229others(73): Show | 77 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.1820-410G>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 7/9 | chr1 | 231208537 | ||||||
| chr1:231208643
|
T | C | 6 | a0001c0003t0006g0069a0001c0003t0006g0089a0001c0003t0006g0090others(3): Show | 6 | HG00423.hp2 NA18941.hp2 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.1820-304T>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 7/9 | chr1 | 231208643 | ||||||
| chr1:231208813
|
A | G | 28 | a0001c0001t0005g0215a0001c0001t0034g0063a0001c0002t0005g0031others(25): Show | 28 | HG00438.hp1 HG00609.hp1 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.1820-134A>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 7/9 | chr1 | 231208813 | ||||||
| chr1:231208843
|
C | T | 45 | a0001c0001t0005g0225a0001c0001t0005g0229a0001c0001t0005g0230others(42): Show | 46 | HG00408.hp2 HG00423.hp1 HG01256.hp1 others(43): Show |
intron_variant | MODIFIER | c.1820-104C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 7/9 | chr1 | 231208843 | ||||||
| chr1:231208884
|
G | T | 1 | a0001c0002t0005g0157 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1820-63G>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 7/9 | chr1 | 231208884 | ||||||
| chr1:231208897
|
T | C | 1 | a0001c0003t0007g0074 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1820-50T>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 7/9 | chr1 | 231208897 | ||||||
| chr1:231208927
|
C | G | 28 | a0001c0001t0005g0215a0001c0001t0034g0063a0001c0002t0005g0031others(25): Show | 28 | HG00438.hp1 HG00609.hp1 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.1820-20C>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 7/9 | chr1 | 231208927 | ||||||
| chr1:231209307
|
C | T | 3 | a0001c0001t0026g0061a0001c0001t0026g0062a0001c0023t0039g0005 | 3 | HG01884.hp2 HG02055.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.2123+57C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 8/9 | chr1 | 231209307 | ||||||
| chr1:231209471
|
G | A | 7 | a0001c0001t0013g0123a0001c0001t0030g0340a0001c0003t0057g0064others(4): Show | 7 | HG01243.hp1 HG03041.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.2123+221G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 8/9 | chr1 | 231209471 | ||||||
| chr1:231209499
|
C | T | 1 | a0001c0001t0001g0337 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2123+249C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 8/9 | chr1 | 231209499 | ||||||
| chr1:231209554
|
A | C | 142 | a0001c0001t0001g0216a0001c0001t0002g0042a0001c0001t0002g0045others(139): Show | 143 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.2123+304A>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 8/9 | chr1 | 231209554 | ||||||
| chr1:231209596
|
T | C | 3 | a0001c0001t0026g0061a0001c0001t0026g0062a0001c0023t0039g0005 | 3 | HG01884.hp2 HG02055.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.2123+346T>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 8/9 | chr1 | 231209596 | ||||||
| chr1:231209692
|
C | T | 1 | a0001c0014t0016g0328 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2123+442C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 8/9 | chr1 | 231209692 | ||||||
| chr1:231209761
|
C | A | 1 | a0001c0009t0035g0029 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2123+511C>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 8/9 | chr1 | 231209761 | ||||||
| chr1:231209795
|
T | A | 2 | a0001c0001t0005g0293a0001c0004t0005g0016 | 2 | HG01891.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.2123+545T>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 8/9 | chr1 | 231209795 | ||||||
| chr1:231209803
|
G | A | 1 | a0001c0001t0044g0177 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2123+553G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 8/9 | chr1 | 231209803 | ||||||
| chr1:231209897
|
T | A | 97 | a0001c0001t0001g0216a0001c0001t0002g0042a0001c0001t0002g0045others(94): Show | 98 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.2123+647T>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 8/9 | chr1 | 231209897 | ||||||
| chr1:231209939
|
T | C | 7 | a0001c0002t0009g0116a0001c0002t0009g0139a0001c0002t0009g0156others(4): Show | 7 | HG02717.hp1 HG02895.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.2123+689T>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 8/9 | chr1 | 231209939 | ||||||
| chr1:231210004
|
C | G | 3 | a0001c0001t0026g0061a0001c0001t0026g0062a0001c0023t0039g0005 | 3 | HG01884.hp2 HG02055.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.2123+754C>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 8/9 | chr1 | 231210004 | ||||||
| chr1:231210007
|
ACACCCCT others(1): Show |
A | 3 | a0001c0001t0026g0061a0001c0001t0026g0062a0001c0023t0039g0005 | 3 | HG01884.hp2 HG02055.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.2123+762_2123+769d others(10): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 231210007 | |||||
| chr1:231210065
|
C | G | 1 | a0001c0001t0001g0212 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2123+815C>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 8/9 | chr1 | 231210065 | ||||||
| chr1:231210145
|
G | A | 1 | a0001c0002t0003g0051 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2123+895G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 8/9 | chr1 | 231210145 | ||||||
| chr1:231210200
|
C | T | 4 | a0001c0001t0024g0043a0001c0001t0024g0247a0001c0001t0045g0169others(1): Show | 4 | HG00280.hp1 HG00323.hp2 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.2123+950C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 8/9 | chr1 | 231210200 | ||||||
| chr1:231210202
|
G | T | 1 | a0001c0004t0005g0016 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2123+952G>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 8/9 | chr1 | 231210202 | ||||||
| chr1:231210368
|
G | C | 1 | a0001c0014t0016g0328 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2123+1118G>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 8/9 | chr1 | 231210368 | ||||||
| chr1:231210420
|
A | G | 176 | a0001c0001t0001g0216a0001c0001t0002g0042a0001c0001t0002g0045others(173): Show | 178 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(175): Show |
intron_variant | MODIFIER | c.2123+1170A>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 8/9 | chr1 | 231210420 | ||||||
| chr1:231210440
|
G | A | 96 | a0001c0001t0001g0216a0001c0001t0002g0042a0001c0001t0002g0045others(93): Show | 97 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.2123+1190G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 8/9 | chr1 | 231210440 | ||||||
| chr1:231210588
|
A | C | 4 | a0001c0001t0024g0043a0001c0001t0024g0247a0001c0001t0045g0169others(1): Show | 4 | HG00280.hp1 HG00323.hp2 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.2123+1338A>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 8/9 | chr1 | 231210588 | ||||||
| chr1:231210796
|
T | C | 10 | a0001c0001t0005g0225a0001c0001t0005g0229a0001c0001t0005g0230others(7): Show | 10 | HG01891.hp1 HG02257.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.2123+1546T>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 8/9 | chr1 | 231210796 | ||||||
| chr1:231210812
|
G | A | 1 | a0001c0001t0001g0216 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2123+1562G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 8/9 | chr1 | 231210812 | ||||||
| chr1:231210908
|
A | G | 2 | a0001c0001t0001g0249a0001c0001t0001g0290 | 2 | NA18944.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.2123+1658A>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 8/9 | chr1 | 231210908 | ||||||
| chr1:231210927
|
GTTTCAGC others(116): Show |
G | 28 | a0001c0001t0005g0215a0001c0001t0034g0063a0001c0002t0005g0031others(25): Show | 28 | HG00438.hp1 HG00609.hp1 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.2123+1681_2123+180 others(4): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 231210927 | |||||
| chr1:231210967
|
T | C | 96 | a0001c0001t0001g0216a0001c0001t0002g0042a0001c0001t0002g0045others(93): Show | 97 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.2123+1717T>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 8/9 | chr1 | 231210967 | ||||||
| chr1:231211027
|
A | T | 7 | a0001c0001t0005g0225a0001c0001t0005g0229a0001c0001t0005g0230others(4): Show | 7 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.2123+1777A>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 8/9 | chr1 | 231211027 | ||||||
| chr1:231211029
|
A | T | 7 | a0001c0001t0005g0225a0001c0001t0005g0229a0001c0001t0005g0230others(4): Show | 7 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.2123+1779A>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 8/9 | chr1 | 231211029 | ||||||
| chr1:231211031
|
A | AAAT | 11 | a0001c0001t0002g0045a0001c0001t0002g0055a0001c0001t0002g0130others(8): Show | 11 | HG00597.hp1 HG00639.hp2 HG01074.hp1 others(8): Show |
intron_variant | MODIFIER | c.2123+1782_2123+178 others(7): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 231211031 | |||||
| chr1:231211031
|
A | ATAT | 81 | a0001c0001t0002g0042a0001c0001t0002g0057a0001c0001t0002g0121others(78): Show | 82 | HG00544.hp1 HG00558.hp1 HG00621.hp2 others(79): Show |
intron_variant | MODIFIER | c.2123+1781_2123+178 others(7): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 8/9 | chr1 | 231211031 | ||||||
| chr1:231211031
|
A | T | 33 | a0001c0001t0001g0032a0001c0001t0001g0034a0001c0001t0001g0035others(30): Show | 33 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.2123+1781A>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 8/9 | chr1 | 231211031 | ||||||
| chr1:231211033
|
T | A | 32 | a0001c0001t0001g0039a0001c0001t0001g0041a0001c0001t0001g0135others(29): Show | 33 | HG00140.hp2 HG00673.hp2 HG01169.hp1 others(30): Show |
intron_variant | MODIFIER | c.2123+1783T>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 8/9 | chr1 | 231211033 | ||||||
| chr1:231211035
|
T | A | 3 | a0001c0001t0001g0205a0001c0001t0001g0255a0001c0003t0006g0114 | 3 | HG00673.hp2 HG02738.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.2123+1785T>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 8/9 | chr1 | 231211035 | ||||||
| chr1:231211040
|
A | G | 1 | a0001c0001t0002g0219 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2123+1790A>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 8/9 | chr1 | 231211040 | ||||||
| chr1:231211044
|
A | G | 1 | a0001c0001t0004g0151 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2123+1794A>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 8/9 | chr1 | 231211044 | ||||||
| chr1:231211048
|
A | T | 15 | a0001c0001t0001g0216a0001c0001t0002g0281a0001c0001t0002g0311others(12): Show | 15 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(12): Show |
intron_variant | MODIFIER | c.2123+1798A>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 8/9 | chr1 | 231211048 | ||||||
| chr1:231211050
|
A | T | 101 | a0001c0001t0001g0216a0001c0001t0002g0042a0001c0001t0002g0045others(98): Show | 102 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.2123+1800A>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 8/9 | chr1 | 231211050 | ||||||
| chr1:231211052
|
T | A | 1 | a0001c0004t0001g0010 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2123+1802T>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 8/9 | chr1 | 231211052 | ||||||
| chr1:231211124
|
G | C | 2 | a0001c0001t0005g0293a0001c0004t0005g0016 | 2 | HG01891.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.2123+1874G>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 8/9 | chr1 | 231211124 | ||||||
| chr1:231211413
|
G | C | 1 | a0001c0001t0004g0152 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2123+2163G>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 8/9 | chr1 | 231211413 | ||||||
| chr1:231211427
|
C | G | 1 | a0001c0001t0001g0049 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2123+2177C>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 8/9 | chr1 | 231211427 | ||||||
| chr1:231211443
|
C | A | 5 | a0001c0003t0012g0068a0001c0003t0012g0070a0001c0003t0012g0071others(2): Show | 5 | HG02074.hp1 HG02165.hp2 NA18961.hp2 others(2): Show |
intron_variant | MODIFIER | c.2123+2193C>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 8/9 | chr1 | 231211443 | ||||||
| chr1:231211730
|
G | A | 99 | a0001c0001t0001g0216a0001c0001t0002g0042a0001c0001t0002g0045others(96): Show | 100 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.2124-2085G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 8/9 | chr1 | 231211730 | ||||||
| chr1:231211752
|
A | T | 1 | a0001c0004t0010g0022 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2124-2063A>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 8/9 | chr1 | 231211752 | ||||||
| chr1:231211768
|
G | T | 38 | a0001c0001t0005g0215a0001c0001t0005g0225a0001c0001t0005g0229others(35): Show | 38 | HG00438.hp1 HG00609.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.2124-2047G>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 8/9 | chr1 | 231211768 | ||||||
| chr1:231212098
|
G | T | 15 | a0001c0001t0001g0041a0001c0001t0001g0135a0001c0001t0001g0226others(12): Show | 15 | HG01243.hp1 HG02300.hp2 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.2124-1717G>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 8/9 | chr1 | 231212098 | ||||||
| chr1:231212272
|
A | G | 3 | a0001c0001t0026g0061a0001c0001t0026g0062a0001c0023t0039g0005 | 3 | HG01884.hp2 HG02055.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.2124-1543A>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 8/9 | chr1 | 231212272 | ||||||
| chr1:231212639
|
G | A | 1 | a0001c0024t0004g0026 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2124-1176G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 8/9 | chr1 | 231212639 | ||||||
| chr1:231212797
|
C | G | 1 | a0001c0001t0001g0035 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2124-1018C>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 8/9 | chr1 | 231212797 | ||||||
| chr1:231212842
|
C | T | 3 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0232 | 3 | HG00280.hp2 HG01256.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.2124-973C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 8/9 | chr1 | 231212842 | ||||||
| chr1:231212998
|
T | C | 1 | a0001c0001t0001g0261 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.2124-817T>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 8/9 | chr1 | 231212998 | ||||||
| chr1:231213185
|
C | T | 1 | a0001c0003t0006g0075 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2124-630C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 8/9 | chr1 | 231213185 | ||||||
| chr1:231213248
|
C | T | 98 | a0001c0001t0002g0042a0001c0001t0002g0045a0001c0001t0002g0046others(95): Show | 99 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.2124-567C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 8/9 | chr1 | 231213248 | ||||||
| chr1:231213300
|
C | G | 1 | a0001c0004t0001g0011 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2124-515C>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 8/9 | chr1 | 231213300 | ||||||
| chr1:231213455
|
A | G | 173 | a0001c0001t0002g0042a0001c0001t0002g0045a0001c0001t0002g0046others(170): Show | 175 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(172): Show |
intron_variant | MODIFIER | c.2124-360A>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 8/9 | chr1 | 231213455 | ||||||
| chr1:231213589
|
G | T | 1 | a0001c0001t0001g0039 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2124-226G>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 8/9 | chr1 | 231213589 | ||||||
| chr1:231213617
|
G | A | 38 | a0001c0001t0005g0215a0001c0001t0005g0225a0001c0001t0005g0229others(35): Show | 38 | HG00438.hp1 HG00609.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.2124-198G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 8/9 | chr1 | 231213617 | ||||||
| chr1:231213628
|
G | A | 3 | a0001c0001t0001g0296a0001c0001t0001g0323a0001c0001t0001g0326 | 3 | HG01168.hp1 HG01169.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.2124-187G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 8/9 | chr1 | 231213628 | ||||||
| chr1:231213810
|
C | T | 1 | a0001c0001t0004g0166 | 1 | HG01993.hp2 | splice_region_variant&intron_variant | LOW | c.2124-5C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 8/9 | chr1 | 231213810 | ||||||
| chr1:231213998
|
G | A | 1 | a0001c0009t0035g0029 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2286+21G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 9/9 | chr1 | 231213998 | ||||||
| chr1:231214015
|
T | C | 3 | a0001c0001t0026g0061a0001c0001t0026g0062a0001c0023t0039g0005 | 3 | HG01884.hp2 HG02055.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.2286+38T>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 9/9 | chr1 | 231214015 | ||||||
| chr1:231214020
|
A | G | 1 | a0001c0001t0017g0338 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2286+43A>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 9/9 | chr1 | 231214020 | ||||||
| chr1:231214137
|
C | A | 6 | a0001c0004t0010g0007a0001c0004t0010g0013a0001c0004t0010g0014others(3): Show | 6 | HG02055.hp2 HG02486.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.2286+160C>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 9/9 | chr1 | 231214137 | ||||||
| chr1:231214168
|
C | A | 95 | a0001c0001t0002g0042a0001c0001t0002g0045a0001c0001t0002g0046others(92): Show | 96 | HG00140.hp2 HG00544.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.2286+191C>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 9/9 | chr1 | 231214168 | ||||||
| chr1:231214172
|
G | A | 1 | a0001c0003t0007g0105 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2286+195G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 9/9 | chr1 | 231214172 | ||||||
| chr1:231214310
|
C | T | 2 | a0001c0001t0001g0213a0001c0001t0001g0242 | 2 | HG01243.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.2286+333C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 9/9 | chr1 | 231214310 | ||||||
| chr1:231214376
|
A | AG | 6 | a0001c0004t0010g0007a0001c0004t0010g0013a0001c0004t0010g0014others(3): Show | 6 | HG02055.hp2 HG02486.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.2286+400dupG | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 231214376 | |||||
| chr1:231214376
|
A | G | 1 | a0001c0010t0021g0097 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.2286+399A>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 9/9 | chr1 | 231214376 | ||||||
| chr1:231214552
|
G | A | 4 | a0001c0001t0024g0043a0001c0001t0024g0247a0001c0001t0045g0169others(1): Show | 4 | HG00280.hp1 HG00323.hp2 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.2286+575G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 9/9 | chr1 | 231214552 | ||||||
| chr1:231214606
|
C | T | 3 | a0001c0001t0026g0061a0001c0001t0026g0062a0001c0023t0039g0005 | 3 | HG01884.hp2 HG02055.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.2286+629C>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 9/9 | chr1 | 231214606 | ||||||
| chr1:231214620
|
C | A | 1 | a0001c0001t0001g0318 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2286+643C>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 9/9 | chr1 | 231214620 | ||||||
| chr1:231214766
|
G | A | 1 | a0001c0001t0001g0272 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2287-609G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 9/9 | chr1 | 231214766 | ||||||
| chr1:231214778
|
C | CA | 35 | a0001c0001t0002g0046a0001c0001t0002g0219a0001c0001t0004g0167others(32): Show | 36 | HG00408.hp2 HG00423.hp1 HG01256.hp1 others(33): Show |
intron_variant | MODIFIER | c.2287-573dupA | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 231214778 | |||||
| chr1:231214778
|
C | CAA | 6 | a0001c0001t0014g0218a0001c0002t0003g0124a0001c0002t0014g0056others(3): Show | 6 | HG01361.hp1 HG02080.hp1 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.2287-574_2287-573d others(4): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 231214778 | |||||
| chr1:231214778
|
CA | C | 30 | a0001c0001t0001g0035a0001c0001t0001g0119a0001c0001t0001g0144others(27): Show | 30 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(27): Show |
intron_variant | MODIFIER | c.2287-573delA | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 231214778 | |||||
| chr1:231214778
|
CAAA | C | 6 | a0001c0004t0010g0007a0001c0004t0010g0013a0001c0004t0010g0014others(3): Show | 6 | HG02055.hp2 HG02486.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.2287-575_2287-573d others(5): Show |
TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 231214778 | |||||
| chr1:231214804
|
A | G | 3 | a0001c0001t0016g0210a0001c0001t0016g0211a0001c0014t0016g0328 | 3 | HG02280.hp2 HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2287-571A>G | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 9/9 | chr1 | 231214804 | ||||||
| chr1:231214952
|
T | C | 6 | a0001c0004t0010g0007a0001c0004t0010g0013a0001c0004t0010g0014others(3): Show | 6 | HG02055.hp2 HG02486.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.2287-423T>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 9/9 | chr1 | 231214952 | ||||||
| chr1:231215081
|
G | C | 2 | a0001c0001t0005g0225a0001c0022t0005g0154 | 2 | HG02615.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2287-294G>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 9/9 | chr1 | 231215081 | ||||||
| chr1:231215088
|
G | A | 1 | a0001c0001t0032g0349 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2287-287G>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 9/9 | chr1 | 231215088 | ||||||
| chr1:231215221
|
A | T | 1 | a0001c0002t0003g0051 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2287-154A>T | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 9/9 | chr1 | 231215221 | ||||||
| chr1:231215289
|
C | A | 5 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0235others(2): Show | 5 | HG02109.hp2 HG02451.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.2287-86C>A | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 9/9 | chr1 | 231215289 | ||||||
| chr1:231215301
|
T | C | 1 | a0001c0002t0005g0170 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2287-74T>C | TRIM67 | ENSG00000119283.16 | transcript | ENST00000366653.6 | protein_coding | 9/9 | chr1 | 231215301 |